Unit 10 DQ

Topic 1: Collaboration for Research and Evidence-based Practice

Consider the role of the nurse as an interdisciplinary team member in completing research and using research findings to inform health care practices.

Review the following:

  • Women’s Health Initiative retrieved from http://www.nhlbi.nih.gov/whi
  • Collaborative strategies to enhance research and evidence-based practice. (see Journal in Reading)

Answer the following questions:

  • Discuss the role of the advanced practice nurse as an interdisciplinary research collaborator and member of the interdisciplinary team obligated to co-participate in the implementation and use of evidence-based practice.
  • End your discussion by providing an example of an evidence-based change that would require the collaborative efforts of nursing and at least two other healthcare disciplines and that would lead to quality improvement in healthcare

Health Policy Due 3/4/2021 800 Words

Health policy 

MUST USE THE TEXTBOOK! Respond to the questions below. Be sure to cite and reference resource with at least 4 references including the book. 

Part 1:

200 words–Question A:  Chapter 5: Public Health is accomplished through the local, state, federal and global agencies, but discuss the involvement by at least 4 other entities or agencies. How are these other entities or agencies involved with Public Health issues, provide specific example?

200 words–Question B: Chapter 6: Discuss the A) types and B) limitations of individual legal rights of health care. C) How did these rights come to health care?

200 words–Question C: Chapter 7—a) What are health harming social conditions? Provide examples  b) Describe the ways in which the law can be both positive and negative in relation to health harming social conditions.

200 words–Part 2:  Address your ‘a-ha moment’ for this week: Something that was a realization for the week that really opened your eyes, changed your perceptions and/or something that you know that you will remember forever, this must be related to the above chapters and topics. Use at least one evidence-based article to support your thoughts.

Series Editor: Richard Riegelman

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and Law Sara E. Wilensky, JD, PhD Department of Health Policy and Management, Milken Institute School of Public Health, The George Washington University

Joel B. Teitelbaum, JD, LLM Department of Health Policy and Management, Milken Institute School of Public Health, The George Washington University

Essentials of

FOURTH EDITION

 

 

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Library of Congress Cataloging-in-Publication Data Names: Teitelbaum, Joel Bern, author. | Wilensky, Sara E., author. Title: Essentials of health policy and law / Sara E. Wilensky, Joel B. Teitelbaum. Description: Fourth edition. | Burlington, Massachusetts: Jones & Bartlett Learning, [2020] | Joel B. Teitelbaum’s name appears first in previous edition. | Includes bibliographical references and index. Identifiers: LCCN 2018058317 | ISBN 9781284151619 Subjects: | MESH: Health Policy—legislation & jurisprudence | Insurance, Health—legislation & jurisprudence | Social Determinants of Health | Health Care Reform | United States Classification: LCC RA395.A3 | NLM WA 33 AA1 | DDC 362.10973—dc23 LC record available at https://lccn.loc.gov/2018058317

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Prologue . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .vii About the Editor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ix Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xi Acknowledgments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .xv About the Authors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xvii Contributors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . xix

PART I Setting the Stage: An Overview of Health Policy and Law 1

Chapter 1 Understanding the Role of and Conceptualizing Health Policy and Law . . . . . . . . . . . . . . . . . . 3

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Role of Policy and Law in Health Care

and Public Health . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Conceptualizing Health Policy and Law . . . . . . . . . . . . . 5

The Three Broad Topical Domains of Health Policy and Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Social, Political, and Economic Historical Context . . . . 6 Key Stakeholders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

Chapter 2 Policy and the Policymaking Process . . . . . . . . . . . 11

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Defining Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

Identifying Public Problems . . . . . . . . . . . . . . . . . . . . . . . . 11 Structuring Policy Options . . . . . . . . . . . . . . . . . . . . . . . . . 12

Public Policymaking Structure and Process . . . . . . . . . 13 State-Level Policymaking . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 The Federal Legislative Branch . . . . . . . . . . . . . . . . . . . . . . 14 The Federal Executive Branch . . . . . . . . . . . . . . . . . . . . . . 21

The Health Bureaucracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 The Federal Government . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 State and Local Governments . . . . . . . . . . . . . . . . . . . . . . 28 Interest Groups . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

Chapter 3 Law and the Legal System . . . . . . . 33 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33 The Role of Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34 The Definition and Sources of Law . . . . . . . . . . . . . . . . . 35

Defining “Law” . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35 Sources of Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35

Key Features of the Legal System . . . . . . . . . . . . . . . . . . 39 Separation of Powers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39 Federalism: Allocation of Federal

and State Legal Authority . . . . . . . . . . . . . . . . . . . . . . . . 40 The Role of Courts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

Chapter 4 Overview of the United States Healthcare System . . . . . . . . . . . . . . . . . . . . . . . 49

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49 Healthcare Finance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

Health Insurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51 Direct Services Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

Healthcare Access . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54 The Uninsured . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54 The Underinsured . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60 Insurance Coverage Limitations . . . . . . . . . . . . . . . . . . . . 61 Safety Net Providers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63 Workforce Issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65

Healthcare Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68 Key Areas of Quality Improvement . . . . . . . . . . . . . . . . . 68 Assessment of Efforts to Improve Quality . . . . . . . . . . . 71

Contents

iii

 

 

Comparative Health Systems . . . . . . . . . . . . . . . . . . . . . . 71 A National Health Insurance System: Canada . . . . . . . 71 A National Health System: Great Britain . . . . . . . . . . . . . 73 A Socialized Insurance System: Germany . . . . . . . . . . . 74 The Importance of Health Insurance Design . . . . . . . . 75

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

Chapter 5 Public Health Institutions and Systems . . . . . . . . . . . . . . . . . . . 81

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81 What Are the Goals and Roles

of Governmental Public Health Agencies? . . . . . . . 81 What Are the 10 Essential Public Health Services? . . . 83 What Are the Roles of Local and State Public

Health Agencies? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85 What Are the Roles of Federal Public Health

Agencies? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87 What Are the Roles of Global Health

Organizations and Agencies? . . . . . . . . . . . . . . . . . . . . 90 How Can Public Health Agencies Work Together? . . . 91 What Other Government Agencies

Are Involved in Health Issues? . . . . . . . . . . . . . . . . . . . . 91 What Roles Do NGOs Play in Public Health? . . . . . . . . 92

Nongovernmental Organizations . . . . . . . . . . . . . . . . . . . 92

How Can Public Health Agencies Partner With Health Care to Improve the Response to Health Problems? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93

How Can Public Health Take the Lead in Mobilizing Community Partnerships to Identify and Solve Health Problems? . . . . . . . . . . 95

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96 Further Reading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 109 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 109 Other Sources Consulted . . . . . . . . . . . . . . . . . . . . . . . . . . 109 Source for Political Affiliation of Senate . . . . . . . . . . . . 109 Source for Political Affiliation of the

House of Representatives . . . . . . . . . . . . . . . . . . . . . . . 109

PART II Essential Issues in Health Policy and Law 111

Chapter 6 Individual Rights in Health Care and Public Health . . . . . . . . . . . . . 113

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113

Background . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114 Individual Rights and Health Care: A Global

Perspective . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 116 Individual Rights and the Healthcare System . . . . . 117

Rights Under Healthcare and Health Financing Laws . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118

Rights Related to Freedom of Choice and Freedom From Government Interference . . . . . . . 119

The Right to Be Free From Wrongful Discrimination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125

Individual Rights in a Public Health Context . . . . . . 128 Overview of Police Powers . . . . . . . . . . . . . . . . . . . . . . . . 128 The Jacobson v. Massachusetts Decision . . . . . . . . . . . . 129 The “Negative Constitution” . . . . . . . . . . . . . . . . . . . . . . . 130

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 132 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 133

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 134

Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health . . . . . . . . . . . . . 137

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 138 Social Determinants of Health . . . . . . . . . . . . . . . . . . . 139

Defining Social Determinants of Health . . . . . . . . . . . 139 Types of SDH . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 139 The Link Between Social Determinants and

Health Outcomes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141

Law as a Social Determinant of Health . . . . . . . . . . . 142 Right to Criminal Legal Representation

vs . Civil Legal Assistance . . . . . . . . . . . . . . . . . . . . . . . . 144

Combating Health-Harming Social Conditions Through Medical-Legal Partnership . . . . . . . . . . . . 146

The Evolution of an “Upstream” Innovation . . . . . . . . 147 The Benefits of MLPs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 148

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 149 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 150

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 151

Chapter 8 Understanding Health  Insurance . . . . . . . . . . . . . . . . . . . . 153

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 153 A Brief History of the Rise of Health

Insurance in the United States . . . . . . . . . . . . . . . . . 154 How Health Insurance Operates . . . . . . . . . . . . . . . . . 156

Basic Terminology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 156 Uncertainty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 157 Risk . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 158 Setting Premiums . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 160 Medical Underwriting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 161

iv Contents

 

 

Managed Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 162 Cost Containment and Utilization Tools . . . . . . . . . . . . 163 Utilization Control Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . 164 Common Managed Care Structures . . . . . . . . . . . . . . . 166 The Future of Managed Care . . . . . . . . . . . . . . . . . . . . . . 169

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 170

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 171

Chapter 9 Health Economics in a Health Policy Context . . . . . . . . . . 173

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 173 Health Economics Defined . . . . . . . . . . . . . . . . . . . . . . . 174

How Economists View Decision Making . . . . . . . . . . . 174 How Economists View Health Care . . . . . . . . . . . . . . . . 176

Economic Basics: Demand . . . . . . . . . . . . . . . . . . . . . . . 176 Demand Changers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 176 Elasticity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 178 Health Insurance and Demand . . . . . . . . . . . . . . . . . . . . 179

Economic Basics: Supply . . . . . . . . . . . . . . . . . . . . . . . . . 180 Costs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180 Supply Changers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180 Profit Maximization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 180 Health Insurance and Supply . . . . . . . . . . . . . . . . . . . . . . 181

Economic Basics: Markets . . . . . . . . . . . . . . . . . . . . . . . . 182 Health Insurance and Markets . . . . . . . . . . . . . . . . . . . . . 182 Market Structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 182 Market Failure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 183

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 187

Chapter 10 Health Reform in the United States . . . . . . . . . . . . . . . . 189

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 189 Difficulty Achieving Health Reform

in the United States . . . . . . . . . . . . . . . . . . . . . . . . . . . . 190 Culture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 191 U .S . Political System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 191 Interest Groups . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193 Path Dependency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 193

Unsuccessful Attempts to Pass  National Health Insurance Reform . . . . . . . . . . . . . 194

The Stars Align (Barely): How the ACA Became Law . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 197

Commitment and Leadership . . . . . . . . . . . . . . . . . . . . . 197 Lessons From Failed Health Reform Efforts . . . . . . . . . 199 Political Pragmatism . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 201

Overview of the ACA . . . . . . . . . . . . . . . . . . . . . . . . . . . . 201 Individual Mandate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 203 State Health Insurance Exchanges/

Marketplaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 206 Employer Mandate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 213 Changes to the Private Insurance Market . . . . . . . . . . 214 Financing Health Reform . . . . . . . . . . . . . . . . . . . . . . . . . . 215 Public Health, Workforce, Prevention,

and Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 216

The U .S . Supreme Court’s Decision in the Case of National Federation of Independent Business v. Sebelius . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 217

States and Health Reform . . . . . . . . . . . . . . . . . . . . . . . . 218 Key Issues Going Forward . . . . . . . . . . . . . . . . . . . . . . . . 219

Congressional Activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 220 Insurance Plan Premium Rates . . . . . . . . . . . . . . . . . . . . 222 ACA Litigation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 224

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 225

Chapter 11 Government Health Insurance Programs: Medicaid, CHIP, and Medicare . . . . . . . . . . . . . . . . 231

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 232 Medicaid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 233

Program Administration . . . . . . . . . . . . . . . . . . . . . . . . . . . 233 Eligibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 234 Benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 238 Amount, Duration, and Scope,

and Reasonableness Requirements . . . . . . . . . . . . . 241 Medicaid Spending . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 242 Medicaid Financing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 243 Medicaid Provider Reimbursement . . . . . . . . . . . . . . . . 244 Medicaid Waivers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 247 The Future of Medicaid . . . . . . . . . . . . . . . . . . . . . . . . . . . . 248

Children’s Health Insurance Program . . . . . . . . . . . . . . . . . . . . . . . . . . . . 248

CHIP Structure and Financing . . . . . . . . . . . . . . . . . . . . . 249 CHIP Eligibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 250 CHIP Benefits and Beneficiary Safeguards . . . . . . . . . . 251 CHIP and Private Insurance Coverage . . . . . . . . . . . . . . 252 CHIP Waivers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 252 The Future of CHIP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 252

Medicare . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 253 Medicare Eligibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 253 Medicare Benefits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 255 Medicare Spending . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 258 Medicare Financing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 258 Medicare Provider Reimbursement . . . . . . . . . . . . . . . . 262 The Future of Medicare . . . . . . . . . . . . . . . . . . . . . . . . . . . . 265

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Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 265 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 265

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 268

Chapter 12 Healthcare Quality Policy and Law . . . . . . . . . . . . . . . . . . . . 271

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 271 Quality Control Through Licensure

and Accreditation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 272 Medical Errors as a Public

Health Concern . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 273 Promoting Healthcare Quality Through the

Standard of Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 275 The Origins of the Standard of Care . . . . . . . . . . . . . . . . 275 The Evolution of the Standard of Care . . . . . . . . . . . . . 276

Tort Liability of Hospitals, Insurers, and MCOs . . . . 278 Hospital Liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 278 Insurer Liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 279 Managed Care Liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . 280

Federal Preemption of State Liability Laws Under ERISA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 281

Overview of ERISA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 281 ERISA Preemption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 282 The Intersection of ERISA Preemption

and Managed Care Professional Medical Liability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 283

Measuring and Incentivizing Healthcare Quality . . . 284 Quality Measure Development . . . . . . . . . . . . . . . . . . . . 286 Quality Measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 286 Public Reporting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 286 Value-Based Purchasing . . . . . . . . . . . . . . . . . . . . . . . . . . . 287 National Quality Strategy . . . . . . . . . . . . . . . . . . . . . . . . . . 288 Private Payer Efforts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 289 Role of Health Information Technology . . . . . . . . . . . . 289

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 290 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 290

Endnotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 291

Chapter 13 Public Health Preparedness Policy . . . . . . . . . . . . . . . . . . . . . . 293

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 293 Defining Public Health Preparedness . . . . . . . . . . . . . 294

Threats to Public Health . . . . . . . . . . . . . . . . . . . . . . . . . 295 CBRN Threats . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 295 Naturally Occurring Disease Threats . . . . . . . . . . . . . . . 299 Natural Disasters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 300 Man-Made Environmental Disasters . . . . . . . . . . . . . . . 303

Public Health Preparedness Policy . . . . . . . . . . . . . . . 303 Federal Response Agencies and Offices . . . . . . . . . . . 303 Preparedness Statutes, Regulations,

and Policy Guidance . . . . . . . . . . . . . . . . . . . . . . . . . . . . 305 Presidential Directives . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 307 International Agreements . . . . . . . . . . . . . . . . . . . . . . . . . 308

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 310 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 311

PART III Basic Skills in Health Policy Analysis 315

CHAPTER 14 The Art of Structuring and Writing a Health Policy Analysis . . . . . . . . . . . . . . . . . . . . 317

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 317 Policy Analysis Overview . . . . . . . . . . . . . . . . . . . . . . . . . 317

Client-Oriented Advice . . . . . . . . . . . . . . . . . . . . . . . . . . . . 317 Informed Advice . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 318 Public Policy Decision . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 318 Providing Options and a

Recommendation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 318 Your Client’s Power and Values . . . . . . . . . . . . . . . . . . . . 318 Multiple Purposes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 319

Structuring a Policy Analysis . . . . . . . . . . . . . . . . . . . . . 319 Problem Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . 320 The Background Section . . . . . . . . . . . . . . . . . . . . . . . . . . 322 The Landscape Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . 323 The Options Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 326 The Recommendation Section . . . . . . . . . . . . . . . . . . . . 330

Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 330 References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 330

Glossary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 331 Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 337

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Prologue The fourth edition of Essentials of Health Policy and Law is a textbook that describes and analyzes the trans- formations taking place across the healthcare delivery and public health systems in the United States. Build- ing on the core content and engaging style of earlier editions, this edition is by necessity influenced by the shifts (both proposed and actual) occurring as a result of the 2016 election cycle, including of course the ways in which the Patient Protection and Affordable Care Act (commonly known as the ACA) is being inter- preted and implemented.

Professors Sara Wilensky and Joel Teitelbaum are both experienced in analyzing and communicating about the ACA and many other aspects of health pol- icy and law, and this edition benefits from their exper- tise. Beyond the issue of national and state health reform, Essentials of Health Policy and Law, Fourth Edition takes a broad approach to the study of health policy and law and provides a coherent framework for grappling with important healthcare, public health, and bioethical issues in the United States.

Health policies and laws are an inescapable and critical component of our everyday lives. The acces- sibility, cost, and quality of health care; the country’s preparedness for natural and human-caused disasters; the safety of the food, water, and medications we con- sume; the right to make individual decisions about one’s own health and well-being; and scores of other important issues are at the heart of health policy and law, and in turn at the heart of individual and commu- nity health and well-being. Health policies and laws have a strong and lasting effect on the quality of our lives as individuals and on our safety and health as a nation.

Professors Wilensky and Teitelbaum do a mar- velous job of succinctly describing not only the nation’s policy- and law-making machinery and the always-evolving healthcare and public health sys- tems, but also the ways in which policy and law affect health care and public health, and vice versa. They have a unique ability to make complex issues accessi- ble to various readers, including those without a back- ground in health care or public health. Their training as policy analysts and lawyers shines through as they

systematically describe and analyze the complex field of health policy and law and provide vivid examples to help make sense of it all.

Equally apparent is their wealth of experience teaching health policy and law at both the undergrad- uate and graduate levels. Between them, they have designed and taught many different health policy and/ or law courses, supplemented the content of health policy and law by integrating writing and analytic skills into their courses, designed and directed a bach- elor of science degree program in public health, and received teaching awards for their efforts. Readers of this textbook are the beneficiaries of their experience, enthusiasm, and commitment, as you will see in the pages that follow.

Essentials of Health Policy and Law, Fourth Edition stands on its own as a text. Even so, the accompanying Essential Readings in Health Policy and Law provides abundant illustrations of the development, influence, and consequences of health policies and laws. The carefully selected articles, legal opinions, and public policy documents in the supplemental reader allow students to delve deeper into the topics and issues explored in this book.

I am pleased that Essentials of Health Policy and Law is a part of the Essential Public Health series. From the earliest stages of the series’ development, Professors Wilensky and Teitelbaum have played a central role. They have closely coordinated efforts with other series authors to ensure that the series provides a comprehensive approach with only intended overlap. This is well illustrated by the numerous additions and revisions that have taken place with the publication of this Fourth Edition, a description of which can be found in the Preface.

I am confident that you will enjoy reading and greatly benefit from Essentials of Health Policy and Law. Whether you are studying public health, public policy, healthcare administration, or a field within the clinical health professions, this textbook is a key com- ponent of your education.

—Richard Riegelman, MD, MPH, PhD Editor, Essential Public Health Series

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About the Editor Richard K. Riegelman, MD, MPH, PhD, is professor of epidemiology-biostatistics, medicine, and health policy, and founding dean of the George Washington University Milken Institute School of Public Health in Washington, DC. He has taken a lead role in developing the Educated Citizen and Public Health initiative, which has brought together arts and sci- ences and public health education associations to

implement the Health and Medicine Division of the National Academies’ recommendation that “all undergraduates should have access to education in public health.” Dr. Riegelman also led the develop- ment of the George Washington University’s under- graduate major and minor and currently teaches Public Health 101 and Epidemiology 101 to under- graduate students.

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Preface

In the context of health care and public health, the dozen years since the first edition of this textbook was published can be summed up in a well-worn phrase: change is the only constant. The first edition of Essentials of Health Policy and Law did not even include mention of the Patient Protection and Afford- able Care Act—commonly known as the Affordable Care Act or ACA—because it was still 3 years from passage. Now hailed as the most important set of changes to health insurance since the 1965 enactment of Medicare and Medicaid, the ACA was signed into law by President Barack Obama in March of 2010. Since that time, the ACA itself has been on quite a journey, given the policy shifts and legal challenges it has undergone in a relatively short time. Broadly speaking, the ACA represents two landmark achieve- ments in health policy: major reform of the private health insurance market and, relatedly, a redistribu- tion of resources to groups and individuals who, by virtue of indigence and/or illness, have historically been excluded from the health insurance market and/ or healthcare system. Additionally, the law includes dozens of other important reforms and programs unrelated to insurance. For example, more efficient and higher-quality health care, population health, healthcare access, long-term care, the health work- force, health disparities, community health centers, healthcare fraud and abuse, comparative effectiveness research, health information technology, and more all receive attention by the ACA. Indeed, it is fair to say that a fully implemented ACA would move the nation toward a more affordable, equitable, and stable insur- ance system, not only for the millions of individuals who have and are expected to gain insurance, but also for the tens of millions of people who no longer face the threat of a loss or lapse of coverage.

▸ Implementation of the ACA Yet, full implementation of the ACA is still just a goal, as many federal and state policymakers and a substantial bloc of the voting public continue their efforts to undermine—if not totally destroy—the law. To understand these efforts, readers must understand

that many ACA reforms required a reordering of the relationships that lie at the heart of the nation’s healthcare and public systems. Individuals, providers, insurers, employers, governments, and others were forced to alter once-normative behaviors in response to the policy and legal decisions underpinning the law. These types of major policy and legal shifts— such as, in the case of the ACA, the creation of the “individual insurance mandate,” new prohibitions that prevent private insurers from using discrimina- tory enrollment practices, the creation of new health insurance “exchanges,” and the expansion of Medicaid eligibility standards—are basically destined to create backlash, given the very nature of how people respond to change and the vast amounts of money that, for some industries, are at stake. Add to this the fact that (as described more fully in Chapter 10) the ACA bill that eventually became law passed in Congress by the slimmest of margins after months of rancorous debate, and fully half the states in the United States actively opposed the ACA’s implementation after its passage. Even now, at the time of this writing, more than 8 years since the ACA became law, courts across the country have ACA-related cases on their dockets, the Trump administration has made a habit of slowing or reversing dozens of Obama-era ACA policy deci- sions, and the ACA continues to be used as a cudgel on the campaign trail. Needless to say, the outcomes of these lawsuits and policy debates will no doubt be discussed in both the national media and in the health policy and law courses in which you register, and they will be devoted space in the pages of this book in future editions.

▸ Other Changes in the Health Care and Public Health Landscape

Of course, the ACA is not the only significant shift in the healthcare/public health landscape since the first edition of this book. Just as that edition did not mention the ACA (for obvious reasons), neither did

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it include the term “social determinants of health,” which is a growing focus of healthcare and public health systems nationwide and now has an entire chapter in this book to show for it. Furthermore, the 2007 edition included just a single reference to pub- lic health emergency preparedness, a topic that also is now rewarded with its own chapter. Back in 2005, when the first outline of the first draft of this book took shape, health informatics and health information technology were, relatively speaking, fringe topics in courses on medical care and public health. Not so today. And finally, of course, the country experienced a mainly unanticipated election at the very top of the ticket in 2016, a result that injected many new poli- cies and legal interpretations into an already complex, costly, and oftentimes inequitable web of healthcare services and public health protections.

▸ Shifts in Public Health Education

Important shifts in public health education have taken place since 2007, as well. One particular change that is relevant to this textbook (and the entire Essentials of Public Health series) is the effort undertaken by the Association of American Colleges and Univer- sities (AAC&U) and the Association of Schools and Programs of Public Health (ASPPH) to develop the Educated Citizen and Public Health Initiative. This initiative seeks to integrate public health perspectives into a comprehensive liberal education framework and to develop and organize publications, presentations, and resources to help faculty develop public health curricula in the nation’s colleges and universities. As a result, public health perspectives generally, and health policy and law specifically, are increasingly being inte- grated into courses as diverse as political science, his- tory, sociology, public policy, and a range of courses that prepare students for the health professions. We are proud that this textbook has played a role in shaping (and supplying) the market for health policy and law education as part of a liberal education framework, and we aim with this Fourth Edition to make the mate- rial as accessible to these diverse audiences as possible.

▸ Addressing Health Policy Challenges

On the topic of health system complexity, we offer four factors for your consideration as you delve into the

chapters that follow. First, like most challenging public policy problems, pressing health policy questions simul- taneously implicate politics, law, ethics, and social mores, all of which come with their own set of competing inter- ests and advocates. Second, health policy debates often involve deeply personal matters pertaining to one’s qual- ity—or very definition—of life, philosophical questions about whether health care should be a market commod- ity or a social good, or profound questions about how to appropriately balance population welfare with closely guarded individual freedoms and liberties. Third, it is often not abundantly clear how to begin tackling a par- ticular health policy problem. For example, is it one best handled by the medical care system, the public health system, or both? Which level of government—federal or state—has the authority or ability to take action? Should the problem be handled legislatively or through regu- latory channels? The final ingredient that makes health policy problems such a complex stew is the rapid devel- opments often experienced in the areas of healthcare research, medical technology, and public health threats. Generally speaking, this kind of rapid evolution is a con- founding problem for the usually slow-moving Ameri- can policy- and law-making machinery.

Furthermore, the range of topics fairly included under the banner of “health policy and law” is breath- taking. For example, what effect is healthcare spend- ing having on national and state economies? How should finite financial resources be allocated between health care and public health? How can we ensure that the trust funds established to account for Medi- care’s income and disbursements remain solvent in the future as an enormous group of baby boomers becomes eligible for program benefits? What kind of return (in terms of quality of individual care and the overall health of the population) should we expect from the staggering amount of money we collectively spend on health? Should individuals have a legal enti- tlement to health insurance? How should we attack extant health disparities based on race, ethnicity, and socioeconomic status? What policies will best pro- tect the privacy of personal health information in an increasingly electronic medical system? Can advanced information technology systems improve the quality of individual and population health? Should the right to have an abortion continue to be protected under the federal Constitution? Should physician assistance in dying be promoted as a laudable social value? Will mapping the human genome lead to discrimination based on underlying health status? How prepared is the country for natural and man-made catastrophes, like pandemic influenza or bioterrorism attacks? What effect will chronic diseases, such as diabetes and

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obesity-related conditions, have on healthcare deliv- ery and financing? How should we harness advancing scientific findings for the benefit of the public’s health?

As seen from even this partial list of questions, the breadth of issues encountered in the study of health policy and law is virtually limitless, and we do not grapple with all of the preceding questions in this book. We do, however, introduce you to many of the policies and laws that give rise to them, provide an intellectual framework for thinking about how to address them going forward, and direct you to additional relevant readings. Given the prominent role played by policy and law in the health of all Americans, and the fact that the Health and Medicine Division of the National Academies recommends that students of public health and other interdisciplinary subjects (for example, public policy or medicine) receive health policy and law training, the aim of this book is to help you under- stand the broad context of American health policy and law, the essential issues impacting and flowing out of the healthcare and public health systems, and how health policies and laws are influenced and for- mulated. Broadly speaking, the goal of health policy is to promote and protect the health of individuals and of populations bound by common circumstances. Because the legal system provides the formal struc- ture through which public policy—including health policy—is debated, effected, and interpreted, law is an indispensable component of the study of health pol- icy. Indeed, law is inherent to the expression of public policy: major changes to policies often demand the creation, amendment, or rescission of laws. As such, students studying policy must learn about policymak- ing and the law, legal process, and legal concepts.

▸ About the Fourth Edition As a result of the changes just described and also in response to comments we received from users of pre- vious editions of the textbook, this edition of Essen- tials of Health Policy and Law has undergone updates to many chapters, including revised and expanded content; updated figures, tables, timelines, and discus- sion questions; and updated references and readings.

Part I Part I of this textbook includes five preparatory chap- ters. Chapter 1 describes the influential role of policy and law in health care and public health and intro- duces various conceptual frameworks through which the study of health policy and law can take place. The

chapter also illustrates why it is important to include policy and law in the study of health care and public health. However, an advanced exploration of health policy and law in individual and population health necessitates both a basic and practical comprehension of policy and law in general—including the policymak- ing process and the workings of the legal system—and an understanding of the nation’s rather fragmented healthcare and public health systems. Thus, Chapter 2 discusses both the meaning of policy and the policy- making process, including the basic functions, struc- tures, and powers of the legislative and executive branches of government and the respective roles of the federal and state governments in policymaking. Chapter 3 then describes the meaning and sources of law and several key features of the American legal sys- tem, including the separation of powers doctrine, fed- eralism, the role of courts, and due process. Chapter 4 provides an overview of the healthcare system, includ- ing basic information on healthcare finance, access, and quality, and examples of how the U.S. system dif- fers from those in other developed nations. Part I closes with an overview, in Chapter  5, of the public health system, including its evolution and core functions.

Part II Part II offers several chapters focusing on key sub- stantive health policy and law issues. Chapter 6 exam- ines the ways in which the law creates, protects, and restricts individual rights in the contexts of health care and public health, including a discussion of laws (such as Medicaid and Medicare) that aim to level the play- ing field where access to health care is concerned. The chapter also introduces the “no- duty-to-treat” princi- ple, which holds that there is no general legal duty on the part of healthcare providers to render care and that rests at the heart of the legal framework pertaining to healthcare rights and duties. Chapter 7 describes how social factors play a critical role in the attainment (or not) of individual and population health, discusses the ways in which law can both exacerbate and ameliorate negative social determinants of health, and introduces readers to the concept of medical-legal partnership. Chapters 8 and 9 cover the fundamentals of health insurance and health economics, respectively, and set up a subsequent thematic discussion in Chapters 10 and 11. Specifically, Chapter 8 describes the function of risk and uncertainty in health insurance, defines the basic elements of health insurance, discusses import- ant health policy issues relating to health insurance, and more; Chapter 9 explains why it is important for health policymakers to be familiar with basic economic

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concepts; the basic tenets of supply, demand, and mar- kets; and the way in which health insurance affects economic conditions.

The focus of Chapter 10 is on health reform, including the ACA. The chapter discusses the reasons why for decades the United States failed to achieve national health reform prior to the ACA, how and why the ACA passed given this history, and what the ACA aims to achieve. Chapter 11 explains how federal and state policymakers have created health insurance programs for individuals and populations who oth- erwise might go without health insurance coverage. The basic structure, administration, financing, and eligibility rules of the three main U.S. public health insurance programs—Medicaid, the Children’s Health Insurance Program, and Medicare—are discussed, as are key health policy questions relating to each pro- gram. Chapter 12 reflects on several important pol- icy and legal aspects of healthcare quality, including the advent of provider licensure and accreditation of health facilities (both of which represent quality con- trol through regulation), the evolution of the stan- dard of care, tort liability for healthcare providers and insurers, preventable medical errors, and, with the ACA as the focal point, efforts to improve healthcare quality through quality improvement and provider incentive programs. Part II concludes with a chapter on public health preparedness policy, including dis- cussions about how to define preparedness, the types of public health threats faced by the United States, policy responses to these threats, and an assessment of where the country stands in terms of preparedness.

Part III The textbook concludes in Part III by teaching the basic skills of health policy analysis. The substance

of health policy can be understood only as the prod- uct of an infinite number of policy choices regarding whether and how to intervene in many types of health policy problems. As such, Chapter 14 explains how to structure and write a short health policy analy- sis, which is a tool frequently used by policy analysts when they assess policy options and discuss rationales for their health policy recommendations.

▸ New to this Edition This Fourth Edition addresses the many changes related to health reform; the health care system; the ACA’s effect on Medicaid, Medicare, and CHIP; as well as health care quality and private payer reform efforts.

The chapter on Public Health Preparedness Policy has been significantly revised, reflecting an increased focus on natural disasters, controlling infectious dis- eases, and military emergencies.

The chapter on writing a policy analysis has been updated with new detailed examples.

For instructors, we offer thoroughly updated PowerPoint lecture slides for classroom use, as well as an updated Test Bank for each chapter.

The resources in the accompanying Navigate  2 Advantage platform have also been thoroughly updated. These are available for either independent student study or for use in an instructor-led, online course. These materials include an interactive eBook with personalization tools such as highlighting, book- marking, notes, and end-of-chapter quizzes to assess learning. Also included are Slides in PowerPoint for- mat, an interactive glossary, practice quizzes, and more. These materials are available by redeeming the code found on the card inside this book.

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Acknowledgments We are grateful to the many people who generously contributed their guidance, assistance, and encour- agement to us during the writing of this book. At the top of the list is Dr. Richard Riegelman, founding dean of the Milken Institute School of Public Health at the George Washington University (GW) and Professor of Epidemiology and Biostatistics, Medicine, and Health Policy. The Essential Public Health series was his brainchild, and his stewardship of the project as Series Editor made our involvement in it both enriching and enjoyable. We are indebted to him for his guidance and confidence.

We single out one other colleague for special thanks. Sara Rosenbaum, the Harold and Jane Hirsh Professor of Health Law and Policy and a past chair of GW’s Department of Health Policy and Management, has been a wonderful mentor, colleague, and friend for decades. We are indebted to her for supporting our initial decision to undertake the writing of this textbook.

During the writing of the various editions of this book, we have been blessed by the help of several

stellar research assistants. The First Edition could not have been completed without V. Nelligan Coogan, Mara B. McDermott, Sarah E. Mutinsky, Dana E. Thomas, and Ramona Whittington; Brittany Plavchak and Julia Roumm were essential to the completion of the Second Edition; Jacob Alexander’s assistance was key to the Third Edition; and Joanna Theiss was instru- mental in updating the current edition. To all of them we send our deep appreciation for their research assis- tance and steady supply of good cheer.

Our gratitude extends also to Mike Brown, pub- lisher for Jones & Bartlett Learning, for his guidance and encouragement, and to his staff, for their patience and technical expertise.

Finally, we wish to thank those closest to us. Sara gives special thanks to Trish Manha—her wife, cheerleader, reviewer, and constant supporter—and to Sophia, and William, who make life fun, surprising, and ever-changing. Joel sends special thanks to his family: Laura Hoffman, Jared Teitelbaum, and Layna Teitelbaum, his favorite people and unending sources of joy and laughter.

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About the Authors Sara Wilensky, JD, PhD, is special services faculty for undergraduate education in the Department of Health Policy and Management at the Milken Institute School of Public Health at the George Washington University (GW) in Washington, DC. She is also the director of the Undergraduate Program in Public Health.

Dr. Wilensky has taught a health policy analysis course and health systems overview course required of all students in the Master of Public Health–Health Policy degree program, as well as the health policy course required of all undergraduate students major- ing in public health. She has been the principal inves- tigator or co-principal investigator on numerous health policy research projects relating to a variety of topics, such as Medicaid coverage, access and financ- ing, community health centers, childhood obesity, HIV preventive services, financing of public hospitals, and data sharing barriers and opportunities between public health and Medicaid agencies.

As director of the Undergraduate Program in Public Health, Dr. Wilensky is responsible for the day- to-day management of the program, including imple- mentation of the dual BS/MPH program. In addition, she is responsible for faculty oversight, course schedul- ing, new course development, and student satisfaction.

Dr. Wilensky is involved with several GW service activities: she has taught a service learning in pub- lic health course in the undergraduate program; she has been heavily involved in making GW’s Writing in the Disciplines program part of the undergradu- ate major in public health; and she is the advisor to students receiving a master in public policy or a mas- ter in public administration with a focus on health policy from GW’s School of Public Policy and Public Administration.

Prior to joining GW, Dr. Wilensky was a law clerk for federal Judge Harvey Bartle III in the Eastern Dis- trict of Pennsylvania and worked as an associate at the law firm of Cutler and Stanfield, LLP, in Denver, Colorado.

Joel Teitelbaum, JD, LLM, is associate professor, director of the Hirsh Health Law and Policy Program,

and co-director of the National Center for Medical-Legal Partnership at the George Washington University Milken Institute School of Public Health in Washington, DC. He also carries a faculty appoint- ment in the GW School of Law, and for 11  years served as vice chair for academic affairs in the School of Public Health’s Department of Health Policy and Management, a role in which he provided oversight of the Department’s graduate degree programs, cur- riculum development, and faculty and student sup- port services. As director of the Hirsh Health Law and Policy Program, he oversees a program designed to foster an interdisciplinary approach to the study of health law, health policy, health care, and public health through educational and research opportuni- ties for law students, health professions students, and practicing lawyers. In his role at the National Center for Medical-Legal Partnership, he helps direct national efforts to embed civil legal services into healthcare delivery as a way of ameliorating social determinants that negatively affect individual and population health.

Professor Teitelbaum has taught law, graduate, or undergraduate courses on healthcare law, healthcare civil rights, public health law, minority health policy, and long-term care law and policy. In 2009 he became the first member of the School of Public Health fac- ulty to receive the University-wide Bender Teaching Award. He is also a member of the GW Academy of Distinguished Teachers and a Fellow in the Universi- ty’s Cross-Disciplinary Cooperative; he has received the School’s Excellence in Teaching Award and was an inaugural member of the School’s Academy of Master Teachers; he was inducted in 2007 into the ASPPH/ Pfizer Public Health Academy of Distinguished Teachers; and he has been named one of the “Stars” of undergraduate teaching at GW by an undergrad- uate leadership group. He is regularly invited to lec- ture at top universities and at national conferences and meetings.

In addition to Essentials of Health Policy and Law, Professor Teitelbaum is co-author of Essentials of Health Justice (2019), also published by Jones & Bartlett Learning. He has authored or co-authored

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dozens of peer-reviewed articles and reports in addi- tion to many book chapters, policy briefs, and blogs on civil rights issues in health care, health reform and its implementation, medical-legal partnership, insurance law and policy, and behavioral healthcare quality, and he has directed many health law and pol- icy research projects. In 2000, he was co-recipient of The Robert Wood Johnson Foundation Investigator Award in Health Policy Research, which he used to explore the creation of a new framework for applying Title VI of the 1964 Civil Rights Act to the modern healthcare system.

In 2016, during President Obama’s second term, Professor Teitelbaum was named to the U.S. Depart- ment of Health and Human Services Secretary’s

Advisory Committee on National Health Promotion and Disease Prevention Objectives for 2030 (i.e., Healthy People 2030, the national agenda aimed at improving the health of all Americans over a 10-year span). He also serves as Special Advisor to the Ameri- can Bar Association’s Commission on Veterans’ Legal Services and as a member of the Board of Advisors of PREPARE, a national advanced care planning organization.

Professor Teitelbaum is a member of Delta Omega, the national honor society recognizing excellence in the field of public health; the American Constitution Society for Law and Policy; the American Society of Law, Medicine, and Ethics; and the Society for Amer- ican Law Teachers.

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Contributors ▸ Chapter 5: Public Health

Institutions and Systems Richard Riegelman, MD, PhD, MPH The George Washington University Washington, DC

▸ Chapter 13: Public Health Preparedness Policy

Rebecca Katz, PhD, and Claire Standley, PhD Georgetown University Washington, DC

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1

PART I

Setting the Stage: An Overview of Health Policy and Law Part I of this textbook includes five contextual chapters aimed at preparing you for the substantive health policy and law discussions in Chapters 6–13 and for the skills-based discussion of policy analysis in Chapter 14. Chapter 1 describes generally the role of policy and law in health care and public health and introduces conceptual frameworks for studying health policy and law. Chapter 2 describes the meaning of policy and also the pol- icymaking process itself. Chapter 3 provides an overview of the meaning and sources of law and of several important features of the legal system. Part I closes with overviews of the U.S. healthcare system (Chapter 4) and public health system (Chapter 5).

 

 

 

CHAPTER 1

Understanding the Role of and Conceptualizing Health Policy and Law

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe generally the important role played by policy and law in the health of individuals and populations ■ Describe three ways to conceptualize health policy and law

▸ Introduction

In this chapter, we introduce the role played by pol-icy and law in the health of individuals and popula-tions and describe various conceptual frameworks with which you can approach the study of health pol- icy and law. In the chapters that follow, we build on this introduction to provide clarity in areas of health policy and law that are neither readily discernable— even to those who use and work in the healthcare and public health systems—nor easily reshaped by those who make, apply, and interpret policy and law.

The goals of this chapter are to describe why it is important to include policy and law in the study of health care and public health and how you might con- ceptualize health policy and law when undertaking your studies. To achieve these goals, we first briefly discuss the vast influence of policy and law in health

care and public health. You will have a much better feel for how far policy and law reach into these areas as you proceed through this text, but we dedicate a few pages here to get you started. We then describe three ways to conceptualize health policy and law which, as you will discover, are interwoven, with no one frame- work dominating the discussion.

▸ Role of Policy and Law in Health Care and Public Health

The forceful influence of policy and law on the health and well-being of individuals and populations is unde- niable. Policy and law have always been fundamental in shaping the behaviors of individuals and industries, the practice of health care, and the environments in which people live and work. They have also been

3

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vital in achieving both everyday and landmark public health improvements.

For example, centuries-old legal principles have, since this country’s inception, provided the bedrock on which healthcare quality laws are built, and today the healthcare industry is regulated in many differ- ent ways. Indeed, federal and state policy and law shape virtually all aspects of the healthcare system, from structure and organization, to service delivery, to financing, to administrative and judicial oversight. Whether pertaining to the accreditation and certifica- tion of individual or institutional healthcare providers, requirements to provide care under certain circum- stances, the creation of public insurance programs, the regulation of private insurance systems, or any other number of issues, policy and law drive the healthcare system to a degree unknown by most people.

In fact, professional digests that survey and report on the subjects of health policy and law typically include in their pages information on topics like the advertis- ing and marketing of health services and products, the impact of health expenditures on federal and state budgets, antitrust concerns, healthcare contracting, employment issues, patents, taxation, healthcare dis- crimination and disparities, consumer protection, bioterrorism, health insurance, prescription drug regulation, physician-assisted suicide, biotechnology, human subject research, patient privacy and confi- dentiality, organ availability and donation, and more. Choices made by policymakers and decisions handed down through the judicial system influence how we approach, experience, analyze, and research all of these and other specific aspects of the healthcare system. Once you have read the next four preparatory chap- ters—one on policy and the policymaking process, one on law and the legal system, and one each covering the structure and organization of the healthcare and pub- lic health systems—and begin to digest the substantive chapters that follow them, the full force of policy and law in shaping the individual healthcare system will unfold. For now, simply keep in the back of your mind the fact that policy and law heavily influence the way in which overall health and well-being are achieved (or not), health care is accessed, medicine is practiced, treatments are paid for, and much more.

The role of policy and law in public health is no less important than in individual health care, but their influence in the field of public health is frequently less visible and articulated. In fact, policy and law have long played a seminal role in everyday public health activi- ties. Think, for example, of food establishment inspec- tions, occupational safety standards, policies related to health services for persons with chronic health

conditions such as diabetes, and policies and laws affecting the extent to which public health agencies are able to gauge whether individuals in a community suffer from certain health conditions. Similarly, policy and law have been key in many historic public health accomplishments such as water and air purification, reduction in the spread of communicable diseases through compulsory immunization laws, reduction in the number of automobile-related deaths through seat belt and consumer safety laws, and several other achievements.a Public health professionals and stu- dents quickly learn to appreciate that combating pub- lic health threats requires both vigorous policymaking and adequate legal powers.

Additionally, in recent years, enhanced fears about bioterrorism and newly emerging infectious diseases have increased the public’s belief that policy and law are important tools in creating an environment in which people can achieve optimal health and safety.

Of course, policies and laws do not always cut in favor of what many people believe to be in the best interests of public health and welfare. A policy or law might, for example, favor the economic interests of a private, for-profit company over the personal interests of residents of the community in which the company is located.b Such situations occur because one main focus of public health policy and law is on locating the appropriate balance between public regulation of private individuals and corporations and the ability of those same parties to exercise rights that allow them to function free of overly intrusive government interven- tion. Achieving this balance is not easy for policymak- ers, as stakeholders disagree on things like the extent to which car makers should alter their operations to reduce environmentally harmful vehicle emissions, or the degree to which companies should be limited in advertising cigarettes, or whether gun manufacturers should be held liable in cases where injuries or killings result from the negligent use of their products.

How do policymakers and the legal system reach a (hopefully) satisfactory balance of public health and private rights? The competing interests at the heart of public health are mainly addressed through two types of policies and laws: those that define the functions and powers of public health agencies and those that aim to directly protect and promote health.c State- level poli- cymakers and public health officials create these types of policies and laws through what are known as their police powers. These powers represent the inherent authority of state and local governments to regulate individuals and private business in the name of public health promotion and protection. The importance of police powers cannot be overstated; it is fair to say that

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they are the most critical aspect of the sovereignty that states retained at the founding of the country, when the colonies agreed to a governmental structure con- sisting of a strong national government. Furthermore, the reach of police powers should not be underesti- mated: they give government officials the authority— in the name of public health and welfare—to coerce private parties to act (or refrain from acting) in certain ways. However, states do not necessarily need to exer- cise their police powers in order to affect or engage in public health–related policymaking. Because the public’s health is impacted by many social, economic, and environmental factors, public health agencies also conduct policy-relevant research, disseminate infor- mation aimed at helping people engage in healthy behaviors, and establish collaborative relationships with healthcare providers and purchasers and with other government policymaking agencies.

Federal policy and law also play a role in public health. Although the word health does not appear in the U.S. Constitution, the document confers powers on the federal government—to tax and spend, for example— that allow it to engage in public health promotion and disease prevention activities. For example, the power to tax (or establish exemptions from taxation) allows Congress to incentivize healthy behaviors, as witnessed by the heavy taxes levied on packages of cigarettes; the power to spend enables Congress to establish executive branch public health agencies and to allocate public- health–specific funds to states and localities.

▸ Conceptualizing Health Policy and Law

You have just read about the importance of taking pol- icy and law into account when studying health care and public health. The next step is to begin thinking about how you might conceptually approach the study of health policy and law.

There are multiple ways to conceptualize the many important topics that fall under the umbrella of health policy and law. We introduce three conceptual frame- works in this section: one premised on the broad top- ical domains of health policy and law, one based on prevailing historical factors, and one focused on the individuals and entities impacted by a particular pol- icy or legal determination (BOX 1-1).

We draw on these frameworks to various degrees in this text. For example, the topical domain approach of Framework 1 is on display in the sections about individual rights in health care and public health and healthcare quality policy and law. Framework 2’s focus

on historical perspectives is highlighted in the chapters on health reform and government health insurance programs. Finally, Framework 3, which approaches the study of health policy and law from the perspec- tives of key stakeholders, is discussed in the policy and policymaking process section and also in the chapter dedicated to the social determinants of health. We turn now to a description of each framework.

The Three Broad Topical Domains of Health Policy and Law One way to conceptualize health policy and law is as consisting of three large topical domains. One domain is reserved for policy and law concerns in the area of health care, another for issues arising in the public health arena, and the last for controversies in the field of bioethics. As you contemplate these topical domains, bear in mind that they are not individual silos whose contents never spill over into the others. Indeed, spill- age of one domain’s contents into another domain is common (and, as noted, is one reason why fixing health policy problems can be terribly complicated). We briefly touch on each domain.

Conceptualizing Health Policy and Law 5

BOX 1-1 Three Conceptual Frameworks for Studying Health Policy and Law

Framework 1. Study based on the broad topical domains of:

a. Health care b. Public health c. Bioethics

Framework 2. Study based on historically dominant social, political, and economic perspectives:

a. Professional autonomy b. Social contract c. Free market

Framework 3. Study based on the perspectives of key stakeholders:

a. Individuals b. The public c. Healthcare professionals d. Federal and state governments e. Managed care and traditional insurance

companies f. Employers g. Healthcare industries (e.g., the pharmaceutical

industry) h. The research community i. Interest groups j. Others

 

 

Healthcare Policy and Law In the most general sense, this domain is concerned with an individual’s access to care (e.g., What poli- cies and laws impact an individual’s ability to access needed care?), the quality of the care the person receives (e.g., Is it appropriate, cost-effective, and non- negligent?), and how the person’s care will be financed (e.g., Is the person insured?). However, “access,” “qual- ity,” and “financing” are themselves rather large sub- domains, with their own sets of complex policy and legal issues; in fact, it is common for students to take semester-long policy and/or law courses focused on just one of these subdomains.

Public Health Policy and Law The second large topical domain is that of public health policy and law. A central focus here is on why and how the government regulates private individuals and cor- porations in the name of protecting the health, safety, and welfare of the general public. Imagine, for example, that the federal government is considering a blanket policy decision to vaccinate individuals across the coun- try against the deadly smallpox disease, believing that the decision is in the best interests of national security. Would this decision be desirable from a national policy perspective? Would it be legal? If the program’s desir- ability and legality are not immediately clear, how would you go about analyzing and assessing them? These are the kinds of questions with which public health policy and law practitioners and scholars grapple.

Bioethics Finally, there is the bioethics domain to health policy and law. Strictly speaking, the term bioethics is used to describe ethical issues raised in the context of med- ical practice or biomedical research. More compre- hensively, bioethics can be thought of as the point at which public policy, law, individual morals, societal values, and medicine intersect. The bioethics domain houses some of the most explosive questions in health policy, including the morality and legality of abortion, conflicting values around the meaning of death and the rights of individuals nearing the end of life, and the policy and legal consequences of mapping the human genetic code.

Social, Political, and Economic Historical Context Dividing the substance of health policy and law into broad topical categories is only one way to conceptual- ize them. A second way to consider health policy and

law is in historical terms, based on the social, polit- ical, and economic views that dominate a particular era.d Considered this way, health policy and law have been influenced over time by three perspectives, all of which are technically active at any given time, but each of which has eclipsed the others during specific peri- ods in terms of political, policy, and legal outcomes. These perspectives are termed professional autonomy, social contract, and free market.e

Professional Autonomy Perspective The first perspective, grounded in the notion that the medical profession should have the authority to regu- late itself, held sway from approximately 1880 to 1960, making it the most dominant of the three perspectives in terms of both the length of time it held favored sta- tus and its effect in the actual shaping of health policy and law. This model is premised on the idea that phy- sicians’ scientific expertise in medical matters should translate into legal authority to oversee essentially all aspects of delivering health care to individuals; in other words, according to proponents of the physi- cian autonomy model, legal oversight of the practice of medicine should be delegated to the medical pro- fession itself. During the period that this perspective remained dominant, policy- and lawmakers were gen- erally willing to allow physicians to control the terms and amount of payments for rendered healthcare services, the standards under which medical licenses would be granted, the types of patients they would treat, the type and amount of information to disclose to patients, and the determination as to whether their colleagues in the medical profession were negligent in the treatment of their patients.

Social Contract Perspective The second perspective that informs a historical con- ceptualization of health policy and law is that of the “modestly egalitarian social contract” (Rosenblatt, Law, & Rosenbaum, 1997, p. 2; the authors write that the American social contract lags behind those of other developed countries, and thus use the phrase “modestly egalitarian” in describing it). This paradigm overshadowed its competitors, and thus guided poli- cymaking, from roughly 1960 to 1980, a time notable in U.S. history for social progressiveness, civil rights, and racial inclusion. At the center of this perspective is the belief that complete physician autonomy over the delivery and financing of health care is poten- tially dangerous in terms of patient care and health- care expenditures, and that public policy and law can and sometimes should enforce a “social contract”

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at the expense of physician control. Put differently, this perspective sees physicians as just one of several stakeholders (including but not limited to patients, employers, and society more broadly) that lay claim to important rights and interests in the operation of the healthcare system. Health policies and laws borne of the social contract era centered on enhancing access to health care (e.g., through the Examination and Treatment for Emergency Medical Conditions and Women in Labor Act), creating new health insurance programs (Medicare and Medicaid were established in 1965), and passing antidiscrimination laws (one of the specific purposes of Title VI of the federal 1964 Civil Rights Act was wiping out healthcare discrimination based on race).

Free Market Perspective The final historical perspective—grounded in the twin notions of the freedom of the marketplace and of mar- ket competition—became dominant in the 1990s and continues with force today (though one could argue that the Affordable Care Act evidences a curbing of the free market perspective and an elevation, again, of the social contract perspective). It contends that the mar- kets for healthcare services and for health insurance operate best in a deregulated environment, and that commercial competition and consumer empower- ment will lead to the most efficient healthcare system. Regardless of the validity of this claim, this perspective argues that the physician autonomy model is falsely premised on the idea of scientific expertise, when in fact most healthcare services deemed “necessary” by physicians have never been subjected to rigorous sci- entific validation (think of the typical treatments for the common cold or a broken leg). It further argues that even the modest version of the social contract theory that heavily influenced health policy and law during the civil rights generation is overly regulatory. Furthermore, market competition proponents claim that both other models are potentially inflationary: in the first case, self-interest will lead autonomous physi- cians to drive up the cost of their services, and in the second instance, public insurance programs like Medi- care would lead individuals to seek unnecessary care.

To tie a couple of these historical perspectives together and examine (albeit in somewhat oversim- plified fashion) how evolving social and economic mores have influenced health policy and law, consider the example of Medicaid, the joint federal–state health insurance program for low-income individuals. In 1965, Medicaid was born out of the prevailing societal mood that it was an important role of government to expand legal rights for the poor and needy. Its creation

exemplified a social contract perspective, which in the context of health promotes the view that individuals and society as a whole are important stakeholders in the healthcare and public health systems. Medicaid entitled eligible individuals to a set of benefits that, according to courts during the era under consider- ation, was the type of legal entitlement that could be enforced by beneficiaries when they believed their rights under the program were infringed.

These societal expectations and legal rights and protections withstood early challenges during the 1970s, as the costs associated with providing services under Medicaid resulted in state efforts to roll back program benefits. Then, in the 1980s, Medicaid costs soared higher, as eligibility reforms nearly doubled the program’s enrollment and some providers (e.g., com- munity health centers) were given higher payments for the Medicaid services they provided. Still, the social contract perspective held firm, and the program retained its essential egalitarian features.

As noted, however, the gravitational pull of the social contract theory weakened as the 1980s drew to a close. This, coupled with the fact that Medicaid spending continued to increase in the 1990s, led to an increase in the number of calls to terminate pro- gram members’ legal entitlement to benefits.f Also in the 1990s, federal and state policymakers dramatically increased the role of private managed care companies in both Medicaid and Medicare, an example of the trend toward free market principles.

Key Stakeholders A third way to conceptualize health policy and law issues is in terms of the stakeholders whose interests are impacted by certain policy choices or by the pas- sage or interpretation of a law. For example, imag- ine that in the context of interpreting a state statute regulating physician licensing, your state’s highest court ruled that it was permissible for a physician to not treat a patient who was in urgent need of care, even though the doctor had been serving as the patient’s family physician. What stakeholders could be impacted by this result? Certainly the patient, as well as other patients whose treatment may be colored by the court’s decision. Obviously the doctor and other doctors practicing in the same state could be impacted by the court’s conclusion. What about the state legis- lature? Perhaps it unintentionally drafted the licensing statute in ambiguous fashion, which led the court to determine that the law conferred no legal responsibil- ity on the physician to respond to a member of a fam- ily that was part of the doctor’s patient load. Or maybe the legislature is implicated in another way—maybe

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it drafted the law with such clarity that no other out- come was likely to result, but the citizenry of the state was outraged because its elected officials have created public policy out of step with constituents’ values. Note how this last example draws in the perspective of another key stakeholder—the broader public.

Of course, patients, healthcare providers, gov- ernments, and the public are not the only key stake- holders in important matters of health policy and law. Managed care and traditional insurance companies, employers, private healthcare industries, the research community, interest groups, and others all may have a strong interest in various policies or laws under debate.

▸ Conclusion The preceding descriptions of the roles played by policy and law in the health of individuals and populations, and of the ways to conceptualize health policy and law, were cursory by design. But what we hope is apparent to you at this early stage is the fact that the study of policy and law is essential to the study of both health care and public health. Consider the short list of major problems with the U.S. health system as described in a book edited and written by a group of leading scholars: the coverage and financing of health care, healthcare quality, health disparities, and threats to population health (Mechanic, Rogut, Colby, & Knickman, 2005, p. 10). All of the responses and fixes to these prob- lems—and to many other healthcare- and public health–related concerns—will invariably and neces- sarily involve creative policymaking and rigorous legal reform (and indeed, the Affordable Care Act, about which you will read in various sections, addressed each of these topics to one degree or another). This fact is neither surprising nor undesirable: policy and law have long been used to effect positive social change, and neither the healthcare nor public health field is immune to it. Thus, going forward, there is little rea- son to expect that policy and law will not be two of the primary drivers of health-related reform.

Policy and legal considerations are not relevant only in the context of major healthcare and public health transformations, however—they are critical to the daily functioning of the health system, and to the health and safety of individuals and communities across a range of everyday life events. Think about pregnancy and childbirth, for example. There are approximately 11,000 births each day in this coun- try, and thus society views pregnancy and childbirth as more or less normal and unremarkable events. In fact, the process of becoming pregnant, accessing and

receiving high-quality prenatal health care, and expe- riencing a successful delivery is crucial not only to the physical, mental, and emotional health and well-being of individuals and families, but to the long-term eco- nomic and social health of the nation. It also implicates a dizzying number of interesting and important policy questions. Consider the following:

■ Should there be a legal right to health care in the context of pregnancy, and, if so, should that right begin at the point of planning to get pregnant, at the moment of conception, at the point of labor, or at some other point?

■ Regardless of legal rights to care, how should the nation finance the cost of pregnancy care? Should individuals and families be expected to save enough money to pay out-of-pocket for what is a predictable event? Should the government help subsidize the cost of prenatal care? If so, in what way? Should care be subsidized at the same rate for everyone, or should subsidy levels be based on financial need?

■ Regarding the quality of care, what is known about the type of obstetrical care women should receive, and how do we know they are getting that care? Given the importance of this type of care, what policy steps are taken to ensure that the care is sound? What should the law’s response be when a newborn or pregnant woman is harmed through an act of negligence? When should clinician errors be considered preventable and their commission thus tied to a public policy response? And what should the response be?

■ What should the legal and social response be to prospective parents who act in ways risky to the health of a fetus? Should there be no societal response because the prospective parents’ actions are purely a matter of individual right? Does it depend on what the actions are?

■ Is it important to track pregnancy and birth rates through public health surveillance systems? Why or why not? If it is an important function, should the data tracking be made compulsory or voluntary?

■ How well does the public health system control known risks to pregnancies, both in communities and in the workplace?

■ Finally, who should answer these questions? The federal government? States? Individuals? Should courts play a role in answering some or all of them, and, if so, which ones? Whose interests are implicated in each question, and how do these stakeholders affect the policymaking process?

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There are scores of topics—pregnancy and child- birth among them, as you can see—that implicate a range of complex health policy questions, and these are the types of questions this text prepares you to ask and address. Before you turn your attention to the essential principles, components, and issues of health policy and law, however, you must understand something about policy and law generally, and about the organization and purposes of the healthcare and public health systems. The next two chapters provide a grounding in policy and law and supply the basic information needed to study policy and law in a health context. In those chapters, we define policy and law, discuss the political and legal systems, introduce the administrative agencies and functions at the heart of the government’s role in health care and public health, and more. With this information at your disposal, you will be better equipped to think through some of the threshold questions common to many policy debates, including the following questions: Which sector— public, private, or not-for-profit (or some combina- tion of them)—should respond to the policy problem? If government responds, at what level— federal or state—should the problem be addressed? What branch of government is best suited to address, or is more attuned to, the policy issue? When the government takes the lead in responding to a policy concern, what is the appropriate role of the private and not-for-profit sectors in also attacking the problem? What legal bar- riers might there be to the type of policy change being contemplated? Once you have the knowledge to crit- ically assess these types of questions, you will be able to focus more specifically on how the healthcare and public health systems operate in the United States, and on the application of policy and law to critical issues in health care and public health.

References Mechanic, D., Rogut, L. B., Colby D. C., & Knickman, J. R.

(Eds.). (2005). Policy challenges in modern health care. New Brunswick, NY: Rutgers University Press.

Rosenblatt, R. E., Law, S. A., & Rosenbaum, S. (1997). Law and the American health care system. Westbury, CT: The Foundation Press.

▸ Endnotes a. See, for example, Parmet W. E. (2006). Intro-

duction: The interdependency of law and pub- lic health. In R. A. Goodman, R. E. Hoffman, W. Lopez, G. W. Matthews, M. A. Rothstein, & K. L. Foster (Eds.), Law in public health practice

(2nd  ed., pp. xxvii–xxvii). Oxford, England: Oxford University Press.

b. For a nonfictional and utterly engrossing exam- ple of the ways in which law and legal process might stand in the way of effective public health regulation, we recommend Harr, J. (1995). A civil action. New York, NY: Vintage Books.

c. See, for example, Gostin, L. O., Thompson, F. E., & Grad, F. P. (2006). The law and the public’s health: The foundations. In R. A. Goodman, R. E. Hoffman, W. Lopez, G. W. Matthews, M. A. Rothstein, & K. L. Foster (Eds.), Law in public health practice (2nd ed., pp. 25–44). Oxford, England: Oxford University Press.

d. The particular historical framework described here was developed to apply to health care rather than to public health. We do not mean to imply, however, that it is impossible to consider public health from a historical, or evolutionary, vantage point. In fact, it is fair to say that public health practice may have just entered its third histori- cal phase. Throughout the 1800s and most of the 1900s, protection of the public’s health occurred mainly through direct regulation of private behavior. In the latter stages of the 20th cen- tury, strict reliance on regulation gave way to an approach that combined regulation with chronic disease management and public health promo- tion, an approach that necessitated a more active collaboration between public health agencies and healthcare providers and purchasers. Now, it appears that public health professionals are adding to this revised practice model another strategic initiative: building collaborative rela- tionships with policymaking agencies whose responsibilities are not directly related to public health—for example, agencies whose primary fields are housing, transportation, or agriculture.

e. The discussion of these perspectives is guided by Rosenblatt, R. E., Law, S. A., & Rosenbaum, S. (1997). Law and the American health care sys- tem (pp. 24–35). Westbury, CT: The Foundation Press; Rosenblatt, R. E. (2004). The four ages of health law. Health Matrix: Journal of Law- Medicine, 14(1), 155–196.

f. By 2005, proponents of weakening Medicaid- enrolled persons’ entitlement to program ben- efits had made significant strides: Congress passed a law called the Deficit Reduction Act that, among other things, granted states the ability to redefine the benefits and services to which Medicaid beneficiaries are entitled.

Endnotes 9

 

 

 

CHAPTER 2

Policy and the Policymaking Process

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe the concepts of policy and policymaking ■ Describe the basic function, structure, and powers of the legislative branch of government ■ Describe the basic function, structure, and powers of the executive branch of government ■ Explain the role of federal and state governments in the policymaking process ■ Explain the role of interest groups in the policymaking process

▸ Introduction

The first steps for any student of health policy are to understand what policy is generally and to learn about the policymaking process. It is vital to consider policy questions in the particular context in which they arise, both in terms of the gen- eral politics of the issue and the values and powers of the policymaker. As you will discover, there is no sin- gle definition of policy. Even so, this chapter arms you with the information needed to know what issues to consider when thinking about a public policy prob- lem, how to account for a variety of competing policy views, and what policy options are possible given the political process in the United States.

The chapter first defines what policy is and then moves to a discussion of the policymaking process by examining the roles and powers of two of the politi- cal branches of government—the legislative and exec- utive branches. As part of this discussion, we intro-

duce you to federal and state agencies that make up the healthcare and public health bureaucracy. We conclude with a discussion about the roles of interest groups in policymaking and the influence they wield in the policymaking process.

▸ Defining Policy In this section we consider various aspects of what we mean by the term policy. Before delving into the policy- making process, we identify which issues fall within the realm of a public policy decision and, generally, what kinds of decisions might be made by policymakers.

Identifying Public Problems Scholars have defined policy in many different ways. Consider a few of them:

■ Authoritative decisions made in the legislative, exec- utive, or judicial branches of government that are

11

© Mary Terriberry/Shutterstock

 

 

intended to direct or influence the actions, behav- iors, and decisions of others (Longest, 2016, p. 10).

■ A course of action adopted and pursued by a gov- ernment, party, statesman, or other individual or organization (Subcommittee on Health and Envi- ronment, 1976, p. 124).

■ Authoritative decisions and guidelines that direct human behavior toward specific goals either in the private or the public sector (Hanley, 1999, p. 125).

The differences in these definitions raise several important issues. The first question to consider is whether private actors make policy or whether poli- cymaking is an activity for the government only. The first definition refers only to governmental policy- makers, the second definition allows for both public and private policymakers, and the third definition is unclear on this issue. Of course, the government is a key player in any policy field, and it is certainly true that decisions by government entities represent public policy. However, in this text we also focus on private actors who make policy, such as commercial insurance companies, private employers, influential individuals, and others who can all be part of health policy. For example, when a major health insurance company decides to cover obesity prevention mea- sures, or when the Bill and Melinda Gates Founda- tion provides grants to develop crops that are high in essential vitamins and minerals to improve the nutri- tion of people in developing countries, they are mak- ing health policy decisions.

Regardless of whether the policymaker is a public or private figure, it is necessary that the decision being made is an authoritative decision. These are decisions made by an individual or group with the power to implement the decision, and there are a variety of lev- els where these kinds of decisions can take place. For example, within government, authoritative decisions may be made by the president, cabinet officials, agency heads, members of Congress, governors, state legisla- tures, public health commissioners, and many others.

But all decisions by public and private individuals or entities are not necessarily policy decisions. The key issue to determining whether a “decision” represents a “policy” is whether the question at hand is an indi- vidual concern or a public policy problem. A public policy problem goes beyond the individual sphere and affects the greater community. Whereas an indi- vidual might decide to take advantage of employer- sponsored health insurance, a public policy question is whether all employers should be required to offer health insurance to their employees. Whereas an indi- vidual might decide to purchase a generic (as opposed to a brand name) drug to save money, a public policy

question is whether patients should be induced to buy less expensive generic drugs. When deciding whether something is a public policy decision, the focus is not only on who is making a decision, but also on what kind of decision is being made.

Furthermore, just because a problem is identified as a public policy problem does not necessarily mean the only solution involves government intervention. For example, consider the problem of an influenza vaccine shortage. Although there are government- oriented solutions to this problem, such as expanding public research and development or creating pro- duction incentives (through tax cuts or subsidies) to encourage private manufacturers to produce more vaccine, other solutions may rely solely on private actors. Private companies may decide to invest in the research and development of new ways to produce vaccines, or to build new plants to increase produc- tion capacity, because they believe they can make a profit in the long run. Just as private individuals and entities can make policy decisions for their own ben- efit, they can also play a central role in solving public policy problems. A lengthier discussion about options for solving public policy problems and arguments for and against government intervention is found in a review of health economics.

Structuring Policy Options Considered broadly, there are different ways to approach public policy problems. For example, some policy options are voluntary, whereas others are man- datory. It is important to recognize that authoritative decisions do not always require others to act or refrain from acting in a certain way. Some of the most import- ant and effective policies are those that provide incen- tives to others to change their behavior. Indeed, the power of persuasion is very important to public offi- cials, particularly those working for the federal gov- ernment, which is limited in its ability to force states and individuals to take certain actions. This limitation stems from the fact that the 10th Amendment of the U.S. Constitution limits Congress and the executive branch to specific powers and reserves all other pow- ers for the states. However, members of the federal government may use their enumerated powers, such as those to tax and spend, to persuade states and oth- ers to act in desired ways.

For example, the Constitution does not give the legislative or executive branches the power to protect the public’s health, meaning that the area is primarily within the purview of states to regulate. As a result, Congress and the president cannot require states to create emergency preparedness plans. Yet, Congress

12 Chapter 2 Policy and the Policymaking Process

 

 

may provide incentives to states to do so by offering them federal money in return for state preparedness plans that meet certain criteria established by the fed- eral government.

In addition, it is important to remember that inaction can also be a policy decision. Deciding to do nothing may be a decision to keep a prior decision in place or not to engage in a new issue. For exam- ple, a governor could decide against trying to change a restrictive abortion law, or a state legislature could choose not to pass a law expanding the allowable scope of practice for nurse practitioners. Both of these inactions result in important policy decisions that will affect the choices and opportunities available to indi- viduals, advocacy organizations, and others.

This brief discussion about policy has raised sev- eral important issues to consider when identifying policy options. The next section provides a detailed discussion of the policymaking process, providing you with the background knowledge necessary to identify and understand the roles and powers of various poli- cymakers.

▸ Public Policymaking Structure and Process

The public policymaking structure refers to the vari- ous branches of government and the individuals and entities within each branch that play a role in making and implementing policy decisions. In this section, we review the structure, powers, and constituency of these branches, with a focus on the U.S. House of Rep- resentatives, the U.S. Senate, and various commissions and agencies that assist Congress, the president, White House staff, and federal executive branch administra- tive agencies. In addition to reviewing the policymak- ing structure, we discuss the processes used by these various individuals and entities for making public pol- icy decisions.

State-Level Policymaking The federal government does not have a monopoly on policymaking. Indeed, important policy decisions are regularly made at the state level as well, espe- cially in the healthcare arena. However, because state governments are similar to the federal government in many ways, the policymaking duties and powers pre- sented in the following discussion can often be applied to a state-level analysis. At the same time, there is a significant amount of variation in how states structure their legislative and executive branches, agencies, and offices, and it is not possible to review the differences

that exist among all 50 states. Accordingly, after a brief discussion of state-level policymaking, this chapter focuses primarily on the federal policymaking struc- ture and process.

Like the federal government, each state has three branches of government. State legislatures pass laws, appropriate money within the state, and conduct over- sight of state programs and agencies. States also have their own judiciary with trial and appellate courts. The governor is the head of the state executive branch and can set policy, appoint cabinet members, and use state administrative agencies to issue regulations that implement state laws. Although there are limits to a state’s power to regulate healthcare issues, state regula- tion is an extremely important aspect of health policy. Just a few examples of the healthcare matters states can regulate include provider licensing, accreditation, some aspects of health insurance, and most public health concerns.

While state governments share these general characteristics, it is important to realize that all state governments are not exactly alike. The governor has more power in some states than in others, agencies are combined in different ways among the states, state legislatures may meet annually or biannually, state leg- islators may be full-time or part-time employees, and so on. Because these differences exist, it is essential for policy analysts to understand the specific structure of the state in which their client resides.

Furthermore, there are important differences between the federal government and the states. Unlike the federal government, almost all states are required to have a balanced budget, and most states cannot borrow money for operating expenses. These rules mean that states must act to raise revenue or cut programs if they project that their budget will be in deficit by the end of the fiscal year. In addition, in 2010, 30 states had at least one tax and expenditure limit rule that restricted the growth of government revenues or spending to a fixed numerical target, sometimes using changes in population level or the inflation rate as guideposts. Further, 15 states require a legislative supermajority or voter approval to raise taxes (a supermajority means that more than a simple majority—over 50%—is required; for example, a two- thirds majority vote could be required) (Waisanen, 2010). As a result, state officials may be more likely than federal officials to make the difficult choice to either limit programs or cut resources from one pro- gram to fund another.

As is evident from this brief discussion, state-level policymaking is both a rich area for discussion and a difficult area to make generalizations about because each state is unique. Having highlighted some of the

Public Policymaking Structure and Process 13

 

 

key differences and similarities among the states and between the state and the federal governments, we now turn to the legislative and executive branches of the federal government.

The Federal Legislative Branch Article I of the U.S. Constitution makes Congress the lawmaking body of the federal government by granting it “All legislative Powers” and the right to enact “ necessary and proper laws” to effect its prerog- atives (U.S. Const. art. I, § 1; U.S. Const. art. I, § 8). Congressional responsibilities are fulfilled by the two chambers of Congress, the Senate and the House of Representatives (“the House”). The Constitution grants specific powers to Congress, including but not limited to the power to levy taxes, collect revenue, pay debts, provide for the general welfare, regulate interstate and foreign commerce, establish federal courts inferior to the Supreme Court, and declare war (U.S. Const. art. I, § 1). The Senate has the specific power to ratify treaties and confirm nominations of public officials.

The Senate consists of 2 elected officials from each state, for a total of 100 senators.a Each senator is elected in a statewide vote for a 6-year term, whereas representatives in the House sit for 2-year terms. Due to the lengthy term of its members, the Senate is con- sidered less volatile and more concerned with long- term issues than the House. A senator must be at least 30 years old, a U.S. citizen for at least 9 years, and a resident of the state he or she is seeking to represent (U.S. Const. art. I, § 3).

The House includes 435 members allocated pro- portionally based on the population of the 50 states, with each state guaranteed at least 1 representative.b For example, in 2018, California was allotted 53 rep- resentatives, while Vermont had only 1. Due to the proportionality rule, members from larger states dominate the House and often hold leadership posi- tions. Members of the House are elected by voters in congressional districts and serve 2-year terms. They must be at least 25 years old, a U.S. citizen for at least 7 years, and a resident of the state where the election takes place (U.S. Const. art. I, § 2).

Leadership Positions Leadership roles in Congress are determined by polit- ical party affiliation, with the party in the majority gaining many advantages. The vice president of the United States is also the president of the Senate and presides over its proceedings. In the vice president’s absence, which is common given the other obliga- tions of the office, the president pro tempore, a mostly

ceremonial position, presides over the Senate. In most cases the vice president is not a major player in Senate voting, but with the power to break a tie vote, the vice president wields an important power. The Speaker of the House (“Speaker”) presides over that chamber and has the authority to prioritize and schedule bills, refer bills to committees, and name members of joint and conference committees. Other than the vice presi- dent’s senatorial role, leadership positions in Congress are not elected by the voters, but determined by the members from the party who have been elected to Congress. Other key Congressional leadership posi- tions include the following:

■ Senate majority leader: Speaks on behalf of the majority party, schedules floor action and bills, works on committees, directs strategy, and tries to keep the party united.

■ House majority leader: Works with the Speaker to direct party strategy and set the legislative schedule.

■ House and senate minority leaders: Speak on behalf of the minority party, direct strategy, and try to maintain party unity; as members of the minority, they do not have the legislative duties of the majority leader/Speaker.

■ House and senate majority and minority whips: Track important legislation, mobilize members to support leadership positions, keep a count of how party members are planning to vote, and generally assist their leaders in managing their party’s legis- lative priorities.

Committees Committees have been referred to as the “workhorses” of Congress; they are where many key decisions are made and legislative drafting takes place. Given the vast array of issues that Congress contends with in any given legislative session, it is impossible for every member to develop expertise on every issue. Although members vote on bills that cover a wide range of issues, members often concentrate on the areas relevant to the committees on which they serve.

Committees have a variety of important roles, including drafting and amending legislation; educat- ing members on key issues; shepherding the commit- tee’s legislation on the floor when it goes before a vote by all the members of one chamber; working with the president, his administration, and lobbyists to gain support for a bill; holding hearings; and conducting oversight of executive branch departments, agencies, commissions, and programs within their purview. Committee members often gain expertise in the areas

14 Chapter 2 Policy and the Policymaking Process

 

 

covered by their committees, and other members often rely on their advice when making voting decisions.

Standing committees are generally permanent com- mittees with specified duties and powers. There are 20 standing committees in the House and 16 in the Senate. House committees tend to be larger than those in the Senate, with about 40 members per committee. Some committees have authorization jurisdiction, allowing them to create programs and agencies. Other commit- tees have appropriation authority, meaning they are responsible for funding various programs and agen- cies. Standing committees also have oversight authority, meaning they monitor how programs are run and funds are spent. Each chamber of Congress has established specific oversight committees for some programs and issues that cut across committee jurisdiction, as well as committees that review the efficiency and economy of government actions (Heitshusen, 2018).

Not surprisingly, some of the most powerful and popular committees are those that deal with appropri- ating money. These include the following:

■ House Ways and Means and Senate Finance committees: These committees have jurisdiction

over legislation concerning taxes, tariffs, and other revenue-generating measures, and over entitle- ment programs such as Medicare and Social Secu- rity. The Constitution requires all taxation and appropriations bills to originate in the House, and House rules require all tax bills to go through the Ways and Means committee.

■ House and Senate Appropriations committees: These committees have responsibility for writing federal spending bills.

■ House and Senate Budget committees: These committees are tasked with creating the overall budget plan that helps guide tax and appropria- tion committee work.

■ House Rules committee: This committee has jurisdiction over the rules and order of business in the House, including rules for the floor debates, amendments, and voting procedures. Unlike in the Senate, all House bills must go to the House Rules committee before reaching the House floor for a vote by all representatives.

TABLE 2-1 identifies the key health committees and subcommittees and their health-related jurisdictions.

Committee/Subcommittee Health-Related Jurisdiction

Senate Finance Committee

■ Subcommittee on Health Care  ■ Department of Health and Human Services • Centers for Medicare and Medicaid Services (includes

Children’s Health Insurance Program [CHIP]) • Administration for Children and Families

■ Department of the Treasury • Group health plans under the Employee Retirement

Income Security Act (ERISA)

Senate Appropriations Committee

■ Subcommittee on Labor, Health, Human Services, Education, and Related Agencies

■ Department of Health and Human Services • All areas except Food and Drug Administration, Indian

Health, and construction activities

■ Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies

■ U.S. Agricultural Department (except Forest Service) • Includes child nutrition programs; food safety and

inspections; nutrition program administration; special supplemental nutrition program for Women, Infants, Children (WIC); Supplemental Nutrition Assistance Program (SNAP)

■ Food and Drug Administration

(continues)

TABLE 2-1 Key Health Committees and Subcommittees

Public Policymaking Structure and Process 15

 

 

Committee/Subcommittee Health-Related Jurisdiction

■ Subcommittee on Interior, Environment, and Related Agencies

■ Department of Health and Human Services • Indian Health Services • Agency for Toxic Substances and Disease Registry

Senate Health, Education, Labor, and Pensions Committee

■ Subcommittee on Children and Families ■ Subcommittee on Primary Health and

Retirement Security

■ Occupational safety and health, public health, Health Resources Services Act, substance abuse and mental health, oral health, healthcare disparities, ERISA

Senate Committee on Agriculture, Nutrition, and Forestry

■ Subcommittee on Nutrition, Specialty Crops, and Agricultural Research

■ Food from fresh waters; SNAP; human nutrition; inspection of livestock, meat, and agricultural products; pests and pesticides; school nutrition programs; other matters related to food, nutrition, and hunger

Senate Committee on Environment and Public Works

■ Subcommittee on Clean Air and Nuclear Safety ■ Air pollution, environmental policy, research and development, noise pollution, water pollution, nonmilitary control of nuclear energy, solid waste disposal and recycling

House Committee on Ways and Means

■ Subcommittee on Health ■ Programs providing payments for health care, health delivery systems, and health research

■ Social Security Act ■ Maternal and Child Health Block Grant ■ Medicare ■ Medicaid ■ Peer review of utilization and quality control of healthcare

organizations ■ Tax credit and deduction provisions of the Internal Revenue

Service relating to health insurance premiums and healthcare costs

■ Subcommittee on Human Resources ■ Social Security Act • Public assistance provisions • Supplemental Security Income provisions • Mental health grants to states

House Committee on Appropriations

■ Subcommittee on Labor, Health and Human Services, Education, and Related Agencies

■ Department of Health and Human Services • Administration for Children and Families • Administration for Community Living • Agency for Healthcare Research and Quality • Centers for Disease Control and Prevention • Centers for Medicare and Medicaid Services

TABLE 2-1 Key Health Committees and Subcommittees

16 Chapter 2 Policy and the Policymaking Process

(continued)

 

 

• Health Resources Services Administration • National Institutes of Health • Substance Abuse and Mental Health Services • Federal Mine Safety and Health Review Commission • Medicaid and CHIP Payment and Access Commission • Medicare Payment Advisory Committee • National Council on Disability • Occupational Safety and Health Review Commission • Social Security Administration

■ Subcommittee on Agriculture, Rural Development, Food and Drug Administration, and Related Agencies

■ Food and Drug Administration ■ Department of Agriculture (except Forestry)

■ Subcommittee on Energy, Water Development, and Related Agencies

■ Department of Energy • National Nuclear Strategy Administration • Federal Energy Regulatory Commission

■ Department of Interior ■ Bureau of Reclamation ■ Defense Nuclear Facilities Safety Board ■ Nuclear Regulatory Commission

■ Subcommittee on Interior, Environment, and Related Agencies

■ Department of Interior ■ Environmental Protection Agency ■ Indian Health Service ■ National Institute of Environmental Health Sciences ■ Chemical Safety and Hazards Investigation Board

House Committee on Agriculture

■ Subcommittee on Nutrition ■ Nutrition programs, including SNAP

■ Subcommittee on Biotechnology, Horticulture, and Research

■ Policies and statutes relating to horticulture, bees, organic agriculture, pest and disease management, bioterrorism, biotechnology

■ Subcommittee on Livestock and Foreign Agriculture

■ Policies and statutes relating to inspections of livestock, dairy, poultry, and seafood; aquaculture; animal welfare

Congressional Commissions and Staff Agencies Although the committee system helps members of Congress focus on particular areas, members often need assistance with in-depth research and policy analysis. Commissions and staff agencies provide members with information they might not otherwise have the time to gather and analyze. There are too many commissions and agencies to list here, but a few key ones include the following:

■ Congressional Budget Office: An agency that provides Congress with cost estimates of bills and federal mandates to state and local governments,

as well as forecasts economic trends and spending levels.

■ Government Accountability Office: An indepen- dent, nonpartisan agency that studies how federal tax dollars are spent and advises Congress and executive agencies about more efficient and effec- tive ways to use federal resources.

■ Congressional Research Service: The public pol- icy research service that conducts nonpartisan, objective research on legislative issues.

■ Medicare Payment Advisory Commission: An independent federal commission that gives Congress advice on issues relating to the Medicare program, including payment, access to care, and quality of care.

Public Policymaking Structure and Process 17

 

 

How Laws Are Made One way that members of Congress indicate their pol- icy preferences is by passing laws that embody their values and the values of their constituents. This is a lengthy process, with many steps along the way that could derail a bill (FIGURE 2-1).

Before a committee considers a bill, it must be introduced by a member of Congress. Once this occurs, the Speaker refers the bill to one or more committees in

the House, and the majority leader does the same in the Senate. The bill may die in committee if there is not suf- ficient support for it, although there are rarely invoked procedures that allow a bill to be reported to the full chamber even without committee approval. While the bill is in committee, members may hold hearings on it or “mark up” the bill by changing or deleting language in the proposed bill or by adding amendments to it. If a majority of the committee members approves a bill, it

FIGURE 2-1 How a Bill Becomes a Law

18 Chapter 2 Policy and the Policymaking Process

Representative introduces bill in the House

Senator introduces bill in the Senate

Bill is read in the House and assigned to a committee by the

Speaker

Bill is read in the Senate and assigned to a committee by the

majority leader

Bill leaves committee, is scheduled for floor

consideration and debate, may be amended

Bill leaves committee, is scheduled for floor

consideration and debate, may be amended

House passes bill Senate passes bill

Bill is sent to Senate Bill is sent to House

A conference committee is created to resolve differences if both chambers do not pass an identical bill

Identical bill is passed by both House and Senate OR one branch agrees to the other branch’s version OR bill is amended and both branches vote again and pass amended version

Bill is presented to the President, who has four options

Option 1: President signs bill into law

Option 2: During congressional

session, bill becomes law after 10 days without presidential signature

Option 3: When not in session, bill

does not become law without presidential

signature

Option 4: President vetoes bill.

Two-thirds vote in House and Senate can override veto

 

 

goes to the full chamber (House or Senate, depending on where the bill originated).

The full House or Senate then debates the mer- its of the bill and puts it to a vote. If a majority does not support the bill, it dies on the chamber floor. If a majority supports the bill, it is sent to the other cham- ber for consideration. The second chamber may pass the exact same bill or a different version of the bill. If the second chamber does not pass any version of the bill, it dies on the chamber floor and no version of the bill moves forward. If the second chamber passes an identical bill, it goes directly to the president for consideration.

If there are differences in the bills passed by the House and Senate, the two chambers must reach a con- sensus through an exchange of amendments for the bill to have a chance of becoming law. Consensus building is facilitated by a “conference committee” made up of members from both chambers. If the committee can- not reach a consensus, the bill dies. If the committee reaches a consensus, the bill is sent back to each cham- ber for a vote on the new version of the bill. If either chamber does not approve it, the bill dies at that point. If both the House and the Senate pass the new version, it is sent to the president for consideration.

The president may choose to sign the bill into law, or the president may choose to veto the bill. If the president chooses not to sign the bill while Congress is in session, the bill becomes law after 10 days; if Congress is not in session and the bill goes unsigned, the bill dies (this is referred to as a “pocket veto”). If the president vetoes the bill, Congress may over- ride the veto with approval of a two-thirds majority in each chamber.

Congressional Budget and Appropriations Process Although the budget and appropriations process may sound dry, it is about much more than numbers and charts. If you take a close look at budget documents, they include narratives that discuss why certain pro- grams are being funded and what the government hopes to achieve by doing so. In many ways, this process is a key policy tool for members of Congress and the pres- ident; they are able to show which programs and issues have their support through their funding decisions.

Given both the amount of money involved in running the United States ($4 trillion in 2017) and the various jurisdictions of congressional commit- tees, it is not surprising that the federal budget pro- cess is fairly complex. The Congressional Budget and Impoundment Control Act of 1974 (“Budget Act”) and subsequent amendments were passed by

Congress to create a process that brings together the numerous committees involved in crafting an over- all budget plan. The budget process works in concert with the appropriations process, which involves con- gressional passage of bills from each of the appropria- tions committees to distribute the funds provided for in the overall budget (House Committee on the Bud- get Majority Caucus, 2001; Senate Committee on the Budget, 1998).

The president is required to submit a budget pro- posal to Congress by the first Monday in February. This proposal is the administration’s request; it is not binding on Congress. Each chamber then passes a budget resolution, identifying how the chamber would spend federal money delineated by different catego- ries of spending (e.g., defense, agriculture, transpor- tation). Members from each chamber then meet to develop a single conference report reflecting a consen- sus agreement on the overall budget. Congress then passes a concurrent budget resolution, which is binding upon the House and Senate as a blueprint for revenue collection and spending. However, it is not a law and the president is not bound by the budget resolution.

Over the 6 weeks subsequent to the passage of the concurrent budget resolution, the House and Sen- ate budget committees hold hearings to discuss the budget, and other committees review the budget as it pertains to their jurisdiction. The latter committees provide the budget committees with their “views and estimates” of appropriate spending and/or revenue levels for the upcoming year. In addition, the Con- gressional Budget Office provides the budget commit- tees with its budget and economic outlook reports and provides the budget and appropriations committees with its analysis of the president’s proposal.

In March, the House and Senate budget commit- tees each craft a budget plan during public meetings known as “markups.” When the markups are com- plete, each committee sends a budget resolution to its respective chamber. The budget resolution contains a budget total, spending breakdown, reconciliation instructions, budget enforcement mechanisms, and statements of budget policy. Budget totals are pro- vided as aggregates and as committee allocations.

The federal budget includes two types of spending: discretionary and mandatory. Discretionary spending refers to money that is set aside for programs that must be funded annually in order to continue. If the programs are not funded by Congress, they will not receive federal dollars to continue their operations. For example, the Head Start program, which provides early childhood education services, is a discretionary program that relies on annual appropriations. Manda- tory spending refers to spending on entitlement and

Public Policymaking Structure and Process 19

 

 

other programs that must be funded as a matter of law. For example, the Medicaid program is an entitlement that provides health insurance to eligible low-income individuals. The authorizing legislation (the law that created the program) for Medicaid includes eligibility rules and benefits. Because Medicaid is an entitlement program, Congress must provide enough money so the Medicaid agency can meet the obligations found in the authorizing legislation.

The appropriations committees write bills to cover discretionary spending. These committees make their decisions based on the amount of funds available and any reconciliation instructions, which direct the appropriate authorizing committee to make changes in the law for mandatory spending programs to meet budgetary goals. Appropriations bills and reconcilia- tion instructions must be signed by the president to become law.

Members of the House and Senate have the opportunity to make changes to the work of the bud- get committees. Once the House and Senate pass their own versions of the budget resolution, they establish a conference committee to resolve any differences. Once the differences are resolved, each full chamber votes on the compromise budget.

Congress often does not meet Budget Act dead- lines (shown in TABLE 2-2). If the appropriations bills are not passed by every October 1—the beginning of the fiscal year—Congress may pass a continuing resolution that allows the government to continue to spend money. If Congress does not pass a continuing resolution or if the president vetoes it, all nonessential activities of federal agencies must stop until additional funds are provided.

Constituents of Legislative Branch With the wide array of issues they take on, members of Congress may have an equally wide array of constitu- ents to be concerned about when making policy deci- sions. Clearly, members are concerned about pleasing the voters who elect them. Even though there may be a variety of policy views to consider, members often prioritize their home constituents. In addition to court- ing their home-state voters, members often try to court independents or voters from the opposing party in their home state to strengthen their appeal. High approval ratings deter challengers from trying to take an incum- bent’s congressional seat and allow members of Con- gress more leeway to pursue their goals and policies.

TABLE 2-2 Federal Budget Process Timeline

First Monday in February President submits budget proposal to Congress.

March House completes its budget resolution.

April Senate completes its budget resolution.

April 15 House and Senate complete concurrent budget resolution.

May Authorizing committees develop reconciliation language when necessary and report legislation to budget committees. House and Senate develop conference report on reconciliation, which is voted on by each chamber.

June 10 House concludes reporting annual House appropriations bills.

June 15 If necessary, Congress completes reconciliation legislation.

June 30 House completes its appropriations bills.

September 30 Senate completes its appropriations bills. House and Senate complete appropriations conference reports and vote separately on the final bills.

October 1 Fiscal year begins.

Modified from House Committee on the Budget Majority Caucus, Basics of the Budget Process, 107th Cong. Briefing Paper, 2001.

20 Chapter 2 Policy and the Policymaking Process

 

 

Although concern for their home-state base may be their first priority, representatives and senators often need to be concerned about supporting their party’s position on issues. Today, elected federal politicians are usually affiliated with the Democratic or Republi- can Party, and voters may be influenced by the party’s stance on issues. Also, if the balance of power between the two parties is close in Congress, the parties usually cannot afford to have members defect from their par- ty’s positions. Members’ concern regarding keeping their party strong is magnified if they hold leadership positions in Congress or are considering running for national office.

Finally, the views of the president may be import- ant for members to consider, depending on whether the member and the president share the same party, the particular issue involved, and the president’s pop- ularity. Members who are in the same party as the sitting president have incentive to help the president remain popular because they will likely advance many of the same policies. In addition, presidents are often prodigious fundraisers and campaigners who may be able to assist members during election season. Even when members disagree with the president, the presi- dent’s power to affect their influence in Congress may be a deterrent to opposing the president. Of course, if the president is exceedingly popular, it is difficult for members of either party to oppose presidential policy goals.

The Federal Executive Branch Article II of the U.S. Constitution establishes the executive branch and vests executive power in the most well-known member of the branch, the presi- dent (U.S. Const. art. II, § 1). Of course, the president does not act alone in running the executive branch. Presidents rely on Executive Office agencies and staff such as the Council of Economic Advisors and Office of Management and Budget, as well as policy development offices such as the National Security Council and Domestic Policy Council (see BOX 2-1 for a description of one such office). In addition, there are 15 cabinet departments led by individuals selected by the president (subject to Senate confir- mation) and additional non– cabinet-level agencies, all of which are responsible for, among other duties, interpreting and implementing the laws passed by Congress. All of these advisors identify issues to be addressed and formulate policy options for the pres- ident to consider. In theory, all of these parts of the executive branch work in furtherance of the goals set by the president.

The Presidency The president is the head of the federal executive branch. As powerful as that may sound, the coun- try’s founders created three distinct branches of gov- ernment and limited the president’s power in order to ensure that no single individual gained too much control over the nation. As you will see, in some ways the president is very powerful, and in other ways his power is quite limited.

Although there have been third-party candidates for president in the past, generally speaking the United States operates with a two-party system, with the Dem- ocratic and Republican parties as the major parties. Each party selects a candidate for president who rep- resents the party in the election. Presidents (and their vice presidents) are elected through a nationwide vote to serve a 4-year term. An individual is limited to serv- ing two 4-year terms as president, which may or may not be consecutive (U.S. Const. amend. XXII, §  1).c To be eligible for election, candidates must be at least 35 years old, a natural-born citizen of the United States, and a resident of the country for at least 14 years.

Presidents have many roles. As the unofficial Chief of State, the president is seen as the symbol of the country and its citizens (H.R. Doc. No. 106–216, 2000, p. 40). As the official Chief Executive Officer, the president man- ages the cabinet and executive branch. The president also holds the position of Commander in Chief of the Armed Forces, and as such is the top-ranking military official in the country. The U.S. Constitution vests the president

BOX 2-1 Office of Management and Budget

The Office of Management and Budget (OMB) reports directly to the president and plays an important role in policy decisions. OMB is responsible for preparing the presidential budget proposal, which includes reviewing agency requests, coordinating agency requests with presidential priorities, working with Congress to draft appropriation and authorization bills, and working with agencies to make budget cuts when needed. In addition to these budgetary functions, OMB provides an estimate of the cost of regulations, approves agency requests to collect information, plays a role in coordinating domestic policy, and may act as a political intermediary on behalf of the president. OMB also has an oversight and evaluation function over select federal agencies as a result of the Government Performance and Results Act, which requires agencies to set performance goals and have their performance evaluated.

Public Policymaking Structure and Process 21

 

 

with other powers, such as the ability to appoint judges to the federal courts, sign treaties with foreign nations, and appoint ambassadors as liaisons to other countries. These powers are all subject to the advice and consent of the Senate (H.R. Doc. No. 106–216, 2000, p. 41).

Agenda Setting. A key tool of the presidency is the ability to put issues on the national agenda and offer a recommended course of action: “Framing agendas is what the presidency is all about” (Davidson, 1984, p. 371). Presidents help set the national agenda because of the role of the president as the country’s leader and the amount of media attention given to presiden- tial actions, decisions, and policy recommendations. Unlike many other politicians or interest groups, the president does not have to work hard to receive media coverage. Whether it is the annual State of the Union address, release of the president’s budget proposal, a major speech, a press conference, a photo shoot with a foreign leader, or the release of a report, the president’s message is continually publicized. In addition, the president’s message can be delivered by the vice pres- ident, cabinet officers, and party leaders in Congress.

The notion of appealing directly to the country’s citizens to focus on a particular issue and to influence legislative debates is referred to as “going public.” In going public, presidents try to use support from the American people to gain the attention of Congress and sway votes on policy decisions. Because mem- bers of Congress are highly concerned about pleasing their constituency to improve their chance for reelec- tion, “the president seeks the aid of a third party—the public—to force other politicians to accept his prefer- ences” (Kernell, 1997, p. 3).

Sometimes it may be advantageous for the pres- ident to place an item on the policy agenda in a less public manner. For example, if a policy is controver- sial with the general public or if members of the pres- ident’s party disagree with a proposal, it may be more effective to promote a policy behind the scenes. The president, either directly or through intermediaries, can carefully let members of Congress know which policies are favored. Using combinations of prom- ises of favors and threats to members’ interests, the president may be able to influence the outcome of pol- icy debates in Congress even without going public.

In addition to deciding whether to approach Con- gress publicly or behind the scenes, the president must choose whether to present a preferred policy decision with more or less detail. A policy can be presented broadly through principles or general guidelines, or specifically through proposed legislation that is pre- sented to Congress. Each method for conveying the president’s goals has pros and cons. If a policy choice is

presented in a broad manner, Congress may interpret the policy in a way that the president dislikes. How- ever, if the president presents Congress with a specific proposal or draft legislation, Congressional members may view the president as infringing upon their role as the legislative body and resist working with him.

Whether presidents are successful in placing pol- icy issues on the national agenda and having them resolved in accordance with their preferences depends in part on how much “political capital” a president has available. Political capital is defined as the strength of the president’s popularity and of his party, in Congress and in other contexts. Members of Congress are more likely to support a popular president who has the abil- ity to mobilize the public’s support, improve members’ standing by association with the president and the president’s party, and raise money for their campaigns.

Even the most popular president cannot always dictate what issues are on the national agenda, how- ever. Events and decisions outside the president’s control often influence what topics most concern the nation. The terrorist attacks of September 11, 2001, the subsequent anthrax scare, and the subway and bus bombings in London and Madrid all served to place combating terrorism at the top of the policy and politi- cal agenda during the George W. Bush administration. Concerns about an avian flu epidemic and numerous food recalls put public health and food safety issues on the national agenda. The devastation wrought by the BP oil spill in the Gulf of Mexico made improved responses to environmental disasters a high priority for a short time. Thus, even the most popular presi- dents must be responsive to national and international events that may be beyond their control.

Presidential Powers. As noted earlier, if Congress passes legislation the president dislikes, he has the power to veto it, thereby rejecting the bill. However, the president does not have to actually use the veto to shape policy. The president may be able to persuade Congress to change a piece of legislation simply by threatening to veto it, especially if it is a law that is expected to pass by only a slim majority. In general, vetoes are used infrequently, with presidents vetoing only 3% of all legislation since George Washington was president (H.R. Doc. No. 106–216, p. 43).

Presidents also have the power to issue executive orders. These are legally binding orders that the presi- dent gives to federal administrative agencies under the control of the Executive Office. In general, these orders are used to direct federal agencies and their officials in how they implement specific laws. Executive orders are controversial because under our system of government, Congress, not the executive, is tasked with making

22 Chapter 2 Policy and the Policymaking Process

 

 

laws. In addition, significant policy decisions can be accomplished by using executive orders. For example, an executive order was used by President Truman to integrate the armed forces, by President Eisenhower to desegregate schools, by President Clinton to desig- nate 1.7 million acres in southern Utah as a national monument, and by President George W. Bush to create the federal Office of Homeland Security (which subse- quently became a cabinet-level department when Con- gress established it through legislation). As is discussed in the Health Reform in the United States chapter, Pres- ident Trump issued several executive orders intended to undermine the Affordable Care Act after Congress was unable to pass a bill to repeal and replace it.

If Congress believes an executive order is contrary to congressional intent, it has two avenues of recourse. It can amend the law at issue to clarify its intent and effectively stamp out the executive order that is now clearly contrary to the law. (Bear in mind that because the president may veto any bill, in effect it takes a two- thirds majority of Congress to override an executive order.) As an alternative, Congress may challenge the executive order in court, claiming that the president’s actions exceed his constitutional powers.

Constituents of the Executive Branch. From this description of the presidency, it is evident that pres- idents have several layers of constituents to consider when making policy choices. Certainly, the president represents every citizen and the country as a whole

as the only nationally elected official (along with the vice president) in the nation. However, the president is also a representative of a particular political party and therefore must consider the views of that party when making policies. The party’s views may be evi- dent from the party platform, policies supported by party leadership in Congress, and voters who identify themselves as party members. In  addition, the pres- ident must keep in mind the foreign policy duties of the office. Depending on the issue, it may be import- ant for the president to take into account the views of other nations or international organizations, such as the United Nations or the World Health Organization.

How does the president decide which policies to pursue? Presidents are driven by multiple goals. They want “their policies to be adopted, they want the poli- cies they put in place to last, and they want to feel they helped solve the problems facing the country” (Weis- sert & Weissert, 2002, p. 82). In addition, presidents often speak of wanting to leave a legacy or ensure their place in history when they leave office.

Given the vast array of constituents that presidents must consider, the president’s policy decision-making process involves several layers. As shown in FIGURE 2-2, presidents consult their agency staff to identify prob- lems, decide which problems are priorities, determine what solutions are available to address those problems, and choose the policy option that is the preferred course of action. In addition, the president’s staff inter- acts with members of Congress and other political

FIGURE 2-2 Executive Agency Policymaking Source: Courtesy of Jeff Levi, Professor of Health Policy, George Washington University.

Public Policymaking Structure and Process 23

Should this be on the agenda?

Agency Staff

What are the options?

Is there a problem?

What is recommended to decision-maker?

Congress

Media

White House

CONSUMERS, CITIZENS, & CONSTITUENCY GROUPS

Political Players

 

 

players to gauge their support for or opposition to various policies. Of course, how the media portrays both the problems and the potential solutions can be an important ingredient in whether politicians and the general public support the president’s initiatives.

In addition, which policies presidents choose to promote may depend in part on when policy decisions are made. First-term presidents must satisfy their con- stituents if they hope to be reelected. Although all presidents want to see their favored policies imple- mented throughout their time in office, second-term presidents may be more willing to support more con- troversial goals because they cannot run for reelection. Yet, second-term presidents may also be constrained by the desire to keep their party in power, even though another individual will hold the presidential office.

Administrative Agencies When studying the structure of our government, it is common to review Congress, the presidency, and the court system. Administrative agencies, however, are often overlooked despite the power they wield over the way our country is run.

Structurally, almost all administrative agencies are part of the executive branch and, thus, are under the power and control of the president. Practically, administrative agencies often work out of the public’s eye to implement the laws passed by Congress and the executive orders signed by the president.

Federal agencies fall into two main categories: executive department agencies and independent agencies. Executive department agencies are under the direct control of the president, and department heads serve at the pleasure of the president. These departments include the 15 cabinet-level departments and their subunits; some of the more well-known executive departments are the Department of Health and Human Services, the Department of Education, the Treasury Department, the Department of State, the Department of Defense, and the Department of Homeland Security. Independent agency heads are appointed by the president and confirmed by the Sen- ate. They serve a fixed term and may be removed only “for cause,” meaning there must be a legitimate rea- son to fire them. Examples of independent agencies include the Securities and Exchange Commission, the U.S. Postal Service, and the National Labor Rela- tions Board.

Overall, the president fills approximately 4,000 federal jobs (Yoder, 2016). In general, these political appointees have short tenures, lasting an average of 2 years (Weissert & Weissert, 2002, p. 161). When the

administration changes hands after an election, new appointees are usually selected to run the agencies. The daily operations of agencies are run by career civil ser- vants, public employees who do not necessarily come and go with each administration but who often remain at an agency for years, gaining expertise and institu- tional knowledge about the agencies in which they work. Frequently, there may be tension between the goals of the political appointee and those of the career bureaucrat, who may have the advantage of familiar- ity with members of Congress and who knows that the political appointee is likely to be replaced in a few years.

Administrative agencies can be created by statute, internal department reorganization, or presidential directive (H.R. Doc. No. 106-216, 2000, p. 50). How- ever they are initially created, agencies must have statutory authority in order to receive appropriations from Congress and act with the force of law. This stat- utory authority, or enabling statute, outlines the agen- cy’s responsibilities and powers.

Agency Powers. By necessity, statutes are usually written broadly. Congress does not have the time or expertise to include every detail about how a new pro- gram should operate or how a new department will be structured. It is up to the executive branch agency to fill in the details, and it does so by issuing policy state- ments, developing rules, and promulgating regulations.

The Affordable Care Act (ACA) is a classic example. Although the statute itself is lengthy (over 2,400 pages), the regulations needed to implement the law have been even more extensive—with some estimates putting the total page number at 20,000. To give just one example for now (a detailed dis- cussion of the ACA occurs in the Health Reform in the United States chapter), the ACA includes a list of essential health benefits that must be provided by health insurance plans offered in state exchanges. The statute outlines numerous such services, includ- ing mental health services, maternity and newborn care services, prevention and wellness services, and chronic disease management services. Even with this level of detail, many unanswered questions remain regarding which services must be covered. Do mental health services include inpatient and outpatient ser- vices? Do prevention and wellness services include contraceptive coverage? Does chronic disease man- agement include all chronic disease management models? These (and many other) questions must be answered through regulations. The ACA includes numerous provisions that require the relevant agen- cies to issue detailed regulations necessary to imple- menting the law.

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In addition, agencies must follow the require- ments set forth in the Administrative Procedure Act of 1946 (APA). The APA contains detailed require- ments compelling agencies to issue a notice of their intent to issue a new rule or change an existing rule, and provide for and respond to public comments on the proposed rule. Some agencies are also required to hold hearings and develop rules based on the evi- dence presented in those hearings (Weissert & Weis- sert, 2002, p. 172). It is important to know that the APA creates procedural standards that require an agency to follow a particular process when promul- gating regulations, but that the APA does not relate to the substance of the regulations. As long as an agency follows the necessary notice and comment require- ments of the APA, it has wide latitude to issue rules within its scope of power, even if many of the public comments opposed the proposed rules. If an agency does not follow the APA requirements, interested parties may sue the agency in court to force compli- ance with the law.

Constituents of Agencies. Agency heads, because they are not elected, do not have constituents in the same way that the president and members of Con- gress do. In theory, as members of the executive branch, agency heads should be concerned only with the wishes of the president. In reality, however, that is not always the case. Some presidents have firmer con- trol of their departments than others. If the president gives the departments and agencies broad discretion

to make policy decisions, the agencies may have few policy constraints. Practically, however, agency heads want their operation to run smoothly, which includes having a good working relationship with the individ- uals or entities regulated by that agency. If an agency antagonizes the people or groups being regulated, they might reach out to their congressional representa- tives to try to change or limit the agency’s personnel or authority. In addition, because Congress appropri- ates funds to and maintains oversight of many agen- cies, agency heads are well served by taking Congress’s interests into account.

TABLE 2-3 summarizes the general public poli- cymaking machinery. We next turn our attention to the specific parts of the government bureaucracy that operate in the health arena.

▸ The Health Bureaucracy The Federal Government Although several federal agencies have healthcare- related responsibilities, three significant health agen- cies include the Department of Health and Human Services (HHS), the Department of Defense (DoD), and the Department of Veterans Affairs (VA). HHS houses many of the major public health insurance programs and health services that provide care, infor- mation, and more to millions of U.S. residents; the DoD and VA operate health insurance programs spe- cifically for military personnel and their families.

TABLE 2-3 Summary of Public Policymaking Entities

Congress President Administrative Agencies

Main function Legislative body Chief executive of the country Implement statutes through rule making

Main tools/ powers

Support/oppose/pass legislation Appropriations Oversight

Agenda setting Persuasion Propose solutions Budget proposals Executive orders Sign legislation into law

Create regulations Provide information

Constituents Voters in state or district Voters in nation if in leadership role or have national aspirations Party President

Nation (all voters) Public who voted for the president Party Other nations International organizations

President Congress Individuals and entities regulated or served by the agency

The Health Bureaucracy 25

 

 

Department of Health and Human Services HHS includes hundreds of programs that cover activ- ities as varied as medical and social science research, preschool education services, substance abuse and pre- vention services, and health insurance programs, just to name a few. As shown in FIGURE 2-3, the department

has 11 operating divisions. The main purpose of each agency is described in TABLE 2-4.

Each operating division has numerous bureaus or divisions that operate health programs. For example, the HIV/AIDS Bureau (HAB) is one of five bureaus in the Health Resources and Services Administration. The HIV/AIDs Bureau implements the Ryan White CARE Act of 1990, which provides health care to

FIGURE 2-3 Department of Health and Human Services Organizational Chart Source: Reproduced from: the U.S. Department of Health and Human Services. HHS Organizational Chart. Retrieved from https://www.hhs.gov/about/agencies/orgchart/index.html#

26 Chapter 2 Policy and the Policymaking Process

Secretary Deputy Secretary

Chief of Staff

The Executive Secretariat (ES)

Office of Health Reform (OHR)

Office of the Secretary

Office of the Assistant Secretary for Administration (ASA)

Administration for Children and Families (ACF)

Administration for Community Living (ACL)

Agency for Healthcare Research and Quality (AHRQ)

Agency for Toxic Substances and Disease Registry (ATSDR)

Centers for Disease Control and Prevention (CDC)*

Centers for Medicare & Medicaid Services (CMS)

Food and Drug Administration (FDA)*

Health Resources and Services Administration (HRSA)*

Indian Health Service (IHS)*

National Institutes of Health (NIH)*

Substance Abuse and Mental Health Services Administration (SAMHSA)*

Office of the Assistant Secretary for Financial Resources (ASFR)

Office of the Assistant Secretary for Health (OASH)

Office of the Assistant Secretary for Legislation (ASL)

Office of the Assistant Secretary for Planning and Evaluation (ASPE)

Office of the Assistant Secretary for Preparedness and Response (ASPR)*

Office of the Assistant Secretary for Public Affairs (ASPA)

Center for Faith-Based and Neighborhood Partnerships (CFBNP)

Office for Civil Rights (OCR)

Departmental Appeals Board (DAB)

Office of the General Counsel (OGC)

Office of Global Affairs (OGA)*

Office of Inspector General (OIG)

Office of Medicare Hearings and Appeals (OMHA)

Office of the National Coordinator for Health Information Technology (ONC)

*denotes the components of the Public Health Service

Operating Divisions

Office of Intergovenmental and External Affairs (IEA)

 

 

TABLE 2-4 Department of Health and Human Services Agencies

Agency Main Purpose of Agency

Administration for Children and Families (ACF)

To promote economic and social well-being of families, children, individuals, and communities through educational and supportive programs

Administration for Community Living (ACL)

To increase access to community support and resources for older adults and people with disabilities

Agency for Healthcare Research and Quality (AHRQ)

To produce evidence to make health care safer, high quality, more accessible, and affordable, and to work with HHS and other partners to make sure the evidence is understood and used

Agency for Toxic Substances and Disease Registry (ATSDR)

To prevent exposure to toxic substances and reduce the adverse health effects associated with such exposure

Centers for Disease Control and Prevention (CDC)

To protect the nation’s health by providing leadership in the prevention and control of diseases and other preventable conditions, and to respond the public health emergencies

Center for Medicare and Medicaid Services (CMS)

To provide oversight of Medicare, the federal portions of Medicaid and CHIP, and the Health Insurance Marketplace, and to engage in quality assurance activities

Food and Drug Administration (FDA) To assure the safety of human and veterinary drugs, biological products, and medical devices, and to ensure the safety and security of the nation’s food supply and products that emit radiation

Health Resources and Services Administration (HRSA)

To provide health care to populations that are geographically isolated, or economically or medically vulnerable

Indian Health Services (IHS) To provide American Indians and Alaska Natives with comprehensive health services

National Institutes of Health (NIH) To support and conduct biomedical and behavioral research, to train promising young researchers, and to promote collecting and sharing knowledge

Substance Abuse and Mental Health Services Administration (SAMHSA)

To improve access to and reduce barriers to high-quality, effective programs for individuals who suffer from addictive or mental disorders, and for their families and communities

Department of Health and Human Services (2015). Source: Department of Health and Human Services. (2015). HHS agencies and offices. Retrieved from https://www.hhs.gov/about/agencies/hhs-agencies-and-offices/index.html

individuals with HIV and AIDS. Similarly, the Food and Drug Administration has several offices or cen- ters; the one whose job is perhaps best known to the general public is the Center for Drug Evaluation and Research, which is responsible for testing and approv- ing new drugs before they can be sold to the public. These are just two examples of the many subagency units that perform vital functions in our federal healthcare bureaucracy.

HHS also includes numerous offices that assist the Secretary of HHS in running the department. The Office of the Assistant Secretary of Health (OASH) is the principal advisor to the HHS secretary on pub- lic health matters. Through the Office of the Surgeon General, OASH oversees the U.S. Public Health Service (PHS), the Commissioned Corps (health profession- als used for both emergency responses and as health promoters), and the Office of Disease Prevention and

The Health Bureaucracy 27

 

 

Health Promotion. The PHS employs both commis- sioned corps members and civilians to run its public health programs.

Nine of the offices and agencies within HHS are part of the PHS. In addition, the PHS employees also work in the Bureau of Prisons, U.S. Coast Guard, National Oceanic and Atmospheric Administration, Environmental Protection Agency (EPA), Division of Immigration Health Services, and U.S. Marshal Ser- vices. HHS also has divisions concerned with planning and evaluation, legislation, administration and man- agement, budget and finance, program support, pub- lic affairs, and global health affairs. Offices concerned with the legality and efficiency of the department’s activities include those of the General Counsel and Inspector General, and the Office of Civil Rights.

As a result of the focus on preventing terrorism, HHS includes an Assistant Secretary for Prepared- ness and Response. This individual is the principal advisor to the Secretary of HHS on matters relating to bioterrorism and other public health emergencies and helps coordinate efforts in these areas at all levels of government. Other federal departments also have a role in public health emergency preparedness. The Department of Homeland Security (DHS), which includes the Federal Emergency Management Agency (FEMA), is tasked with preparing for and coordinat- ing the federal response to emergencies, whether due to natural or human-made disasters. The CDC houses the Strategic National Stockpile of emergency phar- maceutical supplies. Other agencies, such as the EPA, DoD, and VA, play significant roles in emergency pre- paredness and response.

Department of Veterans Affairs and Department of Defense Any veteran who does not receive a dishonorable dis- charge is potentially eligible for healthcare services through the Veterans Health Administration (VHA). The VHA is the largest healthcare delivery system in the country, with hundreds of medical centers, nurs- ing homes, and outpatient clinics that serve over 9 million patients each year (Department of Veterans Affairs, n.d.).

VHA-sponsored health plans offer a wide array of preventive, ambulatory, and hospital services as well as medications and medical and surgical supplies. VHA providers are organized into integrated networks aimed at providing cost-effective services based on local need. There are no premiums (monthly payments) for the plan, but veterans have to make co-payments (a charge per visit) unless they are exempt based on disability or income level. Unlike most healthcare plans, the VHA

system is completely portable, meaning veterans can access VHA facilities anywhere in the country.

Veterans who wish to receive care through the VHA must enroll in the program. Because the VHA receives an annual appropriation from Congress, it may not have sufficient funds to pay for all of the care demanded by eligible veterans. For that reason, the VHA uses a priority system to ensure that veterans who are low-income or have service-related disabili- ties can be enrolled into a plan. Other veterans may have to wait to be enrolled if there are insufficient funds. In addition, priority in accessing care is given to enrolled veterans who need care for service-related disabilities or have a sufficiently severe service-related disability and need care for any health concern. Veter- ans not in a priority group may have to wait to see an appropriate provider once they are enrolled.

Although veterans may receive care through the VHA, they are not required to do so. If eligible, they may choose to obtain services through other public or private healthcare programs or health insurance plans. They may also choose to receive some ser- vices through the VHA and others from non-VHA programs or plans. As a result of scandals pertain- ing to excessive wait times and falsified patient logs, Congress passed several bills to improve the medical care veterans receive. For example, the bipartisan VA Mission Act of 2018 is intended to streamline various VA programs that allow veterans to access care in the private sector and improve payment systems for pro- viders (Rein, 2018).

The VHA does not provide coverage to veterans’ family members, but the DoD does through its TRI- CARE program. TRICARE provides healthcare ser- vices to current and retired military personnel and their families. TRICARE offers a variety of plans with various eligibility requirements and costs to the patient.

State and Local Governments As discussed earlier, the Constitution gives states primary responsibility for protecting the public’s health. States have health-related agencies that deal with health financing, aging, behavioral health, environmental health, children and family services, veterans, facility licensing and standards, provider credentialing, and more. Although all states have agencies that generally cover the same functions, their structure, responsibilities, and lines of author- ity vary greatly.

With the variation among state agencies, it is not surprising that there are significant differences across the states in terms of their approach to public health and health services needs. All states have agencies to

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run their Medicaid and CHIP programs, as well as other state-specific health services programs. Local health departments (LHDs) carry out the public health functions of the state. Most commonly, LHDs are formed by, managed by, and report to a local gov- ernment, such as a county commission or local board of health. This structure provides LHDs with signif- icant latitude to interpret and implement state stat- utes. In some states, the state and local governments jointly oversee the LHD. LHDs may provide services directly or, as is increasingly common, may contract or provide support to others who perform the ser- vices. The services provided by LHDs vary consid- erably, though there is an emphasis on addressing communicable diseases, environmental health, and children’s health issues. LHDs often provide services such as immunizations; infectious disease investi- gations, epidemiology, and surveillance; food safety and inspections; nutrition services; and environ- mental health services. Some also provide diabetes care, glaucoma screening, substance abuse treatment, mental health services, and more (Turnock, 2016, pp. 235–239). (A more detailed discussion of various public health agencies is found in the Public Health Institutions and Systems chapter.)

Interest Groups Before leaving the discussion of policy, the policy- making process, and the health bureaucracy, we must say a few words about interest groups. Interest group is a general term used for a wide variety of organi- zations that are created around a particular issue or population and have the goal of influencing policy and educating others about their views and concerns (Weissert & Weissert, 2002, p. 117). Interest groups are different from most of the other stakeholders that have been discussed because interest groups do not have the power to make policy. Although members of the executive and legislative branches of govern- ment have a key role in determining which policies are adopted, interest groups have the limited, but still significant, role of trying to influence the decisions of policymakers.

There are many types of interest groups, includ- ing trade associations, think tanks, advocacy groups, and lobbying firms. A few examples include the Phar- maceutical Research and Manufacturers of America (n.d), whose mission is to “conduct effective advocacy for public policies that encourage discovery of import- ant new medicines for patients by pharmaceutical and biotechnology research companies” (Our Mission section, para. 1); America’s Essential Hospitals (n.d), which “champions excellence in health care for all,

regardless of social or economic circumstance, and advances the work of hospitals and health systems committed to ensuring access to care and optimal health for America’s most vulnerable people” (Mission and Service section, para. 2); the Center on Budget and Policy Priorities (n.d.), which conducts nonpar- tisan research and pursues “federal and state policies designed both to reduce poverty and inequality and to restore fiscal responsibility in equitable and effec- tive ways” (About the Center section, para. 1); and the Heritage Foundation (n.d.), which strives to “formu- late and promote conservative public policies based on the principles of free enterprise, limited govern- ment, individual freedom, traditional American val- ues, and a strong national defense” (About Heritage section, para. 1).

Just as members of Congress do not have the time or ability to become experts in every issue that comes before them, the same is true for the average citizen. Many people do not have the time and ability to learn about all of the issues that are important to them, develop proposals, rally public support for their positions, monitor current activity, lobby to add or remove issues from the agenda, and reach out to pol- iticians who make policy decisions. Instead, interest groups take on those duties: “Their job is to make the case for their constituents before government, plying the halls of Congress, the executive branch, the courts, and the offices of other interest groups to provide a linkage between citizens and government” (Weissert & Weissert, 2002, p. 119)

Interest Group Powers Interest groups do not have the power to pass laws. However, they can influence policy in a variety of ways throughout the policymaking process. For example, recall all the steps it takes for a bill to become a law. Anywhere along that continuum is an opportunity for interest groups to make their case. The first step for interest groups is often to commission research that they use to support their position. This can be most important in the early stages of policy development, when politicians might have an open mind about var- ious proposals (Weissert & Weissert, 2002, p. 131). However, it does not matter how much information a group has if it is not able to gain access to the deci- sion makers. Even a few minutes with a politician may be a few more minutes than the opposition has to make its case directly to a decision maker (Weissert & Weissert, 2002, p. 131). Finally, interest groups need to develop a persuasive argument, a way to frame the issue that convinces politicians to agree with their view of a policy matter.

The Health Bureaucracy 29

 

 

Interest groups have a variety of tools at their dis- posal when developing strategies for lobbying. They may initiate a grassroots campaign, asking their members to contact their representatives with a particular message. Because interest group members are the voters with the power to reelect public officials, strong grassroots cam- paigns can be quite effective. Or, they may try a grass- tops strategy and harness the influence of community leaders and other prominent individuals (Weissert & Weissert, 2002, p. 1319), or, they may join with other interest groups to create coalitions and strengthen their influence through numbers. Interest groups may start a media campaign to align public sentiment with their goals. Of course, providing candidates with money, often through political action committees, is a time-honored way to try to influence the outcome of policy debates.

Whatever methodology they use, interest groups are an important part of the policymaking process. According to Lindbloom (1980), interest groups are an “indispensable” (p. 85) part of making policy deci- sions. They provide a way to give a voice to their mem- bers, who may not otherwise feel able to participate effectively in the policymaking process.

▸ Conclusion This journey through the policymaking process in the United States was intended to provide you with an understanding of policy and a context for your discus- sions and analysis of health policy issues. It is vital that you become familiar with both the nature of policy and the institutions that make and influence policy. As you have seen, the definition of policy is subject to much debate, yet it is necessary to define what policy means before attempting to engage in policy analysis. We have also walked through the specific duties and powers of the executive and legislative branches of the federal government and included key points about state-level policymaking as well. Finally, all policy students must be aware of and understand the influ- ence of interest groups. They have and use numerous opportunities to influence the policymaking process, and their strength and concerns must be accounted for when analyzing policy issues. As you move further into health policy study, use the information provided in this overview to help you think about and frame your own policy positions.

References Administrative Procedure Act of 1946, 5 U.S.C. § 500 (2018). America’s Essential Hospitals. (n.d.). Mission and service. Retrieved

from https://essentialhospitals.org/about-americas-essential -hospitals/mission-driven-and-ready-to-serve/

Center on Budget and Policy Priorities. (n.d.). About the center. Retrieved from https://www.cbpp.org/about/mission -history

Davidson, R. H. (1984). The presidency and the Congress. In M. Nelson (Ed.), The presidency and the political system (p. 371). Washington, DC: Congressional Quarterly Press.

Department of Veterans Affairs. (n.d.). Veterans Health Administration. Retrieved from https://www.va.gov/health /aboutVHA.asp

Hanley, B. E. (1999). Policy development and analysis. In J. K. Leavitt, D. J. Mason, & M. W. Chaffee (Eds.), Policy and politics in nursing and health care (3rd ed., pp. 125–138). Philadelphia, PA: W. B. Saunders.

Heitshusen, V. (2018). Introduction to the legislative process in the U.S. Congress (CRS Report No. R24843). Retrieved from https://fas.org/sgp/crs/misc/R42843.pdf

Heritage Foundation. (n.d.). About Heritage. Retrieved from https://www.heritage.org/about-heritage/mission

House Committee on the Budget Majority Caucus. (2001). Basics of the budget process. Washington, DC: U.S. Government Printing Office.

H.R. Doc. No. 106-216, at 40–50 (2000). Kernell, S. (1997). Going public: New strategies of presidential

leadership (3rd ed.). Washington, DC: CQ Press. Lindbloom, C. (1980). The policy-making process. Englewood

Cliffs, NJ: Prentice-Hall.

Longest, B. B., Jr. (2016). Health policymaking in the United States (6th ed.). Chicago, IL: Health Administration Press.

Pharmaceutical Research and Manufacturers of America. (n.d.). Our mission. Retrieved from https://www.phrma.org/about /our-mission

Rein, L. (2018, May 23). Congress sends massive veterans bill to Trump, opening door to more private care. The Washington Post. Retrieved from https://www.washingtonpost.com/politics /congress-sends-massive-veterans-bill-to-trump-opening -door-to-more-private-health-care/2018/05/23/48e91220 -5e a8-11e8-a4a4-c070ef53f315_stor y.ht m l?nore dire c t =on&utm_term=.6661a7a87de9

Ryan White Comprehensive AIDS Resources Emergency Act of 1990, 42 U.S.C. § 300ff (2000).

Senate Committee on the Budget. (1998). The congressional budget process: An explanation. Washington, DC: U.S. Government Printing Office.

Subcommittee on Health and Environment of the Committee on Interstate Commerce, U.S. House of Representatives. (1976). A discursive dictionary of health care. Washington, DC: U.S. Government Printing Office.

Turnock, B. J. (2016). Public health: What it is and how it works (6th ed.). Burlington, MA: Jones and Bartlett Learning.

Waisanen, B. (2010). State tax and expenditure limits. Retrieved from http://www.ncsl.org/research/fiscal-policy/state-tax-and -expenditure-limits-2010.aspx

Weissert, C. S., & Weissert, W. G. (2002). Governing health: The politics of health policy (2nd ed.). Baltimore, MD: Johns Hopkins University Press.

U.S. Const. amend. XXII, § 1.

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U.S. Const. art. I, § 1. U.S. Const. art. I, § 2. U.S. Const. art. I, § 3. U.S. Const. art. I, § 8. U.S. Const. art. II, § 1.

Yoder, E. (2016, November 9). Trump and the federal workforce: Five key issues. The Washington Post. Retrieved from https:// w w w. w a s h i n g t onp o s t . c om / n e w s / p ow e r p o s t / w p / 2 0 1 6 /11/09/trump-and-the-federal-workforce-five-key-issues/? noredirect=on&utm_term=.4e8c427f5046

▸ Endnotes a. Under Article 1 of the Constitution, Congress

has jurisdiction over the District of Columbia. Both the Senate and the House have commit- tees that oversee some governmental functions of the District. The District elects two “shadow senators” who are allowed to lobby Congress on issues but who do not have voting rights. In terms of representation, this places the District in a position similar to other political bodies admin- istered by the United States, such as Puerto Rico, the U.S. Virgin Islands, and American Samoa. The District’s shadow senators (and a shadow representative in the House) were created by the citizens of the District in anticipation of the passage of the 1978 District of Columbia Voting Rights amendment to the U.S. Constitution,

which would have granted the District the same voting rights as the states. The amendment never passed, but the District government has main- tained the shadow positions nonetheless.

b. In addition to the 435 representatives, Puerto Rico has a resident commissioner, and the District of Columbia, Guam, the U.S. Virgin Islands, and American Samoa each has a del- egate who is allowed to sponsor legislation and vote in committees, but may not vote on the House floor. The citizens of the District of Columbia also elect a nonvoting shadow repre- sentative.

c. In circumstances where the president serves 2 years or less of the term of another president, that president may hold office for 10 years.

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CHAPTER 3

Law and the Legal System LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe the role of law in everyday life ■ Define the term “law” ■ Identify the various sources of law ■ Describe key features of the legal system

“It is perfectly proper to regard and study the law simply as a great anthropological document.”

—Former U.S. Supreme Court Justice Oliver Wendell Holmes (1899, p. 444).

▸ Introduction

The importance and complexity of law and the legal system in the United States cannot be overstated. Law’s importance stems from its primary purpose: to function as the main tool with which we organize ourselves as an advanced, demo- cratic society. The complexity of law and the legal pro- cess is a function of the multiple sources of law that may apply to any one of the millions of actions and interactions that occur daily in society, the division of legal authority between the federal and state govern- ments and among the branches within them, the lan- guage the law and its players use to express themselves, and more. For all its complexity, however, there is also an undeniable pervasiveness and openness when it comes to law. We are not left to wonder where it comes from or how it is made. Generally speaking, we are privy to lawmakers’ rationales for the laws they write and to judges’ reasoning for their legal opinions, just

as we are generally privy to the process by which law is made, and once made, laws are not hidden from us; to the contrary, they are discussed in the media and catalogued in books and online services available for public consumption. (Indeed, one is expected to know what the law is, since its violation can have potentially severe consequences.) If you want to know more about law than the average person, you can study it formally in law and other schools, or you can consult with one of the million or so lawyers in practice today. In other words, although law is complicated, it is equally acces- sible in a way that may not be clear at first blush.

Furthermore, beyond the law’s sheer pervasive- ness lies another simplicity: as the quotation at the outset of this chapter implies, the study of law is in essence the study of human beings, particularly their evolving customs, beliefs, and value systems. Because law is the key tool with which we regulate social behav- ior, it stands to reason that it also reflects our foremost values and normative standards. Indeed, law “takes an

33

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understanding, a norm, an attitude, and hardens it into muscle and bone” (Friedman, 2002, p. 29); however, this is subject to change, for as our society evolves, so too does our law. A relevant example of legal evolu- tion can be seen in the updating of state public health laws, which before the tragic events of September 11, 2001, and the subsequent anthrax scare had not been updated in most states for over a century. Soon after the 2001 attacks, however, many states, concerned about new risks to the public’s health, reviewed and overhauled these laws (Ziskin & Harris, 2007).

This chapter begins by briefly considering the role law plays in everyday life, and then turns to defin- ing law and describing its multiple sources. It then discusses several key features of the legal system, including the separation of powers among branches of government, federalism (i.e., the separate sovereignty and authority of the federal and state governments), the role of courts, due process, and more.

For some, reading this chapter may bring to mind a course you have taken or a book you have read on civics or government. In this case, the chapter should serve as a helpful refresher. For those of you new to the study of law, consider the following pages a condensed but important introduction to one of the most criti- cal and influential aspects of the society in which you live. In either event, this chapter is designed to better position you to understand the law’s application to the specific fields of health care and public health and to digest the health policy and legal concepts discussed in this textbook.

▸ The Role of Law The law reaches into nearly every corner of American life. Its impact is inescapable from the moment you wake up to the time you go back to sleep at night (and perhaps beyond, if your community has a curfew or other means of controlling activity and noise after dark). Have you ever stopped to think about the regu- lations pertaining to the flammability of the mattress you sleep on, or the safety of the water you shower with, cook with, and drink? How about the consumer protection laws regulating the quality of the food you eat throughout the day, and the quality of the estab- lishments that serve it? Then there are the laws per- taining to the safety of the cars, buses, and subways you travel in each day, and the traffic laws that control their movement. You encounter laws daily pertaining to the environment, property ownership, the work- place, civil rights, copyright, energy, banking, and much more. And these are just the laws implicated by the relatively mundane actions of day-to-day life.

Steering into activities that are not as common—say, international travel, or adoption, or being admitted to a hospital—you encounter the law swiftly and notice- ably. If you need final proof of the ubiquitous nature of law, pick up today’s newspaper and count how many stories have some sort of legal angle to them. Then do it tomorrow and the next day. What you will almost certainly find is that a great majority of the stories concern law or legal process.

The law’s pervasive nature is no surprise, given the important societal role we assign to it—namely, to serve as the tool with which we govern our relation- ships with one another, our government, and society at large. A society as sprawling and complex as ours needs formal, enforceable rules of law to provide a measure of control (for example, the need to regulate entities or actions that are potentially dangerous or invidious—a polluting power plant, or acts of discrimination based on race or gender). Furthermore, many people believe that law should be used not just to organize and con- trol the society in which we live, but to achieve a more just society; in other words, according to this view, the country’s key organizing principle should not simply be grounded in law, but rather grounded in a legal sys- tem designed to affirmatively produce outcomes based on fairness, justice, and equality (Smith, 1991).

The main way the law governs the many kinds of relationships in society is to recognize and establish enforceable legal rights and responsibilities that guide those relationships, and to create the institutions nec- essary to define and enforce them. Take constitutional law, for example. Constitutions are charters establish- ing governments and delineating certain individual and governmental rights and obligations. However, constitutional provisions are triggered only when one party to a relationship works for or on behalf of the gov- ernment, whether federal or state. Thus, constitutional law governs the relationship between individuals and their government—not, for example, the relationship between two private parties, even when one party’s actions are clearly discriminatory or wrongful. Thus, it takes affirmative action by a governmental actor to trigger constitutional protections. So, although it would be a violation of a public school student’s First Amendment right to be forced by his principal to pray in class, forced prayer in private schools passes consti- tutional muster.

A legal right (constitutional or otherwise) denotes a power or privilege that has been guaranteed to an individual under the law, not merely something that is claimed as an interest or something that is a matter of governmental discretion. Conceptually, legal rights derive from the fact that the government sometimes creates what are called individual “property rights”—a

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generic term referring to an entitlement to personal or real property—for specified groups of persons (Reich, 1964). Importantly, legal rights also presup- pose that their enforcement can be achieved through public institutions, including state and federal courts, because a person’s ability to secure a remedy when a legal right is denied, reduced, or terminated goes to the very heart of what it means to be “entitled” to some- thing. Indeed, whether particular healthcare benefits rise to the level of being a legal “right” and whether the healthcare right can be enforced in court are two of the most fundamental legal questions in the area of healthcare law. For example, the federal Medicare program for the aged and disabled confers on eligible individuals not only the right to healthcare services, but also the ability to enforce their right to benefits when program violations occur.

▸ The Definition and Sources of Law

Defining “Law” Although many legal scholars agree on the general function of law in society, there is far less consensus on how to define “the law.” As with many legal terms, there are several plausible interpretations of what is meant by the law, and thus there is no single way to correctly define it. For example, Black’s Law Dictionary includes the following definitions in its primary entry:

That which is laid down, ordained, or estab- lished. A rule or method according to which phenomena or actions co-exist or follow each other. Law, in its generic sense, is a body of rules of action or conduct prescribed by con- trolling authority, and having binding legal force. That which must be obeyed and fol- lowed by citizens subject to sanctions or legal consequences is a law. (Garner, 2014, p. 884)

However, even these commonly accepted defi- nitions are not entirely satisfactory, because “a body of rules” that “must be obeyed” in the face of “sanc- tions or legal consequences” necessarily envisions a process by which the rules are created, disseminated, enforced, violated, disputed, interpreted, applied, revised, and so on. Considered in this way, “the law” essentially amounts to a “legal system”—and a system, by definition, entails regularly interacting or interde- pendent parts and subparts coming together to form a functional, unified whole. As you read this text, think of “the law” not just as words on a page (e.g., codified statutes or regulations), but as the many interacting

parts that are involved in drafting those words in the first place, and in bringing them to life once they have been enacted as laws. Note that this broad conceptu- alization of law as a system squares nicely with the primary purpose of law described previously, because there must, by necessity, be a sizeable system in place if law is going to carry out its role as the primary orga- nizing tool in society. This broad definition of law also encompasses key legal doctrines, like separation of powers and federalism, described later in this chapter.

Sources of Law Regardless of the breadth of the definition attached to the term law, at the core of the nation’s expansive legal system lies a body of enforceable written rules meant to maintain order, define the outer limits of our interactions with one another and with our govern- ments, and delineate legal rights and responsibilities. These rules derive from several sources, which collec- tively are called primary sources of law. The sources of primary legal authority include constitutions, stat- utes, regulations, and common (i.e., judge-made) law. There are also secondary sources of law, which are not laws in the technical sense, but rather are a collection of treatises, law review articles, reports, legal encyclo- pedias, and more that analyze, interpret, and critique primary laws. This section discusses each of the four types of primary sources of law.

Constitutions A constitution is a charter that both establishes a gov- ernment and delineates fundamental rights and obli- gations of that government and of individuals who fall within the territory covered by the constitution. In this country, there is a federal constitution and separate constitutions in each of the 50 states. The Constitution of the United States, completed in 1787 and subse- quently ratified in each of the original 13 states, took effect in 1789. It provided for a federal union of sov- ereign states, and a federal government divided into three branches (legislative, executive, and judicial) to operate the union. This governmental structure was not easily agreed upon. Prior to the creation of the fed- eral Constitution, the colonies of the American War of Independence first adopted, in 1777, the Articles of Confederation, which represented the first formal governing document of the United States and which were ratified in 1781. However, a defining feature of the Articles was a weak national government; fairly quickly, a movement for a stronger central govern- ment took hold, the colonies elected to throw out their original plan, and the Constitutional Convention— and with it the Constitution—was born.

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The federal Constitution is rather short and, for the most part, quite general. One explanation for this is that the framers of the Constitution viewed it as a “document for the ages” that needed to include endur- ing principles to serve a growing, evolving society that has certainly proved to be more complex than it was at the time of the Constitution’s ratification. In the words of former U.S. Supreme Court Justice Robert Jackson, the Constitution is a compilation of “majestic general- ities” that collect meaning over a span of many years (Fay v. New York, 1947).

But the fact that some of the most important con- stitutional provisions are written in broad terms leads to many thorny legal controversies, because there are many competing approaches and theories as to how courts should interpret ambiguous constitutional phrases. Broadly speaking, the leading approaches to constitutional interpretation include the “living constitution,” the “moral constitution,” “originalism,” and “strict constructionism.” The living constitu- tion model reflects a belief that the broadly written Constitution should be interpreted to reflect current moral, political, and cultural values in society, not the values that were predominant at the time of the Con- stitution’s ratification. Under this view, the meaning of the Constitution is not fixed, but instead evolves along with society. Moral constitutionalists infuse their interpretation of constitutional law with princi- ples of moral philosophy. Originalism, technically, is an umbrella term referring to a small group of con- stitutional interpretation theories, all of which share a common belief that constitutional provisions have a fixed and knowable meaning. For example, “original intent,” one well-known theory under the originalism umbrella, adheres to the position that constitutional interpretation should be consistent with the intent of the Constitution’s original drafters. Finally, strict constructionists limit their interpretation to the Con- stitution’s actual words and phrases, and decline to consider contextual factors such as shifts in societal values or the commentaries or intent of the framers. The most well-known interpretational controversy in the area of health pertains to the breadth and reach of the due process clause of the federal Constitution’s 14th Amendment, which prohibits states from depriv- ing “any person of life, liberty, or property, without due process of law” (U.S. Const. amend. XIV, § 1). This provision rests at the heart of the Supreme Court’s “right to privacy” jurisprudence, including the right to obtain an abortion. For readers interested in theories of constitutional interpretation, there is a vast body of literature at your disposal (Baker, 2004; Fallon, 1999).

One of the general principles underpinning the Constitution is that citizens should not be subjected to

arbitrary and oppressive government. Given that the Constitution was drafted on the heels of the Revolu- tionary War, this is no surprise. But one consequence of the prevailing mood of the framers toward the reach of a national government is that they drafted the Constitution with an eye toward limiting federal gov- ernment, as opposed to viewing the Constitution as a vehicle for extending benefits to the public—in other words, that “the men who wrote the Bill of Rights were not concerned that government might do too little for the people but that it might do too much to them” (Jackson v. City of Joliet, 1983). This logic helps explain why several key constitutional provisions were drafted in “negative” terms—the First Amendment prohibits government from abridging free speech, the Fourth Amendment makes unreasonable searches illegal— rather than as conferring positive rights, like a gener- alized right to receive healthcare services. At the same time, the First and Fourth Amendments, along with eight others, make up the Bill of Rights, a series of important, specifically guaranteed rights in the Con- stitution the framers believed to be inalienable.b

In addition to the federal Constitution, each state has its own constitution. All state constitutions are like the federal one in that they provide for the organiza- tional structure of the particular state’s government, and all contain some measure of a state bill of rights. Here the similarities can end, however. Although state constitutions cannot limit or take away rights con- ferred by the U.S. Constitution (or by federal statutes), some state constitutions go further than federal law in conferring rights or extending protections. For exam- ple, under current U.S. Supreme Court case law, the death penalty does not always violate the federal Con- stitution, but the Massachusetts Supreme Court has ruled that the death penalty is prohibited under the state’s constitution in every instance. Maryland’s con- stitution requires that a jury be unanimous in order to convict a person of a crime, a standard that differs from federal criminal law. Furthermore, state consti- tutions are amended much more easily and frequently than is their federal counterpart. While state constitu- tions have been amended, on average, 150 times per state (Dinan, 2018, p. 23), the language of the federal Constitution has not been dramatically altered since its inception; there have been just 27 amendments, and the 10 that make up the Bill of Rights were all added by 1791.

Statutes Statutes are laws written by legislative bodies at all levels of government (federal, state, county, city) that, generally speaking, command or prohibit something.

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It is the fact of their being legislatively created that sets them apart from other sources of law, because legislatures are understood as creating laws that are forward-looking and apply to large numbers of peo- ple. Indeed, the two hallmarks of statutes are their prospectivity and generality. These hallmarks result mainly from the fact that legislatures are in the “reg- ulation business” across an enormous array of issues, and as a result, legislators often lack both the time and the substantive expertise to regulate other than in broad fashion.

Because statutes tend to be written as broad policy statements (and because words on a page can never communicate intent with absolute accuracy), there are few statutes that are utterly unambiguous. This, coupled with the fact that our evolving society con- tinuously presents situations that may not have been foreseeable at the time a statute was written, results in the need for courts to interpret and apply general statutes to millions of specific legal cases or contro- versies. This practice is called “statutory construction.” Although it is a tenet of the separation of powers doc- trine (discussed later under Key Features of the Legal System) that legislatures represent the law-making branch of government and the judiciary’s role is to interpret law, it is commonly understood that judges and courts “make” law as well through statutory con- struction, because the continual interpretation and application of broad policy statements (i.e., statutes) can put a “gloss” on the original product, potentially altering its meaning over time.

As discussed more fully later in the section on federalism, state legislatures have greater ability than does Congress to use statutes to regulate across a broad range of issues, pursuant to states’ plenary authority under the Constitution. For instance, the number of state statutes regarding population health and safety (e.g., disease control and prevention, the creation of public health agencies, the ability of governors to classify public health emergencies) far exceeds con- gressional output on the same topic. Notwithstanding states’ broader regulatory power, however, federal stat- utes have primacy over state statutes.

Administrative Regulations The fact that statutes are written in broad generali- ties has another consequence beyond their need to be interpreted and applied in vast numbers of unique instances: specific regulations must be written to assist with the implementation of statutory directives and to promote statutes’ underlying policy goals. This is where administrative agencies of the executive branch of government come in. Because these federal and

state agencies—the U.S. Department of Health and Human Services, the U.S. Department of Labor, the California Department of Social Services, the Wiscon- sin Department of Commerce, and so on—are orga- nized and created to deal with specific policy subject matters, they have more time and expertise than Con- gress or state legislatures have to enforce statutes and promulgate regulations, rules, and orders necessary to carry out statutory prerogatives. It is important to note that assuming the process for creating the regulations was itself legal, and provided that the regulations do not stray beyond the intent of the enacted statute, reg- ulations have the full force of law.

Administrative law is crucial in the area of health policy and law.c For example, consider the Medicaid program, which functions primarily as a health insur- ance program for low-income individuals. The Medic- aid statute embodies Congress’s intentions in passing the law, including standards pertaining to program eligibility, benefits, and payments to participating healthcare providers. Yet there are literally thousands of administrative regulations and rules pertaining to Medicaid, which over the past 50 years have become the real battleground over the stability and scope of the program. In a very real sense, the Medicaid regulations passed by the federal Department of Health and Human Services and state-level agencies are what bring the program to life and give it vitality. This “operationaliz- ing” function of administrative law can be seen across a wide spectrum of important health issues, including the reporting of infectious diseases, the development of sanitation standards, and the enforcement of envi- ronmental laws (Mensah et al., 2004). In order to be lawful, regulations must be proposed and established in a way that conforms to the requirements of the federal Administrative Procedure Act of 1946 (APA), which provides procedural restrictions for agency rule making and adjudication. Compared to state admin- istrative procedure acts, which tend to be technical and detailed, the APA is broad and sweeping, thus relatively more ambiguous and open to various inter- pretations by federal courts.d Once Congress delegates rule- making authority to an executive branch agency via a statute (known as the “enabling statute”), the APA dictates how the agency must go about promulgating specific rules and regulations, unless the statute itself specifies the procedure an agency must follow. If the enabling statute dictates a formal rule-making process, the APA requires the agency to follow cumbersome procedures, and it can adopt rules only after a trial- like hearing on the proposed rule. If Congress does not specify in an enabling statute how an agency must adopt rules, the APA permits the agency to follow a more informal rule-making process. This requires the

The Definition and Sources of Law 37

 

 

agency to publish the proposed rule in the Federal Reg- ister (the official daily publication for rules, proposed rules, and notices of federal agencies) and provide an opportunity for the public to comment on the pro- posed rule. The agency must take the comments under consideration (though it need not revise the proposed rule in response to them), and once it settles on a final rule, it must be published in the Code of Federal Reg- ulations (which houses permanent federal regulations under 50 separate titles representing broad areas sub- ject to federal oversight).

In delegating authority to an agency through an enabling statute, Congress must provide an “intelligi- ble principle” that the agency can (and must) follow. That said, the amount of direction and discretion given to agencies varies widely. For example, the enabling statute for the Occupational Health and Safety Admin- istration provides broad discretion by delegating the authority to create and enforce workplace safety stan- dards (Occupational Health and Safety Act of 1970). Contrast this with the Americans With Disabilities Act, which has very specific provisions and does not allow agencies much discretion when implementing and enforcing the statutory language.

In addition to the power of rule making, Congress may also delegate adjudicatory and enforcement pow- ers to administrative agencies. Adjudicatory power refers to claims of public rights, which are claims that involve private persons as one party and the govern- ment as the other party (excluding criminal cases). Congress may set up a court, known as an administra- tive court, within an agency to adjudicate these claims. Because these courts are located in the executive, rather than judicial, branch of government, they are not subject to the same rules and procedures as tradi- tional courts, although they still must provide for the rights and protections prescribed by the Bill of Rights (e.g., the right to legal counsel). Administrative hear- ings are often much less formal than judicial trials: there are no juries, and although some evidence may be gathered through witness testimony, the majority of evidence derives from written reports. Decisions by administrative law judges (known as ALJs) often do not represent the final word on the matter being adjudicated, as these decisions are subject to approval or rejection by the agency’s lead official or by a tra- ditional (judicial branch) federal court. At the same time, federal courts generally apply a deferential stan- dard of review to administrative decisions, reviewing only to see whether an agency has acted in an “arbi- trary and capricious” manner.

The third type of authority granted to agencies by Congress is that of enforcement. As this author- ity already inherently resides in the executive branch

under the federal Constitution, Congress uses its power to specify which agencies have authority to enforce certain statutes and substantive areas of law.

Once Congress grants power to agencies to pro- mulgate rules, adjudicate claims, and enforce stat- ues, its ability to constrain agency action is limited. Because agencies are located in the executive branch and thus are under the control of the president, Con- gress is limited to passing a new statute overturning the questioned agency action or investigating agency action for impropriety.

Common Law In each of the prior discussions about constitutions, statutes, and administrative regulations, we pointed out the generality and ambiguity of much of law, and the corresponding responsibility of courts to interpret and apply law to specific cases. It is via the common law—essay-like opinions written by appellate courts articulating the bases for their decisions in individual cases—that courts carry out this responsibility. Com- mon law is also referred to as case law, judge-made law, or decisional law.

Common law is central to legal systems in many countries, particularly those that were territories or colonies of England, which is how the United States came to rely on common law as part of its legal sys- tem. Both historically and in modern times, case law is premised on the traditions and customs of society, the idea being that courts could continuously (and relatively efficiently, compared to the legislative pro- cess) interpret and apply law in such a way as to match the values of a society undergoing constant evolution. At the same time, the common law is heavily influ- enced by legal precedent and the doctrine of stare decisis, which refers to the legal principle that prior case law decisions should be accorded great deference and should not be frequently overturned. The impor- tance and function of stare decisis in American law is discussed later in the section detailing the role courts play in maintaining stability in the law.

Although courts are expected to overturn their own prior decisions only in rare circumstances and lower courts can never overturn decisions by higher courts that have jurisdiction over them, legislatures can modify or even overturn common law decisions interpreting statutes and regulations. Imagine that the U.S. Supreme Court interpreted a federal civil rights statute as protecting individuals from intentional acts of race discrimination, but not from conduct that has the unintended effect of discriminating against racial minorities. If Congress disagreed with the court’s interpretation of the statute, it could effectively

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overturn the court’s decision by amending the statute to make it clear that the law was intended to prohibit intentional discrimination and presumably neutral acts that nonetheless resulted in unintended discrimi- nation. However, because the judicial branch has final authority to determine whether statutes violate the federal Constitution, Congress would be powerless to overturn a federal court decision that ruled the same civil rights statute unconstitutional.

Notice the “checks and balances” at play in this example, with one branch of government acting as a restraint on another. In the next section, we discuss the separation of powers doctrine—including checks and balances—and other key features of the legal system. But first, see TABLE 3-1, which provides a summary of the sources of law.

▸ Key Features of the Legal System

Recall the earlier description of the law as something more than just words on a page, something more than statutes and constitutional provisions. Although the

laws themselves are obviously critical, they are just one component of a complex, interacting legal system that creates the laws in the first instance and brings them to life after they hit the pages of legal code books, texts, and treatises.

All legal systems rest on unique principles, tradi- tions, and customs. This section describes a handful of the most important features and principles of the U.S. legal system, including the separation of powers doctrine, federalism, the role and structure of federal and state courts, judicial review, due process, and con- stitutional standards of review.

Separation of Powers This country’s government, both federal and state, has an underpinning structure of three independent and equally powerful branches, a fact that sets it apart from parliamentary systems of government—such as those found in Canada, Germany, the United Kingdom, and many other countries—in which the legislature appoints the executive. The legal doctrine that sup- ports the arrangement of shared governance among multiple branches is the separation of powers doctrine. This doctrine is considered one of the most important

Key Features of the Legal System 39

TABLE 3-1 Summary of the Primary Sources of American Law

Source of Law Key Points

Constitutions ■ Establish governments and delineate fundamental rights and obligations of government and individuals.

■ There is a federal constitution and separate constitutions in each state. ■ The federal constitution restrains government more than it confers individual rights;

however, the Bill of Rights specifically guarantees several important individual rights. ■ The Supreme Court has the final word on the constitutionality of laws created by the

political branches of government.

Statutes ■ Created by legislatures at all levels of government. ■ Two hallmarks: prospectivity and generality. ■ As broad policy statements, statutes are often ambiguous as applied to specific cases

or controversies, requiring courts to interpret them through the practice of statutory construction.

■ State legislatures can use statutes to regulate across a broader range of issues than can Congress; however, federal statutes have primacy over conflicting state statutes.

Regulations ■ Created by executive branch administrative agencies to implement statutes and clarify their ambiguities.

■ Play a particularly critical role in health policy and law.

Common law ■ Court opinions interpreting and applying law to specific cases. ■ Also referred to as case law, judge-made law, or decisional law. ■ Based on the traditions and customs of society, yet heavily influenced by legal precedent

and the doctrine of stare decisis.

 

 

aspects of both federal and state constitutional design. The framers of the U.S. Constitution were well aware that nothing was more likely to foster tyrannical gov- ernment than the concentration of governing powers in one person or political party. To guard against a concentration of political power, the framers did two related things: they divided governmental powers and responsibilities among separate, coequal branches, and they structured the elections of officials for the two political branches of government (legislative and executive) so that they would take place at different intervals and through different mechanisms (e.g., the president is elected through the electoral college sys- tem, whereas members of Congress are not).

Inherent in the separation of powers doctrine is the important concept of checks and balances. “Checks” refers to the ability and responsibility of one branch of government to closely monitor the actions of the other two, including when one branch grasps at an amount of power not envisioned by the Con- stitution. The “balance” at work in the separation of powers framework prevents one branch from exerting power in an area of responsibility that is the province of another branch.

The constitutional doctrine of separation of pow- ers represents, in the words of one legal scholar, an “invitation to struggle for the privilege” of governing the country (Corwin, 1957, p. 171). Alexis de Tocque- ville, a French philosopher and political theorist who studied American government in the 1830s, viewed the concept of checks and balances in much starker terms:

The president, who exercises a limited power, may err without causing great mischief in the state. Congress may decide amiss with- out destroying the union, because the elec- toral body in which the Congress originates may cause it to retract its decision by chang- ing its members. But if the Supreme Court is ever composed of imprudent or bad men, the union may be plunged into anarchy or civil war. (de Tocqueville, 1835, p. 152)

For example, a fairly common separation of powers debate between Congress and a president concerns the nation’s soaring debt and the appropri- ateness of raising the debt ceiling. Some policymak- ers (and many presidents) maintain that the president can act unilaterally to raise the debt ceiling and allow the federal government to borrow more money, while others argue that such a move is solely within the purview of Congress and beyond the scope of pres- idential power.

Throughout this text, there are health policy and law questions that distinctly highlight our government’s divided powers. For instance, how will the struggle between the executive branch and some members of Congress over implementation of the Affordable Care Act (ACA)—the former attempting to thwart imple- mentation through fiscal, policy, and legal channels, while those in Congress who supported the ACA aim to keep the ACA functioning as fully and efficiently as possible—play out? And how has the Supreme Court applied its constitutional right to privacy jurispru- dence to the matter of abortion in response to federal and state legislative enactments? As you consider these and other health policy and law questions from a sep- aration of powers angle, consider the peculiar roles of each branch of government, taking into account their duties, powers, and limitations. Through this prism, continually reflect on which governmental body is best equipped to effectively respond to health policy problems.e

Federalism: Allocation of Federal and State Legal Authority In the legal system, the powers to govern, make and apply law, and effect policy choices are not just appor- tioned among three governmental branches at both the federal and state levels; they are also divided between the federal government and the governments of the various states. This division of authority—which also plays a key role in the development of health policies and laws—is referred to as federalism. Like the separa- tion of powers doctrine, federalism derives from the U.S. Constitution.

Under the Constitution, the federal government is one of limited powers, while the states more or less retain all powers not expressly given to the federal government. In essence, this was the deal consented to by the states at the time our federal republic was formed: they agreed to surrender certain enumerated powers (like foreign affairs) to the federal government in exchange for retaining many aspects of sovereignty.

The Constitution’s 10th Amendment states that “the powers not delegated to the United States by the Constitution . . . are reserved to the States respec- tively.” For example, because the Constitution does not explicitly define the protection and promotion of the public’s health as a power of the federal govern- ment, public health powers are primarily held by the states. (In fact, compared to the federal government, the states handle the vast majority of all legal matters in this country. Consider just a sampling of typical legal affairs overseen by state government: marriages,

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divorces, and adoptions; law enforcement and crim- inal trials; schooling; driving, hunting, medical, and many other licenses; consumer protection; and much more [Adelson, 2003, pp. 481–488]. Furthermore, the vast majority of all litigation that takes place occurs in state, rather than federal, courts [Refo, 2004, p. 3].) As a result, all states regulate the area of public health through what are known as their “police powers,” which allow state and local governments to (among other things) legislate to protect the common good. Exam- ples of the kinds of laws passed under this authority include childhood immunization standards, infectious disease data collection mandates, and environmental hazard regulations. Moreover, under the 10th Amend- ment, states historically have had the power to regulate the practice of medicine and the licensing of hospitals and other healthcare institutions.

Recall, however, that the federal government also plays a role in regulating health care and public health. The national government’s enumerated powers include the ability to tax, spend, and regulate interstate commerce, all of which have been utilized in ways to improve health care and promote public health. For example, Congress has used its taxing power to increase the cost of cigarettes (in the hopes of driv- ing down the number of smokers) and to generate funds for programs such as Medicare, and congres- sional spending powers are the legal cornerstone for federal health programs like Medicaid. Furthermore, the sharing of power under the 10th Amendment notwithstanding, the Constitution’s supremacy clause declares that federal laws—the Constitution, statutes, and treaties—are the “supreme” law of the land, and thus preempt state laws that conflict with them (U.S. Const. art. VI, para. 2).

While federalism is built solidly into the nation’s political branches through separate federal and state legislatures and executives, it is also on display in the structure of U.S. courts. There are both federal and state court systems, and each has unique authority and jurisdiction: federal courts are limited to ruling only in certain kinds of cases, including those involving federal constitutional or statutory law, those in which the United States is a party to the lawsuit, and those specified by statutory law; state courts, by contrast, have jurisdiction to hear just about any case (unless explicitly precluded from doing so by federal statute), including those over which federal courts also have jurisdiction. State court jurisdiction includes cases implicating state statutory and regulatory law, the state constitution, and the U.S. Constitution.

Over the years, defining the boundaries of feder- alism (i.e., defining the federal government’s sphere

of authority and determining the scope of state sov- ereignty) has been a contentious legal and political issue. At the dawn of the country’s independence, after the colonies scrapped the Articles of Confeder- ation in favor of a stronger central government, the Supreme Court decided federalism cases with a nod toward expansive national powers (much to the dislike of some states). Two famous cases make the point. In the 1819 case of McCulloch v. Maryland, the Supreme Court enhanced the power of the U.S. government by establishing the principle that federal governmental powers are not strictly limited to those expressly pro- vided for in the Constitution. At issue in the case was whether Congress had the power to charter a national bank to help the federal government shoulder war- time debt. In 1824, the court for the first time had the opportunity to review the Constitution’s commerce clause (which grants Congress the authority to reg- ulate interstate commerce) in the case of Gibbons v. Ogden (1824), which resulted from a decision by the state of New York to grant a monopoly to a steam- boat operator for a ferry between New York and New Jersey. Again, the court ruled broadly in favor of the federal government, stating that the commerce clause reserved exclusively to Congress the power to regulate interstate navigation.

By the mid-1800s, however, this approach to defining the relative power of the federal and state gov- ernments gave way to one that was more deferential to states and more willing to balance their sovereign interests against the interests of the federal govern- ment. This approach, in turn, lost ground during the New Deal and civil rights eras, both of which were marked by an acceptance of federal authority to pro- vide social services and regulate the economy. The arrival of Ronald Reagan’s presidency in 1981 marked yet another turning point in the evolution of federal- ism. For 8 years, the Reagan administration acted to restrict national authority over the states, a process that took on even more force after the Republican Party took control of Congress in the mid-1990s. Indeed, since the early 1980s, a defining feature of federalism has been the purposeful devolution of authority and governance over social and economic policy from the federal government to state legislators and regulators.

The Role of Courts Elsewhere, we have discussed the structure and pow- ers of two of the political branches of government: the legislative and executive branches. The third branch is that of the judiciary, made up of justices, judges, mag- istrates, and other “adjudicators” in two separate court

Key Features of the Legal System 41

 

 

systems—one federal, one state. Although the fed- eral and state court systems have critically distinctive authority, they do not look very different structurally. The federal court system has three tiers, with cases proceeding from the lowest-level court (a trial court) to two separate, higher-level courts (appellate courts). Federal trial courts are called district courts, and they exist in varying numbers in each state, with the size of the state determining the actual number of “districts,” and thus the number of federal trial courts. In total, there are nearly 100 federal district courts. After a district court renders a decision, the losing party to a lawsuit is entitled to appeal the decision to a federal circuit court of appeals. There are 13 U.S. circuit courts of appeals—12 with jurisdiction over designated mul- tistate geographic regions, or “circuits,” and a court of appeals for the federal circuit (residing in Washington, DC), which has nationwide appellate jurisdiction over certain kinds of cases, such as patent and international trade disputes. For many individuals, losing a case in a federal circuit court represents the end of the line for their case, since litigants have no entitlement to have their case heard by the U.S. Supreme Court, the high- est court in the country. Although parties have a right to petition the Supreme Court to hear their case, at least four of the nine justices on the court must agree to grant the petition. Although the Supreme Court is undeniably the most important court in the country in terms of its authority, it by no means renders the most decisions. Out of approximately 8,000 petitions annually, the Supreme Court typically accepts only 70 to 80, whereas the 13 circuit courts collectively decide approximately 61,000 cases each year. This fact is more than trivial; it effectively means that in the huge majority of federal cases, lower appellate courts, and not the Supreme Court, have final say over the scope and meaning of federal law.

As mentioned, each state also has its own court system, most of which are organized like the federal system: one trial court, followed by two separate appel- late courts (generally termed “[name of state] court of appeals” and “[name of state] supreme court”). How- ever, some state systems provide for only one appellate court. State systems also tend to include courts that are “inferior” even to their general trial courts; these han- dle relatively minor disputes (think of the small claims courts frequently shown on daytime television). Fur- thermore, state trial courts are sometimes divided by specialty, so that certain courts hear cases that involve only family matters, juvenile matters, and the like.

Within the federal and state court system hier- archy, appellate courts have two powers unavailable to trial courts: reviewing lower court decisions to

determine whether there were errors of law made during the trial that necessitate a new one, and estab- lishing legal precedents that lower courts are bound to follow. But appellate courts lack trial courts’ pow- ers to actually conduct trials, including empanelling juries, hearing testimony from witnesses, reviewing evidence, and the like. Instead, appellate reviews are generally limited to the written record created at trial by the lower court.

Adjudication refers to the legal process of resolv- ing disputes. It is in the context of resolving specific legal disputes that the judiciary interprets and applies the law, and also indirectly “makes” law under its common law authority. The results of adjudication are the common law decisions described earlier. Because U.S. courts are generally not permitted to issue advi- sory opinions, courts in this country effectively only act in response to a specific “case or controversy” that is brought to them by parties to a lawsuit. (Where permitted, advisory opinions are released by courts not in response to a particular legal dispute, but in response to a request from another branch of govern- ment regarding the interpretation or permissibility of a particular law. Federal courts are bound from issu- ing advisory opinions because the Supreme Court has ruled that constitutional provisions establishing the federal courts prevent them from reviewing hypothet- ical or moot disputes. Although a couple exceptions exist, state courts are likewise prohibited from issuing advisory opinions.) This limitation essentially means that in order for a court to rule in a particular case, an individual initiating a lawsuit must assert an enforce- able legal right, a measurable violation of that right, actual damage or harm, and a court-fashioned remedy that could appropriately respond to the lawsuit.

Courts play a vital role in the legal system. This role stems in large part from their responsibility to determine what, ultimately, the Constitution means, permits, and prohibits. In discharging this responsi- bility, courts are asked to protect and enforce indi- vidual legal rights, determine whether the political branches of government have acted in a way that vio- lates the Constitution, and maintain stability in the law through the application of legal precedent. The judicial branch is viewed as uniquely able to fulfill these key responsibilities, at least at the federal level, because it is the branch of government most insu- lated (theoretically) from politics: federal judges are appointed, not elected, and granted life tenure under the Constitution to (theoretically) shield them from political influences that might otherwise interfere with their impartiality.f Most state judges, however, are now subject to popular election, either at the time

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of initial selection or subsequently, when it is deter- mined whether they will be retained as judges (Bren- nan Center for Justice, 2015).g

Enforcing Legal Rights As described earlier, two main functions of the legal system are to establish legal rights and to create insti- tutions to enforce those rights. The primary enforc- ers of individual legal rights, and those in the best position to create remedies for their violation, are the courts. For example, the federal courts (and the Supreme Court in particular) were critical to the suc- cess of the civil rights movement, during which time federal judges expansively interpreted civil rights laws and maintained close oversight of the implementa- tion of their rulings. At the same time, however, the Supreme Court has not often been at the forefront of advancing individual rights. Certainly, there have been times when the court has played an enormous role in advancing societal expectations with respect to indi- vidual equality—Brown v. Board of Education (1954) being the most obvious example—but this decision, and a few others, are actually quite anomalous, and the court has been more a follower of evolving attitudes and expectations.

Among the most important rights courts are expected to uphold and enforce is the constitutional right to due process, which protects individuals from arbitrary and unfair treatment at the hands of govern- ment. Both the 5th and 14th Amendments to the Con- stitution make clear that no person can be deprived of “life, liberty, or property, without due process of law,” with the 5th Amendment applying to the federal government and the 14th applying to the states. An important component of due process is the principle that when government establishes a legal right or enti- tlement for individuals, it may not then decide to deny the right or entitlement unfairly.

When courts consider due process claims, they are often thought of as reviewing how laws operate and why laws have been established in the first place. This results from the fact that the due process clause has been interpreted by the Supreme Court as includ- ing procedural due process (the “how”) and substan- tive due process (the “why”). Procedural due process requires that laws be enacted and applied fairly and equitably, including procedural fairness when individ- uals challenge government infringements on their life, liberty, or property. Thus, due process requirements might be triggered if a law is too vague or is applied unevenly, if government threatens to withdraw a pre- viously granted license, or if an individual’s public

benefits are withheld. For example, before a physician can lose his state-granted license to practice medicine, the state must provide the physician advance notice of the termination and a formal hearing before an impartial examiner with all the usual legal trappings (right to legal representation, right to present evidence in one’s defense, right to appeal the examiner’s deci- sion, etc.). Similarly, Medicaid beneficiaries must be given notice of, and an opportunity to challenge, ben- efit coverage denials made by a managed care com- pany participating in the Medicaid program. And the courts’ most well-known jurisprudence in the area of health-related due process rights concerns abortion, specifically whether federal and state laws impermis- sibly infringe on the right to terminate a pregnancy, which is part of the right to “liberty” under the due process clause.

But that clause has been interpreted by courts to require more than just procedural fairness when a law deprives an individual of life, liberty, or property; it also requires that government provide a sound reason for having invaded personal freedoms in the first place. This form of due process, which is termed substantive due process, serves as a proscription against arbitrary government activity. For instance, when states have been unable to adequately explain the reasoning behind statutes requiring involuntary confinement of mentally ill individuals who were not dangerous to themselves or others, courts ruled the laws unconstitutional on substantive due process grounds. Substantive due pro- cess is unquestionably more controversial than its pro- cedural counterpart, because many critics argue that the former gives courts unrestrained power to inval- idate, on constitutional grounds, government actions with which they simply disagree. In other words, some view this form of due process “as a potentially limitless warrant for judges to impose their personal values on the Constitution” (Lazarus, 1999, p. 474).

Reviewing the Actions of the Political Branches An important piece of the separation of powers puz- zle, and one that grants the courts wide authority to enforce individual legal rights in this country, is the doctrine of judicial review. Judicial review refers to the power of the courts to declare laws unconstitutional and to determine whether the actions of the legislative and executive branches of government are lawful. The theory behind judicial review is that, as the branch of government most independent of the political pro- cess, courts can pass judgment on the actions of the political branches free of partisanship.

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Judicial review has its roots in the famous 1803 case of Marbury v. Madison, in which the Supreme Court ruled that it had the power to review acts of Congress and determine their constitutionality. The facts of the case are fascinating. In 1800, Thomas Jef- ferson won the presidential election, besting incum- bent John Adams. In the final days of President Adams’s term, the Federalist-controlled Congress passed, and Adams signed into law, a statute called the Judiciary Act of 1801. Among other things, the law created several new judgeships, and the idea was to fill the new judicial posts with Federalists before Jeffer- son assumed the presidency. Among the new judicial appointments made by Adams and approved by the Senate before Jefferson took office were 42 justices of the peace, including one for William Marbury. Prior to Jefferson’s taking office, Marbury’s commission was signed by Adams and by John Marshall—who at the time was Secretary of State under Adams—but not delivered. After his inauguration, Jefferson ruled that Marbury’s commission (and those of several other Adams-appointed justices of the peace) were invalid because they had not been delivered during the Adams presidency, and therefore directed his new Secretary of State, James Madison, to withhold deliv- ery. Marbury sued to force delivery of his commission, petitioning the Supreme Court directly to issue a writ of mandamus, which is an order by a court compelling a government officer to perform his duties. Marbury was able to ask the court directly for the writ because the recently enacted Judiciary Act also authorized the Supreme Court to issue writs of mandamus.

The Supreme Court’s decision in Marbury v. Mad- isonh first established the important principle that for every violation of a legal right, there must be a corre- sponding legal remedy. With this principle in place, the court ruled that Marbury was in fact entitled to his commission and to a legal remedy for Jefferson’s decision to withhold it,

since [Marbury’s] commission was signed by the President, and sealed by the secretary of state . . . and the law creating the office, gave the officer a right to hold for five years, inde- pendent of the executive, the appointment. . . . To withhold his commission, therefore, is an act deemed by the court not warranted by law, but violative of a vested legal right.

The Marbury court then did something monu- mental: it established and justified the power of judi- cial review. This outcome flowed from the fact that Marbury had filed his legal petition directly with the Supreme Court, and the court needed to determine

whether Congress acted constitutionally in grant- ing the court power under the Judiciary Act to issue writs of mandamus as a matter of “original jurisdic- tion.” (Original jurisdiction refers to cases on which a court rules before any other court does so, contrasted with situations in which a court reviews a decision of a lower court, which is called “appellate jurisdiction.”)

It was not apparent that the mandamus com- ponent of the new Judiciary Act was constitutional because Article III of the Constitution—which estab- lished the judicial branch of the federal government, including the Supreme Court—says,

In all Cases affecting Ambassadors, other public Ministers and Consuls, and those in which a State shall be a Party, the Supreme Court shall have original Jurisdiction. In all the other Cases [subject to Supreme Court jurisdiction], the Supreme Court shall have appellate Jurisdiction, both as to Law and Fact, with such Exceptions, and under such Regulations as the Congress shall make. (U.S. Const. art. III, § 2, clause 2)

Interpreting this clause, Chief Justice Marshall determined the court could issue a writ of manda- mus under the Constitution only as an exercise of appellate—but not original—jurisdiction, and that Congress had no power to modify the court’s original jurisdiction. As a result, the court held that the Judi- ciary Act of 1801 was in conflict with Article III, and thus unconstitutional.

Marbury represented the first time the Supreme Court exercised the power of judicial review and declared unconstitutional a law passed by Congress. Over the years, the court has exercised this power sparingly, explaining in 1867 that although it clearly had the authority to strike down congressional legis- lation repugnant to the Constitution, this “duty is one of great delicacy, and only to be performed where the repugnancy is clear, and the conflict unreconcilable” (Mayor v. Cooper, 1867).

For example, the Supreme Court invalidated few congressional acts in the first 50 years after Marbury, although the pace picked up somewhat after that, to an average of about one invalidation every 2 years. During William Rehnquist’s term as chief justice (1986–2005), however, the court ruled unconstitu- tional more than 30 laws or statutory provisions, with most of these decisions occurring between 1995 and 2005. This uptick in the court’s use of its most power- ful judicial review tool has led to a discussion about the court’s proper place in the separation of powers framework. As stated in one opinion piece,

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Declaring an act of Congress unconstitutional is the boldest thing a judge can do. That’s because Congress, as an elected legislative body representing the entire nation, makes decisions that can be presumed to possess a high degree of democratic legitimacy. (Ger- witz & Golder, 2005, p. A19)

When determining whether a statute violates the Constitution, courts necessarily take into account the subject of the regulation and Congress’s purpose in regulating. Certain kinds of laws—say, affirmative action laws, or a law that classifies people on the basis of their gender—require a greater level of governmen- tal justification and thus are held to a higher constitu- tional standard of review. In other words, these laws are scrutinized more closely by the court and thus stand a greater chance of failing the constitutionality test.

By way of example, the Supreme Court has devel- oped a tiered standard of review framework for equal protection jurisprudence. Under the Constitution’s equal protection clause, states are prohibited from denying “to any person within its jurisdiction the equal protection of the laws” (U.S. Const. amend. XIV, § 1).

The Court employs one of three standards when it reviews whether a particular law satisfies this con- stitutional mandate. The first, termed rational basis or rational relations review, is applied to everyday legis- lation pertaining to things like public safety, tax rates, and consumer protection and thus is the review stan- dard most frequently used. It is nearly impossible for a law to run afoul of this standard, because as long as the challenged statute is rationally related to any legiti- mate government purpose in passing the law, it will be upheld as constitutional.

The second standard is that of intermediate review. This is the court’s choice when the measure under review classifies individuals or groups on, for example, the basis of gender. The assumption here— and the point of the heightened review standard—is that when politicians legislate with gender (or another potentially baseless characteristic) in mind, there is a greater likelihood they are doing so for nefarious reasons. In order to pass constitutional muster under intermediate review, a statute must serve an import- ant government objective and be substantially related to that objective. A good deal of legislation reviewed under this standard is found to be unconstitutional.

Finally, the court has at its disposal in equal pro- tection lawsuits a review standard known as strict scrutiny. The court reserves this standard for laws that tread on fundamental constitutional rights (defined in part as those that are firmly established in American tradition), including an individual’s

right to be free of governmental discrimination on the basis of race. In theory, otherwise discriminatory laws that are necessary to achieve a compelling gov- ernment interest—meaning that the law in question is the least discriminatory way to meet the legisla- ture’s compelling objective—can survive this intense form of scrutiny. However, of all the equal protection claims measured against this standard, only one sur- vivor emerged—when the Supreme Court permit- ted the federal government to intern individuals of Japanese descent during World War II (Korematsu v. United States, 1944)—and this almost universally vil- ified decision was finally condemned (if not formally overruled) by the Supreme Court in 2018 (Trump v. Hawaii, 2018).i

Maintaining Stability in the Law In addition to enforcing legal rights and passing on the constitutionality of actions of the two political branches of government, courts are expected to main- tain a measure of stability, continuity, and predict- ability in the law. This expectation derives from the idea that those subject to the law should not have to contend with continuous swings in the direction law takes. In theory, the relatively nonpolitical judicial branch of government is in the best position to bring this expectation to fruition.

The way courts implement their responsibility to maintain legal stability is through application of stare decisis, a Latin legal term meaning “let it stand.” Stare decisis is a policy of the courts to stand by existing legal precedent; that is, where rules of law have been established in prior judicial decisions, these decisions should be adhered to in subsequent cases where the questions of law and fact are substantially similar to those in the original case. Stability in the law is consid- ered so important that stare decisis is usually applied, and the original judicial decision given deference, even when the original decision is subsequently deter- mined to be wrongly decided or not legally sound. This is especially true where the original decision is an old one on which society has come to rest, as opposed to a relatively young decision with few deep roots in terms of societal expectations. The role of legal precedent has been described in this way:

Legal doctrines are shaped like family trees. Each generation of decisions is derived from ones that came before as, over time, each branch of the law grows and spreads or, occa- sionally, withers and dies away. The most recent decisions almost always draw their strength by tracing back through an ancestral line,

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choosing among parents, uncles, and cousins according to the aptness of their bloodlines. Rarely, a branch of doctrine is disowned, repu- diated, and left vestigial until perhaps revived in another legal era. (Lazarus, 1999, p. 77)

At the same time, legal precedent is not com- pletely sacred, and prior decisions are sometimes reconsidered and, on occasion, overturned. For instance, changes in societal values might outweigh strict application of stare decisis, as was the case with the Supreme Court’s 1954 decision in Brown v. Board of Education to overturn the invidious idea of “sepa- rate but equal” from the court’s 1896 decision in Plessy v. Ferguson. Stare decisis is, however, generally under- stood to trump mere changes in a court’s makeup. In other words, courts are expected to remain anchored to precedential rules of law even when current indi- vidual members may not be.j Indeed, in a well-known Supreme Court case, former Justice John Marshall Harlan II wrote:

A basic change in the law upon a ground no firmer than a change in our membership invites the popular misconception that this institution is little different from the two polit- ical branches of the Government. No miscon- ception could do more lasting injury to this Court and to the system which it is our abid- ing mission to serve. (Mapp v. Ohio, 1961)

▸ Conclusion This chapter led you on a short journey through the complex world of the legal system. Along the way, you visited several of its essential elements and doc- trines: legal rights, the various types of law, separation of powers, federalism, judicial review, and more. To be sure, the trip was abbreviated and in some cases concepts were oversimplified in an effort to concisely cover a complex and expansive topic.

As you encounter myriad health policy and law topics and concepts that are complex in their own right, bearing in mind a few important details about law might help you achieve a greater measure of clar- ity. First, law’s primary purpose is to organize and control an ever-changing, ever-expanding, ever-more- complex society, and it does this in part by regulating a variety of relationships among parties with often- times competing interests (e.g., individual citizen and government; patient and physician; beneficiary and public program or private insurance company; phy- sician and managed care organization; individual and her family). This function of law helps explain why in the context of a specific relationship, one party has a legal right and the other party has a legal respon- sibility to refrain from acting in a way that infringes that legal right. It also helps explain why an individ- ual can justifiably claim a particular legal right in the context of one specific relationship, but not in others (for example, a patient who believes that he has been treated negligently might have a legitimate legal claim against the physician who provided his care, but not against the hospital where the care was provided).

A second detail worth reflecting on periodically is that law is established, enforced, interpreted, and applied by human beings, and thus one must accept that law and the legal process comprise a certain amount of imperfection. This characteristic of law helps explain why statutes and regulations are some- times difficult to understand, why laws are sometimes enforced sporadically or not at all, why reasonable jurists can disagree about the intended meaning of statutory and constitutional provisions, and why law is too often applied unevenly or inequitably.

Finally, bear in mind the fact that laws and the broader legal system are reflective of the beliefs and values of the society from which they flow. This fait accompli, perhaps more than anything else, provides an object lesson in the role of law across a wide range of subjects, including matters related to health care and public health.

References Adelson, R. G. (2003). The enumerated powers of states. Nevada

Law Journal, 3, 469–494. Administrative Procedure Act of 1946. 5 U.S.C. § 551 et seq. Baker T. E. (2004). Constitutional theory in a nutshell. William

and Mary Bill of Rights Journal, 13(1), 57–123. Brennan Center for Justice. (2015). Judicial selection: Significant

figures. Retrieved from https://www.brennancenter.org /rethinking-judicial-selection/significant-figures

Brown v. Board of Ed., 347 U.S. 483 (1954).

Corwin, E. S. (1957). The president: Office and powers, 1787–1957. New York, NY: New York University Press.

de Tocqueville, A. (1835). Democracy in America (H. Reeve, Trans.). New York, NY: Vintage Books; 1990.

Dinan, J. (2018). State constitutional policies: Governing by amendment in the United States. Chicago, IL: University of Chicago Press.

Fallon, R. H., Jr. (1999). How to choose a constitutional theory. California Law Review, 87(3), 535–579.

46 Chapter 3 Law and the Legal System

 

 

Fay v. New York, 332 U.S. 261 (1947). Friedman, L. M. (1964). Law and its language. George Washington

University Law Review, 33, 563–579. Friedman, L. M. (2002). Law in America: A short history. New

York, NY: The Modern Library. Garner, B. (2014). Black’s law dictionary (10th ed.). Eagan, MN:

Thomson West. Gewirtz, P., & Golder, C. (2005, July 6). So who are the activists?

The New York Times. Retrieved from https://www.nytimes .com/2005/07/06/opinion/so-who-are-the-activists.html

Gibbons v. Ogden, 25 U.S. (9 Wheat.) 1 (1824). Holmes, O. W. (1899). Law in science and science in law. Harvard

Law Review, 12(7), 443–463. Jackson v. City of Joliet, 715 F.2d 1203 (7th Cir. 1983). Korematsu v. United States, 323 U.S. 214 (1944). Lazarus, E. (1999). Closed chambers: The rise, fall, and future of the

modern Supreme Court. New York, NY: Penguin Books. Mapp v. Ohio, 367 U.S. 643 (1961). Marbury v. Madison, 1 Cranch (5 U.S.) 137 (1803). Mayor v. Cooper, 73 U.S. 247 (1867).

McCullough v. Maryland, 17 U.S. (4 Wheat.) 316 (1819). Mensah, G. A., Goodman, R. A., Zaza, S., Moulton, A. D., Kocher,

P. L., Dietz, W. H., . . . Marks, J. S. (2004). Law as a tool for preventing chronic diseases: Expanding the spectrum of effective public health strategies. Preventing Chronic Disease: Public Health Research, Practice, and Policy, 1(2), 1–6.

Occupational Health and Safety Act of 1970. 29 U.S.C. § 655. Plessy v. Ferguson, 163 U.S. 537 (1896). Refo, P. L. (2004). The vanishing trial. Litigation Online, 30(2), 1–4. Reich, C. A. (1964). The new property. The Yale Law Journal, 73(5),

733–787. Smith, S. D. (1991). Reductionism in legal thought. Columbia Law

Review, 91(1), 68–109. Trump v. Hawaii, 138 S. Ct. 923 (2018). U.S. Const. amend. XIV, § 1. U.S. Const. art. III, § 2, clause 2. U.S. Const. art. VI, para. 2. Ziskin, L. Z., & Harris, D. A. (2007). State health policy for

terrorism preparedness. American Journal of Public Health, 97(9), 1583–1588.

▸ Endnotes The language of the law is ever-changing as the courts, Congress, state legislatures, and administrative agencies continue to define, redefine and expand legal words and terms. Furthermore, many legal terms are subject to variations from state to state and again can differ under fed- eral laws. (Garner, 2014, p. iv)

b. For an overview of the Bill of Rights in a public health context, see Gostin, L. O. (2000). Public health law: Power, duty, restraint (pp. 62–65). Berkeley, CA: University of California Press.

c. For a full description of the intertwined nature of administrative and health law, see Jost, T. S. (2004). Health law and administrative law: A marriage most convenient. Saint Louis Univer- sity Law Journal, 49, 1–34.

d. For an in-depth discussion of the relationship between the APA and state administrative pro- cedures, see Bonfield, A. E. (1986). The federal APA and state administrative law. Virginia Law Review, 72(2), 297–336.

e. For a full discussion of each of the govern- ment branches’ role in health policymaking, see Gostin, L. O. (1995). The formulation of health policy by the three branches of government. In R. E. Bulger, E. M. Bobby, & H. V. Fineberg (Eds.), Society’s choices: Social and ethical deci- sion making in biomedicine (pp. 335–357). Washington, DC: National Academy Press.

a. Although the important role that language plays in law is not a topic we delve into in this chapter, it is, particularly for students new to the study of law, one worth thinking about. Words are the basic and most important tool of the law and of lawyers. Without them, how could one draft a law, legal brief, contract, or judicial opinion? Or engage in oral advocacy on behalf of a client, or conduct a negotiation? Or make one’s wishes known with respect to personal matters near the end of life? As one renowned legal scholar puts it, “law is primarily a verbal art, its skills verbal skills” (Friedman, 1964, p. 567).

Of course, one problem with the language of law is that it is full of legal jargon, making it difficult sometimes for laypeople to understand and apply to their own particular situation. For example, if government regulation is to be effec- tive, the language used to do the regulating must be understandable to those being regulated. Another problem relates to the interpretation of words and terms used in the law, because both ambiguity (where language is reasonably capa- ble of being understood in two or more ways) and vagueness (where language is not fairly capable of being understood) are common to laws, leaving those subject to them and those responsible for applying them unsure about their true meaning. Furthermore, as the preface to Black’s Law Dictionary, under the heading “A Final Word of Caution,” states:

Endnotes 47

 

 

f. However, since the 1980s, the selection (by the president) and approval (by the U.S. Senate) process for federal judges has become highly politicized. There is an extensive body of lit- erature on this topic, as evidenced by a simple Internet search.

g. The potential implications of increasingly injecting politics into the court system are very troubling, and there is likewise extensive litera- ture on this topic.

h. The decision was written, as it turned out, by Chief Justice John Marshall—the very same per- son who, as Secretary of State, signed Marbury’s

commission. Marshall was sworn in as Chief Justice of the United States just before Jefferson took office.

i. For a fuller discussion of how the equal protec- tion standards of review operate, see Lazarus, 2004, pp. 293–294.

j. This understanding is often put to the test, how- ever, as seen in the national discussion of the right to abortion that takes place each time a new U.S. Supreme Court nominee is announced whose political stripes seem to clash with the prevailing law that abortion is a constitutionally protected right.

48 Chapter 3 Law and the Legal System

 

 

CHAPTER 4

Overview of the United States Healthcare System

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Identify the key players who provide and finance health care in the United States ■ Identify common characteristics of the uninsured ■ Understand the effect of insurance on access to care and on health status ■ Identify barriers to accessing health care ■ Understand concerns regarding the quality of health care provided in the United States ■ Describe differences in how health care is delivered in various countries

▸ Introduction

Coordinated. Efficient. Cost-effective. Goal oriented. These are words one might use to describe a well- functioning system. Unfortu- nately, they are not words that are often used when discussing how healthcare services are delivered in the United States. Unlike most other developed nations, the United States does not have a unified healthcare system. Even with the passage of the Patient Protection and Affordable Care Act of 2010 (ACA), the first major health reform law passed in this country in nearly 50 years, the United States will continue to provide healthcare services through a patchwork of public and private insurance plans; fed- eral, state, and local governments; and institutions and individual providers who are often unconnected to one other.

The United States has never been accused of provid- ing healthcare services in an efficient or cost-effective manner. On average, this country spends over twice as much on health care per person as other developed countries (Organization for Economic Cooperation and Development [OECD], 2017, p. 133). While the U.S. healthcare system does some things well, it ranks at or near the bottom on important health outcome measures such as life expectancy, infant mortality, and adult obesity rates (OECD, 2017, pp. 47–81). Even though the federal government establishes the nation’s healthcare goals through initiatives such as Healthy People 2020, the lack of coordination within the healthcare system means that all parts of the sys- tem are not working together to achieve these goals (Office of Disease Prevention and Health Promotion, n.d.). The lack of a unified healthcare system makes it difficult to provide a straightforward overview of how

49

© Mary Terriberry/Shutterstock

 

 

healthcare services are delivered and financed. For example, the following are some of the various players in the provision and delivery of health care:

■ Educational institutions such as medical, dental, nursing, and physician assistant programs

■ Research organizations including private entities, public agencies, and nonprofit foundations

■ Private suppliers of goods and services such as hospital equipment manufacturers, home health agencies, and uniform suppliers

■ Private health insurance provided through employers, on the individual market, and through state health exchanges

■ Public health insurance programs such as Medic- aid, Medicare, and TRICARE (the Department of Defense healthcare program for members of the uniformed services and their families)

■ Individual providers such as physicians, dentists, pharmacists, and physical therapists

■ Institutional providers such as hospitals, commu- nity health centers, and skilled nursing facilities

■ Private trade associations representing providers (e.g., the American Medical Association, which represents physicians), institutions (e.g., the National Association of Community Health Cen- ters), and industries (e.g., PhRMA, which rep- resents the pharmaceutical industry)

■ Private accreditation agencies that provide quality certifications to healthcare institutions

■ Consumers of healthcare goods and services

■ Local, state, and federal government agencies that have roles in delivering care, financing care, setting health policy, developing laws and regula- tions, and conducting and funding research

In the absence of a unified system or single govern- ment program to describe, it is easiest to understand the provision of U.S. health care through the concepts of finance (How do individuals pay for health care, and how are providers reimbursed for their services?), access (How do individuals access healthcare services, and what barriers to access exist?), and quality (What is the quality of healthcare services that are provided, and what can be done to improve the quality of care?). It is also helpful to consider the health system choices made by this country against those made by other developed countries. This chapter begins with a dis- cussion of the concepts of finance, access, and quality and then turns to a comparative overview of how other countries have designed their healthcare systems.

▸ Healthcare Finance In 2016, the United States spent $3.3 trillion on aggre- gate healthcare spending, the equivalent of $10,348 per person and 17.9% of the nation’s gross domestic prod- uct (GDP) (FIGURE 4-1). This total represents a 4.3% increase over 2015 spending (Hartman, Martin, Espi- nosa, Catlin, & National Health Expenditures Accounts Team, 2018). Healthcare spending grew slowly during the Great Recession of 2007–2009 and the period

FIGURE 4-1 National Health Expenditures as a Share of Gross Domestic Product, 1987–2016

50 Chapter 4 Overview of the United States Healthcare System

Source: Reproduced from: Centers for Medicare and Medicaid Services, Office of the Actuary. (n.d.). National Health Care Spending in 2016. Retrieved from https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports /NationalHealthExpendData/Downloads/NHE-Presentation-Slides.pdf

10.0

P e rc

e n t o f

G D

P

Calendar Years

17.9%

19 8 7

19 8 8

19 8 9

19 9 0

19 9 1

19 9 2

19 9 3

19 9 4

19 9 5

19 9 6

19 9 7

19 9 8

19 9 9

2 0 0 0

2 0 01

2 0 0 2

2 0 0 3

2 0 0 4

2 0 0 5

2 0 0 6

2 0 0 7

2 0 0 8

2 0 0 9

2 01

0 2 01

1 2 01

2 2 01

3 2 01

4 2 01

5 2 01

6

12.0

14.0

16.0

18.0

July 1990– March 1991 recession

20.0

December 2007– June 2009 recession

March 2001– November 2001 recession

The Share of GDP Devoted to Health Expenditures Was 17.9% in 2016

 

 

shortly thereafter. The implementation of the ACA led to 19 million newly insured individuals from 2014 to 2015. This reduction in the uninsured rate combined with strong prescription drug spending (due, in large part, to increased spending on a new drug for hep- atitis C) resulted in robust spending growth in 2014 and 2015, though growth slowed in 2016. As shown in FIGURE 4-2, spending growth was due to higher medical prices and increased use of health services by newly insured individuals (Hartman et al., 2018).

National health expenditures are expected to average 5.6% growth from 2017 to 2026 and reach 19.7% of the GDP by 2026 (Cuckler et al., 2018). This growth is expected to be driven by an increase in prices for medical goods and services, and increases in Medicare and Medicaid spending due to the aging Baby Boomer population (Cuckler et  al., 2018). Put differently, come 2026, one-fifth of the nation’s econ- omy will be consumed by healthcare spending. This is nothing short of staggering. As shown in FIGURE 4-3, the largest portion of national healthcare spending in 2016 was on hospital services, followed by physician and clinical services.

Health Insurance Having health insurance reduces the risk of financial ruin when expensive health services are needed and often provides coverage for preventive services at low

or no cost. As discussed in the upcoming section on healthcare access, individuals without health insur- ance must pay for services themselves, find services provided at no cost, or go without care. While most people in the United States have health insurance, one of the main goals of the ACA is to decrease the num- ber of uninsured people.

The ACA includes a number of provisions designed to reduce the uninsured rate in this country. While these provisions, as well as the changes that have taken place since the ACA was signed into law, will be discussed in detail in the chapter on health reform, a brief overview is useful here. The ACA attempts to reduce the number of uninsured through three main strategies. First, the law includes mandates on individuals to purchase insurance and on (many) employers to provide insurance. Second, the law expands Medicaid, the federal–state program for the poor, to the poorest uninsured individuals across the country. Third, the ACA created state health insur- ance exchanges, which are aimed at individuals and small businesses that are not able to obtain affordable health insurance through other means.

When President Obama signed the ACA into law in 2010, the uninsured rate was 16.3%, or 49.9 million individuals (U.S. Census Bureau, 2011, pp. 22–23). The ACA was effective in reducing the uninsured rate; by 2016 it had dropped to 8.8%, or 28.1 million individuals (U.S. Census Bureau, 2017). A number of legal and policy developments since the

FIGURE 4-2 Factors Accounting for Growth in per Capita National Health Expenditures, Selected Calendar Years, 2004–2016

Healthcare Finance 51

6.5% 6.0% 5.5% 5.0% 4.5% 4.0% 3.5% 3.0%

0.0%

2004–2007

A n n u a l P

e rc

e n t

C h a n g e

Per Capita Health Spending Grew 3.5% in 2016

5.8%

3.0%

4.3%

5.0%

3.5%

2008–2013 2014 2015 2016

1.0% 0.5%

2.0% 1.5%

2.5%

Age and sex factors Medical prices Residual use and intensity

Notes: Medical price growth, which includes economy-wide and excess medical-specific price growth (or changes in medical-specific prices in excess of economy-wide inflation), is calculated using the chain-weighted national health expenditures (NHE) deflator for NHE. “Residual use and intensity” is calculated by removing the effects of population, age and sex factors, and price growth from the nominal expenditure level.

Source: Reproduced from: Centers for Medicare and Medicaid Services, Office of the Actuary. (n.d.). National Health Care Spending in 2016. Retrieved from https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports /NationalHealthExpendData/Downloads/NHE-Presentation-Slides.pdf

 

 

2016 election have reduced the ACA’s effectiveness. As a result, the Congressional Budget Office (CBO) estimates that the number of individuals younger than 65 years without insurance will increase to 35 million (13%) by 2028 (CBO, 2018). According to the CBO, one of the main reasons for this increase is the 2018 repeal of the penalty associated with the individual mandate. The elimination of this penalty is projected to increase the uninsured rate by 4 million in 2019 and another 3 million by 2021. This is a result of individ- uals choosing not to purchase health insurance while they remain in good health, do not face a penalty for going without coverage, or cannot afford the higher premiums that are expected due to the repeal of the individual mandate penalty (CBO, 2018).

As shown in FIGURE 4-4, most people in the United States are privately insured and obtain their health insurance through their employer. Employer-sponsored insurance plans may be self- funded (meaning employers set aside funds to pay for their employees’ health insurance claims instead of paying a premium to a health insurance carrier) or fully insured (meaning employers pay a premium to a private health insurance company to administer employees’ plans and pay the healthcare claims of the employees). Another significant portion of the popu- lation is publicly insured through Medicaid, the Chil- dren’s Health Insurance Program (CHIP), Medicare, the Veteran’s Administration, and the Department of Defense. Public programs are funded and run by fed- eral and/or state government agencies, depending on the program.

FIGURE 4-5 illustrates how health insurers act as an intermediary between consumers (sometimes referred to as “insureds”) and providers (which refers to both individual providers, such as physicians or nurses, and institutions, such as hospitals and community health centers). The specifics regarding eligibility for a partic- ular insurance plan, choice of plans, how much a plan costs to enroll in or use, what benefits are covered, and how much providers are reimbursed vary by plan or government program. In some circumstances, providers may accept insurance from only a single plan, but often providers will accept patients from a variety of plans.

FIGURE 4-3 The Nation’s Health Dollar, Calendar Year 2016: Where it Went

FIGURE 4-4 Healthcare Coverage in the United States, March 2016

52 Chapter 4 Overview of the United States Healthcare System

Note: “Other spending” includes dental services, other professional services, home health care, durable medical equipment, other nondurable medical products, government public health activities, and investment.

Hospital care, 32%

Physician and clinical services,

20%Nursing care facilities and continuing care

retirement communities, 5%

Prescription drugs, 10%

Government administration and net

cost of health insurance, 8%

Other health, residential, and personal care,

5%

Other spending,

20%

Source: Reproduced from: Centers for Medicare and Medicaid Services, Office of the Actuary. (n.d.). National Health Care Spending in 2016. Retrieved from https://www.cms.gov/Research-Statistics-Data-and-Systems/Statistics-Trends-and-Reports /NationalHealthExpendData/Downloads/NHE-Presentation-Slides.pdf

Employer, 153 million

(47.3%)

Medicare, 55.5 (17.2%)

Medicaid, 49 (15.2%)

Medicaid/CHIP 23.6 (7.3%)

Affordable Care Act 9.1 (2.9%)

Other 4 (1.2%)

Total U.S. population 323.2 million

Uninsured 29 (9%)

Source: Hiltzik, M. (2016, March 29). Where America gets its health coverage: Everything you wanted to know in one handy chart. L.A. Times. Retrieved June 11, 2018 from http://www.latimes.com/business/hiltzik/la-fi-hiltzik-gaba-20160329-snap-htmlstory.html

 

 

Consumers interact with health insurance com- panies or government programs by enrolling into an insurance plan by which they are accepted (in the case of private plans) or for which they are eligible (in the case of public programs), providing payments to the insurance plan for being enrolled (either directly or through a payroll deduction), choosing which pro- vider to see based on plan restrictions or incentives, and working with the plan if they have questions or complaints. Providers that agree to be part of a plan’s “network” (i.e., the group of providers who will see patients insured by the plan) are reimbursed a con- tractually agreed-upon amount from the insurance company and/or the patient for providing services covered under the plan, may accept consumers who are enrolled in the plan, may be subject to plan quali- ty-control measures, and will participate as necessary in plan appeals processes.

Direct Services Programs In addition to providing publicly funded health insurance to certain populations through programs such as Medicare and Medicaid, federal, state, and local governments also fund numerous programs that directly provide healthcare services to vul- nerable populations. Many of these programs also receive private funding and donations to support their operations. Direct service programs generally exist to fill gaps in the private healthcare delivery system. Examples of these types of programs include the following:

■ Federally qualified health centers (FQHCs): These centers are located in medically under- served areas and provide primary care services to individuals on a sliding fee scale (meaning that how much one pays for services depends on the individual’s income level). While anyone may use an FQHC, the health center patient popula- tion is made up of mostly uninsured and pub- licly insured patients. Funding for health centers usually comes from the federal and state govern- ments, and sometimes from local governments and private donations.

■ HIV/AIDS services: The Ryan White HIV/AIDS Program works with states, cities, and local organi- zations to provide services to patients with human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) who do not have health insurance coverage or the financial resources to pay for needed care. The program is federally funded and provides grants to state agen- cies that deliver care to patients. The Ryan White program includes the state AIDS Drug Assistance Program (ADAP), which provides medications to low-income individuals with HIV. A supplemen- tary ADAP for high-need states includes federal funding and a state matching requirement. States often supplement federal funding with state- funded HIV prevention and treatment programs. Some local public health departments provide HIV testing and counseling services and help individuals access treatment. Many programs also accept private donations.

FIGURE 4-5 Insurance Company–Consumer–Provider Interaction

Healthcare Finance 53

Insurance Company

Consumer

Accepts payment Accepts rules

Sets reimbursement rates Sets quality control requirements

Enroll in plan Pays plan Questions

Appeals

Sets plan rules Covers some consumer costs

Provider

Accepts patient Provides services May accept payment

Chooses provider Receives services May pay provider

 

 

■ Family planning services: Title X of the Public Health Service Act provides federal funding for family planning services offered to women who do not qualify for Medicaid, maintains family planning centers, and establishes standards for providing family planning services (although fed- eral dollars may not be used to support abortion services except in the case of rape, incest, or dan- ger to the life of the pregnant woman). In addition, states also fund family planning services. Services provided vary by state but may include contracep- tion, cervical cancer screening, tubal sterilization, sexually transmitted disease screening, HIV test- ing, and abstinence counseling. State laws vary on the use of state funds for abortion services. Local health departments may also offer some of these services as well as help people access family planning services from private providers. Private donations provide revenue to many family plan- ning clinics.

▸ Healthcare Access Access to care refers to the ability to obtain needed health services. There are a variety of factors that can hinder access to care. Barriers may exist if individuals are underinsured and cannot afford the cost sharing required by their health insurance policy, if needed services are not covered by health insurance, if pro- viders will not take a particular insurance plan, or if providers are not available in certain geographic areas. Access problems are exacerbated by provider short- ages, especially in primary care fields (e.g., internal medicine and pediatrics). Many areas of the coun- try already experience workforce shortages, and the influx of newly insured individuals as a result of health reform will make this problem even more pronounced in the years to come.

Of course, one important factor relating to access is lack of health insurance. Individuals with- out health insurance have to pay more for compara- ble services because they do not have the advantage of sharing costs as part of a pool of consumers. Because many individuals without health insurance are low-income, they may be unable to pay for the cost of needed care, and providers are often unwill- ing to accept uninsured patients because of the risk of not being paid for their services. Some provid- ers, referred to as “safety net” providers, focus on providing care to uninsured patients, but gaining access to needed care remains a significant issue for this population.

As noted previously, many changes that took place in 2014 as part of ACA implementation are intended to reduce the number of uninsured people. Even so, it is important to understand the healthcare prob- lems faced by the uninsured due to the uncertainty surrounding the ACA’s future. Furthermore, millions would remain uninsured even with a fully imple- mented ACA. The ACA did not help almost half the uninsured in 2017 because their state did not expand Medicaid, their income was too high to allow them to obtain subsidies, or they were ineligible for insurance or assistance due to immigration restrictions (Foutz, Damico, Squires, & Garfield, 2017). Many of those who could be assisted by the ACA’s provisions also remain uninsured. A 2016 survey conducted by the Common- wealth Fund found that only about half (52%) of the uninsured knew they could look for coverage in a state marketplace, and two-thirds of uninsured adults who knew about state exchanges did not think they could find affordable coverage (Commonwealth Fund, n.d.).

The Uninsured Characteristics of the Uninsured There are many myths relating to the uninsured. It is often assumed that the uninsured do not work or simply choose not to purchase health insurance even though it is available and affordable. Although this assumption may be true in some cases, in most instances it is not. Furthermore, many people believe that all employers offer insurance or that those individuals without private insurance are always eligible for public programs. As you will see, these and other assumptions are also false.

Income Level While the poor saw significant gains in insurance coverage under the ACA, the primary reason people do not have health insurance is still financial—available coverage is simply too expensive (FIGURES 4-6 and 4-7). There was an increase of 17 mil- lion Medicaid and CHIP enrollees from September 2013 to June 2017, accounting for much of the decrease in the uninsured rate among the poor. Not surpris- ingly, between 2013 and 2016, the uninsured rate for nonelderly adults dropped more significantly in states that expanded Medicaid (9.2% decrease) than in states that did not (4.8% decrease) (Foutz et  al., 2017). In addition, another 10 million individuals received pre- mium subsidies to purchase health insurance in a state exchange. These subsidies are available to individu- als whose income is between 100% and 400% of the federal poverty level (FPL) ($20,160 to $80,640 for a family of three in 2016) (Foutz et al., 2017).

54 Chapter 4 Overview of the United States Healthcare System

 

 

Race, Ethnicity, and Immigrant Status Prior to the ACA, the uninsured rate was much higher for His- panics (30.7%) and Blacks (20.8%) than for non-His- panic Whites (11.7%) (U.S. Census Bureau, 2011, pp. 22–23). As shown in Figure 4-6 and FIGURE 4-8,

minority populations experienced significant coverage gains in the early years of the ACA, although Whites continued to have the lowest uninsured rate (U.S. Census Bureau, 2017). These differences are due to a variety of factors, such as language barriers, income level, work status, state of residence, and immigration status (Foutz et al., 2017).

In 2016, noncitizens were three times as likely to be uninsured as were citizens (Foutz et  al., 2017). Restrictive eligibility rules pertaining to immigrants in public programs make it difficult for non-natives to obtain public coverage. While legal immigrants may obtain subsidies to assist with purchasing health insurance through the state exchanges under the ACA, undocumented immigrants are not eligible for federal subsidies and are prohibited from purchasing insur- ance through an exchange, even at full cost.

Employment Status While over half (57%) of employers offered health insurance coverage in 2013, this number has declined significantly since 66% of employers provided this benefit in 1999 (Foutz et  al., 2017). Most of the decrease is due to small businesses dropping coverage. As shown in FIGURE 4-9, premium costs nearly doubled while wages and inflation grew at a much slower pace, meaning coverage became less affordable even for those employees who were offered coverage (Foutz et  al., 2017). While the ACA includes an employer mandate that requires medium and large employers

FIGURE 4-6 Percentage Point Change in Uninsured Rate Among the Nonelderly Population by Selected Characteristics, 2013–2016

FIGURE 4-7 Reasons for Being Uninsured Among Uninsured Nonelderly Adults, 2016

Healthcare Access 55

<1 00

% F

P L

10 0

to 1

99 %

F P L

≥2 00

% F

P L

W hi

te

B la

ck H

is pa

ni c

A si

an C

hi ld

re n

0– 17

N on

el de

rly

ad ul

ts 1

8– 64

Y ou

ng a

du lts

19 –2

5

0.0%

–9.5%

–3.6% –4.8%

–7.4% –7.3%

–1.4%

–8.2%

–12.8%

–11.1%–11.3%

–2.0%

–4.0%

–6.0%

–8.0%

–10.0%

–14.0%

Notes: Includes nonelderly individuals ages 0–64.

–12.0%

Poverty level Race/ethnicity Age

Source: Foutz et al., 2017, Figure 4; Kaiser Family Foundation analysis of the 2013 and 2016 National Health Interview Survey.

0

5

10

15

20

25

30

35

40

45

Share who say they are uninsured because:

Co st is

to o

hi gh

Lo st jo

b or

c ha

ng ed

em pl oy

er s

Lo st m

ed ica

id

Em pl oy

er d

oe s no

t o ffe

r o r

in el ig ib le fo

r c ov

er ag

e

Fa m

ily s ta

tu s ch

an ge

No n

ee d

fo r h

ea lth

co ve

ra ge

4 5 %

23%

12% 10% 9%

2%

Notes: Includes nonelderly adults ages 18–64. Respondents can select multiple reasons. Status change includes marital status change, death of spouse or parent, or ineligible due to age or leaving school.

Source: Kaiser Family Foundation. (n.d.). Key facts about the uninsured population. Retrieved from https://www.kff.org /uninsured/fact-sheet/key-facts-about-the-uninsured-population/

 

 

(those with over 50 full-time- equivalent employ- ees) to provide coverage, the percentage of employ- ers offering health insurance coverage, the number of employees eligible for coverage, and the take-up rate by employees choosing to purchase coverage did not change significantly after the ACA was implemented (Foutz et  al., 2017). This is not sur- prising since medium and large businesses were the most likely to offer coverage before the ACA and concerns about affordability remain the primary obstacle for individuals obtaining insurance.

As shown in FIGURE 4-10, most of the uninsured work or are in families with at least one full-time worker, and many more have part-time workers in the family. In 2017, 74% of nonelderly uninsured workers were not offered health insurance by their employer, and over 40% of uninsured workers were employed by small businesses who were not subject to the ACA’s employer mandate (Foutz et  al., 2017). Most uninsured workers are low-income and/or work in blue-collar fields such as agriculture, construction, and the service industry.

FIGURE 4-8 After 3 Years of the ACA, Uninsured Rates for Blacks, Latinos, and Whites Have Declined Significantly, but Large Numbers of Immigrant Latinos Remain Uninsured

FIGURE 4-9 Cumulative Increase in Family Premiums, Worker Contribution to Premiums, and Worker Earnings, 1999–2017

56 Chapter 4 Overview of the United States Healthcare System

0 White

P e rc

e n t A

d u lts

A g e s

19 – 6 4

U n in

su re

d

16

21

13

36

29

24

47 43

14

9

Black Latino (total)

Latino (U.S.-born)

Latino (foreign-born)

20

10

50

40

30

July-Sept. 2013

Feb.-April 2016

Source: Reproduced from Foutz et al., 2017; The Commonwealth Fund Affordable Care Act Tracking Surveys. July–September 2015 and February–April 2016.

Source: Kaiser/HRET Survey of Employer-Sponsered Health Benefits, 1999-2017; Bureau of Labor Statistics, Consumer Price Index, U.S. City Average of Annual Inflation (April to April), 1999-2017; Bureau of Labor Statistics, Seasonally Adjusted Data from the Current Employment Statistics Survey, 1999-2017 (April to April).

1999

0%

38%

38% 29%

24%

109%

113%

47%

172%

180%

270%

224%

64%

47% 38%

8%

11%

50%

100%

150%

200%

250%

300%

C u m

u la

tiv e G

ro w

th

2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017

Overall inflation Worker earnings

Family premiums Worker contributions

 

 

Age Because Medicaid and CHIP provide extensive coverage to low-income children and Medicare cov- ers older adults, working-age adults between 19 and 64 years are the age group most likely to be uninsured. In 2016, 98.8% of adults older than 65 years and 94.6% of children younger than 19 years were insured, com- pared to 87.9% of working-age adults (U.S. Census Bureau, 2017). Even though many young adults (ages 26–34 years) gained insurance under the ACA, 15.7% of them were still uninsured in 2016.

As young adults transition from school to the workforce, they may become ineligible for their fam- ily’s coverage for the first time, may have entry-level jobs earning too little income to afford a policy, or may work for an employer that does not offer health insurance. The ACA addresses part of this problem by requiring insurers to cover dependents (someone who relies on the primary insured for support) until age 26 years. Although some young adults do not consider health insurance a priority expense because they are relatively healthy, studies have shown that cost is the primary determinant of whether people in this age bracket obtain coverage (Institute of Medicine [IOM], 2001a, pp. 73–74). While adults 55 to 64 years of age are more likely to be insured than are younger adults, the uninsured who fall into this age group are a cause for concern because they are medically high risk and often have declining incomes (IOM, 2001a, p. 72). The disability provisions of Medicaid and Medicare and the availability of employer-based insurance keep the number of uninsured in this group relatively small, which is important because it is very expensive for individuals in this demographic to purchase individ- ual insurance policies in the private market.

Education Level Education level is also an important factor in insurance status because it is easier, for exam- ple, for college graduates to earn higher incomes and obtain jobs that provide affordable employment-based insurance as compared to less-educated individuals (IOM, 2001a, p. 74). The higher the education level, the more likely one is to be insured. In 2016, the uninsured rate was 6.8% for working adults with a bachelor’s degree, compared to 15.2% for high school graduates and 27.3% for those without a high school diploma (U.S. Census Bureau, 2017).

Geography As shown in FIGURE 4-11, residents of the South and West are more likely to be uninsured than are residents of the North and Midwest. There are vari- ations in the uninsured rate from state to state. These differences are based on numerous factors, including racial/ethnic composition, other population charac- teristics, public program eligibility, and employment rates and sectors (Kaiser Family Foundation (KFF) 2017). This trend is likely to continue, at least in the short run, with many states in the South opting not to expand Medicaid coverage under the ACA.

Uninsurance is a particular problem among the 16% of the population who live in rural areas. They are more likely to be poorer, unemployed, or employed in blue-collar jobs and are less likely to have access to employer coverage than are their urban counterparts (Newkirk & Damico, 2014). In addition, rural residents have relatively high healthcare needs—they tend to be older, poorer, and less healthy than urban residents— and there is often a provider shortage in these areas. Because many rural residents live in states that have not chosen to expand Medicaid and also have incomes

FIGURE 4-10 Characteristics of the Nonelderly Uninsured, 2016

Healthcare Access 57

100–199% FPL 25%

200–399% FPL 31%

400%+ FPL 20%

<100% FPL 24%

Total = 27.5 Million Nonelderly Uninsured

Family work status Family income (%FPL)

Race

One or more full-time workers

75%

No workers

15%11% Part-time workers White

44%

Black 15%

Hispanic 33%

Asian/Native Hawaiian or

Pacific Islander 5%

Other 3%

Notes: Includes nonelderly individuals ages 0–64. The U.S. Census Bureau’s poverty threshold for a family with two adults and one child was $19,318 in 2016. Data may not total 100% due to rounding. Persons of Hispanic origin may be of any race; all other race/ethnicity groups are non-Hispanic.

Source: Kaiser Family Foundation analysis of the March 2017 Current Population Survey, Annual Social and Economic Supplement.

 

 

too low to qualify for premium subsidies, insurance is more likely to be unaffordable for them than for urban residents (Newkirk & Damico, 2014).

The Importance of Health Insurance Coverage to Health Status Having health insurance provides tangible health ben- efits. For a variety of reasons discussed in this section,

having health insurance increases access to care and positively affects health outcomes. Conversely, the uninsured, who do not enjoy the benefits of health insurance, are more likely to experience adverse health events and a diminished health-related quality of life and are less likely to receive care in appropriate set- tings or receive the professionally accepted standard of care (Foutz et al., 2017).

Health insurance is an important factor in whether someone has a “medical home,” or consistent source of care. Having a consistent source of care is positively associated with better and timelier access to care, bet- ter chronic disease management, fewer emergency department (ED) visits, fewer lawsuits against EDs, and increased cancer screenings for women (Foutz et  al., 2017; Lambrew, DeFriese, Carey, Ricketts, & Biddle, 1996; Starfield & Shi, 2004). Unfortunately, the uninsured are much less likely to have a usual source of care than are insured individuals (FIGURE 4-12).

The uninsured are also less likely to follow treat- ment recommendations and more likely to forgo care due to concerns about cost (Foutz et  al., 2017). In addition, the uninsured are less likely to receive pre- ventive care and appropriate routine care for chronic conditions (Foutz et  al., 2017). One result of these conditions is that children without insurance are more likely to have developmental delays, often leading to difficulties in education and employment. Also, qual- ity of life may be lower for the uninsured due to their lower health status and anxiety about both monetary and medical problems.

FIGURE 4-11 Uninsured Rates Among the Nonelderly by State, 2016

Source: Reproduced from Centers for Disease Control and Prevention, MMWR 1996;45: 526–528.

58 Chapter 4 Overview of the United States Healthcare System

AK

HI

WA

ID

MT

WY

CO

ND MN

IA

MO

AR

LA

MS AL GA

FL

NJ DE MD DC

SC

NC TN

KY

INIL

WI

MI

OH

PA

WV VA

NY

ME VT

NH MA

CT RI

SD

NE

KS

OK

TX

NMAZ

UT NV

OR

CA

Notes: Includes nonelduals individuals ages 0–64.

<7% (11 states including DC)

7–12% (28 states)

>12% (12 states)

Source: Kaiser Family Foundation analysis of the March 2017 Current Population Survey, Annual Social and Economic Supplement.

BOX 4-1 Discussion Questions

From a policy perspective, are the characteristics just described interrelated, or should they be addressed separately? If you are trying to reduce the number of uninsured, do you believe the focus should be on altering insurance programs or changing the effect of having one or more of these characteristics? Whose responsibility is it to reduce the number of uninsured? Government? The private sector? Individuals?

BOX 4-2 Discussion Questions

The ACA made it a priority to reduce the number of uninsured. At what point, if any, should the government step in to provide individuals with assistance to purchase insurance coverage? Do you think such assistance should be a federal or a state responsibility?

 

 

Because the uninsured are less likely to obtain pre- ventive care or treatment for specific conditions, they have a higher mortality rate overall, have a higher in- hospital mortality rate, and are more likely to be hospi- talized for avoidable health problems (Foutz et al., 2017). Of course, without regular access to care, it is less likely that a disease will be detected early when treatment may be cheaper and more effective. For example, uninsured cancer patients are diagnosed at later stages of the dis- ease and die earlier than insured cancer patients.

Ways to Assess the Cost of Being Uninsured There are several ways to think about the costs of being uninsured. These costs include the health status costs to the uninsured individual, as discussed previously; financial cost to the uninsured individual; financial cost to state and federal governments and to private insurers; financial cost to providers; productivity costs from lost work time due to illness; costs to other pub- lic priorities that cannot be funded because of the resources spent on providing care to the uninsured; and costs to the health status and patient satisfaction of insured individuals.

The financial burden of being uninsured is sig- nificant. Although on average the uninsured spend fewer dollars on health care than the insured, those without insurance spend a greater proportion of their overall income on medical needs. Furthermore, when the uninsured receive care, it is often more expen- sive because the uninsured are not receiving care as

part of an insurance pool with leverage to negotiate lower rates from providers. In fact, the uninsured are charged rates two to four times higher than the rates paid by insurance companies or public programs (Foutz et al., 2017). The uninsured are less likely to be able to pay for healthcare needs because the average uninsured household does not have net assets and half of the uninsured living under the 200% poverty level have no savings (Foutz et al., 2017). Not surprisingly, the uninsured are much more likely to be concerned about being able to pay their medical bills than are their insured counterparts (FIGURE 4-13).

Costs of medical care provided by, but not fully reimbursed to, health professionals are referred to as uncompensated care costs. In 2013, it was estimated that uncompensated care costs surpassed $84 billion in the United States, with federal, state, and local spend- ing covering most of the tab, primarily through “dis- proportionate share” (DSH) payments to hospitals that serve many uninsured individuals and Medicaid bene- ficiaries (Foutz et al., 2017). Under the ACA, however, DSH payments are set to be reduced drastically—a $43 billion reduction between 2018 and 2025 (Foutz et  al., 2017). Although hospitals provide about 60% of all uncompensated care services and receive signif- icant government assistance, most of the uncompen- sated care provided by nonhospital physicians is not subsidized (Foutz et  al., 2017). Every dollar spent by providers, governments, and communities to cover uncompensated care costs is a dollar that is not spent on another public need. There are a variety of high- cost public health needs, such as battling infectious

FIGURE 4-12 Barriers to Health Care Among Nonelderly Adults by Insurance Status, 2016

Healthcare Access 59

0 No usual source

of care Postponed seeking

care due to cost

Note: Includes nonelderly adults ages 18–64. Includes barriers experienced in past 12 months. Respondents who said usual source of care was the emergency room were included among those not having a usual source of care. All differences between uninsured and insurance groups are statistically significant (p < 0.05).

49%

12% 12%

23%

9% 6%

20%

8%

18%

14%

6% 3%

Went without needed care due to cost

Postponed or did not get needed prescription

drug due to cost

10

5

25

30

35

40

45

50

20

15

Uninsured

Medicaid/other public

Employer/other private

Source: Foutz et al., 2017; Kaiser Family Foundation analysis of the 2016 National Health Interview Survey.

 

 

diseases like tuberculosis, engaging in emergency pre- paredness planning, and promoting healthy behaviors. Public and private funds used to cover uncompen- sated care, especially when the care is more expensive than necessary because of the lack of preventive care or early interventions, are resources that are no longer available to meet the country’s other health needs.

An additional cost associated with the uninsured is the cost of lower productivity. This cost refers to the reduced productivity in the workforce stemming from the lower health status associated with being uninsured. Productivity may be reduced when workers are absent or when they are not functioning at their highest level due to illness. In addition, several studies show that pro- viding health insurance helps employers recruit better employees and that workers with health insurance are less likely to change jobs, reducing the costs of hiring and training new employees (Families USA, 2005).

Finally, there is a “spillover” effect of uninsurance for insured individuals. In communities with high rates of uninsured, even insured individuals are less likely to have a usual source of care, schedule an office visit, be satisfied with the quality of care they receive, and obtain needed care (Gresenz & Escarce, 2011; Pauly & Pagán, 2007). This spillover occurs because providers in communities with high uninsured rates may earn less revenue relative to costs. Insured indi- viduals may suffer if subsidies are not available to pro- viders to allow for higher revenue or if government spending on subsidies for the uninsured crowd out spending on services that might benefit the insured (Pauly & Pagán, 2007). In addition, physicians in com- munities with high uninsurance rates may choose to provide fewer types of services or fewer office hours due to profitability concerns. Finally, the insured may suffer if their provider treats them the same as

uninsured patients, who may demand and receive fewer services or lower-quality services from their providers (Gresenz & Escarce, 2011).

The Underinsured While there are disagreements about how to mea- sure the underinsured, in general being underinsured means individuals do not have the financial means to cover the gap between what their insurance coverage pays for and the total cost of their medical bills. As a result, they spend a high proportion of their income on healthcare services. A July 2014 survey found that 23% (31 million) of adults ages 19 to 64 years were under- insured (Collins, Rasmussen, Beutel, & Doty, 2015). Of particular concern are the 45% of underinsured adults younger than 65 years who are on Medicare, because they were the sickest population in the survey. Ninety-one percent of them are in fair or poor health or are disabled, and they are the second-poorest popu- lation after Medicaid beneficiaries (Collins et al., 2015).

The underinsured problem is exacerbated during a recession when more individuals cannot afford to pay their deductibles and co-payments. Insurance status is clearly linked to the decision to delay care due to cost. In the 2014 survey, 57% of uninsured individuals and 44% of underinsured respondents reported avoiding care due to cost, compared to 23% of insured individ- uals (Collins et al., 2015). In addition, over half (51%) of underinsured adults indicated they had problems paying medical bills or were currently paying off med- ical debt, which is twice the rate of other insured adults who are not underinsured (Collins et al., 2015). As a result, everyone ends up paying for the underinsured. Providers attempt to shift the cost associated with the underinsured and uninsured to others who can afford

FIGURE 4-13 Problems Paying Medical Bills by Insurance Status, 2016

60 Chapter 4 Overview of the United States Healthcare System

0 Problems paying or unable to pay

medical bills

Worried about being able to pay costs for normal care

Note: Includes nonelderly adults ages 18–64. All differences between uninsured and insured groups are statistically significant (p < 0.05).

29%

14%

63%

26%

76%

44%

30% 24%

Worried about paying medical bills if get sick

Medical bills being paid off over time

20

10

50

60

70

80

40

30

Uninsured

Insured

Source: Foutz et al., 2017; Kaiser Family Foundation analysis of the 2016 National Health Interview Survey.

 

 

to pay, including the government and insured individ- uals. Institutions such as hospitals may try to negotiate higher reimbursement for their services, which leads insurers to charge higher premiums to their clients to cover the additional costs.

Insurance Coverage Limitations Even individuals with insurance coverage may face healthcare access problems due to coverage limita- tions. These limitations could include high levels of cost sharing, reimbursement and visit caps for specific services, and service exclusions. (Another problem— annual and lifetime dollar limits on coverage—was eliminated by the ACA.)

Cost Sharing A typical insurance plan includes premiums, deduct- ibles, and co-payments (the latter can also be designed as co-insurance). A premium is an annual cost, typ- ically charged monthly, for enrolling in a plan. For those with health insurance through their employer, the premium is often split between employer and employee. The average annual premium for a single coverage was $6,690 in 2017, although individuals in high-deductible plans averaged somewhat less in pre- miums ($6,024) (KFF & Health Research Educational Trust [HRET], 2017). Figure 4-9 and FIGURE 4-14 show the increase in monthly premiums over the last decade and also how much faster premiums have

FIGURE 4-14 Average Annual Premiums for Single and Family Coverage, 1999–2017

Healthcare Access 61

1 9 9 9

2 0 0 0

2 0 0 1

2 0 0 2

2 0 0 3

2 0 0 4

2 0 0 5

2 0 0 6

2 0 0 7

2 0 0 8

2 0 0 9

2 0 1 0

2 0 1 1

2 0 1 2

2 0 1 3

2 0 1 4

2 0 1 5

2 0 1 6

2 0 1 7

$0

$6,000

$8,000

$10,000

$12,000

$18,000

$20,000

$16,000

$14,000

$4,000

$2,000

$ 3 ,3

8 3 *

$ 9 ,0

6 8 *

$ 3 ,6

9 5 *

$ 9 ,9

5 0 *

$ 4 ,0

2 4 *

$ 1 0 ,8

8 0 *

$ 4 ,2

4 2 *

$ 1 1 ,4

8 0 *

$ 4

,4 7 9 *

$ 1 2 ,1

0 6 *

$ 4 ,7

0 4 *

$ 1 2 ,6

8 0 *

$ 5 ,0

4 9 *

$ 1 3 ,7

7 0 *

$ 5 ,4

2 9 *

$ 1 5 ,0

7 3 *

$ 5 ,8

8 4 *

$ 1 6 ,3

5 1 *

$ 6 ,4

3 5

$ 1

8 ,1

4 2

*

$ 6 ,6

9 0 *

$ 1

8 ,7

6 4

*

$ 6 ,2

5 1 *

$ 1 7

,5 4

5 *

$ 6 ,0

2 5

$ 1 6 ,8

3 4

*

$ 5 ,6

1 5 *

$ 1 5 ,7

4 5 *

$ 4 ,8

2 4

$ 1 3 ,3

7 5 *

$ 2 ,6

8 9 *

$ 7 ,0

6 1 *

$ 2 ,4

7 1 *

$ 6 ,4

3 8 *

$ 2 ,1

9 6

$ 5 ,7

9 1

$ 3 ,0

8 3 *

$ 8 ,0

0 3 *

Single coverage

Family coverage

*Estimate is statistically different from estimate for the previous year shown (p < 0.05).

Source: Kaiser/HRET Survey of Employer-Sponsered Health Benefits, 1999–2017.

 

 

risen relative to wages and inflation. A deductible is an amount the insured pays out-of-pocket before the insurance plan assists with the costs of health- care services. There may be an annual deductible for the plan overall or separate deductibles for different types of services covered by the plan, such as inpatient care, outpatient care, and prescription drug coverage. Co-payments refer to a specific dollar amount that patients pay when they receive services or drugs. For example, one might have a $15 co-payment to see a primary care provider for an office visit. Co-insurance refers to a percentage of service cost that patients pay when they receive services or drugs. For example, an insured might have a 20% co-insurance requirement to see a primary care provider for an office visit. If the visit cost $150, a 20% co-insurance requirement would cost $30. Co- payment and co-insurance amounts may vary depending on the service received.

Cost-sharing requirements can vary widely by plan and plan type. Some plans do not have general deductibles, and for those with general deductibles, the amount varies significantly. For example, in 2017 the average deductible for a single worker was $1,505, though deductibles vary by plan type and employer size. Preferred provider organizations (PPOs) had the lowest average deductible ($1,046), while high- deductible health plans averaged $2,304 for single workers. Coverage for single workers in small firms is

much higher ($1,594) than it is for those in large firms ($856) (KFF & HRET, 2017). A significant number of plans have deductibles of $1,000 or more (FIGURE 4-15).

Variation also exists for service-specific costs. It is rare for private plans to have separate deductibles for hospital admissions, outpatient surgery, or ED visits, but patients generally have cost-sharing arrangements for these services. For example, in private plans the average co-payment for ED visits is $180 and the aver- age co-payment for outpatient surgery is $231 (KFF & HRET, 2017). Medicare, on the other hand, charged a $1,340 deductible for the first 60 days of hospital- ization in 2018. Medicare beneficiaries do not pay a per diem for the first 60 days in a hospital, but they then pay $335 per day for the next 3 months. This fee increases for longer stays (Centers for Medicare and Medicaid Services, 2017).

Reimbursement and Visit Caps Insurance plans may limit the amount they will reim- burse for a specific service during the year, with patients responsible for costs that exceed dollar amount limits. In addition, plans may limit the number of times a patient may see a certain type of provider during the year. Visit caps vary by insurance plan. For example, a plan might limit a member to 90 physical therapy vis- its per year per injury, or to 20 visits per calendar year

FIGURE 4-15 Percentage of Covered Workers Enrolled in a Plan With a General Annual Deductible of $1,000 or More for Single Coverage, by Firm Size, 2009–2017

62 Chapter 4 Overview of the United States Healthcare System

80%

40%

30%

20%

10%

0%

50%

P e rc

e n ta

g e o

f C

o ve

re d W

o rk

e rs

60%

70%

2012 2013 2014 2016 20172015201120102009

40%

46% 50% 49%

58%* 61%

63% 65%

58%

51%

48%

51%

45%

46%

39%*

41%

32%

38%

28%

34%

26%

31%

22%*

27%*

17%

22%

13%

*Estimate is statistically different from estimate for the previous year shown (p < 0.05).

Note: These estimates include workers enrolled in HDHP/SOs and other plan types. Average general annual health plan deductibles for PPOs, POS plans, and HDHP/SOs are for in-network services.

All small �rms (3–199 Workers) ALL FIRMS

All large �rms (200 or more workers)

Source: “2017 Employer Health Benefits Survey,” 2017.

 

 

for acupuncture. Once a patient reaches these limits, the insurance plan will not cover additional visits and the patient would have to pay the entire cost of a visit out-of-pocket.

Service Exclusions Health insurance plans may also partially or fully exclude certain types of services from coverage alto- gether. For example, a plan might cover high-dose chemotherapy associated with bone marrow trans- plants for only specified organ and tissue transplants and home health services only if certain conditions are met. Examples of services not covered at all by a plan include nonrigid orthopedic or prosthetic devices such as wigs or elastic stockings, eyeglasses, hearing aids, exercise programs, assisted reproductive tech- nology, or physical exams for obtaining or continuing employment.

Coverage for abortion and family planning ser- vices is also limited in many instances. Federal funds may be used for abortion services only in cases of rape or incest or to save the life of the pregnant woman. The ACA does not include abortion services as part of its essential health benefits package, and any cov- erage of abortion services must be paid with private dollars, not with federal subsidies. As of June 2018, 11 states have enacted laws that restrict abortion cover- age in all private plans in the state, 25 states restrict abortion coverage in private plans offered through their exchange, and 21 states restrict abortion cover- age in public employee plans (Guttmacher Institute, n.d., 2018a).

Regarding contraceptive coverage, the ACA requires most health insurance plans to cover all con- traceptive methods approved by the Food and Drug Administration and related counseling services with- out cost-sharing. Federal regulations exempt religious organizations from having to provide contraceptive coverage and make an accommodation for certain other employers with religious objections to avoid pay- ing for or arranging contraceptive coverage, while still allowing employees to obtain coverage through their health insurance plan (Guttmacher Institute, 2018b). In October 2017, the Trump administration issued regulations that expand the ability of organizations to refuse to provide contraceptive coverage due to reli- gious or moral objections, but these regulations are, at the time of this writing, blocked by court rulings. Due to concerns that federal guarantees for contracep- tive coverage may be limited in the future, many states have passed laws protecting coverage. As of June 2018, 29 states require insurance plans to cover the full range of contraceptive drugs, 9 states prohibit cost-sharing

for contraceptives, and 5 states prohibit other restric- tions and delays by insurers. At the same time, 21 states exempt select employers and insurers from providing contraceptive coverage based on religious objections (Guttmacher Institute, 2018b). Given the litigation relating to contraceptive coverage requirements and exemptions/accommodations, it is not yet clear what requirements, if any, plans will have to follow regard- ing contraceptive coverage in the future.

Safety Net Providers Securing access to care can be difficult for those without comprehensive private insurance. For the uninsured, the high cost of care is often a deterrent to seeking care. For those with public coverage, it is often difficult to find a provider willing to accept their insurance due to the low reimbursement rates and administrative burdens associated with participating in these programs. For these patients and the under- insured, the “healthcare safety net” exists.

The healthcare safety net refers to providers who serve disproportionately high numbers of uninsured, underinsured, and publicly insured patients. Although there is no formal designation indicating that one is a safety net provider, the Health and Medicine Division (HMD) of the National Academy of Sciences (for- merly the Institute of Medicine [IOM]) defines the healthcare safety net as “those providers that organize and deliver a significant level of health care and other related services to uninsured, Medicaid, and other vulnerable populations” (IOM, 2000a, p. 21). “Core” safety net providers are those who serve vulnerable populations and have a policy of providing services regardless of patients’ ability to pay. Some safety net providers have a legal requirement to provide care to the underserved, while others do so as a matter of principle (IOM, 2000a, p. 21).

Who are safety net providers? It is a difficult ques- tion to answer because there is no true safety net “sys- tem.” Safety net providers can be anyone or any entity providing health care to the uninsured and other vul- nerable populations, whether community or teaching hospitals, private health professionals, school-based health clinics, or others. Those providers that fit the narrower definition of “core” safety net providers include some public and private hospitals, commu- nity health centers, family planning clinics, and public health agencies that have a mission to provide access to care for vulnerable populations. Safety net provider patient loads are mostly composed of people who are poor, on Medicaid, or uninsured, and are members of racial and ethnic minority groups. For example, in 2016, 92% of federally qualified community health

Healthcare Access 63

 

 

center (FQHC) patients had incomes at or below 200% FPL, 72% were on Medicaid or uninsured, 23% were African American, and 35% were Hispanic/ Latino (National Association of Community Health Centers [NACHC], 2018a). Of the America’s Essential Hospitals (formerly National Association of Public Hospitals and Health Systems) member hospital inpa- tient discharges, in 2016, about 46% were covered by Medicaid or uninsured, and 68% were racial or ethnic minorities (America’s Essential Hospitals, 2018).

FQHCs provide comprehensive primary medical care services, culturally sensitive care, and enabling services such as transportation, outreach, and trans- lation that make it easier for patients to access ser- vices. Many health centers also provide dental, mental health, and pharmacy services. Because health cen- ters are not focused on specialty care, public hospitals are often the sole source of specialty care for unin- sured and underserved populations (Makaroun et al., 2017). In addition, public hospitals provide traditional healthcare services, diagnostic services, outpatient pharmacies, and highly specialized trauma care, burn care, and emergency services (America’s Essential Hospitals, 2018). Although not all local government health departments provide direct care, many do. Local health departments often specialize in caring for specific populations, such as individuals with HIV or drug dependency, as compared to public hospitals and health centers, which provide a wider range of services (IOM, 2000a, pp. 63–65).

Safety net providers receive funding from a vari- ety of sources, but they often struggle financially. Medicaid is the single largest funding stream for health centers, accounting for 43% of their revenue (NACHC, 2018b). Due to low Medicaid reimburse- ment, Medicaid revenue accounts for only 80% of the cost of providing care to Medicaid patients served by health centers (NACHC, 2018a). Federal grants to health centers are intended to cover the cost of car- ing for the uninsured; however, this grant funding has not kept pace with the cost of provided care. Due to low federal reimbursement, health centers incurred a $1 billion gap in the cost of care for treating the unin- sured in 2016 (NACHC, 2018a). In addition, payment from private insurance is unreliable due to the high- cost-sharing plans held by many privately insured, low-income individuals. Furthermore, Medicare payments to health centers are capped under federal law at an amount that does not match the growth in healthcare spending.

Public hospitals face a similarly difficult eco- nomic picture. Many public hospital services are not fully reimbursed because payments made by indi- viduals or insurers do not match the cost of care. In

2016, Essential Hospitals members provided almost $5.5 billion in uncompensated care, which equals almost 14% of all the uncompensated care provided nationally (America’s Essential Hospitals, 2018). Like health centers, public hospitals receive funds to cover low- income patients, including Medicaid DSH pay- ments, state and local subsidies, and other revenues such as sales tax and tobacco settlement funds. In 2016, Essential Hospitals had an average aggregate operating margin of 4%, compared to 7.8% for all U.S. hospitals. Without DSH payments, Essential Hospitals’ aggre- gate operating margin would dip to –1.4% ( America’s Essential Hospitals, 2018). Thus, the reduction in DSH payments that occurred as part of health reform is particularly concerning for safety net hospitals.

For all the positive work accomplished by safety net providers, they cannot solve all healthcare prob- lems for vulnerable populations. Safety net patients may lack continuity of care, whether because they cannot see the same provider at each visit or because they have to go to numerous sites or through vari- ous programs to receive all the care they need. Even though safety net providers serve millions of patients every year, there are not enough providers in enough places to satisfy the need for their services. While the ACA included an infusion of funds to safety net pro- viders, they also will serve an influx of newly insured patients. Health centers received $11 billion under the ACA and increased their patient population by 10% over 2 years, to serve 24 million patients in 2015 (Rosenbaum et al., 2017). And, as noted earlier, many safety net providers are underfunded and constantly struggling to meet the complex needs of their patient population.

The problems facing the uninsured and the stress- ors on the healthcare safety net highlight the inade- quacies of the current “system” of providing health care, and many of these problems will remain even after the ACA is implemented. Given the country’s patchwork of programs and plans, decisions made in one area can significantly affect another. For example, if Medicaid reimbursement rates are cut or program eligibility is reduced, safety net providers will have a difficult time keeping their doors open while, simul- taneously, more patients will become uninsured and seek care from safety net providers. If more people choose high-deductible private insurance plans that they cannot easily afford, individuals may go without needed services or safety net providers will end up providing an increasing amount of uncompensated care. If employers decide to reduce or end coverage or increase employee cost sharing, previously insured people may fall into the ranks of the uninsured. As  a result, safety net providers and their patients

64 Chapter 4 Overview of the United States Healthcare System

 

 

are affected by many policies that are not directed at them, but still greatly impact their ability to provide or access care.

Workforce Issues Problems accessing care may also occur due to pro- vider shortages and an uneven distribution of provid- ers throughout the country. This problem affects both the uninsured and the insured alike. If a provider is not available to take you as a patient, it matters little if you have an insurance plan that would cover the cost of your care. Of course, if a provider shortage is so great that those with insurance are turned away, the unin- sured will have an even harder time accessing care.

There are a variety of estimates regarding a future healthcare workforce shortage. For example, the Asso- ciation of American Medical Colleges estimates a phy- sician shortfall between 42,600 and 121,300 by 2030 (Dall, West, Chakrabarti, Reynolds, & Iacobucci, 2018). On the other hand, if healthcare delivery approaches that rely heavily on nonphysician providers are used more often in the future, the estimates for physician shortages decline significantly. Two such models are the patient-centered medical home (PCMH), which relies on a team of providers to supply and coordinate care, and the nurse-managed health center (NMHC), which is a clinic with nurse practitioners (NPs) as the primary caregiver (Auerbach et al., 2013). One study estimated that increased use of PCMHs or NMHCs alone would reduce a primary care physician shortage from 45,000 to 35,000. Used together, the combination of approaches could cut the physician shortage in half (Auerbach et al., 2013).

One of the main concerns with the healthcare workforce is a shortage of primary care providers. It is expected that there will be between 14,800 and 49,300 fewer primary care physicians than are needed to meet demand by 2030 (Dall et al., 2018). More providers are choosing specialty care over primary care. About 30%

of physicians practice primary care today, as opposed to 70% 50 years ago (Mitra, 2016). Midlevel provider career choices have followed a similar pattern. From 1974 to 2012, the percentage of physician assistants (PAs) working in primary care declined from 70% to 34% (Dunker, Krofah, & Isasi, 2014). NPs and PAs are more likely to work in hospitals or specialty care offices than to provide services in office-based primary care (Colwill, Cultice, & Kruse, 2008). The long work hours, increased demands (particularly administra- tive demands associated with insurance companies), lack of respect, and comparatively low pay for pri- mary care providers are sending future practitioners to other fields (Castellucci, 2016). For example, one study showed that, over a lifetime, a cardiologist will make $2.7 million more than a primary care physician (Vaughn, DeVrieze, Reed, & Schulman, 2010).

While fewer graduates are turning to primary care, demand for primary care services is expected to increase in the next several years. Most of the increased demand will be due to population growth and aging, with the remaining uptick in demand based on the increase of insured individuals under the ACA (Dall et al., 2018). The U.S. population is aging, with individuals older than 65 years projected to increase from 15% in 2017 to 21% in 2030 (U.S. Cen- sus Bureau, 2018). These older patients are heavy users of healthcare services. Even though older patients made up about 12% of the population in 2008, they accounted for over 45% of all primary care office visits that year (Centers for Disease Control and Prevention [CDC], 2010). Furthermore, geriatric training is lack- ing among primary care providers. An IOM report on aging and the healthcare workforce found medical school curricula on geriatric medicine to be “inade- quate” (IOM, 2008, p. 129). Physicians agree: in a 2002 survey, only half of all responding physicians thought their colleagues could adequately treat a geriatric condition (IOM, 2008, pp. 128–129), and in a 2007 study, only 23% of medical school graduates indicated they received expert geriatric training (Association of American Medical Colleges, 2012).

In addition to provider shortages, access prob- lems may exist because providers are not distributed as needed throughout the country (FIGURES 4-16 through 4-18). In 2013, 29 states had a primary care physician shortage, with Texas and Florida expe- riencing the greatest deficits (over 1,000 full-time- equivalent [FTE] providers). By 2025, it is estimated that 37 states will have a primary care physician shortage, with 12 states experiencing a deficit of 1,000 FTE providers or more (Health Resources Services Administration [HRSA], 2016). In contrast, Massa- chusetts has a primary care physician surplus that it

BOX 4-3 Discussion Questions

Safety net providers mostly serve uninsured and publicly insured low-income patients. Many of the safety net provider features you just read about are in place to assist these patients in accessing health care. Instead of pursuing universal coverage, would it be an equally good strategy to expand the number of safety net providers? Are there reasons for both safety net providers and health insurance to exist? How does having insurance relate to accessing care?

Healthcare Access 65

 

 

expects to maintain through 2025. Similarly, primary care NP and PA shortages vary across the country. In 2013, 23 states had a primary care NP shortage, but no states are projected to have a shortfall by 2025 (HRSA, 2016). Regarding primary care PAs, 22 states

had a shortage in 2013. In 2025, 9 states are expected to have a PA shortage, while 5 states (New York, North Carolina, Texas, California, and Colorado) are projected to have a surplus of more than 1,000 FTE (HRSA, 2016).

AK

HI

WA

ID

MT

WY

CO

ND MN

IA

MO

AR

LA

MS AL GA

FL

SC

NC TN

KY

INIL

WI

MI

OH

PA

WV VA

NYSD

NE

KS

OK

TX

NMAZ

UT NV

OR

CA

*Note: Estimates in states with an RSE > 20% should be used with caution because of large sampling error.

902–4,032

4,033–7,017

7,018–13,986

13,987–26,841

26,842–94,385

RSE 20–29%*

DC

Total number

NJ DE MD

ME VT

NH MA

CT RIWY

ND

FIGURE 4-16 Number of Physicians by State, 2008–2010 Source: See Figure 2 from The US Health Workforce Chartbook, HRSA, 2013, retrieved from https://bhw.hrsa.gov/sites/default/files/bhw/nchwa/chartbookpart1.pdf

AK

HI

WA

ID

MT

WY

CO

ND MN

IA

MO

AR

LA

MS AL GA

FL

NC TN

INIL

WI

MI

OH

PA

WV VA

NYSD

NE

OK

TX

NMAZAZ

UT NV

OR

CA

*Note: Estimates in states with an RSE > 20% should be used with caution because of large sampling error. **Data are not reported at the state level, because the RSE ≥ 30%; estimate does not meet standards of reliability.

597–763

764–1,394

1,394–2,204

Not reportable**

2,205–3,649

3,650–10,198

RSE 20–29%*

DC

Total number

NJ DE MD

ME VT

NH MA

CT RI

ID

MS

WV

NE

OK

NV

KYKY KS

SCSC

KS

LA

IA

FIGURE 4-17 Number of Physician Assistants by State, 2008–2010 Source: See Figure 7 from The US Health Workforce Chartbook, HRSA, 2013, retrieved from https://bhw.hrsa.gov/sites/default/files/bhw/nchwa/chartbookpart1.pdf

66 Chapter 4 Overview of the United States Healthcare System

 

 

Rural areas are particularly susceptible to pro- vider shortages. This is an especially pressing problem because individuals who live in rural areas are more likely to be sicker, older, and poorer than their urban counterparts. Compared to urban dwellers, rural residents are more likely to lack access to a primary care physician, have higher rates of chronic diseases and teen pregnancies, and engage in more unhealthy behaviors such as smoking (National Conference of State Legislatures, 2017).

In 2017, 59% of designated Health Professional Shortage Areas were in rural areas (National Confer- ence of State Legislatures, 2017). The number of spe- cialists in rural areas is only 30 per 100,000 people, compared to 263 per 100,000 in urban areas (National Rural Health Association [NRHA], n.d.). While the gap is not as prominent for primary care physicians, they also prefer urban locations. The patient–primary care physician ratio in rural areas is 39.8 per 100,000, compared to 53.3 per 100,000 in urban areas (NRHA, n.d.). Primary care providers are vital to the health- care workforce in rural areas. While family physicians comprise only 15% of outpatient physicians in the country, they provide 42% of services in rural areas (NRHA, n.d.).

Rural areas are more likely to attract NPs and PAs than physicians, suggesting that alternative care mod- els that focus on nonphysician providers may be partic- ularly useful in addressing access issues in rural areas (Graves et  al., 2016). FQHCs have already embraced this model, hiring NPs, PAs, and nurse–midwives at a

faster rate than physicians (Proser, Bysshe, Weaver, & Yee, 2015).

Shortages also exist within the public health work- force. The public health workforce has been defined to include anyone who is providing 1 of the 10 essen- tial public health functions (discussed in the Public Health Institutions and Systems chapter), regardless of whether their employer is a government agency, not-for-profit organization, private for-profit entity, or some other type of organization (Center of Excellence, 2013). The public health workforce includes profes- sions such as public health physicians and nurses, epi- demiologists, health educators, and administrators. It is difficult to count everyone involved in the public health workforce, given the wide array of jobs and the numerous data sources needed to compile the infor- mation. In 2012, the public health field was estimated to include between 310,000 and 342,000 workers. This represents a worker-to-population ratio of 99 to 110  per 100,000 people, which is substantially lower than the earlier estimates in 1980 (220 per 100,000 people) and 2000 (158 per 100,000 people) (Center of Excellence, 2013).

The ACA contains a number of provisions, intended to address some of the more pressing healthcare and public health workforce issues, which could accomplish the following goals:

■ Increase funding for community health centers ■ Increase funding for the National Health Service

Corps, which provides scholarships and loan

AK

HI

WA

ID

MT

WY

CO

ND MN

IA

MO

AR

LA

MS AL GA

FL

SC

NC TN

KY

INIL

WI

MI

OH

PA

WV VA

NYSD

NE

KS

OK

TX

NMAZ

UT NV

OR

CA

4,296–22,260 Total number

22,261–50,861

50,842–90,663

90,664–167,476

167,477–274,722

DC

NJ DE MD

ME VT

NH MA

CT RI

FIGURE 4-18 Number of Nurse Practitioners by State, 2008–2010 Source: See Figure 21 from The US Health Workforce Chartbook, HRSA, 2013, retrieved from https://bhw.hrsa.gov/sites/default/files/bhw/nchwa/chartbookpart1.pdf

Healthcare Access 67

 

 

repayments to students who agree to become pri- mary care providers and work in medically under- served communities

■ Increase funding for PA and NP training ■ Provide new funding to establish NP-led clinics ■ Provide new funding for states to plan and imple-

ment innovative strategies to boost their primary care workforce

■ Establish a National Health Care Workforce Com- mission to coordinate federal workforce efforts and bolster data collection and analysis

■ Establish teaching health centers ■ Provide payments for primary care residencies in

community-based ambulatory care centers ■ Increase the number of Graduate Medical Educa-

tion slots available to primary providers by redis- tributing unused slots

■ Promote residency training in outpatient settings ■ Provide grants to training institutions to promote

careers in the healthcare sector ■ Increase reimbursement for primary care provid-

ers under Medicare and Medicaid

Given the uncertain political future of the ACA, it remains to be seen whether these provisions will be implemented or funded in the years to come.

▸ Healthcare Quality As noted earlier in this chapter, the United States spends more on health care than most other devel- oped countries, yet frequently the care provided does not result in good health outcomes. Researchers and policymakers have highlighted the need to improve the quality of care provided in this country. A 2003 landmark study raised many quality concerns, includ- ing findings that patients received the appropriate medical care only 55% of the time and that patients were much more likely not to receive appropriate services than to receive potentially harmful care (McGlynn, Asch, & Adams, 2003). The lack of appro- priate care was seen across medical conditions, simi- larly affecting treatments relating to preventive care, acute care, and chronic diseases (McGlynn et al., 2003, p. 2641). The degree to which patients received appro- priate care varied greatly. For example, only 10% of patients with alcohol dependence received the stan- dard of care, as opposed to 78% of those with senile cataracts (McGlynn et al., 2003, p. 2641). In addition, many adults do not receive all of the recommended preventive measures. A 2015 study found that only 8% of respondents age 35 years and older reported receiv- ing all of the recommended preventive measures,

and only 20% reported receiving most (75%) of them (Borsky et al., 2018). On the other hand, 5% reported receiving none of the recommended preventive mea- sures (Borsky et al., 2018).

Key Areas of Quality Improvement In 2001, the IOM (again, now the HMD) released Crossing the Quality Chasm: A New Health System for the 21st Century, which represented nothing less than an urgent call to redesign the healthcare system to improve the quality of care provided (IOM, 2001b). The IOM attributes our inability to provide consistent, high-quality health care to a number of factors, includ- ing the growing complexity of health care, including quickly developing technological advancements; an inability to meet rapid changes; shortcomings in safely using new technology and applying new knowledge to practice; increased longevity among the population, which carries concerns relating to treating chronic conditions in a system better designed to address epi- sodic, acute care needs; and a fragmented delivery system that lacks coordination, leading to poor use of information and gaps in care (IOM, 2001b, pp. 2–4). In its call to redesign the healthcare system to improve quality, the IOM focuses on six areas of improvement: safety, efficacy, patient-centeredness, timeliness, effi- ciency, and equity (IOM, 2001b, p. 43).

Safety In a safe healthcare system, patients should not be endangered when receiving care that is intended to help them, and healthcare workers should not be harmed by their chosen profession (IOM, 2001b, p. 44). In an earlier report, To Err Is Human, the IOM found that deaths due to medical errors in hospitals could be as high as 98,000 annually and cost up to $29 billion, over half of which is attributable to health- care costs (IOM, 2000b, pp. 1–2). A safe healthcare system also means that standards of care should not decline at different times of the day or week or when a patient is transferred from one provider to another. In addition, safety requires that patients and their fami- lies are fully informed and participate in their care to the extent they wish to do so (IOM, 2001b, p. 45).

Efficacy While scientific evidence regarding a particular treat- ment’s effectiveness is not always available, an effective healthcare system should use evidence-based treat- ments whenever possible. This effort includes avoid- ing the underuse of effective care and the overuse of

68 Chapter 4 Overview of the United States Healthcare System

 

 

ineffective care (IOM, 2001b, p. 47). Evidence-based medicine is not limited to findings from random- ized clinical trials, but may use results from a vari- ety of research designs. To promote the use of evidenced-based medicine, healthcare providers and institutions should improve their data collection and analysis capabilities so it is possible to monitor results of care provided (IOM, 2001b, p. 48).

Patient-Centeredness A patient-centered healthcare system is sensitive to the needs, values, and preferences of each patient, includes smooth transitions and close coordination among providers, provides complete information and education at a level and in a language patients can understand, involves the patient’s family and friends according to the patient’s wishes, and, to the extent possible, reduces physical discomfort experienced by patients during care (IOM, 2001b, pp. 49–50). A lan- guage or cultural barrier may be a significant hurdle to receiving high-quality and patient-centered care. In 2013, one in five Americans spoke a language other than English at home (Camarota & Zeigler, 2014). Individuals with language barriers are less likely to adhere to medication regimens, have a usual source of care, and understand their diagnosis and treat- ment, and are more likely to leave a hospital against a provider’s advice and miss follow-up appointments (Speaking Together, 2007). While use of interpreters can improve a patient’s quality of care, when friends or family members serve as interpreters, there is greater risk that the interpreter will misunderstand or omit a provider’s questions and that the patient will not dis- close embarrassing symptoms (Speaking Together, 2007). Similarly, cultural differences between pro- vider and patient can result in patients receiving less than optimal care. Cultural differences can define how healthcare information is received, whether a problem is perceived as a healthcare issue, how patients express symptoms and concerns, and what type of treatment is most appropriate. As a result, healthcare organiza- tions should ensure that patients receive care that is both linguistically and culturally appropriate (Office of Minority Health, n.d.).

Timeliness A high-quality healthcare system will provide care in a timely manner. Currently, U.S. patients experience long waits when making appointments, sitting in doctors’ offices, standing in hallways before receiving procedures, waiting for test results, seeking care at EDs, and appealing billing errors (IOM, 2001b, p. 51).

These delays can take an emotional as well as physical toll if medical problems would have been caught ear- lier with more timely care. Timeliness problems also affect providers because of difficulties in obtaining vital information and delays that result when consult- ing specialists. In addition, lengthy waits are the result of a system that is not efficient and does not respect the needs of its consumers (IOM, 2001b, p. 51).

Efficiency An efficient healthcare system makes the best use of its resources and obtains the most value per dollar spent on healthcare goods and services. The uncoor- dinated and fragmented U.S. system is wasteful when it provides low-quality care and creates higher than necessary administrative and production costs (IOM, 2001b, p. 52). As indicated previously, the high level of spending and poor outcomes relating to prevent- able conditions, the number of patients who do not receive appropriate care, and the high number of med- ical errors make it clear that the quality of healthcare services provided can be improved.

In addition, significant geographic variations in the provision of healthcare services suggest a lack of efficiency in the system; however, this is a complicated issue to understand and solve. For example, the Dart- mouth Atlas Project has studied regional variations in healthcare practices and spending for several decades. Even after controlling for level of illness and prices paid for services, researchers have found a two-fold difference in Medicare spending in the country.

Furthermore, higher spending areas are not asso- ciated with better quality of care, more patient satis- faction, better access to care, more effective care, or improved outcomes (Fisher, Goodman, Skinner, &

BOX 4-4 Discussion Questions

Unfortunately, evidence is not available to support the effectiveness or cost–benefit of every procedure or drug. How should policymakers and providers make decisions when faced with a dearth of evidence? Do you prefer a more cautious approach that does not approve procedures or drugs until evidence is available or a more aggressive approach that encourages experimentation and use of treatments that appear to be effective? What about medical care for children, who are generally excluded from clinical and research trials for ethical reasons? When, if ever, is it appropriate for insurers to cover or the government to pay for treatments that are not proven effective?

Healthcare Quality 69

 

 

Bronner, 2009). Instead, both health system capac- ity and local practice styles appear to be key factors in geographic variations in cost. An IOM report addressing this issue also found that health status, demographics, insurance plan coverage, and market factors did not explain the variation (IOM, 2013). The report highlighted the use of post-acute care and acute care services as a key concern and noted that other factors, such as patient preference and provider dis- cretion, are not included in the data analyzed. In the end, the IOM concluded, “an overall explanation for geographic variation remains elusive” (IOM, 2013). As policymakers try to improve quality of care in the United States, they will have to continue to untangle difficult questions of why some parts of the country spend more on services than others.

The nation also spends close to one-quarter of healthcare expenditures on administration, which is more than twice what the country spends on cardio- vascular disease and three times the amount it spends on cancer (Cutler, 2018). As shown in FIGURE 4-19, this high level of administrative spending dwarfs that of other countries (Bodenheimer, 2005, p. 934; Papanicolas, Woskie, & Jha, 2018). Extensive use of private insurers, who often have high administrative costs relative to public insurance programs, as well as the use of multiple insurers instead of a single-payer system, result in high administrative costs in the United States.

Equity An equitable healthcare system provides essential health benefits to all people and includes universal access to care. Equity can be considered on an indi- vidual level and on a population level (IOM, 2001b, p. 53). While the ACA should improve individual access to services by reducing the number of unin- sured, insurance alone is not sufficient to ensure access to care. The care itself still must be accessible (provid- ers are willing to accept you as a patient), affordable, and available (sufficient providers are available).

Population-level equity refers to reducing health- care disparities among subgroups. In the United States, racial and ethnic minority groups often receive lower-quality care and fewer routine preventive pro- cedures than White people. A 2003 IOM report found that African Americans were less likely than Whites to receive appropriate cardiac medication, undergo necessary artery bypass surgery, and use dialysis or receive a kidney transplant even when controlling for factors such as age, insurance status, income level, and comorbidities. Not surprisingly, African Americans also had higher mortality rates than their White coun- terparts (IOM, 2003, pp. 2–3).

These trends continue. In 2014, African Americans were still more likely than Whites to have asthma, diabetes, cardiovascular disease and AIDS. African American men have the shortest life expectancy

*Or nearest year; data from 2014 for Australia and Canada. No recent data for New Zealand (since 2007). Data reflect current spending on governance and health system and financing administration, in current prices, current PPPs. ‘OECD median’ reflects the median of 34 OECD countries.

34 89 90

123 141 206

255 272 286

787

0

100

200

300

400

500

600

700

800

900

Un ite

d St

at es

Sw itz

er la nd

Fr an

ce

G er

m an

y

Ne th

er la nd

s

Ca na

da

Au st ra

lia

Un ite

d Ki

ng do

m

Sw ed

en

No rw

ay

Dollars ($US)

OECD MEDIAN

Adjusted for Differences in Cost of Living

FIGURE 4-19 Spending on Health Insurance Administration per Capita, 2015 Source: Retrieved from https://www.commonwealthfund.org/publications/publication/2017/nov/multinational-comparisons-health-systems-data-2017

70 Chapter 4 Overview of the United States Healthcare System

 

 

(Orgera & Artiga, 2016). As compared to Whites, His- panics were more likely to be diabetic, experience peri- odontitis, be HIV positive, and be uninsured, and less likely to be screened for colorectal cancer or receive the flu vaccine as an infant (CDC, 2013). Hispanics are more likely than Whites to have asthma, liver disease, tuberculosis, and diabetes, and to die from cervical can- cer, HIV, and end-stage renal disease (Families USA, 2014). In 2016, the Agency for Healthcare Quality and Research (AHQR) found access to care was worse for African Americans on 50% of their measures and for Hispanics on 75% of their measures (AHQR, 2016).

While this country continues to struggle with health disparities, the ACA has made a positive differ- ence. From 2013 to 2015, racial disparities narrowed in terms of percentage of working adults who were uninsured, who skipped care due to cost, and who lacked a usual source of care (Hayes, Riley, Radley, & McCarthy, 2017).

Assessment of Efforts to Improve Quality The IOM has called for sweeping changes to the health- care system to address the numerous ways in which the quality of care could be improved. In 2015, the Depart- ment of Health and Human Services (HHS) issued a progress report on its Action Plan to Reduce Racial and Ethnic Health Disparities, which included a number of activities HHS had already taken and goals for future activities (HHS, 2015). While the ACA makes signifi- cant changes to the healthcare system, the law is focused more on improving access than improving quality or the delivery system. Many of the law’s quality improvement provisions are pilot programs and demonstration proj- ects that may eventually result in significant changes— or fall to the wayside once they expire.

None of the quality improvement tasks the IOM calls for will be simple to achieve, and, at times, they seem to have conflicting goals. For example, making the healthcare system patient-centered may not always result in enhanced efficiency. Furthermore, the IOM’s proposed changes would require increased resources at a time when the United States is facing record defi- cits and unsustainable healthcare spending levels. Improving the quality of the healthcare system is an enormous challenge and one that is likely to remain on the nation’s agenda for years to come.

▸ Comparative Health Systems A review of the U.S. healthcare system and a discus- sion of its flaws often leads one to ask, how do other countries deliver health care, and do they do a better

job? Because the United States spends more overall and more per person on health care comparatively speaking and yet often lags in many quality and out- come indicators, perhaps there are lessons to learn from other countries (FIGURE 4-20). While there are many problems with healthcare delivery in the United States, it is also true that each type of healthcare sys- tem has its advantages and drawbacks.

There are three types of healthcare systems often found in other countries: (1) a national health insur- ance system that is publicly financed, but in which care is provided by private practitioners (e.g., Canada); (2) a national health system that is publicly financed and where care is provided by government employees or contractors (e.g., Great Britain); and (3) a socialized insurance system that is financed through mandatory contributions by employers and employees and in which care is delivered by private practitioners (e.g., Germany) (Shi & Singh, 2019, p. 22). Of course, varia- tions exist within these types of systems in terms of the role of the central government, the presence of private insurance, the way the healthcare system is financed, and how care is administered by providers and accessed by patients. While comparing the systems in the three countries used as examples does not cover all possible permutations of how healthcare systems are designed, it provides an overview of the choices made by policymakers in different countries (TABLE 4-1).

A National Health Insurance System: Canada Canada’s healthcare system is called Medicare. Prior to establishing the Medicare program in 1966, Canada provided insurance in a manner that was similar to the U.S. method, with private plans offering coverage to many, even while millions remained uninsured. Incre- mental changes were made to the Canadian healthcare system until the Medical Care Act of 1966 established Medicare’s framework; it was later modified through the Canadian Health Act of 1984. The Canadian Health Act established five principles for health care delivery: (1) public administration, (2) comprehen- sive coverage, (3) universality, (4) portability across Canada, and (5) uniform and reasonable access to care (Johnson, Stoskopf, & Shi, 2018).

Canada’s healthcare system is largely decentralized, with Canada’s provinces and territories responsible for setting up their own delivery system. As such, Canada’s Medicare system is a collection of single-payer systems governed by the provinces and territories, with the cen- tral government taking a more limited role. The prov- inces and territories set their own policies regarding

Comparative Health Systems 71

 

 

0

2

4

6

8

10

12

14

16

18

1980 1982 1984 1986 1988 1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012 2014

P e rc

e n ta

g e

United States (16.6%)

Switzerland (11.4%)

Sweden (11.2%)

France (11.1%)

Germany (11.0%)

Netherlands (10.9%)

Canada (10.0%)

United Kingdom (9.9%)

New Zealand (9.4%)

Norway (9.3%)

Australia (9.0%)

GDP refers to gross domestic product. Data in legend are for 2014.

FIGURE 4-20 Healthcare Spending as a Percentage of Gross Domestic Product, 1980–2014 Source: Retrieved from https://www.commonwealthfund.org/chart/2017/health-care-spending-percentage-gdp-1980-2014

TABLE 4-1 Comparison of Health Systems Across Four Countries

United States Canada Great Britain Germany

System type No unified system National health insurance

National health system

Socialized health insurance

Universal coverage

Near universal if ACA fully implemented

Yes Yes Yes

Role of private insurance

Significant Supplemental to Medicare, two-thirds purchase

Minimal Minimal

Financing Private payments and tax revenue

Mostly tax revenue (federal, provincial, territorial)

All federal income tax revenue

Mandatory employer and employee contributions to national health fund

Hospital reimbursement

Varies by payer (DRGa, FFSb, capitation, per diem)

Global budget Global budget

DRGa

Physician reimbursement

Fee schedule or capitation

Negotiated fees with provinces/ territories

Salary or capitation

Negotiated fees with funds

DRGa = diagnostic-related group (payment based on bundle of services needed for diagnosis). FFSb = fee for service (payment per service rendered).

72 Chapter 4 Overview of the United States Healthcare System

 

 

many healthcare and other social issues, administer their own individual single-payer systems, reimburse hospitals directly or through regional health authori- ties, and negotiate physician fees schedules with pro- vincial medical associations. Provinces and territories use regional health authorities as their primary payer of healthcare services. While funding methods vary by location, regional health authorities have the abil- ity to tailor funds in a way that best serves the needs of their population. In addition to paying for care, regional health authorities also organize the delivery of care. They hire staff at most acute care facilities and contract for some ambulatory care services. General practitioners and specialists mostly work on a fee-for- service arrangement and in private practice (Allin & Rudoler, n.d.). The federal government has respon- sibility for specific health areas such as prescription drugs, public health, and health research, as well as for providing care to certain populations (e.g., veterans, indigenous peoples) (Allin & Rudoler, n.d.).

Financing for health benefits varies by benefit type. Hospital services, physician services, and public health services are financed through public taxation. Hospitals mostly operate under global budgets they negotiate with a ministry of health or regional health authority, although a few provinces are considering activity-based funding (Allin & Rudoler, n.d.). Cer- tain services, including prescription drugs, home care, and institutional care, are financed through a combi- nation of public taxation and private insurance cov- erage. Other goods and services, such as dental and vision care, over-the-counter drugs, and alternative medicines are covered only through private insurance. Approximately two-thirds of Canadians purchase pri- vate insurance, which is used to cover goods and ser- vices not provided by Medicare (Allin & Rudoler, n.d.).

Tax revenue from the provincial, territorial, and federal governments pays for 70% of total Medicare expenditures, while private insurance reimbursement accounts for 12% of costs, patient out-of-pocket pay- ments cover 14%, and various sources account for the remaining amount (Allin & Rudoler, n.d.). Healthcare spending is expected to reach C$242 billion in 2017 (Canadian Institute for Health Information [CIHI], “How much,” n.d.). Healthcare spending varies con- siderably across the country. For example, Alberta spends C$7,329 per person, compared to Yukon’s C$11,222 per-person costs (CIHI, “How does,” n.d.).

A National Health System: Great Britain Great Britain’s healthcare system was designed by Sir William Beveridge as part of a social reconstruc- tion plan after World War II. The National Health

Services Act of 1946 created the National Health Ser- vice (NHS), a centrally run healthcare system that provides universal insurance coverage to all residents of Great Britain. It was designed based on the princi- ple that the government is responsible for providing equal access to comprehensive health care that is gen- erally free at the point of service (Johnson et al., 2018, pp. 174–176).

The Health and Social Care Act of 2012 intro- duced significant changes to the NHS system. In the prior system, health care was delivered through a variety of trusts that covered services such as primary care, mental health care, acute care, and ambulance services (Johnson et al., pp. 178–179). In the new sys- tem, Primary Care Trusts were replaced with Clinical Commissioning Groups (CCGs), which are led by cli- nicians. CCGs are bodies that consist of general prac- titioners in their service area, and they are responsible for providing urgent and emergency care, elective hos- pital care, community health services that go beyond general practitioner services, maternity and newborn services, and mental health and learning disability services. The 2012 legislation also created an inde- pendent organization called NHS England to focus on improving health outcomes and quality of care. NHS England provides national leadership, supervises CCGs, allocates resources to CCGs, and commissions primary care, certain specialty care, military care, and offender care (Thorlby, Arora, & Nuffield Trust, n.d.).

The NHS is the largest publicly financed national health system in the world. The 2017–2018 budget is £124.7 billion, with only a 1.2% growth rate pro- jected from 2010 to 2021. This is far below the needed growth rate, which is expected to exceed 4% (King’s Fund, 2018). Due to this discrepancy, NHS projects a $6 billion deficit by 2021 (Thorlby et al., n.d.). NHS is using a number of cost containment strategies to address its budgetary concerns, including freezing wages, increasing use of generic drugs, reducing hos- pital payments, lowering administrative costs, and improving hospital management (Thorlby et al., n.d.).

The NHS is financed primarily through general tax revenues. It is NHS England’s responsibility to identify necessary healthcare services and Monitor’s (England’s regulatory body for health care) role to set prices for those services. While most residents receive their care through the NHS, private insurance is also available. Approximately 10.5% of residents have pri- vate health insurance, which provides the same bene- fits as the NHS but allows for reduced waiting times, more convenient care, and greater access to specialists (Johnson et al., 2018, p. 182; Thorlby et al., n.d.).

NHS services are provided by provider organiza- tions that are classified as NHS foundation trusts or

Comparative Health Systems 73

 

 

NHS trusts. NHS foundation trusts are not directed by the government and are free to make financial deci- sions based on a framework established by law and regulation. NHS trusts are directed by the government and are financially accountable to the government (Johnson et al., 2018, p. 181; Thorlby et al., n.d.). Most general practice physicians and nurses are private practitioners who work for the NHS as independent contractors, not salaried employees, while the NHS owns the hospitals and the hospital staff are salaried employees. Patients select a general practitioner in their service area, and this provider is the gateway to NHS services. Almost everyone has a registered gen- eral practitioner, and most patient contact is with this provider (Thorlby et  al., n.d.). Services are provided free of charge, except for specific services designated by law.

The Health and Social Care Act also renewed focus on public health needs. Public Health England was created in 2013 as an autonomous executive agency of the Department of Health. Its role is to protect the public’s health, reduce health disparities, promote health knowledge and information, and ensure that high-quality healthcare services are delivered to the public. In addition, local Health and Wellbeing Boards were created to improve the public’s health and reduce disparities through local government action (Public Health England, n.d.).

In 2014, NHS unveiled the Five Year Forward plan to address challenges to the healthcare system, with a focus on improving early identification of high-risk patients and exploring new payment models. Based on the plan, 50 “vanguards,” or pilot programs, have been established to test ideas such as “scaled-up primary care, enhanced health care in long-term care homes, vertically integrated hospital and community care, and networks to improve emergency care” (Thorlby et  al., n.d.). In addition, the plan includes a diabetes initiative, a commitment to 7-day workweeks by 2020, and “footprints” that bring together purchasers and providers in a local community to provide services under a consolidated budget (Thorlby et al., n.d.).

A Socialized Insurance System: Germany In 1883, Germany’s Otto von Bismarck created the first healthcare system in the world. He viewed a strong health and pension system as a way to build a superior nation, earn support from Germany’s working class, and undermine any attempts by Germany’s socialist party to gain power. The central government is respon- sible for setting health policy and regulating the Social Health Insurance System (SHIS). German healthcare

policy emphasizes solidarity, the idea that all should have equal access to health care regardless of ability to pay (Johnson et al., 2018, pp. 217–223). Germany’s legislature passed several major health reform bills in recent years. These reforms include integration of inpa- tient and ambulatory care, premium payment changes, an insurance mandate, and revised long-term care pol- icies (Johnson et al., 2018, pp. 230–31).

SHIS is composed of a collection of nonprofit regional sickness funds with a standard benefit package that includes inpatient services, outpatient services, medications, rehabilitation therapy, and dental benefits. The funds are organized around industry or geography and are responsible for man- aging healthcare services. Germans must enroll in sickness funds or obtain coverage through private insurance (Blümel & Busse, n.d.). Some populations are required to be under SHIS, including individu- als who earn less than $60,000 per year or are pen- sioners, students, unemployed, disabled, poor, or homeless. Funds may not refuse to cover these indi- viduals, and physicians may not refuse to treat them. Germans who earn more than $60,000 per year for 3 consecutive years or who are self-employed may choose to opt out of SHIS and purchase private cov- erage. Exempt citizens and individuals choosing to opt out of SHIS may purchase private substitu- tive private health insurance (PHI). In 2015, almost 9  million people—often young, wealthy workers who could secure a low-premium plan—enrolled in substitutive PHI (Blümel & Busse, n.d.).

Health care is provided in the public and private sectors. SHIS ambulatory care physicians generally work in private practice and are members of regional associations that negotiate a fee schedule with sick- ness funds. Fee schedules are also used by private insurers, but often at a higher rate than the SHIS fee schedule. Hospitals are split between public, private nonprofit, and private for-profit institutions, with the latter increasing its share of the market in recent years. Hospitals are staffed by salaried providers and reimbursed based on a diagnostic-related group methodology (Blümel & Busse, n.d.; Johnson et  al., 2018, p. 235).

Sickness funds are financed through employer and employee contributions. As of 2016, employer and employees split the 14.6% of gross wage contribution. In addition, there is a supplementary contribution based on income that is set by each sickness fund. The sickness fund contributions are pooled and then real- located to individuals based on a risk-adjusted formula that accounts for age, sex, and morbidity (Blümel & Busse, n.d.). In 2014, Germany spent $492 billion in

74 Chapter 4 Overview of the United States Healthcare System

 

 

concerns and how different residents fared within a system varied by country ( FIGURES 4-21 through 4-25).

While affordability was a key concern in the United States, Americans reported fewer access prob- lems than residents in many other countries. Of those surveyed, a third of U.S. residents went without care due to cost, as compared to 7% of respondents in England and Germany (Osborne et  al., 2016). Cost barriers to accessing dental care were a much big- ger concern for American and Canadian respon- dents than for those living in England or Germany. Low-income adults reported worse health and more cost concerns than wealthier individuals across all of the countries surveyed, with the United States hav- ing the highest rate of low-income respondents indi- cating that cost was a barrier to care. England was the only country where low-income adults did not report greater access problems due to cost (Osborne et  al., 2016). In terms of same-day or next-day appointments, Canadians (53%) and Germans (47%) reported more problems than American (42%) and British (41%) respondents (Osborne et  al., 2016). In addition, about 30% of Canadian adults and 19% of British adults reported having to wait at least 2 months for a specialty appointment, compared to less than 10% of adults in Germany and the United States. Germans obtained care through EDs at a much lower rate (11%) than residents of other countries, with Canadians (41%) and Americans (35%) reporting much higher use of emergency care.

BOX 4-5 Discussion Questions

Do you prefer one of these health systems to the others? Why or why not? Are there features that you think should be incorporated into the U.S. healthcare system? Are there reasons why certain features might be difficult to incorporate into the U.S. healthcare system?

FIGURE 4-21 Cost-Related Access Barriers in the Past Year Source: Retrieved from https://www.commonwealthfund.org/publications/surveys/2016/nov/2016-commonwealth-fund-international-health-policy-survey-adults

health expenditures, mostly through SHIS (Johnson et al., 2018, p. 234).

The Importance of Health Insurance Design Reviewing the healthcare systems of four countries— the United States, Canada, Great Britain, and Germany—shows how varied healthcare systems are around the world. Differences exist regarding the role of government, the ability to purchase private insur- ance, cost-sharing requirements, and how the sys- tem is financed. Even countries that share the same general type of system have variations based on their specific culture, politics, and needs. How a system is designed matters in terms of access to care, financing, and patient satisfaction. A 2016 survey in 11 coun- tries asked residents about their experience with their country’s healthcare system (Obsorne, Squires, Doty, Sarnak, & Schneider, 2016). What issues were primary

Comparative Health Systems 75

7 7 8 8 10

14 16 17

18 22

33

0

20

40

60

Un ite

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m

G er

m an

y

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ay

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lia

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P e

rc e n ta

g e *

*Had a medical problem but did not visit doctor; skipped medical test, treatment, or follow-up recommended by doctor; and/or did not fill prescription or skipped doses

 

 

▸ Conclusion This wide-ranging review of the U.S. healthcare sys- tem was intended to provide readers with a general sense of how health care is accessed, financed, and administered in this country. Understanding the var- ious players in the healthcare system, from providers to researchers to policymakers, is crucial to being able to participate in debates over current issues in health policy and law. While the U.S. system excels on many

fronts, it falls short in many areas relating to access, quality, and efficiency. Perhaps policymakers in this country could learn lessons from successes abroad, but the United States has a unique political environ- ment and it is clear there is no silver bullet that will solve all the problems we face. Specific health policy and law concerns will be described in much greater detail elsewhere, providing a foundation to tackle the many problems that will confront the country in the years ahead.

FIGURE 4-23 Waited 2 Months or Longer for a Specialist Appointment Source: Retrieved from https://www.commonwealthfund.org/publications/surveys/2016/nov/2016-commonwealth-fund-international-health-policy-survey-adults

FIGURE 4-22 Did Not Get Same or Next-Day Appointment Last Time You Needed Care Source: Retrieved from https://www.commonwealthfund.org/publications/surveys/2016/nov/2016-commonwealth-fund-international-health-policy-survey-adults

76 Chapter 4 Overview of the United States Healthcare System

19 22

31

41 41 42 43 44

47 50

53

0

20

40

60

80

100

P e rc

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Base: Excludes adults who did not need to make an appointment to see a doctor or nurse

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3 4 6 7

9 13

19 19 20 28 30

0

20

40

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80

100

P e rc

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Base: Saw or needed to see specialist in past 2 years

Sw itz

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11

20 22 23 24

26 30

33 35 37

41

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20

40

60

80

100

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ay

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8

16 16 20

23 24 28 30 30

31

43

7 6 7 8 7 13

18 14 13

22

32

0

20

40

60

80

100

Low income adults All other adults

P e rc

e n t

*Indicates differences are significant at p<0.05.

Note: “Low income” defined as household income less than 50% the country median. Sample sizes are small (n<100) in the Netherlands and UK.

Ne th

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s*

Ca na

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FIGURE 4-25 Cost-Related Access Barriers in the Past Year, By Income Source: Retrieved from https://www.commonwealthfund.org/publications/surveys/2016/nov/2016-commonwealth-fund-international-health-policy-survey-adults

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National Conference of State Legislatures. (2017). Improving access to care in rural and underserved communities: State workforce strategies. Retrieved from http://www.ncsl.org/research /health/improving-access-to-care-in-rural-and-underserved -communities-state-workforce-strategies.aspx

National Rural Health Association. (n.d.). About rural health care. Retrieved from https://www.ruralhealthweb.org/about-nrha /about-rural-health-care

Newkirk, V., & Damico, A. (2014). The Affordable Care Act and insurance coverage in rural areas. Retrieved from https://www .kff.org/uninsured/issue-brief/the-affordable-care-act-and -insurance-coverage-in-rural-areas/

Office of Disease Prevention and Health Promotion. (n.d.). Healthy People 2020 homepage. Retrieved from https://www .healthypeople.gov/

Office of Minority Health. (n.d.). The national CLAS standards. Retrieved from https://minorityhealth.hhs.gov/omh/browse .aspx?lvl=2&lvlid=53

Organization for Economic Cooperation and Development. (2017). Health at a glance 2017: OECD indicators. Retrieved from http://dx.doi.org/10.1787/health_glance-2017-en

Orgera, K., & Artiga, S. (2018). Disparities in health and health care: Five key questions and answers. Retrieved from https:// w w w.k f f.org/disp ar it ies-p olic y/issue-br ief/disp ar it ies -in-health-and-health-care-five-key-questions-and-answers/

Osborne, R., Squires, D., Doty, M. M., Sarnak, D. O., & Schneider, E. C. (2016). In new survey of eleven countries, US adults still struggle with access to and affordability of health care. Health Affairs, 35(12). doi:10.1377/hlthaff.2016.1088

Papanicolas, I., Woskie, L. R., & Jha, A. K. (2018). Health care spending in the United States and other high-income countries. New England Journal of Medicine, 319(10), 1024 –1039. doi:10.1001/jama.2018.1150

Patient Protection and Affordable Care Act of 2010, 42 U.S.C. § 18001 (2010).

Pauly, M. V., & Pagán, J. A. (2007). Spillovers and vulnerability: The case of community uninsurance. Health Affairs, 5, 1304–1314. doi:10.1377/hlthaff.26.5.1304

Proser, M., Byshhe, T., Weaver, D., & Yee, R. (2015). Community health centers at the crossroads: Growth and staffing needs. Journal of the American Academy of PAs, 28(4), 49–53. doi:10.1097/01.JAA.0000460929.99918.e6

Public Health England. (n.d.). About us. Retrieved from https://w w w.gov.u k/gover nment/organis at ions/public -health-england/about

Rosenbaum, S., Paradise, J., Markus, A., Sharac, J., Tran, C., Reynolds, D., & Shin, P. (2017). Community health centers: Recent growth and the role of the ACA. Retrieved from http:// files.kff.org/attachment/Issue-Brief-Community-Health -Centers-Recent-Growth-and-the-Role-of-the-ACA

Shi, L., & Singh, D. A. (2019). Delivering health care in America: A  systems approach (7th ed.). Burlington, MA: Jones and Bartlett Learning.

Speaking Together. (2007). Addressing language barriers in health care: What’s at stake. Retrieved from https://www .r wjf.org/content/dam/farm/rep or ts/issue_briefs/2007 /rwjf30140

Starfield, B., & Shi, L. (2004). The medical home, access to care, and insurance: A review of evidence. Pediatrics, 113, 1493– 1498. doi:10.1542/peds.113.5.S1.1493

Thorlby, R., Arora, S., & Nuffield Trust. (n.d.). The English health care system. Retrieved from https://international .commonwealthfund.org/countries/england/

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79References

 

 

U.S. Census Bureau. (2017). Health insurance coverage in the United States: 2016 (Current Population Reports, P60-260). Washington, DC: U.S. Government Printing Office.

U.S. Census Bureau. (2018). Demographic turning points for the United States: Population projections from 2020 to 2016 (Current Population Reports, P25-1144). Washington, DC: U.S. Government Printing Office.

U.S. Department of Health and Human Services. (2015). HHS action plan to reduce racial and ethnic health disparities:

Implementation progress report 2011–2014. Retrieved from https://aspe.hhs.gov/basic-report/hhs-action-plan-reduce -racia l-and-et hnic-he a lt h-disp ar it ies-implement at ion -progress-report-2011-2014

Vaughn, B. T., DeVrieze, S. R., Reed, S. D., & Schulman, K. A. (2010). Can we close the income and wealth gap between specialists and primary care physicians? Health Affairs, 29(5), 933–940. doi:10.1377/hlthaff.2009.0675

80 Chapter 4 Overview of the United States Healthcare System

 

 

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© Mary Terriberry/Shutterstock

CHAPTER 5

Public Health Institutions and Systems Richard Riegelman

LEARNING OBJECTIVES

By the end of this chapter you will be able to: ■ Identify goals of governmental public health ■ Identify the 10 essential services of public health ■ Describe basic features of local, state, and federal public health agencies in the United States ■ Identify global public health organizations and agencies and describe their basic roles ■ Identify roles in public health for federal agencies not identified as health agencies ■ Illustrate the need for collaboration by governmental public health agencies with other governmental and

nongovernmental organizations ■ Describe approaches to connecting public health and the healthcare system

▸ Introduction

The cases in BOX 5-1 all reflect the responsibilities of public health agencies at the local, federal, and global levels. While they illustrate public health working the way it is supposed to work, this is of course not always the case. Let us start by taking a look at the goals and roles of public health agencies.

▸ What Are the Goals and Roles of Governmental Public Health Agencies?

Public health is often equated with the work of gov- ernmental agencies. The role of government is only a

portion of what we mean by “public health,” but it is an important component. It is so important, in fact, that we often define the roles of other components in terms of how they relate to the work of governmental public health agencies. That is, we may refer to them as nongovernmental public health.

In 1994, the U.S. Public Health Service put forth the Public Health in America statement, which pro- vided the framework that continues to define the goals and services of governmental public health agencies (Centers for Disease Control and Prevention [CDC], 2018):

■ To prevent epidemics and the spread of disease ■ To protect against environmental hazards ■ To prevent injuries ■ To promote and encourage healthy behaviors

 

 

82 Chapter 5 Public Health Institutions and Systems

BOX 5-1 Vignette

A young man in your dormitory is diagnosed with tuberculosis. The health department works with the student health service to test everyone in the dorm, as well as in his classes, with a tuberculosis skin test. Those who are positive for the first time are advised to take a course of a medicine called INH. You ask, is this standard operating procedure?

You go to a public health meeting and learn that many of the speakers are not from public health agencies, but from the Departments of Labor, Commerce, Housing, and Education. You ask, what do these departments have to do with health?

You hear that a new childhood vaccine was developed by the National Institutes of Health (NIH), approved by the Food and Drug Administration (FDA), endorsed for federal payment by the Centers for Disease Control and Prevention (CDC), and recommended for use by the American Academy of Pediatrics. You ask, do all these agencies and organizations always work so well together?

A major flood in Asia leads to disease and starvation. Some say it is due to global warming, others to bad luck. Coordinated efforts by global health agencies, assisted by nongovernmental organizations (NGOs) and individual donors, help get the country back on its feet. You ask, what types of cooperation are needed to make all of this happen?

A local community health center identifies childhood obesity as a problem in the community. The center collects data demonstrating that the problem begins as early as elementary school. They develop a plan that includes clinical interventions at the health center and also at the elementary school. They ask the health department to help them organize an educational campaign and assist in evaluating the results. Working together, they are able to reduce the obesity rate among elementary school children by 50%. This seems like a new way to practice public health, you conclude. What type of approach is this?

Source: © maxstockphoto/ShutterStock, Inc.

■ To respond to disasters and assist communities in recovery

■ To ensure the quality and accessibility of health services

These are ambitious and complicated goals to achieve. To achieve them, it is important to further define the roles that governmental public health agen- cies themselves play and, by implication, the roles that other governmental agencies and NGOs need to play.

The Public Health in America statement built upon a 1988 report by the Institute of Medicine (IOM;

now called the Health and Medicine Division [HMD]) called The Future of Public Health. The IOM defined three core public health functions that governmental public health agencies need to perform. The concept of “core function” implies that the job cannot be del- egated to other agencies or to NGOs. It also implies that the governmental public health agencies will work together to accomplish these functions, because as a group, they are responsible for public health as a whole; that is, no one agency at the local, state, or fed- eral level is specifically or exclusively responsible for accomplishing the essential public health services.a

 

 

What Are the 10 Essential Public Health Services? 83

The core functions defined by the IOM are (1) assessment, (2) policy development, and (3) assurance (Institute of Medicine [IOM], 1988).

■ Assessment includes obtaining data that define the health of the overall population and specific groups within the population, including defining the nature of new and persisting health problems.

■ Policy development includes developing evidence- based recommendations and other analyses of options, such as health policy analysis, to guide implementation, including efforts to educate and mobilize community partnerships.

■ Assurance includes governmental public health’s oversight responsibility for ensuring that key compo- nents of an effective health system, including health care and public health, are in place even though the implementation will often be performed by others.

The three core functions, while useful in provid- ing a delineation of responsibilities and an intellectual framework for the work of governmental public health

TABLE 5-1 10 Essential Public Health Services

Essential Service Meaning of Essential Service Examples

Core function: assessment

1. Monitor health status to identify and solve community health problems

This service includes accurate diagnosis of the community’s health status; identification of threats to health and assessment of health service needs; timely collection, analysis, and publication of information on access, utilization, costs, and outcomes of personal health services; attention to the vital statistics and health status of specific groups that are at a higher risk than the total population; and collaboration to manage integrated information systems with private providers and health benefit plans.

Vital statistics Health surveys Surveillance, including reportable diseases

2. Diagnose and investigate health problems and health hazards in the community

This service includes epidemiologic identification of emerging health threats; public health laboratory capability using modern technology to conduct rapid screening and high-volume testing; active communicable disease epidemiology programs; and technical capacity for epidemiologic investigation of disease outbreaks and patterns of chronic disease and injury.

Epidemic investigations CDC–Epidemic Intelligence Service State public health laboratories

Core function: policy development

3. Inform, educate, and empower people about health issues

This service includes social marketing and media communications; providing accessible health information resources at community levels; active collaboration with personal healthcare providers to reinforce health promotion messages and programs; and joint health education programs with schools, churches, and worksites.

Health education campaigns, such as comprehensive state tobacco programs

agencies, were not tangible enough to provide a clear understanding or definition of the work of public health agencies. Thus, in addition to the goals of public health, the Public Health in America statement defined a series of 10 essential public health services that build upon the IOM’s core functions, guide day-to-day responsibilities, and provide a mechanism for evaluating whether the core functions are fulfilled. These 10 services have come to define the responsibilities of the combined local, state, and federal governmental public health system.

▸ What Are the 10 Essential Public Health Services?

TABLE 5-1 outlines the 10 essential public health ser- vices and organizes them according to which IOM core function they aim to fulfill (CDC, 2018). A description of each service is presented in column 2, and exam- ples of these essential services are listed in column 3.

(continues)

 

 

84 Chapter 5 Public Health Institutions and Systems

Essential Service Meaning of Essential Service Examples

4. Mobilize community partnerships and action to identify and solve health problems

This service includes convening and facilitating community groups and associations, including those not typically considered to be health-related, in undertaking defined preventive, screening, rehabilitation, and support programs; and skilled coalition-building to draw upon the full range of potential human and material resources in the cause of community health.

Lead control programs: testing and follow-up of children, reduction of lead exposure, educational follow-up, and addressing underlying causes

5. Develop policies and plans that support individual and community health efforts

This service requires leadership development at all levels of public health; systematic community and state-level planning for health improvement in all jurisdictions; tracking of measurable health objectives as a part of continuous quality improvement strategies; joint evaluation with the medical/healthcare system to define consistent policy regarding prevention and treatment services; and development of codes, regulations, and legislation to guide public health practice.

Newborn screening and follow-up programs for PKU and other genetic and congenital diseases

Core function: assurance

6. Enforce laws and regulations that protect health and ensure safety

This service involves full enforcement of sanitary codes, especially in the food industry; full protection of drinking water supplies; enforcement of clean air standards; timely follow-up of hazards, preventable injuries, and exposure-related diseases identified in occupational and community settings; monitoring quality of medical services (e.g., laboratory, nursing home, home health care); and timely review of new drug, biologic, and medical device applications.

Local: Fluoridation and chlorination of water State: Regulation of nursing homes Federal: FDA drug approval and food safety

7. Link people to needed personal health services and ensure the provision of health care when otherwise unavailable

This service (often referred to as “outreach” or “enabling” services) includes ensuring effective entry for socially disadvantaged people into a coordinated system of clinical care; culturally and linguistically appropriate materials and staff to ensure linkage to services for special population groups; ongoing “care management”; and transportation.

Community health centers

8. Ensure the provision of a competent public and personal healthcare workforce

This service includes education and training for personnel to meet the needs of public and personal health services; efficient processes for licensure of professionals and certification of facilities with regular verification and inspection follow-up; adoption of continuous quality improvement and lifelong learning within all licensure and certification programs; active partnerships with professional training programs to ensure community-relevant learning experiences for all students; and continuing education in management and leadership development programs for those charged with administrative/ executive roles.

Licensure of physicians, nurses, and other health professionals

TABLE 5-1 10 Essential Public Health Services (continued)

 

 

What Are the Roles of Local and State Public Health Agencies? 85

Monitor Health

Evaluate

Assure Competent Workforce

Diagnose and

Investigate

Inform, Educate, Empower

Link to / Provide

Care

Enforce Laws

Develop Policies

Mobilize Community

Partnerships

ResearchResearch

A S

S U

R A

N C

E

ASSESSM

EN T

S ys

te m M

anagem en

t

POL ICY

D EV

EL

O P M

E N

T S

FIGURE 5-1 Essential Public Health Services and Institute of Medicine’s Core Functions Source: Centers for Disease Control and Prevention. (2017). The public health system & the 10 essential public health services. Retrieved from https://www.cdc.gov/stltpublichealth/publichealthservices/essentialhealthservices.html

Governmental Public Health

Agencies

Other Government

Agencies

Local

State

Federal

Global

Healthcare Delivery System

Community and Private Organizations

FIGURE 5-2 Framework for Viewing Governmental Public Health Agencies and Their Complicated Connections

FIGURE 5-1 then combines the core functions of pub- lic health with the essential services of public health agencies so that you can see the connections.

Public health services are delivered through a complex web of local and federal agencies, as well as through increasing involvement from global organi- zations. What follows is a description of the work of public health agencies at each of these levels.

FIGURE 5-2 provides a framework to guide our review of the delivery of public health services.

It  diagrams the central role of governmental public health agencies and the complicated connections required to accomplish their responsibilities. We begin by taking a look at the structure and function of governmental public health agencies at the local/ state, federal, and global levels. We then examine the key connections with other governmental agencies, community organizations, and private organiza- tions, and finally the connections with the healthcare delivery system.

▸ What Are the Roles of Local and State Public Health Agencies?

The U.S. Constitution does not mention public health. Because public health is not a delineated federal

9. Evaluate effectiveness, accessibility, and quality of personal and population- based health services

This service calls for ongoing evaluation of health programs, based on analysis of health status and service utilization data, to assess program effectiveness and to provide information necessary for allocating resources and reshaping programs.

Development of evidence-based recommendations

All three IOM core functions

10. Research for new insights and innovative solutions to health problems

This service includes continuous linkage with appropriate institutions of higher learning and research and an internal capacity to mount timely epidemiologic and economic analyses and conduct needed health services research.

NIH, CDC, AHRQ, other federal agencies

Abbreviations: Agency for Healthcare Research and Quality = AHRQ; Centers for Disease Control and Prevention = CDC; Food and Drug Administration = FDA; National Institutes of Health = NIH; phenylketonuria = PKU.

Source: Data from Public Health in America. Essential public health services. Retrieved from http://www.cdc.gov/nphpsp/ essentialservices.html. Accessed October 26, 2015.

 

 

86 Chapter 5 Public Health Institutions and Systems

BOX 5-2 Brief History of Public Health Agencies in the United States

An understanding of the history of U.S. public health institutions requires an understanding of the response of local, state, and federal governments to public health crises and the complex interactions among these levels of government.

The colonial period in the United States saw repeated epidemics of smallpox, cholera, and yellow fever, primarily focused in the port cities. These epidemics brought fear and disruption of commerce, along with accompanying disease and death. One epidemic in 1793 in Philadelphia, which was then the nation’s capital, nearly shut down the federal government. These early public health crises brought about the first municipal boards of health, made up of respected citizens authorized to act in the community’s interest to implement quarantine, evacuation, and other public health interventions of the day. The federal government’s early role in combating epidemics led to the establishment in 1798 of what later became known as the U.S. Public Health Service.

Major changes in public health occurred in the last half of the 1800s, with the great expansion of the understanding of disease and the ability to control it through community actions. The Shattuck Commission in Massachusetts in 1850 outlined the roles of state health departments as responsible for sanitary inspections, communicable disease control, food sanitation, vital statistics, and services for infants and children. Over the next 50 years, the states gradually took the lead in developing public health institutions based on delivery of these services.

Local health departments did not exist outside of the largest cities until the 1900s. The Rockefeller Foundation stimulated and helped fund early local health departments and campaigns, in part to combat specific diseases, such as hookworm. There was no standard model for local health departments; they developed in different ways in the various states and were chronically underfunded.

The federal government played a very small role in public health throughout the 1800s and well into the 20th century. However, an occasional public health crisis stimulated federal action, often as a result of media attention. The founding of the FDA in 1906 resulted in large part from the journalistic activity known as “muckraking,” which exposed the status of food and drug safety. The early years of the 1900s set the stage for expansion of the federal government’s role in public health through the passage of the 16th Amendment to the Constitution, which authorized federal income tax as a major source of federal government funding.

The Great Depression, in general, and the Social Security Act of 1935, in particular, brought about a new era in which federal funding became a major source of financial resources for state and local public health departments and NGOs. The founding of the CDC (which at that time stood for Communicable Disease Center) in 1946 led to a national (and eventually international) leadership role for the CDC, which attempts to connect and hold together the complex local, state, and federal public health efforts and integrate them into global public health efforts.

The Johnson administration’s War on Poverty, as well as the Medicare and Medicaid programs, brought about greatly expanded funding for healthcare services and led many health departments to provide direct healthcare services, especially for those without other sources of care. The late 1980s and 1990s saw a redefinition of the roles of governmental public health, including the IOM definition of core functions and the development of the 10 essential public health services. These documents have guided the development of a broad population focus for public health and a move away from the direct provision of healthcare services by health departments.

The terrorism of September 11, 2001, and the subsequent anthrax scare moved public health institutions to the center of efforts to protect the public’s health through emergency response and disaster preparedness. The development of flexible efforts to respond to expected and unexpected hazards is now a central feature of public health institutions’ roles and funding. The success of these efforts has led to new levels of coordination of local, state, federal, and global public health agencies using state-of-the-art surveillance, laboratory technology, and communications systems.

responsibility, it is an authority retained by the states. States may retain their authority, voluntarily request or accept help from the federal government, or delegate their responsibility and/or authority to local agencies at the city, county, or other local levels.b

BOX 5-2 briefly describes the history of public health agencies in the United States. It is a complex history and has resulted in more structures than there are states—more because large cities often have their own public health systems (Turnock, 2009). In addition, the District of Columbia and several U.S.

territories have their own systems and often have the authority to make public health system decisions as if they were states.

To understand the role of local health depart- ments, it is useful to think of two models (Turnock, 2007). In the first model, which we will call the “home rule” or “local autonomy” model, authority is dele- gated from the state to the local health department. The local health department, or the local government, has a great deal of autonomy in setting its own struc- ture and function and often raising its own funding.

 

 

What Are the Roles of Federal Public Health Agencies? 87

In the second model, which we will call the “branch office” model, the local health department can be viewed as a branch office of the state agency, with little or no independent authority or funding. There are several thousand local health departments across the country. The majority of these lie somewhere in between these two extreme models; however, these models provide a framework for understanding the many varieties of department structures. Thus, when we speak of local public health, we may be speaking of a state agency with branch offices or a relatively inde- pendent local agency. Regardless of which model a state uses, many public health responsibilities of local public health departments are quite similar, and they usually have authority and responsibility for at least the following (Turnock, 2007):

■ Immunizations for those individuals not covered by the private health insurance system

■ Communicable disease surveillance and initial investigation of outbreaks

■ Communicable disease control, often including at a minimum tuberculosis and syphilis case finding and treatment

■ Inspection and licensing of restaurants ■ Environmental health surveillance ■ Coordination of public health screening pro-

grams, including newborn and lead screenings ■ Tobacco control programs ■ Public health preparedness and response to disasters

Health departments in many parts of the United States also serve as the healthcare provider for those without other sources of health care. This function is generally referred to as the healthcare safety net. In recent years, many health departments have reduced or discontinued these services, often transferring them to the healthcare system or integrating their efforts into community health centers. The concept of core functions holds that while these activities can be performed by other organizations or agencies, the public health agencies retain responsibility for ensur- ing access to and the quality of these services.

The work of local public health agencies cannot be viewed in isolation. The state health department usu- ally retains important roles even in those states where the local departments have home rule authority. These responsibilities often include collecting vital statistics, running a public health laboratory, licensing health professionals, administering nutrition programs, and regulating health facilities, such as nursing homes. In addition, drinking water regulation, administration of the state Medicaid program, and the office of the med- ical examiner may also fall under the authority of the state health department.

The 2003 IOM report The Future of the Public’s Health in the 21st Century, in conjunction with the Futures Initiative of the CDC, initiated the establish- ment of a voluntary national accreditation program for state and local health departments to advance quality and performance in health departments. Through these efforts, the Public Health Accredita- tion Board was formed, and in early 2013, the first set of health departments achieved national accred- itation. The accreditation standards and measures address each of the 10 essential public health services to evaluate health department processes and services and their outcomes (Public Health Accreditation Board, 2013).

Today, the federal government has a great deal of involvement in national and global issues of public health and often works closely with local agencies. We now turn to a discussion of the structure and role of the federal government in public health.

▸ What Are the Roles of Federal Public Health Agencies?

The federal government’s role in public health does not explicitly appear in the U.S. Constitution. It has been justified largely by that document’s Interstate Commerce clause, which provides federal government authority to regulate commerce between the states. Federal public health authority often rests on the vol- untary acceptance by the states of funding provided by the federal government. The federal government may require that states take certain actions to qualify for the funding.

The Department of Health and Human Services (HHS) is the central public health agency of the fed- eral government. It includes operating agencies, each of which reports directly to the cabinet-level secretary of HHS. TABLE 5-2 outlines most of these agencies, their roles and authority, and their basic public health structure and activities (U.S. Department of Health and Human Services, 2017).

The NIH, one of the larger agencies within HHS, is devoted to basic science research and the translation of research into clinical practice. Some of the other federal health agencies, such as the Health Resources and Services Administration, the Substance Abuse and Mental Health Services Administration, and the Indian Health Service, provide or fund individually oriented health services in addition to population- oriented preventive services. The Indian Health Ser- vice is unique because it is responsible for both public health and healthcare services for a defined population.

 

 

88 Chapter 5 Public Health Institutions and Systems

The CDC is perhaps the agency most closely iden- tified with public health at the federal level. BOX  5-3 describes its first 50 years, from 1946 to 1996, in a reprint of its official history first published in the Morbidity and Mortality Weekly Report (MMWR),

TABLE 5-2 Key Federal Health Agencies of the Department of Health and Human Services

Agency Roles/Authority Examples of Structures/Activities

Centers for Disease Control and Prevention (CDC) and the Agency for Toxic Substances and Disease Registry (ATSDR)

The CDC is the lead agency for prevention, health data, epidemic investigation, and public health measures aimed at disease control and prevention. The CDC administers the ATSDR, which works with the Environmental Protection Agency to provide guidance on health hazards of toxic exposures.

The CDC and ATSDR work extensively with state and local health departments.

The CDC’s Epidemic Intelligence Service functions domestically and internationally at the request of governments.

National Institutes of Health (NIH)

Serves as lead research agency; also funds training programs and communication of health information to the professional community and the public.

NIH comprises 17 institutes in all—the largest being the National Cancer Institute. The National Library of Medicine is part of NIH Centers, which also include the John E. Fogarty International Center for Advanced Study in the Health Sciences. NIH is the world’s largest biomedical research enterprise, with intramural research at NIH and extramural research grants throughout the world.

Food and Drug Administration (FDA)

Acts as consumer protection agency with authority for safety of foods and safety and efficacy of drugs, vaccines, and other medical and public health interventions.

Divisions of FDA are responsible for food safety, medical devices, drug efficacy, and safety pre- and post-approval.

Health Resources and Services Administration (HRSA)

Seeks to ensure equitable access to comprehensive quality health care.

HRSA funds community health centers, HIV/AIDS services, and scholarships for health professional students.

Agency for Healthcare Research and Quality (AHRQ)

Sets research agenda to improve the outcomes and quality of health care, including patient safety and access to services.

AHRQ supports U.S. Preventive Services Task Force, evidence-based medicine research, and Guidelines Clearinghouse.

Substance Abuse and Mental Health Services Administration (SAMHSA)

Works to improve quality and availability of prevention, treatment, and rehabilitation for substance abuse and mental illness.

SAMHSA provides research, data collection, and funding of local services.

Indian Health Service (IHS)

Provides direct health care and public health services to federally recognized tribes.

IHS provides services to approximately 550 federally recognized tribes in 35 states. It is the only comprehensive federal agency responsibility for health care plus public health services.

a weekly publication of the agency (CDC, 1996). Today, the CDC is a global partner in conducting research and epidemiologic investigations in addition to working closely with states to monitor and pre- vent disease through health surveillance, taking an

 

 

What Are the Roles of Federal Public Health Agencies? 89

Source: Reproduced from Centers for Disease Control and Prevention, MMWR 1996;45: 526–528.

BOX 5-3 History of the CDC

The following is reprinted as it originally appeared in 1996 in the Morbidity and Mortality Weekly Report (CDC, 1996):

The Communicable Disease Center was organized in Atlanta, Georgia, on July 1, 1946; its founder, Dr. Joseph W. Mountin, was a visionary public health leader who had high hopes for this small and comparatively insignificant branch of the Public Health Service (PHS). It occupied only one floor of the Volunteer Building on Peachtree Street and had fewer than 400 employees, most of whom were engineers and entomologists. Until the previous day, they had worked for Malaria Control in War Areas, the predecessor of CDC, which had successfully kept the southeastern states malaria-free during World War II and, for approximately 1 year, from murine typhus fever. The new institution would expand its interests to include all communicable diseases and would be the servant of the states, providing practical help whenever called.

Distinguished scientists soon filled CDC’s laboratories, and many states and foreign countries sent their public health staffs to Atlanta for training. Medical epidemiologists were scarce, and it was not until 1949 that Dr. Alexander Langmuir arrived to head the epidemiology branch. Within months, he launched the first-ever disease surveillance program, which confirmed his suspicion that malaria, on which CDC spent the largest portion of its budget, had long since disappeared. Subsequently, disease surveillance became the cornerstone on which CDC’s mission of service to the states was built and, in time, changed the practice of public health.

The outbreak of the Korean War in 1950 was the impetus for creating CDC’s Epidemic Intelligence Service (EIS). The threat of biological warfare loomed, and Dr. Langmuir, the most knowledgeable person in PHS about this then- arcane subject, saw an opportunity to train epidemiologists who would guard against ordinary threats to public health while watching out for alien germs. The first class of EIS officers arrived in Atlanta for training in 1951 and pledged to go wherever they were called for the next 2 years. These “disease detectives” quickly gained fame for “shoe-leather epidemiology,” through which they ferreted out the cause of disease outbreaks.

The survival of CDC as an institution was not at all certain in the 1950s. In 1947, Emory University gave land on Clifton Road for a headquarters, but construction did not begin for more than a decade. PHS was so intent on research and the rapid growth of the National Institutes of Health that it showed little interest in what happened in Atlanta. Congress, despite the long delay in appropriating money for new buildings, was much more receptive to CDC’s pleas for support than either PHS or the Bureau of the Budget.

Two major health crises in the mid-1950s established CDC’s credibility and ensured its survival. In 1955, when poliomyelitis appeared in children who had received the recently approved Salk vaccine, the national inoculation program was stopped. The cases were traced to contaminated vaccine from a laboratory in California; the problem was corrected, and the inoculation program, at least for first and second graders, was resumed. The resistance of these 6- and 7-year-olds to polio, compared with that of older children, proved the effectiveness of the vaccine. Two years later, surveillance was used again to trace the course of a massive influenza epidemic. From the data gathered in 1957 and subsequent years, the national guidelines for influenza vaccine were developed.

CDC grew by acquisition. When CDC joined the international malaria-eradication program and accepted responsibility for protecting the earth from moon germs and vice versa, CDC’s mission stretched overseas and into space.

CDC then played a key role in one of the greatest triumphs of public health: the eradication of smallpox. In 1962 it established a smallpox surveillance unit, and a year later tested a newly developed jet gun and vaccine in the Pacific island nation of Tonga. CDC also achieved notable success at home tracking new and mysterious disease outbreaks. In the mid- 1970s and early 1980s, it found the cause of Legionnaires disease and toxic-shock syndrome. A fatal disease, subsequently named acquired immunodeficiency syndrome (AIDS), was first mentioned in the June 5, 1981, issue of MMWR.

Although CDC succeeded more often than it failed, it did not escape criticism. For example, television and press reports about the Tuskegee study on long-term effects of untreated syphilis in black men created a storm of protest in 1972. This study had been initiated by PHS and other organizations in 1932 and was transferred to CDC in 1957. Although the effectiveness of penicillin as a therapy for syphilis had been established during the late 1940s, participants in this study remained untreated until the study was brought to public attention. CDC was also criticized because of the 1976 effort to vaccinate the U.S. population against swine flu, the infamous killer of 1918–1919. When some recipients of the vaccines developed Guillain-Barre syndrome, the campaign was stopped immediately; the epidemic never occurred.

As the scope of CDC’s activities expanded far beyond communicable diseases, its name had to be changed. In 1970 it became the Center for Disease Control and in 1981, after extensive reorganization, Center became Centers. The words “and Prevention” were added in 1992 but, by law, the well-known three-letter acronym was retained. In health emergencies, CDC means an answer to SOS calls from anywhere in the world, such as the recent one from Zaire where Ebola fever raged.

Fifty years ago, CDC’s agenda was non-controversial (hardly anyone objected to the pursuit of germs), and Atlanta was a backwater. In 1996, CDC’s programs are often tied to economic, political, and social issues, and Atlanta is as near to Washington as the tap of a keyboard.

 

 

90 Chapter 5 Public Health Institutions and Systems

action-oriented approach to disease prevention, and maintaining health statistics through the National Center for Health Statistics, which has been a part of the CDC since 1987.

The CDC’s role in connecting federal, state, and local governmental public health efforts is central to the success of the system. Approximately half of the CDC’s over $10 billion total budget is channeled to state and local health departments. A key function of the CDC is to provide national leadership and to coordinate the efforts of local/state and federal public health agencies.

To understand the local/state and federal pub- lic health system, it is important to appreciate that less than 5% of all health-related expenditures in the United States goes to governmental public health agencies, and of that, less than half goes to population-based prevention (as opposed to pro- viding safety net healthcare services to individuals). In addition, the role of governmental public health is limited by social attitudes toward government. For instance, there are constitutional limitations on the authority of public health and other government agencies to impose actions on individuals. These may limit public health agencies’ abilities to address issues ranging from tuberculosis and HIV control to responses to emergencies.

The social attitudes of Americans may also limit the authority and resources provided to public health agencies. Americans often favor individual or private efforts over governmental interventions when they believe that individuals and private organizations

are capable of success. For instance, some Americans resist active efforts in schools to provide information and access to contraceptives, while others resist the type of case-finding efforts for HIV/AIDS that have been used successfully in investigating and controlling other communicable diseases.

Today, governmental public health is a global enterprise. As a result, we now turn to a discussion of the roles of global health organizations and agencies.

▸ What Are the Roles of Global Health Organizations and Agencies?

Public health is increasingly becoming a global undertaking. Global governmental efforts have grown dramatically in recent years. The World Health Orga- nization (WHO), created in 1948, has become decid- edly more prominent in the 2000s with the increasing importance of global health issues. WHO is a part of the United Nations organizations, which also include the United Nations International Children’s Emer- gency Fund (UNICEF) and the Joint United Nations Programme on HIV/AIDS (UNAIDS).

Today, the World Bank and other multilateral financial institutions are the largest funding source for global health efforts (World Bank, 2018). National governmental aid programs, including the U.S. Agency for International Development (USAID), also play an important role in public health. TABLE 5-3 outlines the

TABLE 5-3 Global Public Health Organizations

Type of Agency Structure/Governance Role(s) Limitations

World Health Organization

United Nations Organization Seven “regional” semi- independent components (e.g., Pan American Health Organization covers North and South America)

Policy development (e.g., tobacco treaty, epidemic control policies) Coordination of services (e.g., SARS control) Vaccine development Data collection and standardization (e.g., measures of healthcare quality, measures of health status)

Limited ability to enforce global recommendations, limited funding, and complex international administration

Other UN agencies with focused agenda

UNICEF UNAIDS

Focus on childhood vaccinations Focus on AIDS

Limited agendas and limited financing

 

 

What Other Government Agencies Are Involved in Health Issues? 91

structure/governance, roles, and limitations of global public health agencies.

The complexity of local, state, federal, and global public health agencies raises the question of whether these agencies can and do work together. It should not surprise you that close collaboration, while the goal, is often difficult to achieve with so many organizations involved. Thus, it is important to ask: How can public health agencies work together?

▸ How Can Public Health Agencies Work Together?

Coordination among just local, state, and federal pub- lic health agencies has been a major challenge. Increas- ingly, coordination also requires a global aspect. Efforts toward efficient collaboration, on all levels, have a long way to go. There are signs of hope with progress in such fields as tobacco control, food safety, and the response to severe acute respiratory syndrome (SARS). BOX 5-4 discusses the dramatic events of the 2003 SARS epi- demic, providing an example of what can be done and what needs to be done to address future public health emergencies (Duffin & Sweetman, 2006).

Collaboration needs to be an everyday effort, not just a requirement for emergencies or epidemics. Let us look at the relationships and needed collaboration among governmental public health and other gov- ernmental agencies, NGOs, and the healthcare deliv- ery system.

▸ What Other Government Agencies Are Involved in Health Issues?

To address the full range of issues that affect population health, it is important to recognize the important roles that government agencies not designated as health agencies play in public health. Such agencies exist at the local/state, federal, and global levels. To illustrate the involvement of these agencies in health issues, let us begin with the roles of non-health agencies at the federal level.

A number of federal agencies serve public health functions even though they are not defined as health agencies. The roles they play are important, especially when we take the population health perspective, which includes the totality of efforts to promote and protect health and prevent disease, disability, and death.

Environmental health issues are an important part of the role of the Environmental Protection Agency. Reduc- ing injury and hazardous exposures in the workplace are key goals of the Occupational Safety and Health Admin- istration, which is part of the Department of Labor.

Protecting health as part of preparation and response to disasters and terrorism is central to the role of the Department of Homeland Security. The Depart- ment of Agriculture shares with the FDA the role of protecting the nation’s food supply. The Department of Housing and Urban Development influences the built environment and its impacts on health. The  Depart- ment of Energy plays important roles in setting

International financing organizations

The World Bank Other multilateral regional banks (e.g., InterAmerican and Asian Development Banks)

World Bank is largest international funder. Increasingly supports “human capital” projects and reform of healthcare delivery systems and population and nutrition efforts Provides funding and technical assistance, primarily as loans

Criticized for standardized approach with few local modifications

Bilateral governmental aid organizations

USAID Many other developed countries have their own organizations and contribute a higher percentage of their gross domestic product to those agencies than does the United States

Often focused on specific countries and specific types of programs (e.g., the focus on HIV/AIDS in the United States), and maternal and child health

May be tied to domestic politics and global economic, political, or military agendas

Abbreviations: AIDS = acquired immunodeficiency syndrome; HIV = human immunodeficiency virus; SARS = severe acute respiratory syndrome; UN = United Nations; UNAIDS = Joint United Nations Programme on HIV/AIDS; UNICEF = United Nations International Children’s Emergency Fund; USAID = U.S. Agency for International Development.

 

 

92 Chapter 5 Public Health Institutions and Systems

BOX 5-4 SARS and the Public Health Response

The SARS epidemic of 2003 began with little notice, most likely somewhere in the heartland of China, and then spread to other areas of Asia. The world took notice following televised reports of public health researchers who were sent to Asia to investigate the illness subsequently contracting and dying from the disease. Not an easily transmissible disease except for between those in very close contact, such as investigators, family members, and healthcare providers, the disease spread slowly but steadily through areas of China. Among those infected, the case-fatality rate was very high, especially without the benefits of modern intensive care facilities.

The disease did not respond to antibiotics and was thought to be a viral disease by its epidemiologic pattern of spread and transmission, but at first, no cause was known. The outside world soon felt the impact of the brewing epidemic when cases appeared in Hong Kong that could be traced to a traveler from mainland China. Fear spread when cases were recognized that could not be explained by close personal contact with a SARS victim.

The epidemic continued to spread, jumping thousands of miles to Toronto, Canada, where the second-greatest concentration of disease appeared. Soon, the whole world was on high alert, if not quite on the verge of panic. At least 8,000 people worldwide became sick, and nearly 10% of them died. Fortunately, progress came quite quickly. Researchers coordinated by WHO were able to put together the epidemiologic information and laboratory data and establish a presumed cause—a new form of the coronavirus never before seen in humans—leading to the rapid introduction of testing.

WHO and the CDC put forth recommendations for isolation, travel restrictions, and intensive monitoring that rapidly controlled the disease, even in the absence of an effective treatment aimed at a cure. SARS disappeared as rapidly as it emerged, especially after systematic efforts to control spread were put in place in China. Not eliminated, but no longer a worldwide threat, SARS left a lasting global impact. WHO established new approaches for reporting and responding to epidemics, which now have the widespread formal acceptance of most governments.

Once the world could step back and evaluate what happened, it was recognized that the potential burden of disease posed by the SARS epidemic had worldwide implications and raised the threat of interruption of travel and trade. Local, national, and global public health agencies collaborated quickly and effectively. Infection control recommendations made at the global level were rapidly translated into efforts to identify disease at the local level and manage individual patients in hospitals throughout the world. It is a model of communicable disease control that will be needed in the future.

groups organizing to advocate for public health causes, delivering public health services, and providing fund- ing to support public health efforts. In recent years, these efforts have been expanding globally as well.

The American Red Cross and its network of interna- tional affiliates represent a major international effort to provide public health services. The organization plays a central role in obtaining volunteers for blood donations and ensuring the safety and effectiveness of the U.S. and world supply of blood products in collaboration with the FDA. The ability of the Red Cross to obtain dona- tions, mobilize volunteers, and publicize the need for disaster assistance has allowed it to play a central role in providing lifesaving public health services.

Many private organizations provide public health education, support research, develop evidence-based recommendations, and provide other public health services. Many of these organizations are organized around specific diseases or types of disease, such as the American Cancer Association, the American Heart Association, the American Lung Association, and the March of Dimes, which today focuses on birth defects. Other private organizations focus primarily on advo- cacy for individuals with specific diseases, but these organizations also may advocate for specific public health interventions. For instance, Mothers Against Drunk Driving has had a major impact on the passage

radiation safety standards for nuclear power plants and other sources of energy.

When multiple federal agencies are involved in health-related matters, coordination and collabora- tion are required across agencies. This interaction is certainly important when it comes to food safety and disaster planning and response. It is also key for efforts to address problems that cut across agencies, such as childhood lead exposure or efforts to reduce the envi- ronmental causes of asthma.

The collaboration needed to address complex public health issues lends itself to a “health in all pol- icies” approach, which acknowledges that the variety of influences impacting population health are outside the control of the health sector. Collaborative efforts are not restricted to governmental agencies. We will now explore the roles of NGOs in public health.

▸ What Roles Do NGOs Play in Public Health?

Nongovernmental Organizations NGOs play increasingly important roles in public health in the United States and around the world. In the United States, there is a long tradition of private

 

 

93How Can Public Health Agencies Partner With Health Care?

BOX 5-5 National Vaccine Plan

In 1994, a National Vaccine Plan was developed as part of a coordinated effort to accomplish the following goals:

1. Develop new and improved vaccines. 2. Ensure the optimal safety and effectiveness of vaccines and immunizations. 3. Better educate the public and members of the health profession on the benefits and risks of immunizations.

A recent IOM report evaluated progress since 1994 on achieving these goals and made recommendations for the development of a revised National Vaccine Plan (IOM, 2008). The IOM highlighted a number of successes since 1994 in achieving each of the goals of the plan. These successes illustrate the potential for improved collaboration between public health systems and healthcare systems.

In terms of the development of new and improved vaccines since 1994, over 20 new vaccine products resulting from the collaborative efforts of the NIH, academicians, and industry researchers were approved by the FDA. Novel vaccines introduced include vaccines against pediatric pneumococcal disease, meningococcal disease, and the human papillomavirus—a cause of cervical cancer.

In terms of safety, vaccines and vaccination approaches with improved safety have been developed since 1994, including those directed against rotavirus, pertussis (whooping cough), and polio. The FDA Center for Biologics Evaluation and Research, which regulates vaccines, now has an expanded array of regulatory tools to facilitate the review and approval of safe and efficacious vaccines. The FDA and the CDC have collaborated on surveillance for and evaluation of adverse events. Efforts have also been made to increase collaboration with the Centers for Medicare and Medicaid Services, the Department of Defense, and the Department of Veterans Affairs to improve surveillance and reporting of adverse events following immunization in the adult populations these agencies serve.

In terms of better education of health professionals and the public, progress has also been made. The American Academy of Pediatrics collaborates with the CDC for its childhood immunization support. The American Medical

(continues)

and enforcement of drunk-driving laws. HIV/AIDS advocacy groups have influenced policies on confi- dentiality, funding, and public education.

Globally, NGOs increasingly play a key role in providing services and advocating for public health policies. CARE and Oxfam International are exam- ples of the types of organizations involved in global health-related crises. Physician groups, including Physicians for Social Responsibility and Doctors Without Borders, have been active in advocating for public health efforts, seeking funding for public health needs, and addressing the ethical implementation of public health programs.

New combinations of governmental and NGOs are increasingly developing to fill in the gaps. At the global level, the Global Fund to Fight AIDS, Tuber- culosis, and Malaria, which is a public–private effort, provides funding for evidence-based interventions to address these diseases. It is funded not only by govern- ments, but also by private foundations, such as the Bill and Melinda Gates Foundation.

Private foundations have long played major roles in both funding public health efforts and stimulating governmental funding. The Rockefeller Foundation’s efforts were instrumental in developing local health departments and initiating schools of public health in the United States during the early years of the 1900s. The Kellogg Foundation, the Robert Wood Johnson Foun- dation, and most recently the Gates Foundation have

all played key roles in advancing public health efforts in areas ranging from nutrition to tobacco control to the advancement of new public health technologies.

Foundation funding has been the catalyst in initi- ating new funding efforts and sustaining those that are not adequately funded by governments. They cannot be expected, however, to provide long-term support for basic public health services. Thus, additional strat- egies are required. One key strategy is to link public health efforts with the efforts of healthcare profession- als and the healthcare system.

▸ How Can Public Health Agencies Partner With Health Care to Improve the Response to Health Problems?

Clinicians and public health professionals increasingly share a common commitment to evidence-based think- ing, cost-effective delivery of services, and computerized and confidential data systems. They also increasingly share a commitment to provide quality services to the entire population and eliminate health disparities. The potential for successful collaboration between public health and health care is illustrated by the National Vac- cine Plan, which is discussed in BOX 5-5 (IOM, 2008).

 

 

94 Chapter 5 Public Health Institutions and Systems

Association cosponsors the annual National Influenza Vaccine Summit, a group that represents 100 public and private organizations interested in preventing influenza.

Despite the growing collaboration and success in vaccine development and use, new issues have appeared in recent years. Vaccines are now correctly viewed by health professionals and the broader public as having both benefits and harms. In recent years, the public has grown more concerned about the safety of vaccines, including the issue of the use of large numbers of vaccines in children. The limitations of vaccines to address problems, such as HIV/AIDS, have also been increasingly recognized. Hopefully, the continued efforts to develop and implement national vaccine plans will build upon these recent successes and address the new realities and opportunities.

BOX 5-5 National Vaccine Plan

BOX 5-6 Community-Oriented Primary Care

Community-oriented primary care (COPC) is a structured effort to expand the delivery of health services from a focus on the individual to include an additional focus on the needs of communities. Serving the needs of communities brings healthcare and public health efforts together. COPC can be seen as an effort on the part of healthcare delivery sites, such as community health centers, to reach out to their community and to governmental public health institutions.

TABLE 5-4 outlines the six steps in the COPC process and presents a question to ask when addressing each of these steps. Notice the parallels between COPC and the evidence-based approach. A series of principles underlies COPC:

■ Healthcare needs are defined by examining the community as a whole, not just those who seek care. ■ Needed healthcare services are provided to everyone within a defined population or community. ■ Preventive, curative, and rehabilitative care are integrated within a coordinated delivery system. ■ Members of the community directly participate in all stages of the COPC process.

The concept of COPC, if not the specific structure, has been widely accepted as an approach for connecting the organized delivery of primary health care with public health. It implies that public health issues can and should be addressed, when possible, at the level of the community with the involvement of healthcare providers and the community members themselves.

TABLE 5-4 The Six Sequential Steps of Community-Oriented Primary Care

Steps in the COPC Process Questions to Ask

1. Community definition

How is the community defined based on geography, institutional affiliation, or other common characteristics (e.g., use of an Internet site)?

2. Community characterization

What are the demographic and health characteristics of the community, and what are its health issues?

3. Prioritization What are the most important health issues facing the community, and how should they be prioritized based on objective data and perceived need?

4. Detailed assessment of the selected health problem

What are the most effective and efficient interventions for addressing the selected health problem based on an evidence-based assessment?

5. Intervention What strategies will be used to implement the intervention?

6. Evaluation How can the success of the intervention be evaluated?

Data from Mullan, F., & Epstein, L. (2002). Community-oriented primary care: New relevance in a changing world. American Journal of Public Health, 92(11), 1748–1755.

(continued)

 

 

95How Can Public Health Take the Lead in Mobilizing Community Partnerships?

BOX 5-7 Child Oral Health and Community-Oriented Public Health

The problem of childhood dental disease illustrates the potential for COPH. A lack of regular dental care remains a major problem for children in developed, as well as developing, countries. Oral health is often high on the agenda of parents, teachers, and even the children themselves.

The history of public health interventions in childhood oral health is a story of great hope and partial success. Public health efforts to improve oral health go back to the late 1800s and early 1900s, when toothbrushes and toothpaste were new and improved technologies. The public health campaigns of the early 1900s were very instrumental in making

(continues)

In the mid-1990s, the Medicine–Public Health Initiative was implemented to investigate better ways to connect public health with medicine, in particu- lar, and health care, in general. Connecting these two fields has not always been easy or yielded successful results. Additional structures are needed to formalize effective and efficient bonds. Models do exist and new ideas are being put forth to connect clinical care and public health. BOX 5-6 discusses one such model, called community-oriented primary care (COPC) (Gofin & Gofin, 2011).

Despite efforts in the healthcare system to reach out to the community and address public health issues (such as COPC), it remains the pri- mary responsibility of governmental public health to organize and mobilize community-based efforts. Working with NGOs and healthcare professionals and organizations is imperative to effectively and efficiently accomplish the goals of public health. But how exactly can public health agencies accomplish these goals?

▸ How Can Public Health Take the Lead in Mobilizing Community Partnerships to Identify and Solve Health Problems?

An essential service of public health is the mobiliza- tion of community partnerships and action to iden- tify and solve health problems. These efforts by public health agencies are critical to putting the pieces of the health system together to protect and promote health and prevent disability and death.

Increasingly, community members themselves are becoming active participants in addressing health and disease in their communities. One approach

to engage community members in the process is through community-based participatory research (CBPR). Through CBPR, community members are involved in all phases of the research process, con- tributing their expertise while sharing ownership and responsibility over the research, and assisting to build trust, knowledge, and skill to facilitate the research and development and implementation of interventions.

Examples of successful collaboration include state tobacco control programs that have been led by public health agencies but rely heavily on NGOs, healthcare professionals, and other governmental agencies. These efforts have substantially reduced statewide cigarette smoking rates.

Efforts to organize coordinated programs for lead control have also been met with success. Collabora- tive efforts between public health and health care have identified and treated children with elevated lead levels. Cooperation with other agencies has provided for the removal of lead paint from homes and testing and control of lead in playgrounds, water, and, most recently, toys.

It is possible to view the coordinated mobilization of public and private efforts as community-oriented public health (COPH). We can see this as a parallel to COPC. In COPC, healthcare efforts are expanded to take on additional public health roles. In COPH, public health efforts are expanded to collaborate with healthcare delivery institutions, as well as other com- munity and other governmental efforts. Child oral health, an example of COPH, is illustrated in BOX 5-7.

Developing community partnerships is a time- consuming and highly political process that requires great leadership and diplomatic skills. Central author- ity and command and control approaches are generally not effective in the complex organizational structures of the United States. New approaches and new strat- egies are needed to bring together the organizations and individuals who can get the job done.

 

 

96 Chapter 5 Public Health Institutions and Systems

BOX 5-7 Child Oral Health and Community-Oriented Public Health (continued)

toothbrushing a routine part of life in the United States. Unfortunately, the fluoridization of drinking water, despite the well-grounded evidence of its benefits, has not been so readily accepted. The American Dental Association and the American Medical Association have supported this intervention for over half a century. Resistance from those who view it as an intrusion of governmental authority, however, has prevented universal use of fluoridation in this country. After over a half century of effort, fluoridation has reached less than 66% of Americans through the water supply.

Today, new technologies, from dental sealants to more cost-effective methods for treating cavities, have again made oral health a public health priority. However, the number of dentists has not grown in recent years to keep up with the growing population. In addition, dental care for those without the resources to pay for it is often inadequate and inaccessible. Thus, a new approach is needed to bring dental care to those in need. Perhaps a new strategy using a COPH approach can make this happen.

COPH can reach beyond the institutional and geographical constraints that COPC faces when based in a community health center or other institutions serving a geographically defined population or community. COPH as a government- led effort allows a greater range of options for intervention, including those that require changes in laws, incentives, and governmental procedures. Interventions may include authorizing new types of clinicians, providing services in nontraditional settings such as schools, funding innovations to put new technologies into practice, and addressing the regulatory barriers to rapid and cost-effective delivery of services.

▸ Conclusion In summary, the chapter offered a look at the orga- nization of the public health system and the chal- lenges it faces in accomplishing its core functions

and providing its essential services. The role of public health will continue to evolve as current and emerging issues impact the health of the population.

References Centers for Disease Control and Prevention. (1996). History

of CDC. Morbidity and Mortality Weekly Report, 45(25), 526–530.

Centers for Disease Control and Prevention & Centers for State, Tribal, Local, and Territorial Support. (2018). Public health professionals gateway: The public health system and the 10 essential public health services. Retrieved from https://www.cdc.gov/stltpublichealth/publichealthservices /essentialhealthservices.html

Duffin, J., & Sweetman, A. (2006). SARS in context: Memory, history, policy. Montreal, Canada: McGill-Queen’s University Press.

Gofin, J., & Gofin, R. (2011). Essentials of global community health. Sudbury, MA: Jones and Bartlett Learning.

Institute of Medicine. (1988). The future of public health. Washington, DC: National Academies Press.

Institute of Medicine. (2008). Initial guidance for an update of the National Vaccine Plan: A letter report to the national vaccine program office. Washington, DC: National Academies Press.

Public Health Accreditation Board. (2013). Standards and measures. Retrieved from http://www.phaboard.org/accreditation-process /public-health-department-standards-and-measures

Turnock, B. J. (2007). Essentials of public health. Burlington, MA: Jones and Bartlett Learning.

Turnock, B. J. (2009). Public health: What it is and how it works (4th ed.). Burlington, MA: Jones and Bartlett Learning.

U.S. Department of Health and Human Services. (2017). HHS organizational chart. Retrieved from http://www.hhs.gov /about/orgchart

World Bank. (2018). Health. Retrieved from http://www .worldbank.org/en/topic/health

▸ Endnotes a. This does not imply that components of the

work cannot be contracted to nongovernmen- tal organizations. This activity is increasingly occurring. The concept of core function, how- ever, implies that public health agencies remain responsible for these functions even when the

day-to-day work is conducted through con- tracts with an outside organization.

b. This delegation may occur at the discretion of the state government or it may be included in the state’s constitution, providing what is called home rule authority to local jurisdictions. In general, jurisdictions with home rule author- ity exercise substantially more autonomy.

 

 

97PART I ADDENDUM: TIMELINE

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ic al

c ar

e to

m er

ch an

t s ea

m en

.

M ar

bu ry

v . M

ad is

on , 5

U .S

. 1 37

(1 80

3) :

Es ta

bl is

he d

th e

Su pr

em e

C ou

rt ’s

po w

er

of ju

di ci

al re

vi ew

; 1 81

8 O

ffi ce

o f t

h e

Su rg

eo n

G en

er al

e st

ab lis

he d.

 

Im p

o rt

an t

D ev

el o

p m

en ts

in H

ea lt

h

an d

M ed

ic in

e St

at e

Po or

L aw

s re

qu ire

c om

m un

iti es

to c

ar e

fo r r

es id

en ts

w

ho a

re p

hy si

ca lly

o r m

en ta

lly in

ca p

ab le

o f c

ar in

g fo

r th

em se

lv es

; S ta

te s

b eg

in b

ui ld

in g

d is

p en

sa rie

s in

th e

la te

17

00 s

to p

ro vi

d e

m ed

ic at

io n

to th

e p

oo r;

A lm

sh ou

se s

se rv

e as

p rim

iti ve

h os

p ita

ls , p

ro vi

d in

g li

m ite

d c

ar e

to th

e in

d ig

en t;

Pu b

lic h

ea lth

fo cu

se s

on fi

g ht

in g

p la

g ue

, c ho

le ra

, a nd

sm

al lp

ox e

p id

em ic

s, of

te n

th ro

ug h

qu ar

an tin

e.

 

 

98 PART I ADDENDUM: TIMELINE

18 30

s 18

40 s

18 50

s

Po lit

ic al

P ar

ty in

P o

w er

— Fe

d er

al G

o ve

rn m

en t

Pr es

id en

t D

em oc

ra t (

18 29

–1 84

1) W

h ig

(1 84

1– 18

45 );

D em

oc ra

t ( 18

45 –1

84 9)

; W h

ig (1

84 9–

18 53

); D

em oc

ra t (

18 53

–1 86

1)

A n

d re

w J

ac ks

on (1

82 9–

18 37

); M

ar tin

V an

B ur

en

(1 83

7– 18

41 )

W ill

ia m

H en

ry H

ar ris

on (1

84 1)

; Jo

h n

T yl

er (1

84 1–

18 45

); Ja

m es

K .

Po lk

(1 84

5– 18

49 );

Z ac

h ar

y Ta

yl or

(1

84 9–

18 50

)

M ill

ar d

F ill

m or

e (1

85 0–

18 53

); Fr

an kl

in P

ie rc

e (1

85 3–

18 57

); Ja

m es

B uc

h an

an (1

85 7–

18 61

)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es Ja

ck so

n s

(1 82

9– 18

37 );

D em

oc ra

t ( 18

37 –1

84 1)

U .S

. S en

at e

A n

ti- Ja

ck so

n ia

n (1

83 3–

18 35

); Ja

ck so

n ia

n

(1 83

5– 18

37 );

D em

oc ra

t ( 18

37 –1

84 1)

W h

ig (1

84 1–

18 45

) ( 27

th –2

8t h

); D

em oc

ra t (

18 45

–1 86

1) (2

9t h

–3 6t

h )

M aj

o r

So ci

al a

n d

P o

lit ic

al

Ev en

ts In

d u

st ri

al R

ev o

lu ti

o n

(~ 17

90 –1

86 0)

a n

d in

cr ea

se d

u rb

an iz

at io

n

U .S

.– M

ex ic

an W

ar (1

84 6–

18 48

) C

ri m

ea n

W ar

(1 85

3– 18

56 )

K ey

F ed

er al

L eg

is la

ti ve

P

ro p

o sa

ls /L

aw s

an d

K ey

Le

g al

D ec

is io

n s

18 48

Im p

o rt

D ru

g A

ct : I

n iti

at es

d

ru g

re g

ul at

io n

; U .S

. C us

to m

s Se

rv ic

e is

re q

ui re

d to

e n

fo rc

e p

ur ity

s ta

n d

ar d

s fo

r i m

p or

te d

m ed

ic at

io n

s.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d M

ed ic

in e

18 46

F irs

t p ub

lic iz

ed u

se o

f g en

er al

an

es th

et ic

; U se

o f a

n es

th et

ic s

in cr

ea se

s th

e n

um b

er o

f s ur

g er

ie s

p er

fo rm

ed ; 1

84 7

A m

er ic

an M

ed ic

al

A ss

oc ia

tio n

(A M

A ) i

s fo

un d

ed .

St ud

ie s

b y

Ed w

in C

h ad

w ic

k in

E n

g la

n d,

L em

ue l

Sh at

tu ck

in M

as sa

ch us

et ts

, a n

d o

th er

s re

ve al

th at

ov

er cr

ow d

ed a

n d

u n

sa n

ita ry

c on

d iti

on s

b re

ed

d is

ea se

, a n

d a

d vo

ca te

e st

ab lis

h m

en t o

f l oc

al h

ea lth

b

oa rd

s; B

y th

e en

d o

f t h

e 18

00 s,

4 0

st at

es a

n d

se

ve ra

l l oc

al iti

es e

st ab

lis h

h ea

lth d

ep ar

tm en

ts .

 

 

99PART I ADDENDUM: TIMELINE

18 60

s 18

70 s

18 80

s

Po lit

ic al

P ar

ty in

Po

w er

— Fe

d er

al

G o

ve rn

m en

t

Pr es

id en

t Re

p ub

lic an

; D em

oc ra

t Re

p ub

lic an

Re p

ub lic

an (1

88 1–

18 85

); D

em oc

ra t (

18 85

–1 88

9)

A b

ra h

am L

in co

ln (1

86 1–

18 65

); A

n d

re w

J oh

n so

n

(1 86

5– 18

69 )

U ly

ss es

S . G

ra n

t ( 18

69 –1

87 7)

; Ru

th er

fo rd

B . H

ay es

(1 87

7– 18

81 )

Ja m

es A

. G ar

fie ld

(1 88

1) ; C

h es

te r A

. A rt

h ur

(1 88

1– 18

85 );

G ro

ve r C

le ve

la n

d (1

88 5–

18 89

)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es Re

p ub

lic an

(1 85

9– 18

75 )

D em

oc ra

t ( 18

75 –1

88 1)

Re p

ub lic

an (1

88 1–

18 83

); D

em oc

ra t (

18 83

–1 88

9)

U .S

. S en

at e

Re p

ub lic

an (1

86 1–

18 79

) ( 37

th –4

5t h

) D

em oc

ra t (

18 79

–1 88

1) (4

6t h

) Re

p ub

lic an

(1 88

1– 18

93 ) (

47 th

–5 2n

d )

M aj

o r

So ci

al a

n d

Po

lit ic

al E

ve n

ts In

d u

st ri

al R

ev o

lu ti

o n

(~ 17

90 –1

86 0)

a n

d

in cr

ea se

d u

rb an

iz at

io n

U .S

. C iv

il W

ar (1

86 1–

18 65

) a n

d p

os t-

w ar

ex

p an

si on

in in

te rs

ta te

c om

m er

ce U

.S .–

M ex

ic an

W ar

(1 84

6– 18

48 )

C ri

m ea

n W

ar (1

85 3–

18 56

)

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/L aw

s an

d

K ey

L eg

al D

ec is

io n

s

18 62

B u

re au

o f C

h em

is tr

y (fo

re ru

n n

er o

f th

e Fo

od a

n d

D ru

g A

d m

in is

tr at

io n

[F D

A ])

is

es ta

b lis

h ed

a s

a sc

ie n

tifi c

la b

or at

or y

in th

e D

ep ar

tm en

t o f A

g ric

ul tu

re .

18 70

s M

ed ic

al P

ra ct

ic e

A ct

s: E

st ab

lis h

st

at e

re g

ul at

io n

o f p

hy si

ci an

li ce

n si

n g

; 1 87

0 M

ar in

e H

o sp

it al

S er

vi ce

is c

en tr

al iz

ed a

s a

se p

ar at

e b

ur ea

u of

th e

Tr ea

su ry

D ep

ar tm

en t;

18 78

N at

io n

al Q

u ar

an ti

n e

A ct

: G ra

n ts

th e

M ar

in e

H os

p ita

l S er

vi ce

q ua

ra n

tin e

au th

or ity

d

ue to

it s

as si

st an

ce w

ith y

el lo

w fe

ve r

ou tb

re ak

.

18 87

N at

io n

al H

yg ie

n ic

L ab

or at

or y,

p re

d ec

es so

r l ab

to

th e

N at

io n

al In

st itu

te s

of H

ea lth

, i s

es ta

b lis

h ed

in S

ta te

n

Is la

n d,

N ew

Y or

k, b

y th

e N

at io

n al

M ar

in e

H ea

lth S

er vi

ce .

Im p

o rt

an t

D ev

el o

p ­

m en

ts in

H ea

lt h

a n

d

M ed

ic in

e

18 61

F irs

t n ur

si ng

s ch

oo l i

s fo

un d

ed a

nd th

e ro

le o

f n ur

si ng

is e

st ab

lis he

d d

ur in

g th

e C

iv il

W ar

; 18

60 s

Lo ui

s Pa

st eu

r d ev

el op

s th

e g

er m

th eo

ry o

f d

is ea

se ; 1

86 5

an ti

se p

ti c

su rg

er y

is in

tr od

uc ed

b

y Jo

se p

h Li

st er

, d ec

re as

in g

d ea

th ra

te s

fr om

su

rg ic

al o

p er

at io

ns ; W

ith th

e ad

ve nt

o f l

ic en

si ng

, th

e p

ra ct

ic e

of m

ed ic

in e

b eg

in s

to b

ec om

e a

m or

e ex

cl us

iv e

re al

m .

18 77

L ou

is P

as te

ur d

is co

ve rs

th at

a n

th ra

x is

c au

se d

b y

b ac

te ria

; S ci

en tis

ts fi

n d

b

ac te

rio lo

g ic

a g

en ts

c au

si n

g tu

b er

cu lo

si s,

d

ip h

th er

ia , t

yp h

oi d,

a n

d y

el lo

w fe

ve r;

Im m

un iz

at io

n s

an d

w at

er p

ur ifi

ca tio

n

in te

rv en

tio n

s fo

llo w

re ce

n t d

is co

ve rie

s;

St at

e an

d lo

ca l h

ea lth

d ep

ar tm

en ts

c re

at e

la b

or at

or ie

s; S

ta te

s b

eg in

p as

si n

g la

w s

re q

ui rin

g d

is ea

se re

p or

tin g

a n

d e

st ab

lis h

in g

d

is ea

se re

g is

tr ie

s.

18 80

s Fi

rs t h

os p

ita ls

e st

ab lis

h ed

a n

d th

e im

p or

ta n

ce

of h

os p

ita ls

in th

e p

ro vi

si on

o f m

ed ic

al c

ar e

in cr

ea se

s;

18 82

fi rs

t m aj

or e

m p

lo ye

e- sp

on so

re d

m ut

ua l

b en

efi t a

ss oc

ia tio

n w

as c

re at

ed b

y N

or th

er n

P ac

ifi c

Ra ilw

ay , i

n cl

ud es

h ea

lth ca

re b

en efi

t; So

ci al

In su

ra n

ce

m ov

em en

t r es

ul ts

in th

e cr

ea tio

n o

f “ si

ck n

es s”

in su

ra n

ce

th ro

ug h

ou t m

an y

co un

tr ie

s in

E ur

op e;

1 89

5 X-

ra ys

d

is co

ve re

d.

 

 

100 PART I ADDENDUM: TIMELINE

18 90

s 19

00 s

Po lit

ic al

P ar

ty in

P o

w er

— Fe

d er

al

G o

ve rn

m en

t Pr

es id

en t

Re p

ub lic

an (1

88 9–

18 93

); D

em oc

ra t

(1 89

3– 18

97 );

Re p

ub lic

an (1

89 7–

19 01

) Re

p ub

lic an

/P ro

g re

ss iv

e

Be n

ja m

in H

ar ris

on (1

88 9–

18 93

); G

ro ve

r C le

ve la

n d

(1 89

3– 18

97 );

W ill

ia m

M

cK in

le y

(1 89

7– 19

01 )

Th eo

d or

e Ro

os ev

el t (

19 01

–1 90

9)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es Re

p ub

lic an

(1 88

9– 18

91 );

D em

oc ra

t ( 18

91 –1

89 5)

; R ep

ub lic

an (1

89 5–

19 11

)

U .S

. S en

at e

D em

oc ra

t ( 18

93 –1

89 5)

(5 3r

d );

Re p

ub lic

an (1

89 5–

19 13

) ( 54

th –6

2n d

) Re

p ub

lic an

M aj

o r

So ci

al a

n d

P o

lit ic

al E

ve n

ts P

ro g

re ss

iv e

Er a

(1 90

0– 19

20 ):

C h

ar ac

te riz

ed b

y p

op ul

ar s

up p

or t f

or s

oc ia

l r ef

or m

, p ar

t of

w h

ic h

in cl

ud ed

c om

p ul

so ry

h ea

lth in

su ra

n ce

; R oo

se ve

lt ca

m p

ai g

n ed

o n

a s

oc ia

l in

su ra

n ce

p la

tf or

m in

1 91

2.

K ey

F ed

er al

L eg

is la

ti ve

P ro

p o

sa ls

/ La

w s

an d

K ey

L eg

al D

ec is

io n

s 18

90 S

h er

m an

A n

ti tr

u st

A ct

: Pr

oh ib

its in

te rs

ta te

tr us

ts s

o ec

on om

ic

p ow

er w

ou ld

n ot

b e

co n

ce n

tr at

ed in

a

fe w

c or

p or

at io

n s.

H u

rl ey

v . E

d d

in g

fi el

d , 5

9 N

.E . 1

05 8

(In d.

1 90

1) : P

hy si

ci an

s ar

e un

d er

n o

d ut

y to

tr ea

t, an

d a

p hy

si ci

an is

n ot

li ab

le fo

r a rb

itr ar

ily re

fu si

n g

to re

n d

er m

ed ic

al a

ss is

ta n

ce ; 1

90 2

M ar

in e

H ea

lt h

S er

vi ce

re n

am ed

th e

P u

b lic

H ea

lt h

a n

d M

ar in

e H

o sp

it al

S er

vi ce

(P

H M

H S)

a s

its ro

le in

d is

ea se

c on

tr ol

a ct

iv iti

es e

xp an

d s;

1 90

2 B

io lo

g ic

s C

o n

tr o

l A ct

: Re

g ul

at es

s af

et y

an d

e ffe

ct iv

en es

s of

v ac

ci n

es , s

er um

s, e

tc .;

Ja co

b so

n v

. M as

sa ch

u se

tt s,

19

7 U

.S . 1

1 (1

90 5)

: S ta

te s

ta tu

te re

q ui

rin g

c om

p ul

so ry

v ac

ci n

at io

n a

g ai

n st

s m

al lp

ox is

a

co n

st itu

tio n

al e

xe rc

is e

of p

ol ic

e p

ow er

; 1 90

6 Fo

o d

a n

d D

ru g

A ct

( W

ile y

A ct

): G

iv es

re

g ul

at or

y p

ow er

to m

on ito

r f oo

d m

an uf

ac tu

rin g,

la b

el in

g, a

n d

s al

es to

F D

A p

re d

ec es

so r;

19 08

F ed

er al

E m

p lo

ye rs

L ia

b ili

ty A

ct : C

re at

es w

or ke

rs c

om p

en sa

tio n

p ro

g ra

m fo

r s el

ec t

fe d

er al

e m

p lo

ye es

.

Im p

o rt

an t

D ev

el o

p m

en ts

in H

ea lt

h

an d

M ed

ic in

e 19

01 A

M A

re or

g an

iz es

a t l

oc al

/s ta

te le

ve l a

n d

g ai

n s

st re

n g

th , b

eg in

n in

g e

ra o

f “ or

g an

iz ed

m

ed ic

in e”

a s

p hy

si ci

an s

as a

g ro

up b

ec om

e a

m or

e co

h es

iv e

an d

in cr

ea si

n g

ly p

ro fe

ss io

n al

au

th or

ity .

 

 

101PART I ADDENDUM: TIMELINE

19 10

s 19

20 s

Po lit

ic al

P ar

ty in

P o

w er

— Fe

d er

al G

o ve

rn m

en t

Pr es

id en

t Re

p ub

lic an

D em

oc ra

t Re

p ub

lic an

Re p

ub lic

an

W ill

ia m

H . T

af t (

19 09

–1 91

3) W

oo d

ro w

W ils

on (1

91 3–

19 21

) W

ar re

n G

. H ar

d in

g

(1 92

1– 19

23 )

C al

vi n

C oo

lid g

e (1

92 3–

19 29

)

U .S

. H ou

se

of R

ep re

se n

– ta

tiv es

D em

oc ra

t ( 19

11 –1

91 9)

(6 2n

d –6

5t h

) D

em oc

ra t (

19 13

–1 91

9) (6

3r d

–6 5t

h );

Re p

ub lic

an (1

91 9–

19 33

) ( 66

th –7

2n d

) Re

p ub

lic an

(1

91 9–

19 31

) (6

6t h

–7 1s

t)

Re p

ub lic

an

U .S

. S en

at e

Re p

ub lic

an D

em oc

ra t (

19 13

–1 91

9) (6

3r d

–6 5t

h );

Re p

ub lic

an (1

91 9–

19 33

) ( 66

th –7

2n d

) Re

p ub

lic an

Re p

ub lic

an

M aj

o r

So ci

al a

n d

P o

lit ic

al

Ev en

ts W

o rl

d W

ar I

(1 91

4– 19

19 ; U

n ite

d S

ta te

s en

te rs

in 1

91 7)

K ey

F ed

er al

L eg

is la

ti ve

P

ro p

o sa

ls /L

aw s

an d

K ey

L eg

al

D ec

is io

n s

19 12

C h

ild re

n ’s

B u

re au

o f H

ea lt

h e

st ab

lis h

ed in

D

ep ar

tm en

t o f C

om m

er ce

(l at

er m

ov ed

to D

ep ar

tm en

t of

L ab

or );

19 12

P u

b lic

H ea

lt h

a n

d M

ar in

e H

o sp

it al

Se

rv ic

e is

re n

am ed

th e

P u

b lic

H ea

lt h

S er

vi ce

a n

d is

au

th or

iz ed

to in

ve st

ig at

e h

um an

d is

ea se

a n

d s

an ita

tio n

; 19

14 C

la yt

o n

A n

ti tr

u st

A ct

: C la

rifi es

th e

Sh er

m an

A

n tit

ru st

A ct

a n

d in

cl ud

es a

d d

iti on

al p

ro h

ib iti

on s.

19 11

: F irs

t s ta

te w

or ke

rs c

om p

en sa

tio n

la w

e n

ac te

d ; 1

91 8

C h

am b

er la

in ­K

ah n

A ct

: Pr

ov id

es fi

rs t f

ed er

al g

ra n

ts to

s ta

te s

fo r p

ub lic

h ea

lth s

er vi

ce s;

1 92

1 Sw

ee t

A ct

: E st

ab lis

h es

th

e Ve

te ra

n s

A d

m in

is tr

at io

n ; 1

92 2

Sh ep

h er

d ­T

o w

n er

A ct

: P ro

vi d

es g

ra n

ts fo

r t h

e C

h ild

re n’

s Bu

re au

a n

d s

ta te

m at

er n

al a

n d

c h

ild h

ea lth

p ro

g ra

m s,

a n

d is

th e

fir st

d ire

ct fe

d er

al fu

n d

in g

of

h ea

lth s

er vi

ce s

fo r i

n d

iv id

ua ls

.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d M

ed ic

in e

19 10

F le

xn er

R ep

or t o

n M

ed ic

al E

d uc

at io

n c

re at

es

m ed

ic al

s ch

oo l s

ta n

d ar

d s;

“s ic

kn es

s” in

su ra

n ce

es

ta b

lis h

ed b

y Br

ita in

in 1

91 1

an d

R us

si a

in 1

91 2;

So

ci al

is t a

n d

P ro

g re

ss iv

e p

ar tie

s in

th e

U n

ite d

S ta

te s

su p

p or

t s im

ila r “

si ck

n es

s” in

su ra

n ce

.

19 13

A m

er ic

an C

o lle

g e

o f S

u rg

eo n

s (A

C S)

is fo

un d

ed ; 1

91 8

A C

S b

eg in

s ac

cr ed

ita tio

n

of h

os p

ita ls

; 1 91

8– 19

19 p

an d

em ic

fl u

k ill

s ov

er 6

00 ,0

00 p

eo p

le in

th e

U n

ite d

S ta

te s;

1 92

0 A

M A

p as

se s

re so

lu tio

n a

g ai

n st

c om

p ul

so ry

h ea

lth in

su ra

n ce

; A M

A o

p p

os iti

on c

om b

in ed

w

ith e

n tr

y in

to W

or ld

W ar

I (a

n d

th e

an ti-

G er

m an

s en

tim en

ts a

ro us

ed ),

un d

er m

in es

s up

p or

t fo

r n at

io n

al h

ea lth

re fo

rm a

n d

g ov

er n

m en

t i n

su ra

n ce

; 1 92

9 B

lu e

C ro

ss e

st ab

lis h

ed it

s fir

st

h os

p ita

l i n

su ra

n ce

p la

n a

t B ay

lo r U

n iv

er si

ty ; C

h ro

n ic

il ln

es se

s b

eg in

to re

p la

ce in

fe ct

io us

d

is ea

se s

as m

os t s

ig n

ifi ca

n t h

ea lth

th re

at ; W

ith in

n ov

at io

n s

in m

ed ic

al c

ar e,

h ea

lth ca

re c

os ts

b

eg in

to ri

se .

 

 

102 PART I ADDENDUM: TIMELINE

19 30

s 19

40 s

Po lit

ic al

P ar

ty in

Po

w er

— Fe

d er

al

G o

ve rn

m en

t

Pr es

id en

t Re

p ub

lic an

D em

oc ra

t

H er

b er

t H oo

ve r (

19 29

–1 93

3) Fr

an kl

in D

. R oo

se ve

lt (1

93 3–

19 45

)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es D

em oc

ra t (

19 31

–1 94

7) (7

2n d

–7 9t

h )

D em

oc ra

t

U .S

. S en

at e

D em

oc ra

t ( 19

33 –1

94 7)

(7 3r

d –7

9t h

) D

em oc

ra t

M aj

o r

So ci

al a

n d

Po

lit ic

al E

ve n

ts G

re at

D ep

re ss

io n

(1 92

9 th

ro ug

h 1

93 0s

); N

ew D

ea l (

19 33

–1 93

9) W

o rl

d W

ar II

(1 93

9– 19

45 ),

Pe ar

l H ar

b or

1 94

1)

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/L aw

s an

d

K ey

L eg

al D

ec is

io n

s

19 30

N at

io n

al In

st it

u te

s o

f H ea

lt h

e st

ab lis

h ed

; 1 93

3 Fe

d er

al

Em er

g en

cy R

el ie

f A d

m in

is tr

at io

n p

ro vi

d es

li m

ite d

m ed

ic al

s er

vi ce

s fo

r t h

e m

ed ic

al ly

in d

ig en

t; 19

35 S

o ci

al S

ec u

ri ty

A ct

: P ro

vi d

es fe

d er

al

g ra

n t-

in -a

id fu

n d

in g

fo r s

ta te

s to

c re

at e

an d

m ai

n ta

in p

ub lic

h ea

lth s

er vi

ce s

an d

tr ai

n in

g, e

xp an

d s

re sp

on si

b ili

tie s

fo r t

h e

C h

ild re

n’ s

H ea

lth B

ur ea

u,

an d

e st

ab lis

h es

A id

to F

am ili

es w

ith D

ep en

d en

t C h

ild re

n (A

FD C

) w el

fa re

p

ro g

ra m

; 1 93

5 W

o rk

s P

ro je

ct A

d m

in is

tr at

io n

is c

re at

ed , i

n cl

ud in

g

p ro

je ct

s to

b ui

ld a

n d

im p

ro ve

h os

p ita

ls ; 1

93 8

Fo o

d , D

ru g

a n

d C

o sm

et ic

A

ct : E

xp an

d s

re g

ul at

or y

sc op

e of

F D

A to

re q

ui re

p re

m ar

ke t a

p p

ro va

l ( in

re

sp on

se to

d ea

th s

fr om

a n

u n

te st

ed p

ro d

uc t)

; 1 93

9 Pu

b lic

H ea

lth S

er vi

ce

is tr

an sf

er re

d fr

om th

e Tr

ea su

ry D

ep ar

tm en

t t o

th e

n ew

F ed

er al

S ec

ur ity

A

g en

cy .

19 41

M an

h am

A ct

: F un

d s

w ar

tim e

em er

g en

cy b

ui ld

in g

o f h

os p

ita ls

; 1 94

2 N

at io

n al

W ar

L ab

o r

B o

ar d

ru le

s th

at th

e p

ro vi

si on

o f b

en efi

ts , i

n cl

ud in

g

h ea

lth in

su ra

n ce

, d oe

s n

ot v

io la

te w

ag e

fr ee

ze ; 1

94 4

P u

b lic

H ea

lt h

S er

vi ce

A

ct : C

on so

lid at

es th

e la

w s

re la

te d

to th

e fu

n ct

io n

s of

th e

PH S;

1 94

6 H

ill ­

B u

rt o

n A

ct : F

un d

s h

os p

ita l c

on st

ru ct

io n

to im

p ro

ve a

cc es

s to

h os

p ita

l-b as

ed

m ed

ic al

c ar

e; 1

94 6

Th e

C o

m m

u n

ic ab

le D

is ea

se C

en te

r (C

D C

) o p

en s

as p

ar t

of th

e Pu

b lic

H ea

lth S

er vi

ce ; 1

94 9

Tr um

an ’s

n at

io n

al h

ea lth

in su

ra n

ce p

ro p

os al

is

d ef

ea te

d.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

Th e

G re

at D

ep re

ss io

n th

re at

en s

fin an

ci al

s ec

ur ity

o f p

hy si

ci an

s, h

os p

ita ls

, an

d in

d iv

id ua

ls ; C

om m

er ci

al in

su ra

n ce

in d

us tr

y ris

es in

th e

ab se

n ce

o f

g ov

er n

m en

t- sp

on so

re d

in su

ra n

ce p

la n

s; In

th e

la te

1 93

0s th

e Bl

ue C

ro ss

(h

os p

ita l s

er vi

ce s)

a n

d B

lu e

Sh ie

ld (p

hy si

ci an

s er

vi ce

s) h

ea lth

in su

ra n

ce p

la n

cr

ea te

d ; P

re p

ai d

g ro

up h

ea lth

p la

n s/

m ed

ic al

c oo

p er

at iv

es g

ai n

p op

ul ar

ity

w ith

s om

e p

ro vi

d er

s an

d c

on su

m er

s, b

ut a

re o

p p

os ed

b y

A M

A .

(1 93

2– 19

72 ) T

u sk

eg ee

S yp

h ili

s St

u d

y

19 45

N ob

el P

riz e

in M

ed ic

in e

aw ar

d ed

fo r d

ev el

op m

en t o

f p en

ic ill

in tr

ea tm

en t

fo r h

um an

s, w

h ic

h is

u se

d e

xt en

si ve

ly in

th e

w ar

; 1 94

5 Ka

is er

P er

m an

en te

, a

la rg

e p

re p

ai d,

in te

g ra

te d

h ea

lth p

la n

is o

p en

ed to

th e

p ub

lic ; 1

94 6

th e

Em er

so n

Re

p or

t r el

ea se

d p

ro p

os in

g o

ve ra

ll p

la n

fo r p

ub lic

h ea

lth in

th e

U n

ite d

S ta

te s;

19

48 A

M A

o p

p os

es T

ru m

an ’s

p la

n fo

r n at

io n

al h

ea lth

in su

ra n

ce a

n d

s en

tim en

ts

ag ai

n st

n at

io n

al h

ea lth

re fo

rm a

ls o

fu el

ed b

y th

e C

ol d

W ar

; E m

p lo

ye r-

b as

ed

h ea

lth in

su ra

n ce

g ro

w s

ra p

id ly

w ith

n o

n at

io n

al h

ea lth

in su

ra n

ce p

ro g

ra m

a n

d

as e

m p

lo ye

rs c

om p

et e

fo r a

s h

or t s

up p

ly o

f e m

p lo

ye es

d ue

to th

e w

ar a

n d

b

ec au

se h

ea lth

b en

efi ts

a re

e xe

m p

te d

fr om

th e

w ag

e fr

ee ze

; A ft

er W

W II,

la b

or

un io

n s

g ai

n ed

th e

rig h

t t o

b ar

g ai

n c

ol le

ct iv

el y,

le ad

in g

to a

n ot

h er

e xp

an si

on in

em

p lo

ye e

h ea

lth p

la n

s; C

om m

er ci

al in

su ra

n ce

h as

ta ke

n o

ve r 4

0% o

f t h

e m

ar ke

t fr

om B

lu e

C ro

ss .

 

 

103PART I ADDENDUM: TIMELINE

19 50

s 19

60 s

Po lit

ic al

P ar

ty in

Po

w er

— Fe

d er

al

G o

ve rn

m en

t

Pr es

id en

t D

em oc

ra t

Re p

ub lic

an D

em oc

ra t

D em

oc ra

t

H ar

ry S

. T ru

m an

(1 94

5– 19

53 )

D w

ig h

t D . E

is en

h ow

er (1

95 3–

19 61

) Jo

h n

F . K

en n

ed y

(1 96

1– 19

63 )

Ly n

d on

B . J

oh n

so n

(1 96

3– 19

69 )

U .S

. H ou

se

of R

ep re

se n

– ta

tiv es

Re p

ub lic

an (1

94 7–

19 49

) ( 80

th );

D em

oc ra

t ( 19

49 –1

95 3)

(8 1s

t– 82

d )

Re p

ub lic

an (1

95 2–

19 55

) ( 83

rd );

D em

oc ra

t ( 19

55 –1

99 4)

(8 4t

h –1

03 rd

) D

em oc

ra t

D em

oc ra

t

U .S

. S en

at e

Re p

ub lic

an (1

94 7–

19 49

) (8

0t h

); D

em oc

ra t (

19 49

–1 95

3)

(8 1s

t– 82

n d

)

Re p

ub lic

an (1

95 3–

19 55

) ( 83

rd );

D em

oc ra

t ( 19

55 –1

98 1)

(8 4t

h –9

6t h

) D

em oc

ra t

D em

oc ra

t

M aj

o r

So ci

al

an d

P o

lit ic

al

Ev en

ts

C ol

d W

ar id

eo lo

g y

an d

M cC

ar th

yi sm

(1 95

0– 19

54 );

K o

re an

W ar

(1 95

0– 19

53 )

Ec on

om ic

d ow

n tu

rn

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/L aw

s an

d K

ey L

eg al

D

ec is

io n

s

19 53

D ep

ar tm

en t

o f H

ea lt

h , E

d u

ca ti

o n

, a n

d W

el fa

re (H

EW ) i

s cr

ea te

d

fr om

th e

Fe d

er al

S ec

ur ity

A g

en cy

, a n

d th

e Pu

b lic

H ea

lth S

er vi

ce is

tr an

sf er

re d

to

H EW

; 1 95

4 In

te rn

al R

ev en

ue S

er vi

ce d

ec la

re s

th at

e m

p lo

ye rs

c an

p ay

h

ea lth

in su

ra n

ce p

re m

iu m

s fo

r t h

ei r e

m p

lo ye

es w

ith p

re -t

ax d

ol la

rs ; B

ro w

n

v. B

o a

rd o

f E d

u ca

ti o

n , 3

47 U

.S . 4

83 (1

95 4)

: R ac

ia l s

eg re

g at

io n

in p

ub lic

ed

uc at

io n

v io

la te

s th

e Eq

ua l P

ro te

ct io

n C

la us

e of

1 4t

h A

m en

d m

en t;

19 56

D

ep en

d en

ts M

ed ic

al C

ar e

A ct

: C re

at es

g ov

er n

m en

t m ed

ic al

c ar

e p

ro g

ra m

fo

r m ili

ta ry

a n

d d

ep en

d en

ts o

ut si

d e

th e

Ve te

ra n

s A

ff ai

rs s

ys te

m ; 1

95 6

So ci

al

Se cu

ri ty

A ct

is a

m en

d ed

to p

ro vi

d e

So ci

al S

ec ur

ity D

is ab

ili ty

In su

ra n

ce .

19 62

A

m en

d m

en ts

t o

Fo

o d

, D ru

g a

n d

C

o sm

et ic

A ct

s re

q ui

re th

at n

ew

d ru

g s

b e

“e ffe

ct iv

e. ”

19 60

K er

r­ M

ill s

p ro

g ra

m p

ro vi

d es

fe d

er al

fu n

d in

g th

ro ug

h

ve n

d or

p ay

m en

ts to

s ta

te s

fo r m

ed ic

al ly

in d

ig en

t e ld

er ly

; Si

m p

ki n

s v.

M o

se s

H . C

o n

e M

em o

ri al

H o

sp it

al , 3

23 F

.2 d

9 59

(4

th C

ir. 1

96 3)

: R ac

ia l s

eg re

g at

io n

in p

riv at

e h

os p

ita ls

re ce

iv in

g

fe d

er al

H ill

-B ur

to n

fu n

d s

vi ol

at es

th e

Eq ua

l P ro

te ct

io n

C la

us e

of th

e 14

th A

m en

d m

en t;

19 64

: C iv

il R

ig h

ts A

ct p

as se

d ;

19 65

M ed

ic ar

e an

d M

ed ic

ai d

p ro

g ra

m s

cr ea

te d

th ro

ug h

So

ci al

S ec

ur ity

A m

en d

m en

ts ; G

ri sw

o ld

v . C

o n

n ec

ti cu

t, 3

81

U .S

. 4 79

(1 96

5) : T

h e

C on

st itu

tio n

p ro

te ct

s a

rig h

t t o

p riv

ac y,

st

at e

la w

fo rb

id d

in g

th e

us e

of c

on tr

ac ep

tiv es

o r p

ro vi

si on

of

th em

to m

ar rie

d c

ou p

le s

vi ol

at es

a c

on st

itu tio

n al

ri g

h t t

o m

ar ita

l p riv

ac y;

1 96

6 C

iv ili

an H

ea lt

h a

n d

M ed

ic al

P ro

g ra

m

fo r

th e

U n

if o

rm ed

S er

vi ce

s (C

H A

M PU

S) c

re at

ed .

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

19 51

J o

in t C

o m

m is

si o

n o

n A

cc re

d it

at io

n o

f H o

sp it

al s

(J C

A H

) i s

cr ea

te d

to

p ro

vi de

v ol

un ta

ry a

cc re

di ta

tio n;

1 95

3 Sa

lk c

re at

es p

ol io

v ac

ci ne

; 1 95

4 fir

st

or ga

n tr

an sp

la nt

is p

er fo

rm ed

; C on

tin ue

d pr

og re

ss io

n in

m ed

ic al

s ci

en ce

a nd

te

ch no

lo gy

le ad

s to

in cr

ea se

d co

st s;

Po lit

ic al

fo cu

s tu

rn s

to K

or ea

n W

ar a

nd a

w ay

fro

m m

ed ic

al c

ar e

re fo

rm .

19 65

: M ed

ic ar

e an

d M

ed ic

ai d

c re

at ed

; 1 96

7 fir

st h

um an

h ea

rt tr

an sp

la n

t.

 

 

104 PART I ADDENDUM: TIMELINE

19 70

s 19

80 s

Po lit

ic al

P ar

ty

in P

o w

er —

Fe d

er al

G

o ve

rn m

en t

Pr es

id en

t Re

p ub

lic an

Re p

ub lic

an D

em oc

ra t

Re p

ub lic

an

Ri ch

ar d

M . N

ix on

(1

96 9–

19 74

) G

er al

d R

. F or

d (1

97 4–

19 77

) Ji

m m

y C

ar te

r (1

97 7–

19 81

) Ro

n al

d R

ea g

an (1

98 1–

19 89

)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es D

em oc

ra t

D em

oc ra

t D

em oc

ra t

D em

oc ra

t

U .S

. S en

at e

D em

oc ra

t D

em oc

ra t

D em

oc ra

t Re

p ub

lic an

(1 98

1– 19

87 ) (

97 th

–9 9t

h );

D em

oc ra

t (1

98 7–

19 95

) ( 10

0t h

–1 03

rd )

M aj

o r

So ci

al

an d

P o

lit ic

al

Ev en

ts

19 89

“N ew

F ed

er al

is m

” o f t

h e

Re ag

an a

d m

in is

tr at

io n

; Be

rli n

W al

l f al

ls

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/ La

w s

an d

K ey

Le

g al

D ec

is io

n s

Pr es

id en

t N ix

on ’s

p ro

p os

ed c

om p

re h

en si

ve h

ea lth

in su

ra n

ce p

la n

fa ils

; 19

71 p

ro p

os ed

H ea

lth S

ec ur

ity A

ct fr

om S

en at

or E

d w

ar d

K en

n ed

y (D

-M A

) f ai

ls ; 1

97 0

C om

m un

ic ab

le D

is ea

se C

en te

r i s

re n

am ed

th e

C en

te rs

fo r

D is

ea se

C o

n tr

o l;

19 72

S o

ci al

S ec

u ri

ty A

m en

d m

en ts

ex

te n

d M

ed ic

ar e

el ig

ib ili

ty a

n d

c re

at e

Su p

p le

m en

ta l S

ec ur

ity In

co m

e (S

SI ) p

ro g

ra m

; C a

n te

rb u

ry v

. S p

en ce

, 4 64

F .2

d 7

72 (D

.C . C

ir. 1

97 2)

: Es

ta b

lis h

ed m

od er

n la

w o

f i n

fo rm

ed c

on se

n t b

as ed

o n

a re

as on

ab le

p

at ie

n t s

ta n

d ar

d ; R

o e

v. W

ad e,

4 10

U .S

. 1 13

(1 97

3) : C

on st

itu tio

n al

ri g

h t

to p

riv ac

y en

co m

p as

se s

a w

om an

’s d

ec is

io n

to te

rm in

at e

h er

p re

g n

an cy

; 19

73 H

ea lt

h M

ai n

te n

an ce

O rg

an iz

at io

n A

ct : S

up p

or ts

g ro

w th

o f

h ea

lth m

ai n

te n

an ce

o rg

an iz

at io

n s;

1 97

4 Em

p lo

ym en

t R

et ir

em en

t In

co m

e Se

cu ri

ty A

ct (E

R IS

A ) p

as se

d ; 1

97 7

H ea

lt h

C ar

e Fi

n an

ci n

g

A d

m in

is tr

at io

n (H

C FA

) i s

cr ea

te d

to a

d m

in is

te r t

h e

M ed

ic ar

e an

d

M ed

ic ai

d p

ro g

ra m

s.

19 79

C ar

te r

in tr

od uc

es a

N

at io

n al

H ea

lth P

la n

to

C on

g re

ss ; 1

97 9

D ep

ar tm

en t

o f

H ea

lt h

a n

d H

u m

an

Se rv

ic es

(H H

S)

is c

re at

ed fr

om a

re

or g

an iz

ed H

EW .

19 83

M ed

ic ar

e im

p le

m en

ts p

ro sp

ec tiv

e p

ay m

en t s

ys te

m

fo r r

ei m

b ur

si n

g h

os p

ita ls

; 1 98

6 Em

er g

en cy

M ed

ic al

Tr

ea tm

en t

an d

A ct

iv e

La b

o r

A ct

(E M

TA LA

): E

n su

re s

ac ce

ss to

e m

er g

en cy

s er

vi ce

s in

M ed

ic ar

e- p

ar tic

ip at

in g

h

os p

ita ls

re g

ar d

le ss

o f a

b ili

ty to

p ay

; 1 98

6 H

ea lt

h

C ar

e Q

u al

it y

Im p

ro ve

m en

t A

ct : C

re at

es th

e N

at io

n al

Pr

ac tit

io n

er D

at ab

an k;

1 98

6 C

o n

so lid

at ed

O m

n ib

u s

B u

d g

et R

ec o

n ci

lia ti

o n

A ct

(C O

B R

A ):

In cl

ud es

h

ea lth

b en

efi t p

ro vi

si on

s th

at e

st ab

lis h

c on

tin ua

tio n

of

e m

p lo

ye r-

sp on

so re

d g

ro up

h ea

lth c

ov er

ag e;

1 98

9 M

ed ic

ar e

C at

as tr

o p

h ic

C o

ve ra

g e

A ct

o f 1

98 8:

In

cl ud

es o

ut p

at ie

n t p

re sc

rip tio

n d

ru g

b en

efi t a

n d

o th

er

ch an

g es

in M

ed ic

ar e

(r ep

ea le

d  1

98 9)

.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

H ea

lth ca

re c

os ts

c on

tin ue

to ri

se d

ra m

at ic

al ly

, d ue

to a

d va

nc es

in m

ed ic

al te

ch no

lo g

y, h

ig h-

te ch

ho

sp ita

l c ar

e, th

e ne

w p

oo l o

f p ay

in g

p at

ie nt

s fro

m M

ed ic

ai d

a nd

M ed

ic ar

e, in

cr ea

se d

u til

iz at

io n

of

se rv

ic es

, a nd

in cr

ea se

d p

hy si

ci an

s p

ec ia

liz at

io n;

1 97

2 co

m p

ut ed

to m

og ra

p hy

(C T

) s ca

n fir

st u

se d

; 19

78 fi

rs t b

ab y

co nc

ei ve

d th

ro ug

h in

v itr

o fe

rt ili

za tio

n is

b or

n.

19 80

W or

ld H

ea lth

A ss

em b

ly d

ec la

re s

sm al

lp ox

er

ad ic

at ed

; 1 98

1 Sc

ie n

tis ts

id en

tif y

A ID

S; 1

98 7

th e

Jo in

t C

om m

is si

on o

n A

cc re

d ita

tio n

o f H

os p

ita ls

c h

an g

es n

am e

to th

e Jo

in t C

om m

is si

on o

n A

cc re

d ita

tio n

o f H

ea lth

ca re

O

rg an

iz at

io n

s (J

C A

H O

); Sh

ift a

w ay

fr om

tr ad

iti on

al fe

e- fo

r- se

rv ic

e in

su ra

n ce

p la

n s

an d

to w

ar d

m an

ag ed

c ar

e.

 

 

105PART I ADDENDUM: TIMELINE

19 90

s

Po lit

ic al

P ar

ty in

Po

w er

— Fe

d er

al

G o

ve rn

m en

t

Pr es

id en

t Re

p ub

lic an

D em

oc ra

t

G eo

rg e

Bu sh

(1 98

9– 19

93 )

W ill

ia m

J . C

lin to

n (1

99 3–

20 01

)

U .S

. H ou

se

of R

ep re

se n

– ta

tiv es

D em

oc ra

t *F

irs t t

im e

si nc

e 19

55 th

at b

ot h

ho us

es a

re R

ep ub

lic an

; R ep

ub lic

an (1

99 5–

20 05

) ( 10

4t h

–1 08

th )

U .S

. S en

at e

D em

oc ra

t Re

p ub

lic an

(1 99

5– 20

05 ) (

10 4t

h –1

08 th

[J an

. 3 –2

0, 2

00 1,

a n

d J

un e

6, 2

00 1–

N ov

. 1 2,

2 00

2 D

em oc

ra t]

)

M aj

o r

So ci

al a

n d

Po

lit ic

al E

ve n

ts 19

90 –1

99 1

G ul

f W ar

Fo re

ig n

c ris

es in

H ai

ti an

d B

os n

ia ; 1

99 3

N or

th A

m er

ic an

F re

e Tr

ad e

A g

re em

en t (

N A

FT A

); W

h ite

w at

er

in ve

st ig

at io

n ; 1

99 5

O kl

ah om

a C

ity b

om b

in g

; 1 99

8 Pr

es id

en t C

lin to

n im

p ea

ch ed

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/L aw

s an

d K

ey L

eg al

D

ec is

io n

s

19 89

A g

en cy

fo r

H ea

lt h

ca re

P o

lic y

an d

R es

ea rc

h

cr ea

te d

; 1 99

0 A

m er

ic an

s W

it h

D is

ab ili

ti es

A ct

(A D

A ):

Pr

ov id

es p

ro te

ct io

n a

g ai

n st

d is

ab ili

ty d

is cr

im in

at io

n ; 1

99 0

R ya

n W

h it

e C

A R

E A

ct : C

re at

es fe

d er

al s

up p

or t f

or A

ID S-

re la

te d

s er

vi ce

s; C

ru za

n v

. D ir

ec to

r, M

is so

u ri

. D ep

’t o

f H

ea lt

h , 4

97 U

.S . 2

61 (1

99 0)

: F irs

t “ rig

h t t

o d

ie ” c

as e

b ef

or e

Su p

re m

e C

ou rt

, i n

w h

ic h

th e

C ou

rt h

el d

th at

a c

om p

et en

t p

er so

n h

as a

c on

st itu

tio n

al ly

p ro

te ct

ed li

b er

ty in

te re

st in

re

fu si

n g

m ed

ic al

tr ea

tm en

t.

19 93

P re

si d

en t C

lin to

n’ s

p ro

p os

ed H

ea lt

h S

ec u

ri ty

A ct

is d

ef ea

te d

; 1 99

5 PH

S re

or g

an iz

ed to

re

p or

t d ire

ct ly

to th

e Se

cr et

ar y

of H

H S;

1 99

6 H

ea lt

h In

su ra

n ce

P o

rt ab

ili ty

& A

cc o

u n

ta b

ili ty

A ct

(H

IP A

A ):

In cl

ud es

p riv

ac y

ru le

s to

p ro

te ct

p er

so n

al h

ea lth

in fo

rm at

io n

, a tt

em p

ts to

s im

p lif

y co

d in

g fo

r h

ea lth

b ill

s, m

ak es

it d

iffi cu

lt to

e xc

lu d

e p

at ie

n ts

fr om

in su

ra n

ce p

la n

s d

ue to

p re

ex is

tin g

c on

d iti

on s;

Pe

rs o

n al

R es

p o

n si

b ili

ty a

n d

W o

rk O

p p

o rt

u n

it y

R ec

o n

ci lia

ti o

n A

ct o

f 1 99

6 re

p la

ce s

A FD

C

w ith

th e

Te m

p or

ar y

A ss

is ta

n ce

fo r N

ee d

y Fa

m ili

es (

TA N

F) p

ro g

ra m

; 1 99

6 M

en ta

l H ea

lt h

P ar

it y

A ct

: R eq

ui re

s in

su ra

n ce

c ar

rie rs

th at

o ffe

r m en

ta l h

ea lth

b en

efi ts

to p

ro vi

d e

th e

sa m

e an

n ua

l a n

d

lif et

im e

d ol

la r l

im its

fo r m

en ta

l a n

d p

hy si

ca l h

ea lth

b en

efi ts

; 1 99

7 Fo

o d

a n

d D

ru g

A d

m in

is tr

at io

n

M o

d er

n iz

at io

n A

ct : R

el ax

es re

st ric

tio n

s on

d ire

ct -t

o -c

on su

m er

a d

ve rt

is em

en ts

o f p

re sc

rip tio

n

d ru

g s;

1 99

7 B

al an

ce d

B u

d g

et A

ct : A

d d

s M

ed ic

ar e

p ar

t C , t

h e

M ed

ic ar

e m

an ag

ed c

ar e

p ro

g ra

m , a

n d

cr

ea te

s th

e St

at e

H ea

lth In

su ra

n ce

P ro

g ra

m , w

h ic

h a

llo w

s st

at es

to e

xt en

d h

ea lth

in su

ra n

ce c

ov er

ag e

to a

d d

iti on

al lo

w -in

co m

e ch

ild re

n ; T

h e

Ti ck

et t

o W

o rk

a n

d W

o rk

In ce

n ti

ve s

Im p

ro ve

m en

t A

ct

o f 1

99 9:

C re

at es

a n

ew s

ta te

o p

tio n

to h

el p

in d

iv id

ua ls

w ith

d is

ab ili

tie s

st ay

e n

ro lle

d in

M ed

ic ai

d o

r M

ed ic

ar e

co ve

ra g

e w

h ile

re tu

rn in

g to

w or

k.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

En ro

llm en

t i n

m an

ag ed

c ar

e d

ou b

le s;

G re

at er

u se

o f o

ut p

at ie

n t s

er vi

ce s;

R at

e of

h ea

lth s

p en

d in

g is

re

la tiv

el y

st ab

le a

t r ou

g h

ly 1

2% to

1 3%

o f g

ro ss

d om

es tic

p ro

d uc

t; D

ire ct

-t o

-c on

su m

er a

d ve

rt is

in g

o f

p h

ar m

ac eu

tic al

s in

cr ea

se s

d ra

m at

ic al

ly a

n d

th e

In te

rn et

is u

se d

a s

a so

ur ce

o f m

ed ic

al in

fo rm

at io

n ;

19 94

O re

g on

H ea

lth P

la n

ra tio

n s

M ed

ic ai

d s

er vi

ce s

th ro

ug h

a p

rio rit

iz ed

li st

o f m

ed ic

al tr

ea tm

en ts

a n

d

co n

d iti

on s;

1 99

7 Ia

n W

ilm ut

c lo

n es

a s

h ee

p fr

om a

d ul

t h um

an c

el ls

.

 

 

106 PART I ADDENDUM: TIMELINE

20 00

s

Po lit

ic al

P ar

ty in

Po

w er

— Fe

d er

al

G o

ve rn

m en

t

Pr es

id en

t Re

p ub

lic an

D em

oc ra

t

G eo

rg e

W . B

us h

(2 00

1– 20

09 )

Ba ra

ck O

b am

a (2

00 9–

20 17

)

U .S

. H ou

se o

f Re

p re

se n

– ta

tiv es

Re p

ub lic

an (2

00 5–

20 07

) ( 10

9t h

); D

em oc

ra t (

20 07

–2 00

9) (1

10 th

) D

em oc

ra t (

20 09

–2 01

1) (1

11 th

); Re

p ub

lic an

2 01

1– (1

12 th

)

U .S

. S en

at e

Re p

ub lic

an (2

00 5–

20 07

) ( 10

9t h

); D

em oc

ra t (

20 07

–2 00

9) (1

10 th

) D

em oc

ra t (

20 09

–2 01

5) (1

11 th

–1 13

th )

M aj

o r

So ci

al a

n d

Po

lit ic

al E

ve n

ts Se

p te

m b

er 1

1, 2

00 1,

te rr

or is

t a tt

ac ks

o n

W or

ld T

ra d

e C

en te

r i n

N ew

Y or

k an

d th

e Pe

n ta

g on

; 20

01 U

.S . m

ili ta

ry a

ct io

n in

A fg

h an

is ta

n ; 2

00 3

Ira q

W ar

b eg

in s

G re

at R

ec es

si on

(b eg

an in

D ec

em b

er 2

00 7)

, i n

cl ud

in g

fi n

an ci

al

cr is

is a

n d

c ol

la p

se o

f h ou

si n

g m

ar ke

t; Pa

ss ag

e of

th e

20 10

P at

ie n

t Pr

ot ec

tio n

a n

d A

ffo rd

ab le

C ar

e  A

ct

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/L aw

s an

d K

ey L

eg al

D

ec is

io n

s

C on

g re

ss io

n al

a tt

en tio

n a

n d

s p

en d

in g

tu rn

s to

in te

rn at

io n

al a

n d

s ec

ur ity

c on

ce rn

s, li

tt le

d

is cu

ss io

n o

f h ea

lth re

fo rm

; 2 00

2 H

o m

el an

d S

ec u

ri ty

A ct

tr an

sf er

s so

m e

H H

S fu

n ct

io n

s,

in cl

ud in

g th

e St

ra te

g ic

N at

io n

al S

to ck

p ile

o f e

m er

g en

cy p

h ar

m ac

eu tic

al s

up p

lie s

an d

th e

N at

io n

al D

is as

te r M

ed ic

al S

er vi

ce , t

o th

e n

ew D

ep ar

tm en

t o f H

om el

an d

S ec

ur ity

; 2 00

3 M

ed ic

ar e

M o

d er

n iz

at io

n A

ct : A

d d

s a

p re

sc rip

tio n

d ru

g b

en efi

t t o

M ed

ic ar

e b

eg in

n in

g

in 2

00 6;

2 00

4 P

ro je

ct B

io Sh

ie ld

A ct

: P ro

vi d

es fu

n d

in g

fo r v

ac ci

n es

a n

d m

ed ic

at io

n s

fo r

b io

d ef

en se

a n

d a

llo w

s ex

p ed

ite d

F D

A re

vi ew

o f t

re at

m en

ts in

re sp

on se

to a

tt ac

ks ; 2

00 5

D efi

ci t

R ed

u ct

io n

A ct

: M ak

es c

h an

g es

to M

ed ic

ai d

c os

t s h

ar in

g, p

re m

iu m

s, b

en efi

ts , a

n d

a ss

et

tr an

sf er

s; 2

00 6

M ed

ic ar

e P

ar t

D P

re sc

ri p

ti o

n D

ru g

P la

n g

oe s

in to

e ffe

ct ; 2

00 8

M en

ta l

H ea

lt h

P ar

it y

A ct

a m

en d

ed to

re q

ui re

in su

re rs

to tr

ea t m

en ta

l h ea

lth c

on d

iti on

s on

th e

sa m

e b

as is

a s

p hy

si ca

l c on

d iti

on s.

 

C on

g re

ss io

n al

fo cu

s on

h ea

lth re

fo rm

, s p

en d

in g

c ut

s; P

re si

d en

t O

b am

a es

ta b

lis h

es th

e O

ffi ce

o f H

ea lt

h R

ef o

rm ; 2

00 9

A m

er ic

an R

ei n

ve st

m en

t an

d R

ec o

ve ry

A ct

(A R

R A

) c re

at es

in

ce n

tiv es

to h

el p

d ev

el op

h ea

lth in

fo rm

at io

n te

ch n

ol og

y an

d

ex p

an d

th e

p rim

ar y

ca re

w or

kf or

ce , a

m on

g o

th er

th in

g s;

2 00

9 C

h ild

re n

’s H

ea lt

h In

su ra

n ce

P ro

g ra

m R

ea u

th o

ri za

ti o

n

A ct

e xt

en d

in g

(f or

4 .5

y ea

rs ) a

n d

e xp

an d

in g

th e

p ro

g ra

m ;

20 10

P at

ie n

t P

ro te

ct io

n a

n d

A ff

o rd

ab le

C ar

e A

ct (A

C A

):

C om

p re

h en

si ve

h ea

lth re

fo rm

in cl

ud in

g a

n “i

n d

iv id

ua l m

an d

at e”

to

p ur

ch as

e in

su ra

n ce

c ov

er ag

e, M

ed ic

ai d

e xp

an si

on , c

re at

io n

o f

st at

e h

ea lth

in su

ra n

ce e

xc h

an g

es , a

n d

m uc

h m

or e.

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

A ft

er t

h e

Se p

te m

b er

1 1,

2 00

1, a

tt ac

ks , p

u b

lic h

ea lth

b ec

o m

es fo

cu se

d o

n e

m er

g en

cy

p re

p ar

ed n

es s;

2 0

0 3

S eq

u en

ci n

g o

f h u

m an

g en

o m

e co

m p

le te

d ; 2

0 0

3 S

A RS

e p

id em

ic

an d

2 00

4 flu

v ac

ci n

e sh

o rt

ag e

ra is

es c

o n

ce rn

s ab

o u

t p

u b

lic h

ea lth

re ad

in es

s; W

o rld

w id

e co

n ce

rn a

b o

u t

a p

o ss

ib le

A vi

an fl

u e

p id

em ic

; H ig

h le

ve l o

f c o

n ce

rn in

t h

e U

n ite

d S

ta te

s ab

o u

t th

e ris

in g

ra te

o f o

b es

it y;

2 0

0 6

G ar

d as

il va

cc in

e p

ro te

ct in

g a

g ai

n st

t w

o s

tr ai

n s

o f

th e

h u

m an

p ap

ill o

m av

iru s,

w h

ic h

is a

ss o

ci at

ed w

ith c

er vi

ca l c

an ce

r, ap

p ro

ve d

b y

th e

FD A

; 2

0 0

7 In

te rn

at io

n al

H ea

lth R

eg u

la tio

n s,

p as

se d

b y

th e

W o

rld H

ea lth

O rg

an iz

at io

n in

2 00

5, a

re

im p

le m

en te

d b

y m

em b

er s

ta te

s.

Ra te

o f h

ea lth

s p

en d

in g

c on

tin ue

s to

s ky

ro ck

et , a

cc ou

n tin

g in

20

09 fo

r 1 7%

o f t

h e

g ro

ss d

om es

tic p

ro d

uc t;

20 09

H 1N

1 sw

in e

flu v

iru s

p an

d em

ic .

 

 

107PART I ADDENDUM: TIMELINE

20

10 s

Po lit

ic al

P ar

ty

in P

o w

er —

Fe d

er al

G

o ve

rn m

en t

Pr es

id en

t D

em oc

ra t

Re p

ub lic

an

Ba ra

ck O

b am

a (2

00 9–

20 17

) D

on al

d T

ru m

p (2

01 7–

)

U .S

. H ou

se o

f Re

p re

se n

ta tiv

es Re

p ub

lic an

2 01

1– Pr

es en

t ( 11

2t h

–1 15

th )

 

U .S

. S en

at e

Re p

ub lic

an 2

01 5

(1 14

th –1

15 th

)

M aj

o r

So ci

al

an d

P o

lit ic

al

Ev en

ts

G

re at

R ec

es si

o n

e n

d ed

b ut

m an

y n

ot p

ro sp

er in

g d

ur in

g th

e re

co ve

ry ;

C o

n ti

n u

ed p

o lit

ic al

d eb

at e

re g

ar d

in g

t h

e A

C A

, i n

cl ud

in g

d eb

at es

in n

ea rly

h

al f t

h e

st at

es c

on ce

rn in

g w

h et

h er

to a

d op

t t h

e A

C A

’s M

ed ic

ai d

e xp

an si

on ; S

ev er

al

st at

es c

on tin

ue to

e xp

er ie

n ce

fi n

an ci

al a

n d

/o r t

ec h

n ic

al is

su es

in th

e es

ta b

lis h

m en

t an

d o

p er

at io

n o

f A C

A in

su ra

n ce

e xc

h an

g es

; I n

cr ea

si n

g p

ol iti

ca l a

n d

le g

al

ac ce

p ta

n ce

o f s

am e-

se x

m ar

ria g

e lik

el y

to im

p ac

t u se

a n

d c

os t o

f h ea

lth in

su ra

n ce

an

d p

ub lic

h ea

lth p

ro g

ra m

s; G

ro w

th o

f I SI

S as

a te

rr or

is t t

h re

at ; U

.S . S

u p

re m

e C

o u

rt J

u st

ic e

A n

to n

in S

ca lia

d ie

s su

d d

en ly

in F

eb ru

ar y

20 16

, a ft

er w

h ic

h

th e

U .S

. S en

at e,

u n

d er

R ep

ub lic

an p

ow er

, r ef

us es

to c

on si

d er

P re

si d

en t O

b am

a’s

re p

la ce

m en

t n om

in at

io n

u n

til a

ft er

th e

20 16

e le

ct io

n .

M ai

n ly

u n

an ti

ci p

at ed

o u

tc o

m e

in 2

01 6

n at

io n

al e

le ct

io n

re su

lts in

a b

ru p

t sh

ift in

fe d

er al

p ol

ic ym

ak in

g, v

ie w

s ab

ou t e

n tit

le m

en t a

n d

w el

fa re

p ro

g ra

m s,

an

d re

vi se

d im

m ig

ra tio

n p

ol ic

ie s,

a m

on g

o th

er k

ey n

at io

n al

p ol

iti ca

l a n

d s

oc ia

l is

su es

; R ac

ia l t

en si

o n

s es

ca la

te ; R

o b

er t

M u

el le

r ap

p o

in te

d a

s Sp

ec ia

l C

o u

n se

l i n

2 01

7 to

in ve

st ig

at e

th e

al le

g ed

ro le

o f R

us si

an in

te rf

er en

ce in

th e

20 16

n at

io n

al e

le ct

io n

; N ei

l G o

rs u

ch c

o n

fi rm

ed to

ta ke

J us

tic e

Sc al

ia ’s

se at

on

th e

U .S

. S up

re m

e C

ou rt

; U .S

. S u

p re

m e

C o

u rt

J u

st ic

e A

n th

o n

y K

en n

ed y

re ti

re s

at th

e en

d o

f t h

e 20

17 –2

01 8

te rm

, i s

re p

la ce

d b

y B

re tt

K av

an au

g h

b

y th

e sm

al le

st m

ar g

in fo

r a S

up re

m e

C ou

rt J

us tic

e si

n ce

1 88

1 an

d a

ft er

a

d ee

p ly

tr ou

b lin

g a

n d

p ol

ar iz

in g

n om

in at

io n

p ro

ce ss

; N at

io n

al e

co n

om y

m ai

n ly

re

co ve

rs fr

om G

re at

R ec

es si

on , y

et in

co m

e in

eq u

al it

y co

n ti

n u

es t

o g

ro w

.

K ey

F ed

er al

Le

g is

la ti

ve

P ro

p o

sa ls

/ La

w s

an d

K

ey L

eg al

D

ec is

io n

s

C

on gr

es si

on al

fo cu

s co

nt in

ue s

to b

e on

d eb

at in

g th

e A

C A

a s

w el

l a s

in te

rn at

io na

l se

cu rit

y is

su es

; D o

n’ t A

sk D

o n’

t T el

l R ep

ea l A

ct o

f 2 01

0 en

d ed

th e

d is

cr im

in at

or y

m ili

ta ry

p ol

ic y

re g

ar d

in g

g ay

s er

vi ce

m em

b er

s; 20

12 N

FI B

v . S

eb el

iu s,

S up

re m

e C

ou rt

h el

d th

at th

e A

C A

’s in

d iv

id ua

l i ns

ur an

ce re

q ui

re m

en t w

as c

on st

itu tio

na l

b ut

a ls

o ru

le d

th at

th e

A C

A ’s

re q

ui re

m en

t t ha

t a ll

st at

es e

xp an

d M

ed ic

ai d

w as

un

d ul

y co

er ci

ve ; 2

01 4

B ur

w el

l v . H

ob by

L ob

by , t

he S

up re

m e

C ou

rt h

el d

th at

o ne

p

ro vi

si on

o f t

he A

C A

v io

la te

d fe

d er

al la

w b

y re

q ui

rin g

c lo

se ly

h el

d c

or p

or at

io ns

to

p ay

fo r i

ns ur

an ce

c ov

er ag

e fo

r c er

ta in

ty p

es o

f c on

tr ac

ep tio

n; M

ed ic

ar e

an d

C H

IP

R ea

u th

o ri

za ti

o n

A ct

o f 2

01 5

re p

la ce

d th

e Su

st ai

na b

le G

ro w

th R

at e

fo rm

ul a

us ed

fo

r p hy

si ci

an p

ay m

en t a

nd fu

nd ed

C H

IP th

ro ug

h 20

17 ; 2

01 5

O b

er ge

fe ll

v. H

o dg

es ,

th e

Su p

re m

e C

ou rt

h el

d th

at th

e fu

nd am

en ta

l r ig

ht to

m ar

ria g

e is

g ua

ra nt

ee d

to

sa m

e- se

x co

up le

s; In

2 01

5 in

B ur

w el

l v . K

in g

th e

Su p

re m

e C

ou rt

u p

he ld

th e

A C

A ’s

st at

ut or

y an

d re

g ul

at or

y sc

he m

e p

er m

itt in

g fe

d er

al s

ub si

d ie

s to

fl ow

th ro

ug h

b ot

h

st at

e- ru

n an

d fe

d er

al ly

fa ci

lit at

ed in

su ra

nc e

ex ch

an g

es ; T

he G

lo b

al F

o o

d S

ec u

ri ty

A

ct o

f 2 01

6 au

th or

iz ed

a c

om p

re he

ns iv

e, s

tr at

eg ic

a p

p ro

ac h

fo r U

.S . f

or ei

gn

as si

st an

ce to

d ev

el op

in g

c ou

nt rie

s to

re d

uc e

g lo

b al

p ov

er ty

a nd

h un

g er

, a ch

ie ve

fo

od s

ec ur

ity , p

ro m

ot e

su st

ai na

b le

a gr

ic ul

tu ra

l-l ed

e co

no m

ic g

ro w

th , a

nd im

p ro

ve

nu tr

iti on

al o

ut co

m es

, p ar

tic ul

ar ly

fo r w

om en

a nd

c hi

ld re

n; T

he 2

1s t C

en tu

ry C

u re

s A

ct b

ec am

e la

w in

2 01

6 an

d w

as d

es ig

ne d

to h

el p

a cc

el er

at e

m ed

ic al

p ro

d uc

t d

ev el

op m

en t a

nd b

rin g

n ew

in no

va tio

ns a

nd a

d va

nc es

to p

at ie

nt s

w ho

n ee

d th

em

fa st

er a

nd m

or e

effi ci

en tly

; I n

W ho

le W

om an

’s H

ea lt

h v.

H el

le rs

te dt

(2 01

6) , t

he

Su p

re m

e C

ou rt

s tr

uc k

d ow

n st

ric t T

ex as

a b

or tio

n re

g ul

at io

ns , r

ul in

g th

at a

b or

tio n

p

ro vi

d er

re g

ul at

io ns

m us

t b e

b as

ed o

n co

nv in

ci ng

m ed

ic al

e vi

d en

ce a

nd c

an no

t un

d ul

y b

ur d

en a

w om

an ’s

rig ht

to a

b or

tio n.

A ft

er P

re si

d en

t T ru

m p’

s in

au g

ur at

io n

, m ul

tip le

R ep

ub lic

an e

ff o

rt s

to r

ep ea

l an

d r

ep la

ce t

h e

A ff

o rd

ab le

C ar

e A

ct fa

il (t

h o

ug h

s ev

er al

e xe

cu tiv

e/ re

g ul

at o

ry a

ct io

n s

h al

t o r l

im it

th e

re ac

h o

f t h

e A

C A

); C

H IP

r ea

u th

o ri

ze d

an

d fu

n d

ed th

ro ug

h 2

02 7;

T h

e Ta

x C

u ts

a n

d J

o b

s A

ct o

f 2 01

7 re

p re

se n

ts

th e

b ig

g es

t f ed

er al

ta x

ov er

h au

l i n

3 0

ye ar

s— am

o n

g o

th er

th in

g s,

it c

ut th

e m

ax im

um c

o rp

o ra

te in

co m

e ta

x ra

te to

2 1%

, e lim

in at

ed th

e ta

x o

n p

eo p

le

w h

o d

o n

o t o

b ta

in a

d eq

ua te

h ea

lth in

su ra

n ce

c ov

er ag

e, a

n d

in cr

ea se

d th

e st

an d

ar d

d ed

uc tio

n a

n d

th e

es ta

te ta

x ex

em p

tio n

, w h

ic h

to g

et h

er w

ill re

d uc

e fe

d er

al re

ve n

ue s

b y

si g

n ifi

ca n

t a m

o un

ts a

n d

li ke

ly m

ak e

th e

d is

tr ib

ut io

n o

f af

te r-

ta x

in co

m e

m o

re u

n eq

ua l.

In C

o o

p er

v . H

a rr

is (2

01 7)

, t h

e Su

p re

m e

C o

ur t r

ul ed

th at

ra ci

al g

er ry

m an

d er

in g

v io

la te

d th

e rig

h ts

o f v

o te

rs to

e q

ua l

p ro

te ct

io n

o f t

h e

la w

s; T

h e

Su p

re m

e C

o ur

t r ul

ed 5

–4 th

at P

re si

d en

t T ru

m p

h ad

th

e le

g al

a ut

h o

rit y

to re

st ric

t t ra

ve l f

ro m

s ev

er al

m o

st ly

M us

lim c

o un

tr ie

s in

th e

20 18

c as

e o

f T ru

m p

v . H

aw a

ii; In

M as

te rp

ie ce

C ak

es h

o p

v . C

o lo

ra d

o C

iv il

R ig

h ts

C o

m m

is si

o n

(2 01

8) , t

h e

Su p

re m

e C

o ur

t r ul

ed in

fa vo

r o f a

C o

lo ra

d o

b ak

er w

h o

re fu

se d

to c

re at

e a

w ed

d in

g c

ak e

fo r a

g ay

c o

up le

, d et

er m

in in

g

th at

th e

b ak

er h

ad b

ee n

m is

tr ea

te d

b y

th e

st at

e ci

vi l r

ig h

ts c

om m

is si

on b

as ed

on

re m

ar ks

o f o

n e

of it

s m

em b

er s

in d

ic at

in g

h os

til ity

to re

lig io

n ; I

n 2

01 8,

th

e Su

p re

m e

C ou

rt ru

le d

5 –4

th at

fo re

ig n

c or

p or

at io

n s

m ay

n ot

b e

su ed

in

A m

er ic

an c

ou rt

s fo

r c om

p lic

ity in

h um

an ri

g h

ts a

b us

es a

b ro

ad (J

es n

er v

. A ra

b

B a

n k)

.

 

 

108 PART I ADDENDUM: TIMELINE

20

10 s

Im p

o rt

an t

D ev

el o

p m

en ts

in

H ea

lt h

a n

d

M ed

ic in

e

20

10 c

h ol

er a

ou tb

re ak

in H

ai ti,

o n

e of

th e

w or

st o

ut b

re ak

s in

re ce

n t h

is to

ry ; 2

01 2

em er

g en

ce o

f M ER

S- C

oV , a

v ira

l r es

p ira

to ry

il ln

es s

th at

is n

ew to

h um

an s,

fi rs

t re

p or

te d

in th

e M

id d

le E

as t b

ut la

te r s

p re

ad to

s ev

er al

c ou

n tr

ie s

in cl

ud in

g th

e U

n ite

d S

ta te

s; 2

01 3

h ea

lth ca

re s

p en

d in

g re

ac h

ed a

lm os

t $ 3

tr ill

io n

a n

d a

cc ou

n te

d

fo r 1

7. 4%

o f t

h e

g ro

ss d

om es

tic p

ro d

uc t;

20 14

E b

ol a

ou tb

re ak

w as

th e

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Endnotes 109

Other Sources Consulted American Medical Association. (n.d.). Chronology of AMA history.

Retrieved from https://www.ama-assn.org/ama-history U.S. Food and Drug Administration. (n.d.). A history of the FDA

and drug regulation in the United States. Retrieved from https://www.fda.gov/downloads/drugs/resourcesfor you /consumers/buyingusingmedicinesafely/understandingover -the-countermedicines/ucm093550.pdf

U.S. National Library of Medicine. (2012). History of medicine. Retrieved from http://www.nlm.nih.gov/exhibition/phs _history/contents.html

Source for Political Affiliation of Senate U.S. Senate. (n.d.). Party division. Retrieved from http://www

.s enate.gov/p agelayout/histor y/one_item_and_te as ers /partydiv.htm

Source for Political Affiliation of the House of Representatives U.S. House of Representatives. (n.d.). House history timeline.

Retrieved from http://history.house.gov/Education/Timeline /Timeline/

Further Reading For more on these and other related historical timeline details and

trends, see the following: Day, J. G. (1997). Managed care and the medical profession: Old

issues and old tensions the building blocks of tomorrow’s health care delivery and financing system. Connecticut Insurance Law Journal, 3(1), 60–78.

Hall, M. A. (1999). Health care corporate law: Formation and regulation. New York, NY: Aspen Law & Business.

Public Broadcasting System. (n.d.). Healthcare crisis: Healthcare timeline. Retrieved from http://www.pbs.org/healthcarecrisis /history.htm

Wing, K. R., Jacobs, M. S., & Kuszler, P. C. (1998). The law and American health care. New York: Aspen Law & Business.

References Birn, A. (2003). Struggles for national health reform in the United

States. American Journal of Public Health, 93(1), 86–94. Institute of Medicine. (2002). The future of the public’s health in

the 21st century (pp. 96–177). Washington, DC: National Academies Press (Ch. 3).

Shi, L., & Singh, D. A. (2004). Delivering health care services in America: A systems approach. Sudbury, MA: Jones and Bartlett Learning.

Sultz, H., & Young, K. (2003). Health care USA: Understanding its organization and delivery (4th ed.). Sudbury, MA: Jones and Bartlett Learning.

 

 

 

111

PART II

Essential Issues in Health Policy and Law Part I of this book introduced frameworks for conceptualizing health policy and law and described basic aspects of policy, the policymaking process, law, the legal system, and the healthcare and public health sys- tems. Part II covers many of the essential issues in health policy and law. Chapter 6 addresses individual rights in health care and public health, Chapter 7 describes how law itself is a determinant of health and how law relates to other social determinants of health, and Chapters 8 and 9 cover the fundamentals of health insurance and health econom- ics, respectively. Chapter 10 provides an overview of national health reform. Chapters 11 through 13 cover government insurance programs, healthcare quality, and public health preparedness, respectively. After completing Part II, among other things you will understand how social factors influence individual and population health, how health insur- ance functions, why private employer-based coverage dominates the health insurance market, why gaps in health insurance coverage remain, the importance of health economics to health policymaking, key provi- sions in the Affordable Care Act, various policy and legal dimensions to healthcare quality, and the role of public health in preparing for and responding to national and global emergencies.

© Mary Terriberry/Shutterstock

 

 

 

113

© Mary Terriberry/Shutterstock© Mary Terriberry/Shutterstock

CHAPTER 6

Individual Rights in Health Care and Public Health

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe the meaning and importance of the “no-duty to treat” principle ■ Explain generally how the U.S. approach to health rights differs from that of other developed countries ■ Describe the types and limitations of individual legal rights associated with health care ■ Describe the balancing approach taken when weighing individual rights against the public’s health

▸ Introduction

The real-life scenarios in BOX 6-1 touch upon the key issues you will confront in this chapter: namely, the ways in which the law creates, pro- tects, and restricts individual rights in the contexts of health care and public health. Individuals are deeply impacted by law on a daily basis, and this fact is no less true when they navigate the healthcare system, or when an individual’s actions are measured against the broader interests of the public’s health. Over many decades, legal principles have been rejected, developed, and refined as the law continually struggles to define the appro- priate relationship between individuals and the physi- cians, hospitals, managed care companies, and others they encounter in the healthcare delivery system, and between individuals and government agencies charged with protecting public health and welfare. These balanc- ing acts are made all the more difficult as the legal sys- tem bumps up against the quick pace of technological

advancements in medicine and against amorphous, potentially deadly risks to the public’s health, such as bioterrorism and fast-spreading influenzas.

After a background section, this chapter consid- ers individual legal rights in health care, beginning with a brief overview of health rights under interna- tional and foreign law. This sets up a much lengthier discussion of healthcare rights in the United States, which for purposes of this chapter are classified according to an important distinction: legal rights to health care and rights that individuals can claim only within the context of the healthcare system—that is, only once they have found a way to access needed care.a Examples of the latter type of rights include the right to refuse unwanted treatment, the right to autonomy in making personal healthcare decisions, and the right to be free from wrongful discrimina- tion when receiving care. Finally, the chapter turns to a discussion of individual rights in the context of government- initiated public health efforts. This topic

 

 

114 Chapter 6 Individual Rights in Health Care and Public Health

is dominated by the role and scope of government “police powers,” which permit governments, when acting to promote or protect public health, to curtail individual freedoms and liberties.

▸ Background Lurking behind any discussion of individual rights in a health context is one of the most basic principles in U.S. health law: generally speaking, individuals have no legal right to healthcare services (or to public health insur- ance), and, correspondingly, there exists on the part of healthcare providers no general legal duty to provide care. This is referred to as the “no-duty” or “no-duty-to- treat” principle, which is aptly described by the Indiana Supreme Court in the well-known 1901 case of Hurley v. Eddingfield, the facts of which were referred to in the first vignette in Box 6-1. In its decision, the court wrote that the state law permitting the granting of a medical license

provides for . . . standards of qualification . . . and penalties for practicing without a license. The [state licensing] act is preventive, not a

compulsive, measure. In obtaining the state’s license (permission) to practice medicine, the state does not require, and the licensee does not engage, that he will practice at all or on other terms than he may choose to accept. (Hurley v. Eddingfield, 1901)

In other words, obtaining a license to practice medicine does not obligate an individual to actually practice, or to practice in a particular fashion or with a particular clientele; the licensure requirement exists instead to filter out individuals who may not have the requisite knowledge or skills to practice medicine. The same can be said for obtaining a law license, or even a driver’s license: the former does not obligate a law- yer to practice, or to choose certain types of clients or cases; the latter does not require that a person actually drive, or drive a certain make of car. As with a medical license, the point of a law or driver’s license is to guar- antee that should the licensee choose to practice law or operate a motor vehicle, he or she is qualified to do so. Furthermore, you will recall from the facts provided in the vignette that Dr. Eddingfield was Mrs. Burk’s family physician, and many students believe that this fact is enough to establish a sufficient legal relationship between the two to hold Dr. Eddingfield accountable for the death of Mrs. Burk. However, the general legal rule is that physician–patient relationships are specific to “spells of illness” and that past treatment is not tan- tamount to an existing physician–patient relationship. Put another way, under the law a physician–patient relationship does not exist as a general, continuous matter—even with one’s family physician, internist, primary care physician, and so on—but rather it exists for a specific period of time and must be established (or renewed) accordingly.

Note that this basic premise—that there is no fun- damental right to healthcare services in the United States—was not altered by the passage in 2010 of the Affordable Care Act (ACA). While it is arguable that the ACA moves the country in a direction that makes a legal right to health care more plausible down the road (Friedman & Adashi, 2010), and while there can be no arguing that it makes health care more accessible to mil- lions of people by virtue of its health insurance reforms (as discussed later in this chapter and in greater detail elsewhere), the ACA does not create a right to care.

As you begin to think through the significance and implications of the no-duty principle, it is import- ant to understand that there are many other legal principles and health laws that define the relation- ship between an individual and another health system stakeholder (e.g., a physician, hospital, or government program). In fact, there are several federal and state

BOX 6-1 Vignette

At the turn of the 20th century, an Indiana physician named George Eddingfield repeatedly refused to come to the aid of Charlotte Burk, who was in labor, even though he was Mrs. Burk’s family physician. Doctor Eddingfield conceded at trial that he made this decision for no particular reason and despite the facts that he had been offered monetary compensation in advance of his performing any medical services and that he was aware that no other physician was available to provide care to Mrs. Burk. Unattended by any medical providers, Mrs. Burk eventually fell gravely ill, and both she and her unborn child died. It was determined upon trial and subsequent appeals that Dr. Eddingfield did not wrongfully cause either death.

Around the same time as the scenario just described, the Cambridge, Massachusetts, Board of Health ordered everyone within city limits to be vaccinated against the smallpox disease under a state law granting local boards of health the power, under certain circumstances, to require the vaccination of individuals. After refusing to abide by the Cambridge Board’s order, Henning Jacobson was convicted by a state trial court and sentenced to pay a $5 fine. Remarkably, Mr. Jacobson’s case not only made its way to the U.S. Supreme Court, it resulted in one of the court’s most important public health rulings and a sweeping statement about limitations to fundamental individual rights in the face of threats to the public’s health.

 

 

Background 115

laws that narrow the scope of the no-duty principle. For example, a federal law called the Examination and Treatment for Emergency Medical Conditions and Women in Labor Act enables all individuals to access some hospital care in medical emergencies, irrespec- tive of the individual’s ability to pay for that care or a hospital’s willingness to treat the individual. Also, both federal and state laws that generally prohibit cer- tain forms of discrimination (say, based on race or dis- ability) apply in the context of health care and might thus result in access to health services that otherwise would not be forthcoming. Furthermore, some public health insurance programs—Medicaid and Medicare, most prominently—create entitlements (a legal con- cept denoting a legal claim to something) to services for individuals who meet the programs’ eligibility cri- teria (Jost, 2003), and some health insurance products obligate physicians participating in the plan’s networks to extend care to plan members. Finally, some states implemented universal healthcare coverage programs, such as Maine’s Dirigo Health Reform Act, which was designed to provide access to health coverage to every person in Maine (and which ended at the end of 2014 as residents of the state were transitioned into the health insurance exchanges created by the ACA).

When thinking about the law’s no-duty principle, you must also take into account the role of medical ethics, which might require more of a healthcare pro- fessional than does the law. For example, no law man- dates that licensed physicians aid a stranger in medical distress, but many believe an ethical obligation exists in this instance. And although legally the no-duty princi- ple would dictate otherwise, many healthcare provid- ers consider themselves ethically obligated to furnish at least some level of care to those who cannot pay for it. In short, although there is no universal legal right to health care in the United States, certain situations give rise to healthcare rights, and specific populations may be entitled to health care or receive it purely through the magnanimity of ethics-conscious providers.

Perhaps because of the federal and state laws that chip away at the no-duty-to-treat principle, many students new to the study of health law erroneously assume that the principle is a legal anomaly, borne solely of the incredible historical power and auton- omy of the medical profession and without mod- ern precedent. In this case, it is instructive to place the principle in a broader “welfare rights” context. During the 1960s, public-interest lawyers, social reform activists, and others pressed for an interpreta- tion of the federal Constitution that would have cre- ated an individual right to welfare. Under this view, the government must provide individuals with min- imally adequate levels of education, food, housing,

health care, and so on (Davis, 1993). But in a series of cases, the Supreme Court rejected the notion of a constitutional right to welfare.

Consider the right to education. Even though every state provides free public schools and makes education for minors compulsory, there is no national, generalized legal right to education. In the case of San Antonio Independent School District v. Rodriguez (1973), the Supreme Court ruled that education is not a fundamental right under the federal Constitution’s Equal Protection Clause. The plaintiffs in the Rodri- guez case were Mexican-American parents whose children attended elementary and secondary schools in an urban San Antonio school district. They had attacked as unconstitutional Texas’s system of financ- ing public education and filed the suit on behalf of school children throughout the state who were mem- bers of minority groups or who resided in relatively poor school districts. But the court turned the plain- tiffs’ argument away, noting that although education is one of the most important services states perform,

it is not among the rights afforded explicit protection under our Federal Constitution. Nor do we find any basis for saying it is implicitly so protected. . . . [T]he undisputed importance of education will not alone cause this Court to depart from the usual standard for reviewing a State’s social and economic legislation. (San Antonio Indep. School Dist. v. Rodriguez, 1973)

In the wake of the Rodriguez decision, several states interpreted their own constitutions as prohibit- ing inequitable methods of financing public education, thereby recognizing on some level a right to a mini- mally “meaningful” education. Subsequently, lawyers and social activists seeking to promote equal access to all manner of critical services seized on these state determinations, arguing that an egalitarian approach to constitutional interpretation should not be limited to education (Stacy, 1993). Note, for example, how one author’s writings about the right to education could just as well have been written with respect to health care:

Requiring an adequate education will help to fulfill our nation’s promise, articulated in Brown [v. Board of Education], that an indi- vidual be free to achieve her full potential. Ensuring educational adequacy will pro- mote children’s emotional and intellectual development, their career path and earning potential and thus their success throughout life. A meaningful education offers the hope that children can escape the degradation of

 

 

116 Chapter 6 Individual Rights in Health Care and Public Health

poverty and its lack of opportunity, and attain pride, participation in this country’s economic and political life, and financial and emotional success. (Smith, 1997, p. 825)

However, efforts around ensuring adequate edu- cation have not been emulated in other social policy areas, such as health care. In fact, health care is treated not as a right, but as a commodity (like televisions or vacuum cleaners) subject to private market forces and socioeconomic status. During the public debate in 1993 over President Bill Clinton’s failed attempt at national health reform, U.S. Representative Dick Armey (R-TX) stated that “health care is just a com- modity, just like bread, and just like housing and every- thing else” (Reinhardt, 1996, p. 102). But why should this be the case, particularly when the private health insurance market has presumably found equilibrium at a point that continually leaves tens of millions of Americans uninsured, and particularly because health care (like education) is different from vacuum clean- ers and other everyday goods in that it has “a funda- mental bearing on the range of one’s opportunities to realize one’s life plans”? (Stacy, 1993, p. 80).

There is no single answer to the question of why health care is generally treated in this country as some- thing less than an individual legal right. Many factors beyond the scope of this chapter are implicated: the nature and interpretation of the federal Constitution, politics, a weak labor movement, powerful interest groups, the nation’s free market philosophies, the pub- lic’s often negative view of the government, and more (Blum et al., 2003; Rich, 2000; Vladeck, 2003). In this chapter, we limit the discussion to describing the kinds of health rights that do exist, and how they operate in the context of the healthcare delivery system and when considered against government-initiated public health efforts. Before we explore in depth the scope of indi- vidual health-related rights under U.S. law, however, we briefly describe these same types of rights under international law and under the law of other countries. Through this examination, we provide a backdrop for understanding this country’s approach to legal rights in the context of health.

▸ Individual Rights and Health Care: A Global Perspective

Despite being the world leader in terms of the devel- opment of medical technologies and the quantity of medical services, the United States is one of the only high-income nations that does not guarantee health

care as a fundamental right, and it is the only devel- oped nation that has not implemented a system for insuring at least all but the wealthiest segment of its population against healthcare costs (Jost, 2003, p. 3). In essence, other high-income nations with social democracies treat the provision of health care as a social goodb (i.e., something that could be supported through private enterprise but is instead supported by the government and financed from public funds). Fur- thermore, it is worth noting that nations that provide universal healthcare entitlements have not been bank- rupted as a result. In fact, according to Professor Tim- othy Jost, “all of the other developed nations spend less on health care than does the U.S., in terms of both dollars per capita and proportion of gross domestic product” (Jost, 2003, p. 3).

A foreign nation’s universal healthcare rights— whether an unlimited right to health, a right to med- ical care generally or to a basic package of services, a right to healthcare insurance, or something else—exist as the result of either a commitment to human rights principles generally or fidelity to the particular coun- try’s own constitution. When recognized by govern- ments, human rights accrue to all individuals because the rights are based on the dignity and worth of the human being; thus, technically, a human right exists regardless of whether positive law (a constitution or statute) has given it expression (Barnes & McChrystal, 1998). Examples of positive expressions of health as a human right include Article 25 of the 1948 Univer- sal Declaration of Human Rights, which states that “everyone has the right to a standard of living ade- quate for the health and well-being of himself and of his family, including . . . medical care . . . and the right to security in the event of . . . sickness [or] disability” (Claiming Human Rights, 2010), and the Constitution of the World Health Organization, which says that “the enjoyment of the highest attainable standard of health is one of the fundamental rights of every human being without distinction of race, religion, political belief, economic or social condition” (World Health Organi- zation, 2006).

In terms of national constitutions, some two- thirds of constitutions worldwide specifically address health or health care, and almost all of them do so in universal terms, rather than being limited to certain populations (Kinney & Clark, 2004). For example, consider the health-related aspects of the constitutions of four politically and culturally diverse countries— Italy, the Netherlands, South Africa, and Poland—that have some type of “right to health”: Italy’s Constitution guarantees a right to health; under the Dutch Consti- tution, the government is mandated “to promote the

 

 

Individual Rights and the Healthcare System 117

health of the population”; the Constitution of South Africa imposes on government the obligation to pro- vide access to health services; and under Polish con- stitutional law, citizens are guaranteed “the right to health protection” and access to publicly financed healthcare services (Littell, 2002).

Of course, including language respecting health rights in a legal document—even one as profound as a national constitution—does not guarantee that the right will be recognized or enforced. As in the United States, multiple factors might lead a foreign court or other tribunal to construe rights-creating language narrowly or to refuse to force implementation of what is properly considered a right. Examples of these fac- tors include the relative strength of a country’s judicial branch vis-a-vis other branches in its national gover- nance structure and a foreign court’s view of its coun- try’s ability to provide services and benefits inherent in the health right.

▸ Individual Rights and the Healthcare System

The “global perspective” you just read was brief for two reasons. First, a full treatment of international and foreign health rights is well beyond the scope of this chapter, and second, historically speaking, international law has played a limited role in influ- encing this nation’s domestic legal principles. As one author commented, “historically the United States has been uniquely averse to accepting international human rights standards and conforming national laws to meet them” (Yamin, 2005, p. 1156). This fact is no less true in the area of health rights than in any

other major area of law. As described earlier in this chapter, universal rights to health care are virtually nonexistent in this country, even though this stance renders it almost solitary among the world’s devel- oped nations.

This is not to say that the United States has not contemplated health care as a universal, basic right. For instance, in 1952, a presidential commission stated that “access to the means for attainment and preser- vation of health is a basic human right” (President’s Commission, 1983, p. 4). Medicaid and Medicare were the fruits of a nationwide debate about universal healthcare coverage. And during the 1960s and 1970s, the claim that health care was not a matter of privi- lege, but rather of right, was “so widely acknowledged as almost to be uncontroversial” (Starr, 1982, p. 389). Nor is it to say that certain populations do not enjoy healthcare rights beyond those of the general public. Prisoners and others under the control of state gov- ernments have a right to minimal health care (Wing, 1993), some state constitutions expressly recognize a right to health or healthcare benefits (for example, Montana includes an affirmative right to health in its constitution’s section on inalienable rights), and indi- viduals covered by Medicaid have unique legal enti- tlements. Finally, it would be inaccurate in describing healthcare rights to cover only rights to obtain health care in the first instance, because many important healthcare rights attach to individuals once they man- age to access needed healthcare services.

The remainder of this section describes more fully the various types of individual rights associated with the healthcare system. We categorize these rights as follows:

1. Rights related to receiving services explicitly provided under healthcare, health financ- ing, or health insurance laws—for example, the Examination and Treatment for Emer- gency Medical Conditions and Women in Labor Act, Medicaid, and the ACA

2. Rights concerning freedom of choice and freedom from government interference when making healthcare decisions—for example, choosing to have an abortion

3. The right to be free from unlawful discrim- ination when accessing or receiving health care—for example, Title VI of the federal Civil Rights Act of 1964, which prohibits discrimination on the basis of race, color, or national origin by entities that receive federal funding (Annas, 2004; Barnes & McChrystal, 1998, p. 12)

BOX 6-2 Discussion Question

Depending on one’s personal experience in obtaining health care, or one’s view of the role of physicians in society, of law as a tool for social change, of the scope of medical ethics, or of the United States’ place in the broader global community, the no-duty principle might seem appropriate, irresponsible, or downright wrong. Imagine you are traveling in a country where socialized medicine is the legal norm, and your discussion with a citizen of that country turns to the topic of your countries’ respective health systems. When asked, how will you account for the fact that health care is far from being a fundamental right rooted in American law?

 

 

118 Chapter 6 Individual Rights in Health Care and Public Health

Rights Under Healthcare and Health Financing Laws We begin this discussion of rights-creating health laws with the Examination and Treatment for Emergency Medical Conditions and Women in Labor Act (also referred to as EMTALA, which is the acronym for the law’s original name—the Emergency Medical Treat- ment and Active Labor Act—or, for reasons soon to become clear, the “patient anti-dumping statute”). We then briefly discuss the federal Medicaid program in a rights-creating context and wrap up this section with a brief discussion of the ACA.

Rights Under Healthcare Laws: EMTALA Because EMTALA represents the only truly universal legal right to health care in this country—the right to access emergency hospital services—it is often described as one of the building blocks of health rights. EMTALA was enacted by Congress in 1986 to prevent the practice of “patient dumping”—that is, the turning away of poor or uninsured persons in need of hospital care. Patient dumping was a common strategy among private hospitals aiming to shield themselves from the potentially uncompensated costs associated with treating poor and/or uninsured patients. By refusing to treat these individuals and instead “dump- ing” them on public hospitals, private institutions were effectively limiting their patients to those whose treatment costs would likely be covered out-of-pocket or by insurers. Note that the no-duty principle made this type of strategy possible.

EMTALA was a conscious effort on the part of elected federal officials to chip away at the no-duty principle: by creating legally enforceable rights to emergency hospital care for all individuals regardless of their income or health insurance status, Congress created a corresponding legal duty of care on the part of hospitals. At its core, EMTALA includes two related duties, which technically attach only to hospitals that participate in the Medicare program (but then again, nearly every hospital in the country participates). The first duty requires covered hospitals to provide an “appropriate” screening examination to all individu- als who present at a hospital’s emergency department seeking care for an “emergency medical condition.” Under the law, an appropriate medical screening is one that is nondiscriminatory and that adheres to a hospi- tal’s established emergency care guidelines. EMTALA defines an emergency medical condition as a

medical condition manifesting itself by acute symptoms of sufficient severity (including

severe pain) such that the absence of imme- diate medical attention could reasonably be expected to result in (i) placing the health of the individual (or, with respect to a preg- nant woman, the health of the woman or her unborn child) in serious jeopardy, (ii) serious impairment to bodily functions, or (iii) seri- ous dysfunction of any bodily organ or part; or with respect to a pregnant woman who is having contractions, that there is inadequate time to effect a safe transfer to another hospi- tal before delivery, or that transfer may pose a threat to the health or safety of the woman or the unborn child. (Examination and Treat- ment, 2011)

The second key duty required of hospitals under EMTALA is to either stabilize any condition that meets the preceding definition or, in the case of a hospital without the capability to treat the emer- gency condition, undertake to transfer the patient to another facility in a medically appropriate fashion. A proper transfer is effected when, among other things, the transferring hospital minimizes the risks to the patient’s health by providing as much treatment as is within its capability, a receiving medical facility has agreed to accept the transferred patient, and the trans- ferring hospital provides the receiving facility all rele- vant medical records.

The legal rights established under EMTALA are accompanied by heavy penalties for their violation. The federal government, individual patients, and “dumped-on” hospitals can all initiate actions against a hospital alleged to have violated EMTALA, and the federal government can also file a claim for civil money penalties against individual physicians who negligently violate an EMTALA requirement.

Rights Under Healthcare Financing Laws: Medicaid Many laws fund programs that aim to expand access to health care, such as state laws authorizing the establishment of public hospitals or health agencies, and the federal law establishing the vast network of community health clinics that serve medically under- served communities and populations. However, the legal obligations created by these financing laws are generally enforceable only by public agencies, not by individuals.

The Medicaid program is different in this respect. (Medicaid is covered elsewhere in greater depth, but because of its importance in the area of individual

 

 

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healthcare rights, we mention it also in this context.) Although most certainly a law concerning health- care financing, Medicaid is unlike most other health financing laws in that it confers the right to individ- ually enforce program obligations through the courts (Rosenblatt, Law, & Rosenbaum, 1997, pp. 419–424). This right of individual enforcement is one of the rea- sons why Medicaid, 50 years after its creation, remains a hotly debated public program. This is because the legal entitlements to benefits under Medicaid are viewed as a key contributor to the program’s high cost. Yet whether Medicaid’s legal entitlements are any more of a factor in the program’s overall costs than, say, the generally high cost of health care, is not clearly established.

Rights Under Health Insurance Laws: The ACA As you will learn in subsequent chapters, the ACA is far more than a law that concerns only health insurance; it is a sweeping set of reforms that touch on healthcare quality, public health practice, health disparities, com- munity health centers, healthcare fraud and abuse, comparative effectiveness research, the health work- force, health information technology, long-term care, and more. However, for purposes of this chapter, we mention it briefly in terms of its impact on the rights of individuals to access health insurance and to equi- table treatment by their insurer. Details concerning the ACA’s effect on the public and private insurance markets are discussed elsewhere.

Through a series of major reforms to existing pol- icies, the ACA reshapes the private health insurance market, transforming private health insurance from a commodity that regularly classified (and rejected) individuals based on their health status, age, disabil- ity status, and more into a social good whose avail- ability is essential to individual and population health (Rosenbaum, 2011). The key elements of this shift include a ban on exclusion and discrimination based on health status or preexisting health conditions; new protections that ensure that, once covered by insur- ance, individuals will have access to necessary care without regard to artificial annual or lifetime expen- diture caps; a guarantee that once insurance coverage is in place, it cannot be rescinded except in cases of applicant fraud; a ban on additional fees for out-of- network emergency services; the provision of finan- cial subsidies to help low- and moderate-income individuals and small businesses purchase insurance coverage; the inclusion, in the individual and small group insurance markets, of a package of “essential

health benefits” that must be covered; and the creation of state health insurance “exchanges” through which individuals and small employer groups can purchase high-quality health insurance in a virtual market- place that is substantially regulated and that simplifies the job of learning about, selecting, and enrolling in insurance plans.

The ACA also reforms the public health insurance market, primarily through an expansion of Medicaid eligibility to cover all non-elderly low-income persons who are legal residents or citizens (this expansion is now voluntary on the part of states, as the result of a Supreme Court decision described in a subsequent chapter). If fully implemented, this reform would substantially close one of Medicaid’s last remain- ing coverage gaps for the poor—namely, the pro- gram’s historical denial of coverage for nonpregnant, working-age adults without minor children—and in so doing would provide insurance coverage (and the resulting access to health care that often follows cov- erage) to many millions of people.

Rights Related to Freedom of Choice and Freedom From Government Interference EMTALA and Medicaid are remarkable in terms of the rights to health care that they each provide, though as mentioned earlier in this chapter, individual rights that attach within the context of healthcare provision can be equally important. Important individual rights within health care include the right to make informed healthcare decisions and the right to personal privacy and autonomy.

The Right to Make Informed Healthcare Decisions One of the most important healthcare rights is the right of individual patients to make informed deci- sions about the scope and course of their own care. This includes the right to refuse treatment, regard- less of the treatment’s nature or urgency. That is, the right to refuse treatment exists whether the patient is considering ingesting prescribed medication for minor pain, undergoing a minimally invasive test or procedure, or consenting to a major, potentially life- sustaining operation like the removal of a brain tumor. However, the right pertaining to informed decision making does not come without qualifiers and excep- tions, as described here.

Modern notions of informed consent have their roots in the Nuremberg Code, which derived from the Nuremberg trials in the late 1940s of German

 

 

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physicians who performed horrendous experiments on prisoners in Nazi concentration camps during the Second World War. The code spells out principles of research ethics, including the need to secure in advance the voluntary consent of the research subject. These principles have been codified and expanded in American federal statutory and regulatory law con- cerning federally funded biomedical research (Protec- tion of Human Subjects, 2009). But if the Nuremberg Code can be thought of as the roots of U.S. informed consent law, then the decision in Canterbury v. Spence (1972) can be thought of as the trunk.

In 1959, Jerry Canterbury was a 19-year-old suffering from severe back pain. His neurosurgeon, Dr. William Spence, informed him that he would need a laminectomy—a surgical procedure in which the roofs of spinal vertebrae are removed or trimmed to relieve pressure on the spinal cord—to correct what the doctor believed was a herniated disc. However, Dr.  Spence did not inform Canterbury of any risks associated with the surgery. The day after the opera- tion, while appearing to recuperate normally, Canter- bury fell from his hospital bed while no attendant was on hand and a few hours later began suffering paral- ysis from the waist down. This led to a second spinal surgery, but Canterbury never fully recovered; years later, he needed crutches to walk and he suffered from paralysis of the bowels.

Canterbury sued Dr. Spence, alleging negligence in both the performance of the laminectomy and the doctor’s failure to disclose risks inherent in the oper- ation. The federal trial judge ruled in Dr. Spence’s favor and Canterbury appealed, setting the stage for the now-famous decision in 1972 by the federal Court of Appeals for the District of Columbia Circuit (con- sidered second in national importance to the Supreme Court).c The decision includes two important determi- nations pertinent to this chapter. The first is that “as a part of the physician’s overall obligation to the patient, [there exists a] duty of reasonable disclosure of the choices with respect to proposed therapy and the dan- gers inherently and potentially involved.” The court viewed this duty as a logical and modest extension of a physician’s existing general duty to his patients. Importantly, the court discarded the notion that “the patient should ask for information before the physi- cian is required to disclose.” In other words, the duty to disclose requires more than just answering patient questions; it demands voluntary disclosure on the part of the physician of pertinent medical information.

The Canterbury court’s second key determination concerns the actual scope of the disclosure required— in other words, once the physician’s duty to disclose is

triggered, what information satisfies the legal require- ment? On this matter the court made several obser- vations: that the patient’s right of “self-decision” is paramount, that the right to consent can be properly exercised only if the patient has sufficient information to make an “intelligent choice,” that the sufficiency test is met when all information “material to the decision” is disclosed, and that the disclosure’s legality should be measured objectively, not subjectively from the perspective of a particular physician or patient. From these observations, the court settled on three required pieces of disclosed information: a proposed treat- ment’s inherent and potential risks, any alternatives to a proposed treatment, and the likely outcome of not being treated at all. Applying these criteria, the court ruled that Dr. Spence’s failure to disclose even the tini- est risk of paralysis resulting from the laminectomy entitled Canterbury to a new trial.

As mentioned earlier, the right to make informed healthcare decisions is not boundless. For example, the court in Canterbury wrote that where disclosure of a treatment’s risks would pose a threat of harm to the patient (for example, because it would severely complicate treatment or psychologically damage the patient) as to become “unfeasible or contraindicated from a medical point of view,” the physician’s duty to disclose could be set aside. Furthermore, a patient’s competency from a legal vantage point plays a major role in his or her ability to consent to treatment.

The Canterbury decision and its progeny have over the years been interpreted expansively, and today the right to make informed healthcare decisions has many facets beyond a clear explanation of proposed treat- ments, potential risks and complications, and the like. For example, patients have the right to know whether outside factors, such as research interests or finan- cial considerations, are coloring a physician’s think- ing about a proposed course of treatment; patients whose first language is not English have the right to an interpreter; and patients have the right to designate in advance their treatment wishes, whether through written advance directives or another individual.

The Right to Personal Privacy Another right related to freedom of choice and free- dom from government interference is the constitu- tional right to personal privacy. Although the federal Constitution makes no explicit mention of the right to privacy, the Supreme Court has recognized some form of it since the 1890s.d The court has taken a more or less two-pronged approach to the right. The first approach defines the protected personal interest as

 

 

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“informational privacy,” meaning the limiting of oth- ers’ access to and use of an individual’s private infor- mation.e The second approach—the focus of this section—is concerned with individual autonomy and freedom from governmental interference in making basic personal decisions. This right is one of the most debated in law, both because of its implicit nature (constitutionally speaking) and because it has served as the legal underpinning of several divisive social issues, including abortion, intimate associations, and the decisions as to whether, when, and how to end one’s life.

The right to privacy achieved prominence begin- ning with the Supreme Court’s landmark 1965 deci- sion in Griswold v. Connecticut (1965), in which the court considered the constitutionality of a state law criminalizing the provision of contraception to mar- ried couples. In the early 1960s, Estelle Griswold, the Executive Director of the Planned Parenthood League of Connecticut, and one of her colleagues were convicted of aiding and abetting “the use of a drug, medicinal article, or instrument for the purpose of preventing conception” by providing contraceptives to a married couple in violation of Connecticut law. The court determined that although the Constitution does not explicitly protect a general right to privacy, certain provisions in the Bill of Rights create “penumbras,” or zones, of guaranteed privacy, and that Connecticut’s law constituted an undue intrusion into one of these zones (i.e., marriage).

After the Griswold decision, advocates of the con- stitutional right to privacy flooded the federal courts with cases designed to expand the scope of the right. Quickly, laws banning interracial marriage were struck down (Loving v. Virginia, 1967), as were laws

prohibiting unmarried individuals from using contra- ception (Eisenstadt v. Baird, 1972). At the same time, federal courts were confronted with cases asking them to determine how the right to privacy applied in the context of abortion. The remainder of this section analyzes the courts’ response to this particular issue. We selected the constitutional right to abortion as the focal point of the right to privacy discussion because it is not only one of the most contested rights in a health context, but also one of the most contested areas of public policy generally.

The Roe v. Wade Decision. Few judicial decisions have affected this country’s legal, political, and social landscape as much as Roe v. Wade (1973).f In 1970, an unmarried pregnant woman filed a lawsuit under the pseudonym “Roe” challenging the constitutional- ity of a Texas criminal law that prohibited procuring or attempting an abortion at any stage of pregnancy, except for the purpose of saving the pregnant woman’s life. Roe was joined in the lawsuit by a doctor who per- formed abortions in violation of the law. They argued that the constitutional right to privacy articulated in Griswold and its progeny included a woman’s right to choose to obtain an abortion. Texas, through district attorney Henry Wade, claimed that the law was per- missible because the state had a compelling interest in protecting women from an unsafe medical proce- dure and in protecting prenatal life. The federal trial court agreed with Roe and declared the law unconsti- tutional, and Texas immediately appealed to the U.S. Supreme Court, which agreed to hear the case (in rare circumstances, the Supreme Court will hear a case without an intermediate appellate court ruling).

At the Supreme Court, the work of drafting the majority opinion in Roe v. Wade fell to Justice Harry Blackmun, who earlier in his legal career had been counsel to a well-known and highly regarded medi- cal clinic. By a 7–2 margin, the court ruled that the constitutional right to privacy, which in its view most strongly emanates from the 14th Amendment’s due process protections, is broad enough to encompass a woman’s decision to terminate her pregnancy.

Once the court established that a woman has a constitutional right to obtain an abortion, it went on to discuss the limits of that right. Roe had argued that the right to obtain an abortion is absolute and that no state or federal law abridging the right could be enacted. The court did not agree. Justice Blackmun wrote that states have both an interest in protecting the welfare of its citizens and a duty to protect them and that the duty extends to the unborn. According to the court, “a State may properly assert important

BOX 6-3 Discussion Questions

Go back to the first legal principle drawn from the Canterbury decision: namely, that physicians have a duty of reasonable disclosure to include therapy options and the dangers potentially involved with each. Do you agree with the court that this duty is both a logical and modest extension of physicians’ “traditional” obligation to their patients? Why or why not? Depending on your answer, are you surprised to learn that some states have opted not to follow the Canterbury court’s patient-oriented standard of informed consent, relying instead on the more conventional approach of measuring the legality of physician disclosure based on what a reasonable physician would have disclosed?

 

 

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interests in safeguarding health, in maintaining medi- cal standards, and in protecting potential life. At some point in pregnancy, these respective interests become sufficiently compelling to sustain regulation of the fac- tors that govern the abortion decision” (Roe v. Wade, 1973). The court then linked both a woman’s “right to choose” and states’ interest in protecting potential life to the viability of the fetus, setting forth the following “trimester framework” that enhances state power to regulate the abortion decision and restricts a pregnant woman’s right as the fetus grows older:

a. For the stage prior to approximately the end of the first trimester, the abortion deci- sion and its effectuation must be left to the medical judgment of the pregnant woman’s attending physician.

b. For the stage subsequent to approximately the end of the first trimester, the State, in promoting its interest in the health of the mother, may, if it chooses, regulate the abortion procedure in ways that are reason- ably related to maternal health.

c. For the stage subsequent to viability, the State, in promoting its interest in the poten- tiality of human life may, if it chooses, reg- ulate, and even proscribe, abortion except where it is necessary, in appropriate medical judgment, for the preservation of the life or health of the mother (Roe v. Wade, 1973).

As a matter of both policy and law, the Roe deci- sion has been vigorously criticized (Barzelay & Hey- mann, 1973; Bopp & Coleson, 1989; Ely, 1979; Regan, 1979). For example, detractors claim that the court improperly made social policy by “finding” an expan- sive constitutional right to privacy (one broad enough to include the right to terminate a pregnancy) where one did not expressly exist. As a legal matter, many have argued that the decision relied too heavily on medical concepts that would be rendered obsolete as medical technology advanced and that would, in turn, result in a narrowing of the constitutional right advanced in the decision.g

Regardless of these and other criticisms, the Roe decision was monumental beyond its legal implica- tions. It galvanized political forces opposed to abortion and prompted a movement to create ways to discour- age the practice through state policies designed to regulate the factors involved in the abortion decision. For example, as described next, Pennsylvania enacted a law that imposed a series of requirements on women seeking abortion services, and it was this law that nearly 20 years after Roe set the stage for another

battle at the Supreme Court over abortion and the right to privacy.

The Planned Parenthood of Southeastern Penn- sylvania v. Casey Decision. At issue in the 1992 case of Planned Parenthood of Southeastern Pennsylvania v. Casey were several amendments to Pennsylvania’s Abortion Control Act that made it more difficult for a pregnant woman to obtain an abortion: one provi- sion required that a woman seeking an abortion be provided with certain information at least 24 hours in advance of the abortion; a second stated that a minor seeking an abortion had to secure the informed con- sent of one of her parents, but included a “judicial bypass” option if the minor did not wish to or could not obtain parental consent; a third amendment required that a married woman seeking an abortion had to sub- mit a signed statement indicating that she had notified her husband of her intent to have an abortion, though certain exceptions were included; and a final provision imposed new reporting requirements on facilities that offered abortion services. The revised law exempted compliance with these requirements in the event of a “medical emergency.”

Before any of the new provisions took effect, they were challenged by five Pennsylvania abortion clinics and a group of physicians who performed abortions. The federal trial court struck down all of the provi- sions as unconstitutional violations under Roe. On appeal, the Third Circuit Court of Appeals reversed and upheld all of the provisions, except for the hus- band notification requirement, as constitutional. The plaintiffs appealed to the Supreme Court, which agreed to hear the case.

The court’s 5–4 decision in favor of the plaintiffs in Casey expressly acknowledged the widespread confu- sion over the meaning and reach of Roe, and it used its opinion in Casey to provide better guidance to legisla- tures seeking to regulate abortion as a constitutionally protected right. Specifically, the court in Casey sought to define more precisely both the constitutional rights of pregnant women and the legitimate authority of states to regulate some aspects of the abortion deci- sion. The deeply divided court wrote the following:

It must be stated at the outset and with clar- ity that Roe’s essential holding, the holding we reaffirm, has three parts. First is a recognition of the right of the woman to choose to have an abortion before viability and to obtain it without undue interference from the State. Before viability, the State’s interests are not strong enough to support a prohibition of

 

 

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abortion or the imposition of a substantial obstacle to the woman’s effective right to elect the procedure. Second is a confirmation of the State’s power to restrict abortions after fetal viability, if the law contains exceptions for pregnancies which endanger the woman’s life or health. And third is the principle that the State has legitimate interests from the outset of the pregnancy in protecting the health of the woman and the life of the fetus that may become a child. These principles do not con- tradict one another; and we adhere to each. (Planned Parenthood of Southeastern Pennsyl- vania v. Casey, 1992)

Notice how, in interpreting Roe, the court in Casey makes some remarkable alterations to the contours of the right to choose to have an abortion. First, trimesters were replaced by fetal viability as the regulatory touch- stone. Second, the pregnant woman, not her attending physician, makes the abortion decision. Third, a state’s interest in protecting pregnant women and fetuses now attaches “from the outset of the pregnancy,” not at the beginning of the second trimester. Fourth, and perhaps most important, the court’s invalidation of the trimester framework enabled the establishment of a new “undue burden” standard for assessing the con- stitutionality of state abortion regulations. Under this new standard, a state may not prohibit abortion prior to fetal viability, but it may promulgate abortion regu- lations as long as they do not pose a “substantial obsta- cle” to a woman seeking to terminate a pregnancy. The court did not, however, alter its decision in Roe that, post-viability, a state may proscribe abortion except when pregnancies endanger a woman’s life or health. Taken together, these alterations both maintain a pregnant woman’s basic constitutional right to obtain an abortion pre-viability and enhance state interest in protecting the potentiality for human life.

Once the court established the undue burden standard for assessing the constitutionality of state abortion regulations, it applied the standard to each constitutionally questionable amendment to Penn- sylvania’s Abortion Control Act. In the end, only the spousal notification provision was struck down as an unconstitutional burden; the court determined that some pregnant women may have sound reasons for not wishing to inform their husbands of their decision to obtain an abortion, including fear of abuse, threats of future violence, and withdrawal of financial support. As a result, the court equated the spousal notification requirement to a substantial obstacle because it was likely to prevent women from obtaining abortions.

The court majority in Casey provided a new tem- plate for lower courts to use in deciding the consti- tutionality of state abortion regulations. Likewise, the opinion offered guidance to state legislatures as to what kinds of abortion restrictions were likely to withstand a constitutional attack. Nonetheless, some state legislatures have tested the boundaries of Casey by enacting bans on a procedure known as “partial birth” abortion, an issue to which we now turn.

The Stenberg v. Carhart Decision. The undue bur- den standard articulated in Casey for assessing the constitutionality of abortion regulations was put to the test in Stenberg v. Carhart (2000). At issue in the case was a Nebraska criminal law banning “an abor- tion procedure in which the person performing the abortion partially delivers vaginally a living unborn child before killing the unborn child and completing the delivery.” It further defined “partially delivers vag- inally a living unborn child before killing the unborn child” to mean “deliberately and intentionally deliv- ering into the vagina a living unborn child, or a sub- stantial portion thereof, for the purpose of performing a procedure that the person performing such proce- dure knows will kill the unborn child and does kill the unborn child.” The Nebraska law penalized physicians who performed a banned abortion procedure with a prison term of up to 20 years, a fine of up to $25,000, and the automatic revocation of the doctor’s license to practice medicine in Nebraska.

Dr. Leroy Carhart, a Nebraska physician who per- formed abortions, filed a lawsuit seeking a declara- tion that the Nebraska law violated the constitutional principles set forth in Roe and Casey. After a lengthy trial, a federal district court agreed with Dr. Carhart and declared the Nebraska law unconstitutional. The Court of Appeals for the Eighth Circuit agreed, con- cluding that Nebraska’s statute violated the Constitu- tion as interpreted by the Supreme Court in Casey. The Supreme Court then granted review.

The court was unequivocal in its opinion in Sten- berg that the case was not a forum for a discussion on the propriety of Roe and Casey, but rather an appli- cation of the rules stated in those cases. In applying the undue burden standard to pre-viability abor- tions, the court considered trial court testimony from expert witnesses regarding several different abortion procedures that were then current in medical prac- tice to flesh out the procedures’ technical distinctions and to determine whether the procedures fell within Nebraska’s definition of “partial birth” abortion. The court determined that two distinct abortion proce- dures were relevant—dilation and evacuation (D&E),

 

 

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and dilation and extraction (D&X)—and that the Nebraska law’s vague definition of “partial birth” abor- tion effectively banned both procedures.

Again by a 5–4 majority, the Supreme Court struck down the Nebraska law as unconstitutional on two separate grounds. First, the court concluded that the statute created an undue burden on women seeking pre- viability abortions. The court reasoned that ban- ning the most commonly used method for pre-viability second trimester abortions—the D&E procedure— unconstitutionally burdened a woman’s ability to choose to have an abortion. Second, the court invali- dated the state law because it lacked an exception for the preservation of the health of the pregnant woman. The court rejected Nebraska’s claim that the banned procedures were never necessary to maintain the health of the pregnant woman and held that “significant med- ical authority” indicated that the D&X procedure is in some cases the safest abortion procedure available.

At the time Stenberg was decided, nearly 30 states had laws restricting D&E- and D&X-type abortions in some manner. Attempts to enact bans on these abor- tion procedures, however, have not been made only by state legislatures. Congress has tried numerous times to promulgate a federal ban, and after Stenberg was handed down, congressional opponents to abortion vowed to craft a ban that would pass constitutional muster. This effort culminated in the Partial Birth Abortion Ban Act of 2003 (PBABA).

Partial Birth Abortion Ban Act of 2003. PBABA represented Congress’s third attempt since 1996 to ban “partial birth” abortions. Previous bills were vetoed by President Bill Clinton in 1996 and 1997, but in late 2003, PBABA easily passed both houses of Congress and was signed into law by President George W. Bush. Immediately, the constitutionality of PBABA was challenged in federal court, and the Supreme Court ultimately decided the law’s fate in 2007, as described here.

PBABA establishes criminal penalties for “any physician who . . . knowingly performs a partial birth abortion and thereby kills a human fetus.” Attempt- ing to avoid the definitional vagueness that affected the Nebraska law’s constitutionality, the drafters of the federal law used more precise language in an effort to ban only D&X procedures, although PBABA does not specifically refer to any medical procedure by name. Instead, the law defines a “partial birth” abortion as

an abortion in which the person performing the abortion deliberately and intentionally vaginally delivers a living fetus until, in the case of a headfirst presentation, the entire

fetal head is outside the body of the mother, or, in the case of a breech presentation, any part of the fetal trunk past the navel is out- side the body of the mother, for the purpose of performing an overt act that the person knows will kill the partially delivered living fetus. (PBABA, 2003)

PBABA contains an exception allowing for these otherwise illegal abortions when necessary to pro- tect a pregnant woman’s life, but not health. The law’s authors claim that the banned procedure is never nec- essary to protect the health of a pregnant woman and thus that an exception is not required.

Separate lawsuits challenging PBABA were filed in federal courts in California, Nebraska, and New York. All three federal trial courts concluded that the lack of a health exception necessarily rendered the law unconstitutional under Supreme Court prece- dent. With enforcement of PBABA halted, the federal government appealed all three cases. The appellate courts that examined PBABA all found that substan- tial medical authority exists supporting the necessity of the banned procedure and declared PBABA uncon- stitutional because of its lack of a health exception. As noted, the fate of PBABA was then decided by the Supreme Court.

The Gonzales v. Carhart Decision. The Supreme Court upheld the constitutionality of the PBABA in Gonzales v. Carhart, another 5–4 decision. The court rejected the reasoning of the appellate courts and found that PBABA was not on its face “void for vagueness” (a doctrine that permits courts to reject statutes under which a layperson could not generally understand who is being regulated or what is being prohibited) and did not pose an undue burden on the right to receive an abortion under Casey. Although the court reaffirmed again the various basic principles of Roe and Casey—that women have an unfettered right to an abortion pre-viability, that the government has the power to restrict abortions post-viability, and that the government has an interest from the outset of pregnancy in protecting the health of the woman and the fetus—the court in Carhart focused on the latter and held that the government’s legitimate interest in promoting fetal life would be hindered if the act was invalidated.

The court first ruled that PBABA was not void for vagueness simply because the law prohibits per- forming intact D&Es. According to the court, the law puts doctors on notice of the prohibited conduct by adequately describing the intact D&E procedure and requiring that the doctor have knowledge that he is

 

 

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performing the intact D&E for the purpose of destroy- ing the fetus. The court also found that PBABA did not impose an undue burden for being overly broad. To distinguish it from the Nebraska law in Stenberg, the court majority stated that PBABA targets extraction of the entire fetus, as opposed to the removal of fetal pieces beyond a specific anatomic point in the preg- nant woman.

The court then held that PBABA did not pose a “substantial obstacle” to obtaining an abortion under Casey’s undue burden test. According to the court, the ban on partial birth abortions furthers the govern- ment’s interest in protecting fetal life and the govern- ment has the ability to prohibit practices ending fetal life that are similar to condemned practices. Finally, in a major shift that received relatively little attention by the court majority, the court ruled that the fact that PBABA did not contain language protecting the health of the woman did not render the law uncon- stitutional. Deferring to Congress because there are other safe procedures besides intact D&E that a doctor may use to perform an abortion and because accord- ing to the court PBABA promotes fetal life, the court simply declared the law constitutional notwithstand- ing the missing language.

The Right to Be Free From Wrongful Discrimination We now transition to the final topic in the discussion of individual legal rights to and within health care— namely, the topic of healthcare discrimination.h Like discrimination generally, healthcare discrimination has a lurid and lengthy history in this country. Prior to the Brown v. Board of Education decision in 1954 and the civil rights movement of the 1960s, health- care injustice and exclusion based on race and other factors were commonplace, dating to slavery times and plantation-based racially segregated health care. After the end of the First Reconstruction, states passed so-called Jim Crow laws, cementing in place legally segregated health care. As a result, hospitals, physician practices, medical/nursing/dental schools, and pro- fessional medical societies were all separated based on race. In places where Jim Crow laws had not been passed, corporate bylaws and contracts between pri- vate parties often had the same discriminatory effect, and these “Jim Crow substitutes” were generally hon- ored and enforced by the courts that interpreted them.

Federal law also played a role in perpetuating racially segregated health care. For example, the Hos- pital Survey and Construction Act of 1946 (more commonly known as the Hill–Burton Act, after the

key congressional sponsors of the measure) provided federal money to states to build and refurbish hospi- tals after World War II, but explicitly sanctioned the construction of segregated facilities:

A hospital will be made available to all per- sons residing in [its] territorial area . . . with- out discrimination on account of race, creed, or color, but an exception shall be made in cases where separate hospital facilities are provided for separate population groups, if the plan makes equitable provision on the basis of need for facilities and services of like quality for each such group. (Hospital Survey and Construction Act, 1946)

This provision was not ruled unconstitutional until the 1963 case of Simkins v. Moses H. Cone Memo- rial Hospital, which has been referred to as the “Brown v. Board of Education of health care” (Smith, 1999). Simkins also helped fuel the passage of the Civil Rights Act of 1964, this country’s most important civil rights legislation of the 20th century. For purposes of health care, Title VI of the 1964 Act was of specific impor- tance. Title VI is discussed in more depth later in this chapter; in sum, this portion of the Civil Rights Act makes it illegal for programs and activities that receive federal funding to discriminate on the basis of race, color, or national origin.

Notwithstanding the healthcare rewards brought about by the civil rights movement—Title VI, the pas- sage of Medicaid and Medicare, the establishment of federally financed community health centers—the focus on healthcare civil rights was waning as early as 1968. Several factors led to this decline, but what is most striking is that compared to the progress made by public and private civil rights efforts over the past 45 years in education, employment, and housing, civil rights enforcement in the healthcare field has been anything but sustained.

Of course, even an enduring and well-funded enforcement effort is no guarantee of wiping out dis- crimination, regardless of its social context. There are, unfortunately, vestiges of discrimination in many important aspects of American society, including the healthcare system. Moreover, although historically healthcare discrimination on the basis of race and eth- nicity has received the most attention, the existence of discrimination in health care on the basis of socio- economic status, disability, age, and gender also raises troubling questions. The remainder of this section touches briefly on each of these areas, describing laws (where applicable) or legal theories used to combat the particular healthcare discrimination at issue.

 

 

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Race/Ethnicity Discrimination The fact that healthcare discrimination premised on race or ethnicity has dominated the healthcare civil rights landscape should not be surprising, because racist beliefs and customs have infected health care no less so than other areas of life, such as education, employment, and housing. This fact is chronicled to a staggering degree by W. Michael Byrd and Linda A. Clayton, two physician-researchers at the Har- vard School of Public Health (2000; 2002). Byrd and Clayton paint a complex and disturbing picture of a healthcare system that itself perpetuates racism in health care in three distinct ways: by not destroying the myth that minority Americans should be expected to experience poorer health relative to Caucasians; by organizing itself as a private, for-profit system that marginalizes the indigent and minorities; and by refusing to acknowledge the historical and ongoing problem of racial exclusion in health care.

One key problem that in part results from the design of the healthcare system is that of racial and ethnic health disparities—differences in healthcare access, treatment, and outcomes between popula- tions of color and Caucasians. In 2003, the Institute of Medicine (IOM; now called the Academy of Med- icine) released an influential report that included overwhelming evidence of racial and ethnic health disparities and documented that these disparities could not be explained solely by the relative amount of health care needed by populations of color and nonminority populations (Smedley, Stith, & Nelson, 2003). For example, the report concluded that Afri- can Americans are relatively less likely to receive treatment for early-stage lung cancer, publicly insured Latinos and African Americans do not receive coro- nary artery bypass surgery at rates comparable to pub- licly insured nonminorities, and Latino and African American children on Medicaid experience relatively higher rates of hospitalization.

Furthermore, the IOM study revealed that even when relevant patient characteristics are controlled for, racial and ethnic differences arise not only in terms of accessing care initially, but also after individuals have entered the healthcare system, a finding that supports

the notion that both the system itself and physician practice style contribute to disparities. This notion is, of course, quite controversial, because it suggests that physician decision making and clinical practice can increase the likelihood of racially disparate outcomes.

The key federal law used to combat race and eth- nicity discrimination in health care is Title VI of the 1964 Civil Rights Act, which states that “no person in the United States shall, on the ground of race, color, or national origin, be excluded from participation in, be denied the benefits of, or be subjected to discrimina- tion under any program or activity receiving federal financial assistance.” Because it attaches only to recip- ients of federal funding, Title VI does not reach, for example, health professionals who do not directly par- ticipate in government-sponsored health programs; nor does it reach physicians whose only participation in federal assistance programs is under Medicare Part B (the basis for this exemption is historical and purely political, and the exemption is not codified in Title VI statutory or regulatory law [Smith, 1999, pp. 115– 128]). Nonetheless, Title VI has long had the potential to greatly impact the field of health care, because an enormous amount of federal funding has been poured into the healthcare enterprise over the past 50 years.

The concept of “discrimination” under Title VI applies both to intentional acts and to actions or pol- icies that unintentionally have the effect of discrimi- nating against racial and ethnic minorities. This is so because federal regulations implementing the Title VI statute (which explicitly prohibits only intentional discrimination) reach actions that, even if neutral on their face, have a disproportionate adverse impact (or effect) on members of minority groups. In the case of healthcare access and delivery, you can imagine sev- eral types of conduct that might potentially violate the Title VI disproportionate impact regulations. For example, were a hospital to segregate patients by source of payment—say, by maintaining a ward or floor that treated only patients covered under Medicaid—racial and ethnic minorities may be adversely impacted, given the overall makeup of the Medicaid population. Similarly, the Title VI regulations could be violated if a managed care organization enrolled both privately and publicly insured persons but allowed participat- ing providers to refuse to accept as patients those indi- viduals covered by Medicaid.

The disproportionate impact regulations are cru- cial to realizing Title VI’s full force, because much of the racism in post-1954 America does not take the form of overt, intentional acts. However, as a result of the 2001 Supreme Court decision in Alexander v. Sandoval, these regulations were severely undercut.

BOX 6-4 Discussion Question

If you were asked to distill, down to their most essential parts, the constitutional right to privacy and the right to privacy as it applies to abortion, what elements would you include?

 

 

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Under Alexander, private individuals were barred from bringing a lawsuit under the disparate impact regulations, leaving the federal government as the sole enforcer when racial or ethnic minorities allege a vio- lation of the regulations.i

Physical and Mental Disability Discrimination Like discrimination based on race or ethnicity, health- care discrimination premised on disability has a long, sad history in this country and, as with race, the health system itself is partly to blame for its perpetuation. For instance, historically, persons with mental disabilities were viewed from a medical standpoint as having little to offer to society, and they were, as a matter of prac- tice, shipped to mental asylums isolated from commu- nities. Those with physical disabilities were not spared discriminatory practices, either; because individuals with Down syndrome were viewed by medical practi- tioners as “Mongoloid idiots” and children with cere- bral palsy or other serious physical limitations were regularly viewed as unable to contribute to society, they were all simply institutionalized. These historical practices and perspectives resonate even in the mod- ern healthcare system, in which treatment opportuni- ties for the disabled are skewed toward institutional, rather than community, settings, and disease-specific limitations in health insurance are commonplace.

However, passage of the Americans With Disabil- ities Act (ADA) in 1990 alleviated at least some of the problems associated with disability discrimination in health care. Like Title VI, the ADA is not specifically a “health law”; its intent is to extend to the disabled the maximum opportunity for community integra- tion in many sectors of society, including employ- ment, public services, public accommodations (i.e., privately owned entities open to the public), telecom- munications, and more. For this reason, it prohibits discrimination generally against disabled individuals who satisfy the essential requirements of a particular job, or who meet the qualification standards for a pro- gram, service, or benefit.

But the ADA’s impact on health care for disabled individuals is notable, in large part because the law defines “places of public accommodation” to include private hospitals and other private healthcare provid- ers. So, for example, a dentist in private practice who does not receive any federal funds for his services is nonetheless prohibited from discriminating against a person who is HIV-positive, as the well-known case of Bragdon v. Abbott (1990) makes clear. This rep- resents an important expansion of federal disability

law because prior to the ADA, only recipients of fed- eral funds were proscribed from discriminating on the basis of disability. Note also how this expanded con- cept of public accommodations differs from Title VI of the Civil Rights Act, which still requires the receipt of federal money on the part of the offending entity to trigger protections for racial and ethnic minorities.

Although the ADA has dramatically altered the disability law landscape, it is not without limita- tions. For example, the regulations implementing the ADA’s statutory text require entities that implement public programs and services to make only “reason- able modifications”—but not “fundamental alter- ations”—to those programs and services. Under the ADA, a fundamental alteration is one that would change the essential nature of a public program or service. Whether a requested change to a public pro- gram or service by a disabled individual amounts to a “reasonable” or a “fundamental” one is potentially determinative to the outcome of the request. Why? Because if a court determines that the request would alter the essential nature of the program or service at issue, it is powerless under the ADA to order the change. Another way of understanding this reason- able modification/fundamental alteration dichotomy is to recognize that fundamental alterations to public services—alterations that might actually be necessary to achieve at least the spirit of the ADA’s loftiest goals and meet the expectations of a modern, enlightened society—could be made only by the political branches of government, not by the courts.

Another important limitation of the ADA (at least as it has been interpreted by most courts) is that it does not prohibit arbitrary insurance coverage lim- its attached to certain medical conditions. A stark example of this is found in the case of Doe v. Mutual of Omaha Insurance Company (1999), in which a fed- eral appellate court ruled that a lifetime benefit limita- tion in a health insurance policy of $25,000 for AIDS or AIDS-related conditions did not violate the ADA, even though the very same policy set a $1 million life- time limit for other conditions.

Socioeconomic Status Discrimination Compared to race or disability discrimination in healthcare access and treatment, healthcare discrim- ination based on class gains little attention—even though socioeconomic status is independently asso- ciated with health status, and the negative effects of poverty on health and healthcare access are incontro- vertible. Class-related healthcare discrimination can take many forms. For example, healthcare providers

 

 

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might refuse to accept as patients individuals who are covered under Medicaid, or low-income individuals might fall victim to the practice of redlining, which refers to discrimination based on geographic location when companies offer goods and services to consum- ers. (Although insufficient data exist to know the extent of redlining in healthcare-related goods and services, industries such as home health care, pharmaceuticals, and managed care have come under particular scru- tiny [Perez, 2003].) Another example stems from the fact that healthcare providers (e.g., physician and den- tal practices, hospitals) sometimes elect to not operate in relatively poor communities, leaving residents of these communities at heightened risk for experiencing a shortage of adequate healthcare resources.

Gender Discrimination Discrimination against women is also a problem in health care. This bias appears to be of particular concern in the area of coronary heart disease (Bess, 1995), in which delayed or disparate care could have severe conse- quences. While it may seem that gender discrimination in health care could be remedied under the Equal Pro- tection Clause of the federal Constitution, Equal Protec- tion claims are difficult to win because they require proof of both state action (a sufficient government connection to the discriminatory acts) and proximate causation (a cause-and-effect link between the discrimination and the harm suffered). Also, consider the fact that health- care practitioners who receive federal funds cannot face suit under Title VI for even obvious gender discrimina- tion, because Title VI’s prohibitions relate only to race, color, and national origin discrimination.

Age Discrimination Finally, the medical care system also seems to be biased against older adults. Just one of several disturbing facts on the treatment front is that older adults sometimes do not receive needed surgical care because health professionals wrongfully assume that the chances of recovery are not good (Smith, 1996). Another concern pertains to insurance coverage, in that many employ- ers are attempting to rescind lifetime health coverage benefits to retired workers, even where the benefits had been promised as part of negotiated labor con- tracts. At first blush, this may not seem like a critical issue, because many retirees are at or beyond the age required for Medicare eligibility. But some retirees are not yet 65 years old, a retiree’s employer-sponsored benefits might provide more or different coverage than Medicare, and employer benefits might cover a retiree’s dependents, which Medicare does not do.

▸ Individual Rights in a Public Health Context

The discussion thus far has focused on healthcare legal rights that individuals can claim in the con- text of access, receipt of services, freedom of choice, and antidiscrimination. In each of these areas, how- ever, the right claimed is not absolute. For exam- ple, EMTALA does not make illegal all transfers of indigent patients from private hospitals to public ones; rather, it requires that patients be medically stabilized before a transfer can occur. Even eminent civil rights laws do not provide blanket protections, because they might be triggered only where federal funding is present, or where the assistance requested would not fundamentally alter a government health program.

In this section, we consider restrictions on indi- vidual rights and liberties of a different sort: those that derive not from the limitations of specific laws, but rather from governmental police pow- ers used to protect the general public’s health and welfare. One simple way to think about individual rights in a public health context is to use a balancing approach—what might the appropriate legal trade- offs be between private rights and public welfare? Public discussion of this trade-off intensified after the terrorist attacks of September 11, 2001, because many government actions taken in their wake— the passage of new laws, the tightening of existing regulations, the detainment of alleged terrorists— starkly raised the question of where to draw the line between individual autonomy and government authority to restrain that autonomy in the name of public welfare and national security. The attacks raised new questions relating to public health law as well, including whether the potential for a bioterror- ist attack using smallpox should compel the federal government to vaccinate individuals—even against their will—against the virus in order to protect the public at large in the event of an attack.

Overview of Police Powers Police powers represent state and local government authority to require individual conformance with established standards of conduct. These standards are designed to promote and protect the public’s health, safety, and welfare, and to permit government con- trol of personal, corporate, and other private interests. The government’s police powers are broad and take many forms. Healthcare professionals are required to obtain licenses from government agencies. Healthcare

 

 

Individual Rights in a Public Health Context 129

facilities face accreditation standards. Food establish- ments are heavily regulated. Employers are bound by numerous occupational health and safety rules. Busi- nesses are constrained by pollution control measures. Tobacco products can be marketed in only certain ways. The purchase of guns is controlled, buildings have to abide by certain codes, motorcyclists must wear helmets. The list goes on and on.

The government’s police powers are oftentimes invasive, a result that stems in part from the fact that the American colonies were battling multiple com- municable diseases during the time of the writing of the Constitution, and its drafters were thus well aware of the need for pervasive governmental public health powers. At the same time, the government may not overreach when restricting private autonomy in the name of public health promotion and protection. For example, police powers cannot be used as a form of punishment, they cannot be used arbitrarily and capriciously, and they cannot be used for purposes unrelated to public health and welfare.

A key principle inherent to the use of police powers is that of coercion. This is so because, in a country founded upon the twin ideals of individu- alism and a limited government, many individu- als and businesses do not respond kindly to being told to conform with public health regulations that limit their actions. For example, sometimes a public health concern (e.g., pollution) requires a response (enhanced governmental regulation) that may not be in the best economic interests of an implicated party (a refinery). This is not to say that individuals and businesses do not voluntarily assume responsi- bilities and measures that are in the public’s interest. For instance, one effect of poor exercise habits— obesity—has enormous implications for the public’s health and for national healthcare costs. As a result, the government would prefer that all individuals exercise for a minimum amount of time each week, but there is of course no law requiring this; rather, voluntarism is the guiding principle when it comes to personal exercise. Nonetheless, personal coercion and industrial regulation have long been adopted (and accepted) practices of public health officials, and all of the major communicable disease outbreaks have been combated with some combination of com- pulsory screening, examination, treatment, isolation, and quarantine programs.

The Jacobson v. Massachusetts Decision The fact that government coercion can be justified by important public health goals does not answer the

question of where to draw the line between personal/ economic freedom on the one hand, and the public welfare on the other. This question was taken up by the Supreme Court in Jacobson v. Massachusetts (1905), perhaps the most famous public health law decision in the court’s history and the one to which we alluded in the second factual scenario in Box 6-1 at the opening of this chapter.

The facts in Jacobson are straightforward enough. At the turn of the 20th century, the state of Massa- chusetts enacted a law granting local health boards the power to require vaccination when necessary to protect the public’s health or safety. In 1902, the Cam- bridge Board of Health, in the throes of attempting to contain a smallpox outbreak, took the state up on its offer and issued an order requiring all adults in the city to be vaccinated against the disease. Henning Jacobson refused vaccination on the ground that he previously suffered negative reactions to vaccinations. Jacobson was fined $5 for his refusal, a penalty upheld by the state’s highest court. Jacobson appealed to the U.S. Supreme Court, setting the stage for a decision that, more than 100 years later, remains both controversial and at least symbolically forceful (Gostin, 2005).

Like the enduring tension between private inter- ests and public welfare underpinning public health law generally, the Jacobson decision amounts to “a classic case of reconciling individual interests in bodily integrity with collective interests in health and safety” (Mariner, Annas, & Glantz, 2005). The 7–2 decision went the state’s way, with the Supreme Court recognizing that police powers were generally broad enough to encompass forced vaccination. Respond- ing to Jacobson’s argument that the Massachusetts law impermissibly infringed on his constitutional right to liberty, the court wrote the following:

The liberty secured by the Constitution of the United States to every person within its jurisdiction does not import an absolute right in each person to be, at all times and in all circumstances, wholly freed from restraint. There are manifold restraints to which every person is necessarily subject for the common good. On any other basis organized society could not exist with safety to its members. Society based on the rule that each one is a law unto himself would soon be confronted with disorder and anarchy. (Jacobson v. Massachusetts, 1905)

Due to this and other language used by the court in the decision, Jacobson is often described as sweep- ingly deferential to public health officials and their

 

 

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use of police powers. And without question, social compact theory (the idea that citizens have duties to one another and to society as a whole) animates the court’s decision. However, the Jacobson decision also recognizes the individual liberties protected by the Constitution, and in fact requires a deliberative gov- ernmental process to safeguard these interests.

According to the Jacobson court, public health powers must be exercised in conformity with four standards in order to pass constitutional muster:

■ The first standard, that of “public health necessity,” requires that government use its police powers only in the face of a demonstrable public health threat.

■ The second standard, termed “reasonable means,” dictates that the methods used when exercising police powers must be designed in such a way as to prevent or ameliorate the public health threat found to exist under the first standard.

■ “Proportionality” is the third Jacobson standard; it is violated when a particular public health mea- sure imposes a burden on individuals totally dis- proportionate to the benefit to be expected from the measure.

■ Finally, and axiomatically, the public health reg- ulation itself should not pose a significant health risk to individuals subject to it. This is the stan- dard of “harm avoidance.”

These standards have never been explicitly over- turned, but it can be argued that they have at the very least been implicitly replaced, given that in the 100- plus years since Jacobson was decided, the Supreme Court has developed a much more complex approach to applying constitutional provisions to cases impli- cating individual autonomy and liberty.

The “Negative Constitution” The discussion of police powers up to this point might reasonably lead you to believe that the Constitution obligates the government to protect the public’s health and welfare through affirmative use of its powers. This view, however, has never been adopted by the Supreme Court. Instead, the prevailing view is that the Constitution empowers government to act in the name of public health, but does not require it to do so. This interpretation of the Constitution refers to what is known as the “negative constitution”—that is, the idea that the Constitution does not require government to provide any services, public health or otherwise. This approach to constitutional law derives from the fact that the Constitution is phrased mainly in negative terms (e.g., the First Amendment prohibits govern- ment abridgment of free speech). Professor Wendy Parmet describes the “negative constitution” this way:

In the century that has witnessed Auschwitz and Chernobyl, it is easy to see the dangers posed by state power. This recognition tem- pers enthusiasm for public authority and leads us to use law as a limiting device. In our legal tradition, this view of law is integral to constitutional structure, with its emphasis on separation of powers, checks and balances, procedural protections, and individual rights. We rely on the Constitution to limit the power of the government to restrain our free- doms and cause us harm. In this sense, law is a negative force that prevents the state from intruding upon the individual. This negative conception of law, which sees legal rights as a restraint upon the state, has played a domi- nant role in the formulation of contemporary American public health law. It explains the central pillars of constitutional public health law: the search for limits on governmental authority to restrain individual freedoms in the name of public health, and the concom- itant assumption that government has no obligation to promote public health. (Parmet, 1993, pp. 267, 271)

In two important decisions, DeShaney v. Win- nebago County Department of Social Services (1989) and Town of Castle Rock, Colorado v. Gonzales (2005), the Supreme Court has advanced this view of the nega- tive constitution. In the former case, 1-year-old Joshua DeShaney was placed in his father’s custody after his parents divorced. Two years later, the father’s second wife complained to county officials in Wisconsin that

BOX 6-5 Discussion Question

Jacobson v. Massachusetts is a product of the early 20th century, and the public health law principles supporting it are vestiges of an even earlier time. This, coupled with a century of subsequent civil liberties jurisprudence and societal advancement, has led some commentators to question whether Jacobson should retain its paradigmatic role in terms of the scope of government police powers. At the same time, other public health law experts call for Jacobson’s continued vitality, arguing that it is settled doctrine and a still-appropriate answer to the private interest/collective good question. What do you think?

 

 

Individual Rights in a Public Health Context 131

the father had been abusing Joshua physically. Social service workers opened a file on the case and inter- viewed Joshua’s father, but the county did not pursue the matter further after the father denied the charges. One year after that, an emergency department physi- cian treating Joshua alerted social services of his sus- picion that Joshua’s injuries were the result of abuse. The county again investigated but decided that insuffi- cient evidence of child abuse existed to remove Joshua from his father’s custody. This emergency department scenario played out two additional times over the next several months, but Joshua’s caseworkers still believed that they had no basis on which to place Joshua in court custody. Some months later, when Joshua was 4 years old, he suffered a beating so severe that he fell into a life-threatening coma. He survived but was left with permanent, severe brain damage, and he was expected to live his life in an institution for the pro- foundly mentally disabled. Joshua’s father was subse- quently convicted of child abuse.

Joshua’s mother filed a civil rights claim on Josh- ua’s behalf against the county officials who failed to take the boy into their custody. The lawsuit was based on the Due Process Clause of the federal Constitu- tion, which prohibits states from depriving any per- son of property without due process of law. However, the Supreme Court in DeShaney concluded that the “substantive” component of the Due Process Clause— which focuses on challenges to government conduct— could not be read to provide Joshua with a property interest in having state child welfare officials protect him from beatings by his father. For a 6–3 majority, Chief Justice Rehnquist held that state officials had no affirmative constitutional duty to protect Joshua:

Nothing in the language of the Due Pro- cess Clause itself requires the State to pro- tect the life, liberty, and property of its citizens against invasion by private actors. The Clause is phrased as a limitation on the State’s power to act, not as a guarantee of cer- tain minimal levels of safety and security. It forbids the State itself to deprive individuals of life, liberty, or property without “due pro- cess of law,” but its language cannot fairly be extended to impose an affirmative obligation on the State to ensure that those interests do not come to harm through other means. (Deshaney, 1989)

The majority further rejected the argument that the state’s knowledge of the danger Joshua faced, and its expression of willingness to protect him against that

danger, established a “special relationship” that gave rise to an affirmative constitutional duty to protect.

In dissent, three justices in DeShaney argued that through the establishment of its child protec- tion program, the state of Wisconsin undertook a vital duty and effectively intervened in Joshua’s life, and its failure to live up to its child protection duty amounted to a constitutional violation. According to the dissenters, the majority opinion “construes the Due Process Clause to permit a State to displace private sources of protection and then, at the crit- ical moment, to shrug its shoulders and turn away from the harm that it has promised to try to prevent” (Deshaney, 1989).

Sixteen years after DeShaney, the Supreme Court in Castle Rock v. Gonzales had an opportunity to again consider whether the government has a duty to affir- matively protect its citizens. This time, however, the court was concerned not with substantive due process, but rather with procedural due process, which man- dates that when a state establishes a benefit or right for its citizens, it is not entitled to deny individuals the benefit or right in an arbitrary or unfair way.

Unfortunately, the facts in Gonzales are as tragic as those in DeShaney. In May 1999, Jessica Gonzales received a court order protecting her and her three young daughters from her husband, who was also the girls’ father. On June 22, all three girls disappeared in the late afternoon from in front of the Gonzales home, and Jessica suspected that her husband had taken them in violation of the restraining order. This suspicion was confirmed in a phone conversation she had with her husband. In two initial phone conver- sations with the Castle Rock Police Department, she was told there was nothing the police could do and to wait until 10:00 p.m. to see if her husband brought the girls home.

Shortly after 10:00 p.m., Jessica called the police to report that her children were still missing, but this time she was told to wait until midnight to see what transpired. She called the police again at midnight, reported that her children were still missing, and left her home to go to her husband’s apartment. Finding nobody there, she called the police again at 12:10 a.m. and was told to wait for an officer to arrive. Thirty minutes later, after no officer showed up, she went to the police station to submit a report. According to the Supreme Court decision, the officer who wrote up the report “made no reasonable effort to enforce the [restraining order] or locate the three children. Instead, he went to dinner.” A couple of hours later, Jessica’s husband pulled his truck up to, and began shooting at, the Castle Rock Police Department. After

 

 

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he was killed by police during the gunfight, the three Gonzales daughters were found dead in the back of the truck; they had been murdered by their father hours earlier.

Jessica sued the police department, claiming that her constitutional right to procedural due process was violated by the department’s inaction. She argued that the restraining order she received was her “prop- erty” under the Constitution’s Due Process Clause and that it was effectively “taken” from her without due process. Overturning the federal appellate court that ruled in her favor, the Supreme Court decided by a 7–2 margin that Jessica did not have a property interest in police enforcement of the restraining order against her husband.

The court said it was not clear that even if it had found an individual entitlement to enforcement of a restraining order under a Colorado state statute requiring officers to use every reasonable means to enforce restraining orders, that this entitlement would constitute a protected “property” interest that triggers due process protections under the federal Constitution. Justice Antonin Scalia wrote that the Due Process Clause does not protect all government “benefits,” including those things that government officials have discretion to grant or deny. Applying this standard, the court ruled that Colorado’s pro- tection order law did not create an individual enti- tlement to police enforcement of restraining orders, explaining that police have discretion to act or not act under many circumstances, including when to enforce a restraining order (e.g., police officers have discretion to consider whether a violation of a pro- tection order is too “technical” or minor to justify enforcement). Furthermore, the court noted that if the Colorado legislature included statutory language making police enforcement of a restraining order “mandatory,” even that would not necessarily mean that Mrs. Gonzales had a personal entitlement to its enforcement, given that the statute makes no men- tion of an individual’s power to demand—or even request—enforcement.

In dissent, two justices in Gonzales argued that restraining orders amount to a personal, enforce- able property interest. They asserted that the major- ity opinion wrongly ruled that a citizen’s interest in government-provided police protection does not resemble a “traditional conception” of property. Look- ing to the legislative history and text of Colorado’s own protection order law and to the purpose of the state’s domestic violence legislation, the dissent con- cluded that a particular class of individuals was indeed entitled beneficiaries of domestic restraining orders.

▸ Conclusion This chapter offered a snapshot of the current state of health-related legal rights. But, as alluded to early on in the chapter, there were times in its relatively short his- tory that this country was closer to recognizing broader individual healthcare rights than is currently the case, just as there have been times (as the aftermath of Sep- tember 11, 2001, proved) when concerns for the pub- lic’s health and safety have eclipsed the nation’s more natural inclinations toward individualism and a dereg- ulated marketplace. That this is so is of no surprise: legal rights are, by nature, subject to shifts in the polit- ical and social terrain. For example, the Aid for Fam- ilies With Dependent Children program (commonly known as AFDC), the federal welfare entitlement pro- gram for low-income populations, was dismantled in 1996 after more than 60 years in existence. Originally enacted under a slightly different name as part of the New Deal in 1935, the AFDC was replaced with the Temporary Assistance for Needy Families (TANF) pro- gram by a moderate Democrat (President Bill Clinton) and a conservative, Republican-controlled Congress. Compared to the AFDC, TANF dramatically limited the receipt of individual benefits and focused much more heavily on creating work opportunities for needy

BOX 6-6 Discussion Questions

The “negative constitution” is a concept over which reasonable people can easily disagree. Notwithstanding the “defensive” manner of some of the Constitution’s key provisions, there are several arguments in support of more affirmative action on the part of government health and welfare officials than current Supreme Court jurisprudence requires. For example, the dissent in DeShaney argues persuasively that Wisconsin’s implementation of a child protection program effectively created a constitutional duty to actually protect children from seemingly obvious danger. As one leading scholar put it,

If an agency represents itself to the public as a defender of health, and citizens justifiably rely on that protection, is government “responsible” when it knows that a substantial risk exists, fails to inform citizens so they might initiate action, and passively avoids a state response to that risk? (Gostin, 2000)

What do you think of this argument? Can you think of other arguments that call into question the soundness of the negative theory of constitutional law?

 

 

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Berkeley, CA: University of California Press. Gostin, L. O. (2005). Jacobson v. Massachusetts at 100 years: Police

powers and civil liberties in tension. American Journal of Public Health, 95(4), 576–581.

Griswold v. Connecticut, 381 U.S. 479 (1965). Halpern, S. A. (2004). Medical authority and the culture of rights.

Journal of Health Politics, Policy and Law, 29(4-5), 835–852. Hospital Survey and Construction Act of 1946, 42 U.S.C. § 291e(f )

(1946). Hurley v. Eddingfield, 59 N.E. 1058 (Ind. 1901). Jacobson v. Massachusetts, 197 U.S. 11 (1905). Jost, T. S. (2003). Disentitlement? The threats facing our public

health-care programs and a rights-based response. New York, NY: Oxford University Press.

Kinney, E. D., & Clark, B. A. (2004). Provisions for health and health care in the constitutions of the countries of the world. Cornell International Law Journal, 37(2), 285–355.

Littell, A. (2002). Can a constitutional right to health guarantee universal health care coverage or improved health outcomes? A survey of selected states. Connecticut Law Review, 35(1), 289–318.

Loving v. Virginia, 388 U.S. 1 (1967). Mariner, W. K., Annas, G. J., & Glantz, L. H. (2005). Jacobson v.

Massachusetts: It’s not your great-great-grandfather’s public health law. American Journal of Public Health, 95(4), 581–590.

families. Like legal rights generally, health-related legal rights are similarly subject to changing political cur- rents. For example, at the time of this writing, several state legislatures continue to pass bills that protect health professionals from providing care that conflicts with their personal beliefs, reflecting the current polit- ical power of social conservatives.j

Of course, changes to legal rights are not always represented by restrictions of those rights. The enact- ment of Medicaid and Medicare, which created new health-related rights, is an obvious example. Other major examples include EMTALA and expanded state consumer rights for persons in managed care. On a less noticed scale, legal rights for persons with HIV/AIDS have expanded since the 1980s (Halpern, 2004), and federal courts now review the constitution- ality of the treatment provided in, and conditions of,

psychiatric hospitals (Wyatt v. Stickney, 1972). These are just a few of many examples.

Nonetheless, vast challenges remain. After all, many scholars, politicians, and consumers point to the millions of uninsured Americans as just one example of not only a failing healthcare financing and delivery sys- tem, but also a failing of the legal system. To reduce this nation’s huge uninsured population takes not just polit- ical will, but also an enormous undertaking to change the law, as witnessed with the ACA. A “rights revolu- tion” in a health context, like other major legal upheav- als, requires something else, too: a substantial amount of general economic and social unrest (Friedman, 1971). As historian Brooks Adams once noted, “Law is merely the expression of the will of the strongest for the time being, and therefore laws have no fixity, but shift from generation to generation” (Nash & Zullo, 1995).

 

 

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▸ Endnotes a. These competing concepts were given life in

Paul Starr’s influential 1982 book, The Social Transformation of American Medicine: The Rise of a Sovereign Profession and the Making of a Vast Industry. Incidentally, The Social Transfor- mation of American Medicine should be read by all students with an interest in the history of medicine; the book’s significance across a range of disciplines is hard to overstate. See Wailoo and Schlesinger, 2004.

b. For an interesting article describing the impor- tance of political structures in determining

the level of equalities/inequalities in a society, including the level of government-provided healthcare coverage, see Navarro and Shi, 2003.

c. Incidentally, the Canterbury decision was authored by Spottswood Robinson, III, who, prior to becoming a highly regarded federal judge, was instrumental in the fight for civil rights, in part as one of the National Associa- tion for the Advancement of Colored People (NAACP) lawyers who initially brought suit in one of the cases that eventually morphed into Brown v. Board of Education.

Nash, B., & Zullo, A. (Eds.) (1995). Lawyer’s wit and wisdom: Quotations on the legal profession, in brief. Philadelphia, PA: Running Press.

Navarro, V., & Shi, L. (2003). The political context of social inequalities and health. In R. Hofrichter (Ed.), Health and social justice: Politics, ideology, and inequity in the distribution of disease. San Francisco, CA: Jossey-Bass.

Parmet, W. (1993). Health care and the constitution: Public health and the role of the state in the framing era. Hastings Constitutional Law Quarterly, 20(2), 267–335.

Partial Birth Abortion Ban Act, 18 U.S.C. §§ 1531 (a)-(b) (2003). Perez, T. E. (2003). The civil rights dimension of racial and ethnic

disparities in health status. In B. D. Smedley, A. Y. Stith, & A. R. Nelson. (Eds.), Unequal treatment: Confronting racial and ethnic disparities in health care (pp. 626–663). Washington, DC: The National Academies Press.

Planned Parenthood of Southeasten Pa. v. Casey, 505 U.S. 833 (1992). President’s Commission for the Study of Ethical Problems in

Medicine and Biomedical and Behavioral Research. (1983). Securing access to health care: A report on the ethical implications of differences in the availability of health services. Washington, DC: The National Academies Press.

Protection of Human Subjects, 45 C.F.R. Part 46 (2009). Regan, D. H. (1979). Rewriting Roe v. Wade. Michigan Law Review,

77, 1569–1646. Reinhardt, U. (1996). The debate that wasn’t: The public and the

Clinton health care plan. In H. Aaron (Ed.), The problem that won’t go away: Reforming U.S. health care financing (pp. 70–109). Washington, DC: Brookings Institution.

Rich, R. F. (2000). Health policy, health insurance and the social contract. Comparative Labor Law Policy Journal, 21, 397–421.

Roe v. Wade, 410 U.S. 113 (1973). Rosenbaum, S. (2011). Realigning the social order: The patient

protection and affordable care act and the U.S. health insurance system. Suffolk Journal of Health and Biomedical Law, 7, 1–31.

Rosenbaum, S., & Teitelbaum, J. (2003). Civil rights enforcement in the modern healthcare system: Reinvigorating the role of the federal government in the aftermath of Alexander v. Sandoval. Yale Journal of Health Policy, Law, and Ethics, 3(2), 215.

Rosenblatt, R. E., Law, S. A., & Rosenbaum, S. (1997). Law and the American health care system. Westbury, CT: The Foundation Press.

San Antonio Indep. School Dist. v. Rodriguez, 411 U.S. 1 (1973).

Simkins v. Moses H. Cone Memorial Hospital, 323 F.2d 959 (4th Cir. 1963).

Smedley, B. D., Stith, A. Y. & Nelson, A. R. (Eds.). (2003). Unequal treatment: Confronting racial and ethnic disparities in health care. Washington, DC: The National Academies Press.

Smith, D. B. (1999). Health care divided: Race and healing a nation. Ann Arbor, MI: The University of Michigan Press.

Smith, G. P. (1996). Our hearts were once young and gay: Health care rationing and the elderly. University of Florida Journal of Law and Public Policy, 8, 1.

Smith, P. S. (1997). Addressing the plight of inner-city schools: The federal right to education after Kadrmas v. Dickinson Public Schools. Whittier Law Review, 18, 825–835.

Stacy, T. (1993). The courts, the constitution, and a just distribution of health care. Kansas Journal of Law and Public Policy, 3, 77–94.

Starr, P. (1982). The social transformation of American medicine: The rise of a sovereign profession and the making of a vast industry. New York, NY: Basic Books.

Stein, R. (2006, January 30). Health workers’ choice debated: Proposals back right not to treat. Washington Post. Retrieved from http://www.washingtonpost.com/wp-dyn/content/article /2006/01/29/AR2006012900869.html

Stenberg v. Carhart, 530 U.S. 914 (2000). Teitelbaum, J. B. (2005). Health care and civil rights: An

introduction. Ethnicity and Disease, 15(2, supp. 2), 27–30. Town of Castle Rock, Colorado v. Gonzales, 545 U.S. 748 (2005). Vladeck, B. (2003). Universal health insurance in the United States:

Reflections on the past, the present, and the future. American Journal of Public Health, 93(1), 9–16.

Wailoo, K., & Schlesinger, M. (2004). Transforming American medicine: A twenty-year retrospective on The Social Transformation of American Medicine. Journal of Health Politics, Policy, and Law, 29(4–5), 1005–1019.

Wing, K. R. (1993). The right to health care in the United States. Annals of Health Law, 2, 161–193.

World Health Organization. (2006). Constitution of the World Health Organization. Retrieved from http://www.who.int /governance/eb/who_constitution_en.pdf

Wyatt v. Stickney, 344 F. Supp. 373 (M.D. Ala. 1972). Yamin, A. E. (2005). The right to health under international law

and its relevance to the United States. American Journal of Public Health, 95(7), 1156–1161.

 

 

Endnotes 135

d. A now-famous 1890 Harvard Law Review arti- cle titled “The Right to Privacy,” written by Sam- uel Warren and Louis Brandeis, is often credited with introducing the constitutional “right to be let alone.”

e. In a health context, this type of privacy is embodied by the Health Insurance Portability and Accountability Act (HIPAA) of 1996, found in large part at 29 U.S.C. §§ 1181–1187, 42 U.S.C. §§ 300gg et seq. and 42 U.S.C. §§ 1320a et seq., which creates a federal right to main- tain the confidentiality of one’s personal health information.

f. For a compelling look at what the case has meant to society, see Garrow, 1994.

g. For example, notice how the Supreme Court linked states’ power to ban abortions (with cer- tain exceptions) to fetal viability, even though the progression of medical knowledge and tech- nology could push back the point of viability earlier into pregnancy. Also, who appears to hold the power, under “(a),” to decide whether an abortion should occur? The physician, a fact often overlooked by those who hail Roe as a seminal women’s rights case and one that calls into question how the pregnant woman’s

constitutional right to privacy could be effectu- ated by her treating physician.

h. This section was adapted from Teitelbaum, 2005.

i. For a discussion of the implications of the Alexander decision in a healthcare context, see Rosenbaum and Teitelbaum, 2003.

j. These bills represent a

surge of legislation that reflects the inten- sifying tension between asserting indi- vidual religious values and defending patients’ rights. . . . The flurry of political activity is being welcomed by conserva- tive groups that consider it crucial to pre- vent health workers from being coerced into participating in care they find mor- ally repugnant—protecting their “right of conscience” or “right of refusal.” . . . The swell of propositions is raising alarm among advocates for abortion rights, family planning, AIDS prevention, the right to die, gays and lesbians, and others who see the push as the latest manifes- tation of the growing political power of social conservatives. (Stein, 2006)

 

 

 

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© Mary Terriberry/Shutterstock

CHAPTER 7

Social Determinants of Health and the Role of Law in Optimizing Health

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe the meaning of social determinants of health and the significance of social factors on individual and population health

■ Describe how law can create or perpetuate health-harming social conditions ■ Explain how law can be used to ameliorate health-harming social conditions ■ Understand how innovative interventions to improve health, such as medical-legal partnership, can help

address health-harming social conditions at the individual and population levels

BOX 7-1 Vignette

Living through brief periods without heat or electricity is a fact of life for most of us, perhaps as a result of a powerful weather system or a blown generator. But have you thought about what it would be like to be without heat or electricity more chronically, due to homelessness, inadequate housing, or an unscrupulous landlord who neglects a property without concern for tenants? Even for the healthiest among us, this social factor would be incredibly challenging; for those with chronic illness, it can mean increased asthma attacks, severe pain associated with sickle cell disease, an inability to refrigerate needed medicine, and much more, including death. The social factors just noted— homelessness, dilapidated homes, slum landlords—and many others have nothing to do with biology, genetics, personal choice, or access to healthcare services, but have a great deal to do with individual and public health.

 

 

138 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

▸ Introduction

Disparities in health and health care are a sys-temic and deeply challenging problem in the United States (Smedley, Stith, & Nelson, 2003). While related, the two terms have different meanings. A health disparity exists when one popula- tion group experiences a higher burden of disability or illness relative to another group; a healthcare dispar- ity, by contrast, tends to denote differences in access to healthcare services or health insurance, or in the quality of care actually received (Kaiser Family Foun- dation, 2012). What makes both types of disparities so invidious—and a major social justice concern—is that they can exist even when patient needs or treatment recommendations do not differ across populations (Hoffman, Trawalter, Axt, & Oliver, 2016). As long as these disparities exist, a society cannot achieve what is known as health equity—a situation in which every- one has the opportunity to attain his or her full health potential.

Many different factors can contribute to health and healthcare disparities. Individual behaviors, healthcare provider bias, cultural expectations and differences, the location and financing of healthcare systems, social factors, and more can all be contrib- utors. Furthermore, health and healthcare disparities appear through many different lenses; researchers have documented disparities based on race, ethnic- ity, socioeconomic status, age, geography, language, gender, disability status, citizenship status, and sexual identity and orientation.

In 2010 the U.S. Department of Health and Human Services developed a series of strategies and goals for eliminating health disparities based on race and eth- nicity (National Partnership for Action, n.d.) and, as described most prominently in the Health Reform in the United States chapter, the Affordable Care Act (ACA) includes many provisions aimed at improving the health of vulnerable individuals and populations, including several programs specifically directed at reducing health disparities. In addition, many states, localities, and private organizations have agendas for combating and eliminating various types of health and healthcare disparities.

Too often overlooked in discussions about health and health disparities, however, is a striking fact about American society that both differentiates it from other developed countries and appears to deeply affect individual and population health: aside from expenditures related to the direct provision of indi- vidual healthcare  services, the United States spends far less on social services (e.g., housing and food pro- grams, support services for older adults, disability and

sickness benefits, employment programs, unemploy- ment benefits, homeless shelters, utility assistance programs) than do other developed countries. For every $1 spent on health care, the United States ded- icates approximately $0.90 to other social services; in the 33 other Organisation for Economic Co- operation and Development countries (a multinational organi- zation, of which the United States is a member, that strives to fight poverty and achieve economic growth and employment in member countries), the typical spending ratio is $1 on health care to $2 on other social services. As it turns out, the latter ratio is sig- nificantly associated with better health outcomes, including less infant mortality, less premature death, longer life expectancy, and fewer low-birth-weight babies (Bradley, Elkins, Herrin, & Elbel, 2011). At the same time, despite spending two to three times more per capita on direct healthcare services than nearly all of our European counterparts, the United States has significantly worse health outcomes in many respects, particularly among the poorest individuals and fami- lies (Tobin-Tyler, 2012).

As evidence mounts that interventions target- ing social, economic, and environmental factors can account for sizable reductions in morbidity and mor- tality (Gostin, Jacobson, Record, & Hardcastle, 2011), healthcare payers and policymakers are increasingly aiming to tie these nonmedical interventions to new models of healthcare delivery that create economic incentives for providers to incorporate social inter- ventions into their approach to care by linking pay- ments to overall health outcomes (Bachrach, 2014); for example, “accountable care organizations,” or ACOs, are an evolving concept in which various types of healthcare providers collaborate in the pro- vision of care and accept collective accountability for the cost and quality of care delivered to a popula- tion of patients. While it will take time to implement and test these new models, early results indicate that these multifaceted approaches to health and health care can result in cost savings, higher patient satis- faction, more provider productivity, and improved employee satisfaction (Bachrach, 2014).

BOX 7-2 Discussion Questions

Do you think trying to achieve wide-scale health equity is a laudable goal? Why or why not? If yes, what do you think are the keys to achieving it? And what about people who are given the opportunity to achieve optimal health but do not take advantage of it; should they face consequences of some sort?

 

 

Social Determinants of Health 139

▸ Social Determinants of Health Defining Social Determinants of Health According to the federal Centers for Disease Control and Prevention (CDC), determinants of health are “factors that contribute to a person’s current state of health” (2013). Included within this broad category are biologic factors (e.g., carrying a genetic mutation that could increase one’s chances of developing a particular disease, such as sickle cell anemia), psychosocial fac- tors (e.g., conflicts within one’s family that may lead to stress, anger, and/or depression), behavioral factors (e.g., alcohol/drug use, smoking, unprotected sex), and finally, social factors. Social determinants of health (SDH), broadly speaking, are the social conditions into which people are born and that affect their daily lives and overall well-being as they move through the various stages of life. The World Health Organization (WHO) defines SDH as “the conditions in which people are born, grow, live, work and age” (2018), and the CDC notes that SDH are shaped by the distribution of money, power, and resources at both local and national levels.

Resources that enhance the quality of one’s life— such as the availability of healthy foods, access to edu- cation, and an environment free of toxins—all shape individual and population health. These and many other SDH are transient across the life cycle, with some social determinants becoming more pertinent depend- ing on one’s stage of life. For example, proximity to a high-quality school would be more meaningful for a child, while one’s actual education level would be more significant to an adult who is either seeking work or to increase his or her income to better support his or her family. Social determinants include factors that may have led to an individual’s disadvantaged state to begin with—institutional racism, exposure to crime and vio- lence, a lack of available community-based resources, and many other factors can all be health harming.

As you have likely gleaned already, social factors that influence health cover a wide swath of topics and life events, many of which remain outside the control of individuals and populations affected by them. As a result, it is not always easy to define exactly what role SDH—whether one individual social factor, or many at once—play in shaping health. Researchers have for decades explored such questions as these: Why are some populations more predisposed than others to develop and suffer from certain ailments? Why do dif- ferences persist in healthcare quality among racial and ethnic groups? Why do people in low-income fami- lies sometimes experience lower-quality care com- pared to high-income families? Why do studies show incremental improvements in health as one rises in

social status? In some capacity, it is likely that social factors are at play in all of these situations, but defin- ing their role is a challenge. Before delving into some of the more specific research findings concerning the health effects of certain social factors, let’s take a more detailed look at some different types of SDH.

Types of SDH The Healthy People 2020 Initiative lists many differ- ent examples of SDH (U.S. Department of Health and Human Services, 2018). We summarize several of them here to provide context for the discussion that follows.

■ Access to high-quality educational opportu- nities: Individuals with access to consistent, high-quality educational opportunities are more likely to obtain higher-income jobs, and comple- tion of undergraduate and graduate studies affords a sheer greater number of these higher-paying opportunities. Many middle and high schools in low-income areas, however, have high dropout rates or do not adequately prepare students for higher education, and many of these areas do not have adequate access to job training resources for those seeking training in a vocation, which can provide a path to a well-paying career in the absence of a 4-year college degree. Furthermore, many low-paying positions do not offer health insurance as a job benefit, making it all the more difficult for individuals in these positions to access routine and specialty physician services. Overall, educational attainment and corresponding income levels tend to be strong predictors of individual and population health. From an early age, educational attainment and income provide valuable resources that protect individuals against stressors that tend to lead to health complications later in life.

■ Access to medical care services: Individuals who do not live close to medical care providers (e.g., primary care doctors, clinics, hospitals) are less likely to see a physician regularly and will often seek care only in emergencies, eschewing preven- tive care. Access is also not just about geography— it entails affordability as well. People who do not receive health insurance coverage as a job-related benefit and cannot purchase it on their own can forgo seeing a doctor for several years before pre- senting to the emergency department for an acute problem, which can possibly lead to a lengthy hos- pitalization and/or decreased quality of life.

■ Access to social media and other technologies (e.g., the Internet, cell phones): The Internet and cell phones are becoming increasingly use- ful in individual and population health, from

 

 

140 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

appointment time reminders, to learning more about one’s symptoms and diagnoses, to buying insurance through state exchanges established under the ACA, to finding providers who are accepting new patients. In addition, many peo- ple connect to support groups or other valuable health-related resources through the Internet, and providers are increasingly making health records available via Internet portals.

■ Availability of community-based resources and opportunities for recreational activities: Community-based resources can connect resi- dents to local health providers and recreational/ physical activities, both of which increase the like- lihood that people will lead healthier lives overall. The absence of leisurely activities in one’s life can lead to increased stress, which in turn is associ- ated with poorer health outcomes overall.

■ Availability of resources to meet daily needs (e.g., access to local food markets): The further an indi- vidual lives from a grocery store that offers healthy food options, like fruits and vegetables, the more likely it is that the individual will consume fast foods or other relatively unhealthy options. Geographic areas that have no or few healthy food options are referred to as “food deserts.” Food deserts tend to be identified based on their shortages of whole food providers and their abundance of “quick marts” and fast-food establishments that stock processed, sugar-heavy, and fat-laden foods that contribute to a poor diet and can lead to higher levels of obesity and other diet-related diseases, such as diabetes and heart disease. Due to the enormous individual and public health effects of food deserts, the U.S. Depart- ment of Agriculture has developed a map of the nation’s food deserts and many resources aimed at reducing their number (2017).

■ Culture: By way of example, some cultures rely heavily on time-honored approaches to illness, such as teas and other homemade remedies. While these can be effective, some commonly ingested herbals can in fact be quite dangerous when taken in conjunction with other regularly prescribed medications; for example, St. John’s wort—a plant that is used for medicinal purposes in this country and many others—can have drastic effects when taken alongside certain antidepressant medica- tions. So while traditions can have important pos- itive effects in treating illness, cultural norms can also impact health in unseen ways.

■ Language/literacy: If adequate translation and interpretation services are not in place in health- care facilities, foreign language–speaking patients may be discouraged from seeking out care. Even

when they do, many patients struggle to under- stand clinicians and medication or other treat- ment protocols.

■ Public safety: Individuals who live in dangerous neighborhoods tend to remain indoors, which can close off opportunities for exercise and social interaction. People who must pass through a dangerous neighborhood in order to reach pub- lic transportation often have to make a choice between their own safety and attending work or a doctor’s appointment. Furthermore, alcohol, drugs, violence, and the adverse health outcomes associated with them tend to be more prevalent in relatively unsafe neighborhoods.

■ Residential segregation: Physicians may preferen- tially set up their practices in locations dominated by certain demographics. As a result, some patient populations—often minority and low-income populations—suffer from a lack of healthcare facil- ities and resources in their neighborhoods, a par- ticularly strident problem in rural areas.

■ Social norms and attitudes (e.g., discrimination, racism, distrust of government): Discrimina- tory attitudes remain a cause of health disparities (Tobin-Tyler & Teitelbaum, 2019). Multiple stud- ies have shown that physicians are more likely to recommend medical best practices based on race, gender, and age (Schulman et al., 1999; van Ryn, Burgess, Malat, & Griffin, 2006). These studies demonstrate that bias (unconscious or otherwise) in physicians and other health professionals still plays a significant role in how patients of certain races, ethnicities, social statuses, and education levels are treated. Patient attitudes about the medical pro- fessions can also affect health. The most infamous example of discriminatory practice creating nega- tive patient attitudes toward the medical commu- nity stems from the Tuskegee syphilis experiment. In this experiment, hundreds of syphilis-infected, African American men in rural Alabama were used as unwitting research subjects by the U.S. Public Health Service, which wanted to study untreated syphilis in humans. The men were given free med- ical care but were never told they had the disease, nor were any of them treated with penicillin once it became the accepted course of treatment for syphi- lis. The study lasted a stunning 40 years, from 1932– 1972, and has affected the attitudes and healthcare decisions of many African Americans ever since. In 1997 President Bill Clinton issued a formal apology for the Tuskegee Study, but government healthcare programs have been hard-pressed to earn back the trust of millions of patients that was shattered once the study was revealed.a

 

 

Social Determinants of Health 141

■ Socioeconomic conditions (e.g., concentrated poverty and the stressful conditions that accom- pany it): While the link between poverty and poor health is discussed below, suffice it to say here that the connection between the two is well docu- mented and undeniable, and the health effects of extreme financial hardship in childhood can be lifelong even in the event that people eventually escape poverty. A similar phenomenon, though with far different health effects, can be seen at the other end of the socioeconomic spectrum: greater wealth correlates with lower rates of morbidity and longer life spans.

■ Transportation options: Many individuals miss medical appointments because they cannot afford private transportation and live long distances from reliable public transportation. It is common for patients without their own cars to spend hours on buses in an effort to reach medical appointments.

The Link Between Social Determinants and Health Outcomes While it is well beyond the scope of this chapter to provide a full discussion of the myriad ways in which social factors play important roles in individual and population health, we provide in this section a flavor of the types of links that researchers have drawn in this respect. We note at the outset that these links are not usually linear and directly causative: social deter- minants do not usually act alone or in “‘simple addi- tive fashion,’ but rather in concert with one another in complex, interdependent, bidirectional relationships” (McGovern, Miller, & Hughes-Cromwick, 2014, p. 3). Indeed, “most diseases and injuries have multiple potential causes and several factors and conditions may contribute to a single death. Therefore, it is a challenge to estimate the contribution of each factor to mortality” (Mokdad, Marks, Stroup, & Gerberding, 2004, p. 1238). That said, “the overwhelming weight of evidence demonstrates the powerful effects of socio- economic and related social factors on health, even

when definitive knowledge of specific mechanisms and effective interventions is limited” (Braveman & Gottlieb, 2014, p. 22).

Links can be drawn between social determi- nants and both physical and mental health. Among many examples on the physical health front, research indicates that while half of all deaths in the United States involve behavioral causes (McGinnis & Foege, 1993), evidence shows that health-related behav- iors are strongly shaped by three important social factors: income, education level, and employment (Braveman, Egerter, & Barclay, 2011; Stringhini, et al., 2010). Another study concluded that the num- ber of U.S. deaths in 2000 attributable to low educa- tion, racial segregation, and low social support was comparable with the number of deaths attributable to heart attack, cerebrovascular disease, and lung cancer, respectively (Galea, Tracy, Hoggatt, DiMag- gio, & Karpati, 2011). The CDC has regularly found that individuals among the lowest levels of income and education suffered the greatest age-adjusted prevalence and incidence rate of diagnosed diabe- tes (CDC, 2013). Similarly, associations have been demonstrated between lower socioeconomic status and increased prevalence of disease, morbidity, and mortality in persons with arthritis and rheumatic conditions (Callahan et al., 2011).

Access to safe, quality, affordable housing rep- resents one of the most influential SDH. Indeed, for individuals and families trapped in a cycle of housing instability, this determinant can almost completely dictate their ability to achieve and maintain a healthful state (Corporation for Supportive Housing, 2014). Sev- eral studies demonstrate that linking healthcare man- agement to supportive housing—an evidence-based practice that combines permanent affordable housing with relevant support services—leads to improved health outcomes. For example, a study out of Denver, Colorado, found that 50% of supportive housing res- idents experienced improved health status, 43% had better mental health outcomes, and 15% reduced sub- stance use (Perlman & Parvensky, 2006).

Regardless of income or housing cost, living in a predominately minority neighborhood increases the likelihood of having poor access to healthy food choices (Jack, Jack, & Hayes, 2012). For example, one study found that African American urban neighbor- hoods have only 41% of the chain supermarkets found in comparable white neighborhoods (Powell, Slater, Mirtcheva, Bao, & Chaloupka, 2007), and minority neighborhoods have an overabundance of fast-food restaurants known for relatively inexpensive but unhealthful food options (Fleischhacker, Evenson, Rodriguez, & Ammerman, 2011).

BOX 7-3 Group Activity

Each student should begin by rank-ordering a list of the half-dozen social determinants (from those listed in this chapter or otherwise; broad or specific) that he or she believes most significantly affect individual health. Then get together in groups of three or four people to compare lists, discussing disagreements and making the case for some determinants over others.

 

 

142 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

As noted, social determinants play a significant role in mental health outcomes, as well. Emotional stressors—such as neighborhood violence, poverty, or familial abuse—during key developmental years in childhood can lead to severe consequences later in life. For example, several studies have been con- ducted regarding the mental health outcomes of chil- dren who have been subject to abuse, including one showing that survivors of childhood sexual abuse have higher levels of both general distress and major psychological disturbances, including personality disorders (Schneiderman, Ironson, & Siegel, 2005). One particularly fascinating but worrisome study demonstrated that the brains of children in low- income families actually had less surface area than did the brains of children from families who were wealthier—specifically, 6% less surface area in chil- dren whose families made less than $25,000 a year compared with children whose families made more than $150,000 (Layton, 2015). One theory behind this finding was that children from poor fami- lies tend to be malnourished and have less access to high-quality education than their richer peers. Another theory proposed that poorer families tend to lead more chaotic lives, which can inhibit brain development in children.

▸ Law as a Social Determinant of Health

Up to this point, we’ve described generally various types of SDH and some correlations between those determinants and the health of people who live in communities in which SDH may be relatively more compromised. We turn now to a more nuanced discus- sion of one very influential SDH: the law. Throughout the nation’s history, law has played an integral role in causing, exacerbating, and alleviating health- harming social conditions, from the legally sanctioned, racially segregated—and horribly unequal—medical care sys- tems used during slavery time, to the expansion of building codes in the 1920s, to the War on Poverty legislation of the 1960s, to the ACA’s focus on health equity. Because the law’s reach in this regard is so expansive, we provide only an overview for purposes of this chapter.

Whether embodied in constitutions, statutes, reg- ulations, executive orders, administrative agency deci- sions, or court decisions, the law plays a profound role in shaping life circumstances and, in turn, health. The ways in which this occurs can be broken down into five categories.

1. The law can be used to design and per- petuate social conditions that can have terrible physical, mental, and emotional effects on individuals and populations. One obvious example in this category is the “separate but equal” constitutional doctrine that allowed racial segregation in hous- ing, health care, education, employment, transportation, and more. Indeed, injus- tices in healthcare access and quality were commonplace in the United States prior to the civil rights movement. Racially seg- regated health care dates to slavery times, when plantations had on-site facilities to care for slave laborers. After the slaves were freed but also after the First Reconstruction ended in the late 1870s, Jim Crow laws ush- ered in a new era of discriminatory health- care access and delivery through separate hospitals and physician practices; separate medical, nursing, and dental schools; and separate professional medical societies. For example, Alabama once had a law that stated: “No person or corporation shall require any White female nurse to nurse in wards or rooms in hospitals, either public or private, in which Negro men are placed” (Ferris State University, 2012).

2. The law can be used as a mechanism through which behaviors and prejudices are transformed into distributions of well-being among populations. By way of example, although black and white people use illicit drugs at approximately the same rate, drug crime incarceration rates are far higher for black people. Thus, who is cho- sen for surveillance and arrest, and how the arrested are selected for either punishment or treatment, turns out to be an important driver of how a supposedly neutral law dif- ferentially impacts people and communi- ties, and in turn their health (Burris, 2011). Healthcare provider discrimination and bias reside in this category, as well. Health- care discrimination and bias can take many forms: it can be based on race, ethnicity, disability, age, gender, and class (or socio- economic status). Class-related healthcare discrimination alone can take multiple forms. For example, some healthcare pro- viders might refuse to accept as patients individuals who are covered under Medic- aid (because the Medicaid population tends

 

 

Law as a Social Determinant of Health 143

to be disproportionately poor and of color), or low-income individuals might fall victim to the practice of redlining, which refers to situations in which healthcare entities relo- cate from poor neighborhoods to wealthier ones (Yearby, 2013).

3. Laws can be determinative of health through their under-enforcement. For example, a perfectly good set of housing regulations aimed at keeping housing units safe, clean, and quiet are of little value to individual and group health if there is nei- ther the will, nor the resources, to enforce them. Substandard housing conditions, including the presence of rodents, mold, peeling lead paint, exposed wires, and insufficient heat—all of which are common among low-income housing units—can cause or exacerbate asthma, skin rashes, lead poisoning, fires, and common illnesses, yet none of these housing problems can be “cured” by a clinical encounter. While their consequences can be treated medically, the causes require robust enforcement of exist- ing laws (Tobin-Tyler, Lawton, Conroy, Sandel, & Zuckerman, 2011).

4. Laws can be determinative of health through their interpretation. In 2012, the U.S. Supreme Court was asked by half the states in the country to rule on whether the Medicaid expansion in the ACA was unlawfully coercive (National Federation of Independent Business v. Sebelius, 2012; note that this decision is discussed in more detail in the Health Reform in the United States chapter). As originally passed into law, the ACA permitted the secretary of the U.S. Department of Health and Human Ser- vices to terminate all of a state’s Medicaid funding if the state failed to implement the Medicaid expansion—even those Medicaid funds that a state would receive that were unconnected to the expansion. While deter- mining that the Medicaid expansion itself was perfectly legitimate, the court ruled that Congress unconstitutionally forced states to potentially have to choose between the Medicaid expansion and a total loss of Medicaid funding. This ruling had the effect of making the ACA’s Medicaid expansion optional, rather than mandatory, and states have been deciding individually whether to implement the expansion ever since. At the

time of this writing, 33 states and the Dis- trict of Columbia have adopted the ACA’s Medicaid expansion, while 17  states have not; thus, the court’s interpretation of a stat- ute has contributed to the fact that other- wise eligible individuals in “non- expansion states” do not have access to Medicaid ben- efits in the same way that individuals in “expansion states” do.

5. Finally, the law can be used to structure direct responses to health-harming social needs that result from factors like impov- erishment, illness, market failure, and individual behavior that harms others. For example, the Emergency Medical Treatment and Active Labor Act (EMTALA) requires Medicare-participating hospitals to provide needed stabilization services to individuals who have an emergent condition. Notably, EMTALA’s requirements are universal— meaning they have to be fulfilled by hospi- tals irrespective of the presenting patient’s socioeconomic or insurance status—and were written into law because many private hospitals had long turned away emergent patients who were uninsured and could not pay out-of-pocket for their care.

Many financing laws that subsidize healthcare services for vulnerable popula- tions also fit into this category. Medicaid is an obvious example, and the Public Health Service Act includes funding for commu- nity health centers, persons with HIV/ AIDS, persons with mental illness or sub- stance abuse disorders, and project grants to provide preventive and immunization services, and breast and cervical cancer screening and detection. Title VI of the 1964 Civil Rights Act prohibits discrimina- tion on the basis of race, color, or national origin by any recipient of federal financing, including healthcare providers and facil- ities. Finally, public health departments funded under state and local legal authority provide primary and preventive healthcare services, such as childhood immunizations, to underserved populations. Programs such as the National Health Service Corps (NHSC) and the Indian Health Service (IHS) were established under federal law to address the lack of providers in rural and other underserved areas. The NHSC was founded in order to incentivize graduates

 

 

144 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

of medical school and other health profes- sions programs to practice primary care in underserved areas, because starting in the 1950s medical graduates began gravitating in large numbers to large cities to practice a medical specialty. The IHS is the princi- pal federal healthcare provider and health advocate for Indian people, providing com- prehensive health services to approximately 1.9 million American Indians and Alaska Natives.

Furthermore, through their police powers, states directly regulate individual and corporate behavior in order to protect and promote the public’s health. For exam- ple, states regulate the food supply and food establishments, enforce occupational safety rules, curb pollution, control the sale of firearms, restrict the marketing of tobacco products, and accredit healthcare profes- sionals and facilities. Indeed, at the local, state, and federal levels, the law has played important roles in all of the 10 most note- worthy public health achievements of the 20th century, as selected by the CDC (1999): control of infectious diseases, motor vehi- cle safety, fluoridation of drinking water, tobacco use control, vaccinations, decline in deaths due to coronary heart disease and stroke, food safety, improvements in mater- nal and child health, family planning, and safer workplaces.

Taken together, the preceding discussion illus- trates how using law to achieve better health is well suited to what is called a “health in all policies” (HIAP) strategy. This strategy is based on the recogni- tion that several pressing health-related challenges— inequities, chronic disease, skyrocketing costs, the need for insurance reform, and so on—are often com- plex, multidimensional, and linked to one another. As a result, HIAP relies on a collaborative govern- mental (and sometimes nongovernmental) approach to health improvement by incorporating health con- siderations into an array of policy decisions, and by engaging governments and other stakeholders in a multisector approach to shaping the economic, phys- ical, and social environments in which people live, work, and play.

In thinking about how law could be used to foster a HIAP approach, consider the number of rule-making departments and agencies at just the federal level that can (and do) serve healthcare and public health functions even though they are not

commonly identified as health agencies. The Envi- ronmental Protection Agency plays an obviously important role in environmental health. Reducing injuries and hazards in the workplace is the key goal of the Occupational Safety and Health Administra- tion, which is part of the Department of Labor. The Department of Homeland Security protects health when it prepares for and responds to disasters and terrorism. The Department of Agriculture (along with the Food and Drug Administration) plays an important role in the protection of the nation’s food supply. The Department of Housing and Urban Development influences the built environment, which in turn influences health. The Department of Energy sets radiation safety standards for nuclear power plants and other sources of energy. Again, these are just federal agencies, and they are all part of the executive branch of government; legislative branch committees at the federal, state, and local levels that are also not typically considered “health” committees could also craft legislation with a HIAP approach in mind. The involvement of multiple branches and agencies in health-related matters plainly shows that the variety of influences impact- ing individual and population health are outside the control of the health sector alone.

Right to Criminal Legal Representation vs. Civil Legal Assistance Appreciating the law’s power to ameliorate social conditions that negatively affect health requires an understanding of the difference between using law to design broad policies (e.g., Title VI of the Civil Rights Act, firearm regulations, federal housing pol- icy, the ACA) and leveraging the legal system as an individual who is aiming to redress his or her own hardship. In the case of the latter, it helps to under- stand the difference between rights that attach in the area of criminal legal representation versus those that

BOX 7-4 Group Activity

Get together in groups of three or four people. As a group, take 20 minutes to make a list of all the specific ways you can think of that the law has been used to directly respond to health-harming social needs (examples exist in category 5 in this section). When time is up, compare lists across groups, discuss disagreements, and see which group thought of the greatest number of legal interventions.

 

 

Law as a Social Determinant of Health 145

exist in the realm of civil legal assistance, because it is through civil legal assistance that many types of SDH can been ameliorated.

Criminal Legal Representation The government is required to provide legal counsel to all federal defendants who are unable to afford their own attorneys; this right is explicit in the Sixth Amend- ment to the U.S. Constitution. The right to counsel in state criminal prosecutions was established by the U.S. Supreme Court (though only for serious offences) in the famous 1963 case of Gideon v. Wainwright. The case arose out of an everyday burglary at a Florida pool hall, for which Clarence Earl Gideon was arrested not- withstanding the flimsy evidence against him. Because Gideon was indigent and could not afford private coun- sel, he appeared in court alone. He requested counsel but was denied, and as a result acted as his own lawyer at trial. A jury found him guilty and the Florida trial court sentenced Gideon to serve 5 years in state prison.

From prison, Gideon appealed his conviction to the U.S. Supreme Court, arguing that his constitutional rights had been violated when he was denied counsel. The Supreme Court agreed to hear Gideon’s constitu- tional claim and assigned him a well-known lawyer, Abe Fortas, who himself would one day become a U.S. Supreme Court Justice. Building on previous right to counsel cases (for example, in the event of a state prosecution where the death penalty was sought), the court ruled that the assistance of counsel, if desired by an indigent defendant, was a fundamental right under the U.S. Constitution that was required in state prosecutions of serious crimes. Gideon received a new trial and—with the assistance of a lawyer supplied at government expense—was acquitted of all charges just 5 months after the Supreme Court’s ruling.

The decision in Gideon v. Wainwright spawned many changes in the representation of indigent crim- inal defendants, including in misdemeanor and juve- nile proceedings. The decision effectively created the need for public defenders (lawyers employed at public expense in criminal trials), and it lies at the heart of a series of cases dealing not only with legal representa- tion at trial and on appeal, but also with police interro- gation tactics and the right to remain silent.

Civil Legal Assistance While the right to legal representation exists in crim- inal matters, no such right exists on the other side of the legal ledger: there is no right to the assistance of a lawyer in civil matters, even when the most basic human needs are at stake. Common civil legal

matters involve immigration status, domestic vio- lence, disability law, family law (e.g., child custody cases), housing needs, public benefits (e.g., Medicaid, food stamps, Social Security), employment disputes, and special education needs. In all of these types of disputes—which can be incredibly complex from a legal perspective and which can have life-altering consequences—low-income individuals and families can have no expectation that an attorney will pro- vide them with assistance. (We should note, however, that under some state laws individuals have a right to counsel in limited civil situations, such as with the termination of parental rights or involuntary com- mitments to mental health facilities.) In civil matters, indigent people (and, increasingly, more members of the middle class and a rising number of small busi- nesses who cannot afford legal fees)b can apply for what is known as civil legal aid or civil legal services, which are provided by a network of publicly funded legal aid agencies, private lawyers and law firms prac- ticing on a pro bono basis, law school clinics and professional organizations (the latter group includes organizations such as the American Bar Association, the National Legal Aid and Defender Association, and the American Bar Foundation).

This network is the heart and soul of what is termed the access to justice movement, which pro- motes strategies to address the severe gap in access to both criminal and civil justice for low-income and other vulnerable populations.c One of the goals of this movement is to establish a “civil Gideon”—in other words, to create a mandate for legal representation of the poor in civil lawsuits. For example, the American Bar Association’s House of Delegates passed in 2006 a resolution backing the concept of “civil Gideon”:

RESOLVED, That the American Bar Associa- tion urges state, territorial and federal jurisdic- tions to provide counsel as a matter of right at public expense to low-income persons in those categories of adversarial proceedings where basic human needs are at stake, such as those involving shelter, sustenance, safety, health or child custody, as determined by each jurisdic- tion.d (American Bar Association, 2006)

Because the combined resources of the civil legal services community are very limited, services are approved on the basis of financial need, meaning that only those individuals with very low incomes receive assistance. Indeed, reports on the legal aid community routinely describe situations in which 80% of civil legal needs for low-income families were not being met, and legal services programs typically turn away over half of

 

 

146 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

the low-income individuals that seek assistance. Con- gress is most to blame for legal aid’s financial predic- ament; it provides the vast majority of the budget for the Legal Services Corporation (LSC), a not-for-profit corporation established by federal law in 1974 as the single largest funder of civil legal aid for low-income Americans. Considering LSC’s annual appropriations from Congress in constant 2015 dollars, its appro- priation in 1976 was approximately $386 million; in 2015, its appropriation was $375 million (Legal Ser- vices Corporation, 2015).e So even as need has soared over time—the U.S. Census Bureau’s 2012 statistics on poverty show that over 63 million Americans could qualify for civil legal assistance funded by LSC—the key element of legal aid funding has been treated as an afterthought (Legal Services Corporation, 2018).

The link between civil legal assistance and indi- vidual and population health is exemplified by a study of the civil justice experiences of the American public, called the Community Needs and Services Study (San- defur, 2014). The study uncovers widespread incidence of events and situations that have civil legal aspects and for which people receive no formal or expert legal assistance: fully two-thirds of a random sample of adults in a middle-sized American city reported experiencing at least one of 12 different categories of civil justice situations in the previous 18 months (the average number of situations reported was 3.3, and poor people, African Americans, and Hispanics were more likely to report civil justice situations than were middle- or high-income earners and white peo- ple). Unsurprisingly, the most commonly reported situations concerned problems with employment, finances and government benefits, health insurance, and housing. Importantly, respondents indicated that almost half of the civil justice situations they experi- enced resulted in a significant negative consequence such as feelings of fear, a loss of confidence, damage to physical or mental health, or verbal or physical vio- lence or threats of violence. In fact, adverse impacts on health were the most common negative consequence, reported for 27% of situations. Also important is the fact many of those who responded indicated that they didn’t even know that the problems they were experi- encing were rightly considered “legal” in nature.

For all of the reasons just discussed—the lack of a right to needed civil legal services, the misunder- standings among those most in need, and the lack of resources in the civil legal aid community—it is paramount that the nation develop and implement innovative, upstream approaches to addressing social conditions that harm health. One such innovation that has taken root is medical-legal partnership.

▸ Combating Health-Harming Social Conditions Through Medical-Legal Partnershipf

“Do you have any concerns about your housing con- ditions? Are you concerned about having enough food to eat? Is your child receiving proper supports at school? Do you feel safe at home?” These types of ques- tions are asked of low-income patients with regularity, and their medical care providers know well that the answers speak volumes about patients’ health. When the answers come back, however, healthcare providers are too often powerless to do as much as they would like to help remedy these “life circumstances.”

Training doctors, nurses, and allied health pro- fessionals to reframe these circumstances can help. By now, you probably recognize many of these types of determinants of health for what they are: social condi- tions whose improvement would benefit from civil legal assistance. Yet despite the connection between poverty, health, and legal needs, and despite the fact that health- care and civil legal aid professionals commonly provide services to overlapping vulnerable populations, the professions too infrequently attempt to address their populations’ needs in a coordinated fashion.

Medical-legal partnership (MLP) aims to bridge this divide. At a practical level, MLPs function as a patient care team that includes both medical and legal professionals; a legal services attorney is liter- ally embedded in a medical care setting (e.g., a hos- pital, community health center) to address underlying social conditions that negatively affect patient health but whose remediation is outside the expertise of tra- ditional healthcare providers. At a more fundamental level, the goal of the MLP movement is to help cre- ate an interconnected care system that focuses on the whole patient (rather than just on biology and behav- ior), including the ways in which myriad social con- ditions factor into individual and population health. Thus, the work of MLP lawyers is quite different from

BOX 7-5 Discussion Questions

What do you think about the differences that exist between rights that attach in the area of criminal legal representation versus those that exist in the realm of civil legal assistance? Does it seem fair to you? Why or why not? Even if you believe it is fair, do you think all individuals should have access to at least a baseline level of civil legal assistance?

 

 

147Combating Health-Harming Social Conditions Through Medical-Legal Partnership

that of a general counsel or compliance officer who normally inhabits hospitals and clinics: a general counsel typically provides legal advice to clinicians on matters of medical liability and informed consent and represents them in insurance and disciplinary matters; corporate compliance officers ensure that the facility meets all governmental, environmental, and licensing regulations.

The Evolution of an “Upstream” Innovation The modern MLP movement has its roots in the late 1960s, when visionary physicians H. Jack Geiger and Count Gibson were funded by the federal government to form the nation’s first community health centers in Mississippi and Massachusetts. The government’s community health center program grew out of the civil rights movement, when the federal Office of Economic Opportunity (the agency created to administer many of President Lyndon Johnson’s War on Poverty programs, and whose programs continue in large part to this day under the auspices of the U.S. Department of Health and Human Services) established “neighborhood health centers” to provide health and social services to medically underserved populations. In designing the earliest centers, Drs. Geiger and Gibson recognized the importance of spending some of their federal funding on lawyers, who assisted African American health cen- ter patients battling housing discrimination.

The second prominent instance of the blending of medical and legal services for low-income populations occurred in the early 1980s when, faced with devastat- ing death tolls from HIV/AIDS, some health clinics began providing on-site legal assistance to patients who needed to quickly grapple with end-of-life issues (e.g., medical decision making, asset distribution, family and custody matters). A few pioneering clinics held on to this blended model even after the national AIDS crisis abated, offering comprehensive legal ser- vices to all patients in need.

Building on these examples, the first formal MLP was created in the early 1990s in a Boston hospital to intervene on behalf of pediatric patients with chronic conditions who were suffering the consequences of inadequate housing. From that point through 2006, MLPs sprouted up a few at a time, mainly in pediatric healthcare settings, where the model had proven effec- tive in Boston. Since 2006, however, use of the MLP model has expanded considerably. Fueled by the cre- ation of the National Center for Medical-Legal Part- nership (NCMLP), the focus by social scientists on the importance of social factors in determining health, and the ACA’s focus on disease prevention and professional

collaboration, MLP is now practiced in 46  states by more than 300 hospitals and health centers, in settings as diverse as veteran care facilities, American Indian reservations, and correction facilities (National Center for Medical-Legal Partnership, 2018).

Under the MLP model, public interest lawyers work with healthcare workers to screen for health-related legal problems, often encompassing family matters (divorce, domestic violence), housing problems (eviction, hab- itability, utility advocacy), special education advocacy, immigration issues, disability issues, employment instability, receipt of public benefits (health insurance, Supplemental Security income), food security con- cerns, and additional problems that can lead to stress or injury or that can exacerbate existing health problems. FIGURE 7-1 lays out the key types of patient problems that make up the practice of a typical, comprehensive MLP, using the mnemonic “I-HELP”: Income, Housing and utilities, Education and employment, Legal status, and Personal and family stability (Marple, 2015).

The MLP approach is built on the understanding not only that many SDH require legal interventions, but that moving “upstream” to assist vulnerable populations with legal needs is preferable to waiting until a legal cri- sis erupts (for example, remediating a housing problem prior to the receipt of an eviction notice). It is similar to preventive health care: it is often more cost effective— and of course more beneficial to the patient, both physi- cally and emotionally—to help a patient remain healthy, rather than treat the patient post-illness. At MLPs, healthcare and legal professionals are trained side by side about the intersection of health and legal needs and ways to screen for health-harming legal needs. Because MLPs recognize that social determinants contributing to poor health require both health system and public pol- icy change, MLP lawyers utilize on-site legal assistance provided to patients to identify patterns of systemic need, transform institutional practices, and advocate for improved population health policies. FIGURE 7-2 portrays this upstream MLP approach. Similar to the movement to integrate behavioral healthcare services into primary care, the integration of civil legal aid with healthcare delivery can improve access to services, build team capacity, and promote patient-centered care.

MLPs have become more integrated over time, with healthcare and legal partners sharing patient and institutional data, jointly developing service and training priorities, and establishing cross-sector communication processes. The more collaboration and integration that occurs, the more likely it is that upstream detection of the social conditions that lead to poor health can occur. Deep collaboration and integration also present an opportunity for healthcare

 

 

148 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

providers and lawyers—two learned professions that, historically, have not been the closest of colleagues— to work together when policymakers design fixes for health-harming social and legal problems.

The Benefits of MLPs Due to the relatively recent growth of MLPs, the effects of the MLP model have not been regularly tested in for- mal, large-scale studies. However, several small-scale studies have been conducted (Beeson, McAllister, & Regenstein, 2013; Martinez et al., 2017) and offer pre- liminary evidence of the benefits of the model in three areas: impact on patient health and well- being, finan- cial impact on partners and patients, and impact on knowledge and training of health providers.

A handful of studies make the case for MLPs by demonstrating the positive impact they can have on patient health and well-being. One such study, focused on home visit/nurse-based interventions for

Housing & Utilities

Education & Employment

Legal Status

Income

$ $$

Personal & Family Stability

1. Less violence at home means less need for costly emergency healthcare services. 2. Stable family relationship signi�cantly reduce stress and allow for better decision-making, including decisions related to health care.

1. Clearing a person’s criminal history or helping a veteran change their discharge status helps make consistent employment and access to public bene�ts possible. 2. Consistent employment provides money for food and safe housing, which helps people avoid costly emergency healthcare services.

1. A quality education is the single greatest predicator of a person’s adult health. 2. Consistent employment helps provide money for food and safe housing, which also helps avoid costly emergency healthcare services. 3. Access to health insurance is often linked to employment.

1. A stable, decent, affordable home helps a person avoid costly emergency room visits related to homelessness. 2. Consistent housing, heat and electricity helps people follow their medical treatment plans.

1. Increasing someone’s income means s/he makes fewer trade-offs between affording food and health care, including medications. 2. Being able to afford enough healthy food helps people manage chronic diseases and helps children grow and develop.

Education & Employment Units: Secure specialized education services; Prevent and remedy employment discrimination and enforce workplace rights

Bene�ts Unit: Appeal denials of food stamps, health insurance, cash bene�ts, and disability bene�ts

Housing Unit: Secure housing subsidies; Improve substandard conditions; Prevent eviction; Protect against utility shut-off

Family Law Unit: Secure restraining order for do- mestic violence; Secure adoption, custody and guardianship for children

Veterans & Immigration Units: Resolve veteran discharge status; Clear criminal/credit histories; Assist with asylum applications

Civil Legal Aid Interventions That

Help

Availability of resource to meet daily basic needs

Access to the opportunity to learn

and work

Healthy physical environments

Access to the opportunity to work

Expose to violence

Common Social Determinant of

Health

Impact of Civil Legal Aid Intervention on Health /Health Care

I-HELP ® Issue

JOB

FIGURE 7-1 Framing Legal Care as Health Care Source: Reproduced from: Marple, K. Framing Legal Care as Health Care. National Center for Medical-Legal Partnership. http://medical-legalpartnership.org/new-messaging-guide-helps-frame-legal-care-health-care/. Published January 21, 2015. Accessed August 27, 2015.

Train & Identify Need

Treat Patients with direct legal assistance

Transform Clinic Practice through enhanced screening, toolkits, and EHR template letters

Improve Population Health through joint policy advocacy

FIGURE 7-2 The Medical-Legal Partnership Approach to the Social Determinants of Health Source: Reproduced from: The MLP Approach to the Social Determinants of Health. National Center for Medical-Legal Partnership. 2013.

 

 

Conclusion 149

prenatal and postpartum patients, demonstrated bet- ter prenatal health behaviors, better pregnancy out- comes, lower rates of child abuse and neglect, and higher rates of maternal employment among partic- ipants as a result of MLP services (Williams, Costa, Odunlami, & Mohammed, 2008). A second study found a 91% reduction in emergency department visits and hospital admissions of inner-city asthmatic adults after a medical-legal intervention. In the same study, over 91% of patients also dropped two or more classes in asthma severity (O’Sullivan et al., 2012). Another study focused on cancer patients in an MLP showed a reduction in stress for 75% of the patients, an increase in treatment adherence for 30% of them, and greater ease in keeping appointments for 25% of patients (Fleishman, Retkin, Brandfield, & Braun, 2006). Yet another study showed that by redressing complex social issues through legal advocacy, patients experienced less stress, improved access to preventive health care, and a greater feeling of general well-being (Wang, Conroy, & Zuckerman, 2009).

Several MLP studies have focused on the financial benefits of the model—in other words, on the “return on investment” that accrues to institutions that invest in an MLP. One such study found that an MLP tar- geting the needs of cancer patients generated nearly $1 million by resolving previously denied health insur- ance benefit claims (Rodabaugh, Hammond, Myszka, & Sandel, 2013). Similarly, a separate study highlighted four MLP programs, each of which demonstrated suc- cessful recovery of previously unreimbursed funds as a result of improperly denied Medicaid or Social Security Disability claims (Knight, 2008). More strik- ing still is evidence of the financial impact that MLPs could have on patients: an MLP in Illinois helped to relieve $4 million in patients’ healthcare debt, and claimed $2 million in additional awarded Social Secu- rity benefits for patients (Teufel et al., 2012).

Finally, multiple articles have addressed how MLPs can benefit practitioners and patients alike through interdisciplinary training and education. One article, focused on strategies for teaching cultural compe- tence, interdisciplinary practice, and holistic problem solving in legal and medical curricula, describes a legal clinic that increased knowledge about avenues of legal assistance among doctors and of the clinical impact of SDH among lawyers (Tobin-Tyler, 2008). A sec- ond paper describes how medical residents working in clinics with social/legal resources were more con- fident in their knowledge regarding public benefits, and how these same residents were more likely than residents without these resources to ask patients about their social history, use of public benefits, and hous- ing situation (O’Toole, Burkhardt, Solan, Vaughn, &

Klein, 2012). Finally, medical residents who had social work or MLP resources on-site were more confident regarding their personal knowledge of SDH, and as a result were found to screen for them more frequently than other residents (O’Toole et al., 2012).

▸ Conclusion Recall from the start of this chapter the concept of health equity—essentially, an environment in which all people have an equal opportunity to attain their full health potential. While the nation is far from achiev- ing a state of health equity, it should be everyone’s goal to orient society in this direction, even if incremen- tally. More evidence of whether this is in fact the case will come in a few years, when it will be clearer as to whether most Americans accept the ACA’s main goals as ones worth striving for. (Note one final time the law’s role as social determinant of health: should the ACA achieve near-complete implementation—and public acceptance along the lines of, say, the Medicare program—the nation, in our view, will be healthier than if the ACA continues to be subjected to politi- cal and legal attacks, and to implementation battles in more than a dozen states.)

Whether the nation strives for full health equity aggressively or half-heartedly, there is little doubt that increasing our collective focus on the link between social factors and health would benefit millions of individuals and, in turn, the public more generally. Considering that American children, in particular, experience a high prevalence of social conditions that compromise their care and development— including insufficient family income to meet basic living needs, food insecurity, unstable housing, environmental toxins, and a lack of high-quality child care—this type of reorientation is nothing less than a moral imperative (Miller, Sadegh-Nobari, & Lillie-Blanton, 2011).

One facet of this transformation is reframing civil legal services for vulnerable populations as a critical component of health care. Civil legal aid, after all, is first and foremost about promoting the enforce- ment of existing laws that protect vulnerable popu- lations (Houseman, 2015). If health is at the core of well-being for all people, then reducing barriers to good health should be an obvious societal goal, and for low-income and other vulnerable populations this means reducing the health-harming effects of social conditions that they struggle with disproportionately. To address this inequality, the civil legal community should closely align its activities and priorities with healthcare and public health partners.

 

 

150 Chapter 7 Social Determinants of Health and the Role of Law in Optimizing Health

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Bronner, E. (2013, March 15). Right to lawyer can be empty promise for poor. The New York Times. Retrieved from https:// www.nytimes.com/2013/03/16/us/16gideon.html

Burris, S. (2011). Law in a social determinants strategy: A public health law research perspective. Public Health Reporter, 126(supp. 3), 22–27.

Callahan, L. F., Martin, K. R., Shreffler, J., Kumar, D., Schoster, B., Kaufman, J., & Schwartz, T. (2011). Independent and combined influence of homeownership, occupation, education, income and community poverty on physical health in persons with arthritis. Arthritis Care & Research, 63(5).

Centers for Disease Control and Prevention. (1999). Ten great public health achievements—United States, 1900–1999. Morbidity and Mortality Weekly Report, 48(12), 241–243.

Centers for Disease Control and Prevention. (2013). CDC health disparities and inequalities report. Morbidity and Mortality Weekly Report, 62(supp. 3), 1–187.

Corporation for Supportive Housing. (2014). Housing is the best medicine: Supportive housing and the social determinants of health. Retrieved from https://www.csh.org/wp-content /uploads/2014/07/SocialDeterminantsofHealth_2014.pdf

Ferris State University. (2012). What was Jim Crow. Retrieved from http://www.ferris.edu/jimcrow/what.htm

Fleischhacker, S. E., Evenson, K. R., Rodriguez, D. A., & Ammerman, A. S. (2011). A systematic review of fast food access studies. Obesity Review, 12(5), e460–e471.

Fleishman, S. B., Retkin, R., Brandfield, J., & Braun, V. (2006). The attorney as the newest member of the cancer treatment team. Journal of Clinical Oncology, 24(13), 2123–2126.

Galea, S., Tracy, M., Hoggatt, K. J., DiMaggio, C., & Karpati, A. (2011). Estimated deaths attributable to social factors in the United States. American Journal of Public Health, 101(8), 1456–1465.

Gideon v. Wainwright, 372 U.S. 335 (1963). Gostin, L. O., Jacobson, P. D., Record, K., & Hardcastle, L. (2011).

Restoring health to health reform: Integrating medicine and public health to advance the population’s well-being. University of Pennsylvania Law Review, 159, 1777–1823.

Hoffman, K. W., Trawalter, S., Axt, J. R., & Oliver, M. N. (2016). Racial bias in pain assessment and treatment

recommendations, and false beliefs about biological differences between blacks and whites. Proceedings of the National Academy of Sciences, 113(6), 4296–4301.

Houseman, A. (2015). Civil legal aid in the United States: An update for 2015. Retrieved from https://repository.library .georgetown.edu/bitstream/handle/10822/761858/Houseman _Civil_Legal_Aid_US_2015.pdf

Jack, L., Jack, N. H., & Hayes, S. C. (2012). Social determinants of health in minority populations: A call for multidisciplinary approaches to eliminate diabetes-related health disparities. Diabetes Spectrum, 25(1), 9–13.

Jones, J. H. (1993). Bad blood: The Tuskegee syphilis experiment. New York, NY: The Free Press.

Kaiser Family Foundation. (2012). Disparities in health and health care: Five key questions and answers. Retrieved from https:// kaiserfamilyfoundation.files.wordpress.com/2012/11/8396 -disparities-in-health-and-health-care-five-key-questions -and-answers.pdf

Knight, R. (2008). Health care recovery dollars: A sustainable strategy for medical-legal partnerships? Retrieved from https:// static1.squarespace.com/static/5373b088e4b02899e91e9392 /t/53cd59cae4b02facb9407e39/1405966794425/Medical-Legal +Partnership+Health+Care+Recovery+Dollars.pdf

Layton, L. (2015, April 15). New brain science shows poor kids have smaller brains than affluent kids. The Washington Post. Retrieved from http://www.washingtonpost.com/local / e du c at i on / ne w – br ai n – s c i e nc e – show s – p o or- k i d s – h ave -smaller-brains-than-affluent-kids/2015/04/15/3b679858 -e2bc-11e4-b510-962fcfabc310_story.html

Legal Services Corporation. (2015). Congressional appropriations. Retrieved from http://www.lsc.gov/about-lsc/who-we-are/ congressional-oversight/congressional-appropriations

Legal Services Corporation. (2018). Who we are. Retrieved from http://www.lsc.gov/about/what-is-lsc

Marple, K. (2015). Framing legal care as health care. Retrieved from http://medical-legalpartnership.org/new-messaging-guide -helps-frame-legal-care-health-care/

Martinez, O., Boles, J., Muñoz-Laboy, M., Levine, E. C., Ayamele, C., Eisenberg, R., & Draine, J. (2017). Bridging health disparity gaps through the use of medical-legal partnerships in patient care: A systematic review. Journal of Law, Medicine and Ethics, 45(2), 260–273.

McGinnis, J. M., & Foege, W. H. (1993). Actual causes of death in the United States. Journal of the American Medical Association, 270(18), 2207–2212.

McGovern, L., Miller, G., & Hughes-Cromwick, P. (2014). Health policy brief: The relative contribution of multiple determinants to health outcomes. Retrieved from https://www.rwjf.org /content/dam/farm/reports/issue_briefs/2014/rwjf415185

Miller, W. D., Sadegh-Nobari, T., & Lillie-Blanton, M. (2011). Healthy starts for all: Policy prescriptions. American Journal of Preventive Medicine, 40(1 supp. 1), S19–S37.

Mokdad, A. H., Marks, J. S., Stroup, D. F., & Gerberding, J. L. (2004). Actual causes of death in the United States, 2000. Journal of the American Medical Association, 291(10), 1238–1245.

National Center for Medical-Legal Partnership. (2018). Partnerships across the U.S. Retrieved from http://medical -legalpartnership.org/partnerships/

National Federation of Independent Business v. Sebelius, 567 U.S. 519 (2012).

 

 

Endnotes 151

▸ Endnotes a. For a full account of the Tuskegee Study, see

Jones, 1993. b. According to the World Justice Project, a not-

for-profit group promoting the rule of law, the United States ranks 66th out of 98 countries in the access to and affordability of civil legal ser- vices (Bronner, 2013).

c. For more information, see, for example, U.S. Department of Justice, n.d.

d. See American Bar Association (2006) for the resolution and an accompanying report on achieving equal justice in the United States.

e. Note that LSC’s heyday was back in the late 1970s and early 1980s, when their budget topped $800 million dollars in 2015 terms.

f. In the interest of disclosure, Professor Teitelbaum is co-principal investigator of the National Cen- ter for Medical-Legal Partnership at The George Washington University’s Milken Institute School of Public Health. For more information about medical-legal partnership and the National Cen- ter, visit http://www. medical-legalpartnership.org/

National Partnership for Action to End Health Disparities. (n.d.). Home page. Retrieved from http://minorityhealth.hhs.gov/npa/

O’ Sullivan, M. M., Brandfield, J., Hoskote, S. S., Segal, S. N., Chug, L., Modrykamien, A., & Eden, E. (2012). Environmental improvements brought by the legal interventions in the homes of poorly-controlled inner-city adult asthmatic patients: A proof-of-concept study. Journal of Asthma, 49(9), 911–917.

O’Toole, J. K., Burkhardt, M. C., Solan, L. G., Vaughn, L., & Klein, M. D. (2012). Resident confidence addressing social history: Is it influenced by availability of social and legal resources? Clinical Pediatrics, 51(7), 625–631.

Perlman, J., & Parvensky, J. (2006). Denver housing first collab- orative cost benefit analysis and program outcomes report. Retrieved from http://shnny.org/uploads/Supportive_Housing _in_Denver.pdf

Powell, L. M., Slater, S., Mirtcheva, D., Bao, Y., & Chaloupka, F. J. (2007). Food store availability and neighborhood characteristics in the United States. Preventive Medicine, 44(3), 189–195.

Rodabaugh, K. J., Hammond, M., Myszka, D., & Sandel, M. (2013). A medical-legal partnership as a component of a palliative care model. Journal of Palliative Medicine, 13(1), 15–18.

Sandefur, R. L. (2014). Accessing justice in the contemporary USA: Findings from the community needs and services study. Retrieved from http://www.americanbarfoundation.org /uploads/cms/documents/sandefur_accessing_justice_in _the_contemporary_usa._aug._2014.pdf

Schneiderman, N., Ironson, G., & Siegel, S. D. (2005). Stress and health: Psychological, behavioral, and biological determinants. Annual Review of Clinical Psychology, 1, 607–628.

Schulman, K. A., Berlin, J. A., Harless, W., Kerner, J. F., Sistrunk, S., Gersh, B. J., . . . Escarce, J. J. (1999). The effect of race and sex on physicians’ recommendations for cardiac catheterization. New England Journal of Medicine, 340, 618–626.

Smedley, B. D., Stith, A. Y., & Nelson, A. R. (Eds.). Unequal treatment: Confronting racial and ethnic disparities in health care. Washington, DC: The National Academies Press.

Stringhini, S., Sabia, S., Shipley, M., Brunner, E., Nabi, H., Kivimaki, M., & Sing-Manoux, A. (2010). Association of socioeconomic position with health behaviors and mortality. Journal of the American Medical Association, 303(12), 1159–1166.

Teufel, J. A., Werner, D., Goffinet, D., Thorne, W., Brown, S. L., & Gettinger, L. (2012). Rural medical-legal partnership and

advocacy: A three-year follow-up study. Journal of Health Care for the Poor and Underserved, 23(2), 705–714.

Tobin-Tyler, E. (2008). Allies not adversaries: Teaching collaboration to the next generation of doctors and lawyers to address social inequality. Journal of Health Care Law and Policy, 11, 249–294.

Tobin-Tyler, E. (2012). Aligning public health, health care, law and policy: Medical-legal partnership as a multilevel response to the social determinants of health. Journal of Health and Biomedical Law, 8(2), 211–247.

Tobin-Tyler, E., Lawton, E., Conroy, K., Sandel, M., & Zuckerman, B. (Eds.). (2011). Poverty, health and law: Readings and cases for Medical-Legal Partnership. Durham, NC: North Carolina Press.

Tobin-Tyler, E., & Teitelbaum, J. (2019). Essentials of Health Justice: A Primer. Burlington, MA: Jones & Bartlett Learning.

U.S. Department of Agriculture. (2017). Food access research atlas. Retrieved from http://www.ers.usda.gov/data/fooddesert

U.S. Department of Health and Human Services. (2018). Social determinants of health. Retrieved from http:// w w w. h e a lt hy p e opl e. gov / 2 0 2 0 / topi c s – o bj e c t ive s / topi c /social-determinants-health

U.S. Department of Justice. (n.d.) Office for Access to Justice. Retrieved from https://www.justice.gov/archives/atj

van Ryn, M., Burgess, D., Malat, J., & Griffin, J. (2006). Physicians’ perceptions of patients’ social and behavioral characteristics and race disparities in treatment recommendations for men with coronary artery disease. American Journal of Public Health, 96(2), 351–357.

Wang, C. J., Conroy, K. N., & Zuckerman, B. (2009). Payment reform for safety-net institutions—Improving quality and outcomes. New England Journal of Medicine, 361(19), 1821–1823.

Williams, D. R., Costa, M. V., Odunlami, A. O., & Mohammed, S. A. (2008). Moving upstream: How interventions that address the social determinants of health can improve health and reduce disparities. Journal of Public Health Management and Practice, 14, s8–s17.

World Health Organization. (2018). Social determinants of health. Retrieved from http://www.who.int/social_determinants /sdh_definition/en/

Yearby, R. (2013). Breaking the cycle of “unequal treatment” with health care reform: Acknowledging and addressing the continuation of racial bias. Connecticut Law Review, 44(4), 1281–1324.

 

 

 

© Mary Terriberry/Shutterstock

CHAPTER 8

Understanding Health Insurance

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Understand the role of risk and uncertainty in insurance ■ Define the basic elements of health insurance ■ Differentiate various insurance products ■ Discuss incentives created for providers and patients in various types of insurance arrangements ■ Discuss health policy issues relating to health insurance

▸ Introduction

Unlike many other countries, the United States does not have a national healthcare deliv-ery system; whether individuals have access to healthcare services—and whether they receive health care of appropriate quantity and quality—often depends on whether they are insured. Even if an indi- vidual is insured, the kind of coverage he or she has can affect his or her ability to obtain care. Understand- ing health insurance, however, requires more than understanding its importance to healthcare access.

Policymakers must also know how providers, sup- pliers, employers, states, and others respond to changes in the health insurance market. For example, if policy- makers decide to reduce the number of uninsured by creating a new state health insurance exchange (essen- tially, an online marketplace) for the sale and purchase of private insurance coverage (as happened under the

ACA), they must know whether providers will partic- ipate in the program and what features will make it more or less attractive to providers. Or, if policymak- ers want to reduce the number of uninsured by man- dating that employers offer health insurance (as also happened under the ACA), they must know which requirements will make it more or less likely that more employees will be covered under such a mandate. In either case, policymakers might also want to know whether an initiative will affect the financial viability of public hospitals or health centers.

Several themes emerge when considering these types of health-insurance–related policy questions. First, insurance is rooted in the concepts of uncertainty and risk; reducing uncertainty and risk by, for exam- ple, offering a health insurance product, participating as a provider in a health insurance plan, or purchasing health insurance coverage as a consumer creates vari- ous incentives for insurers, the insured, providers, and

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governments to act or refrain from acting in certain ways. As noted in BOX 8-1, one goal of the ACA is to reduce the risk of insuring small businesses and indi- viduals by creating a large purchasing pool through state health insurance exchanges (Patient Protection and Affordable Care Act [ACA], 2010). Second, to a large extent, insurance carriers choose the design of their health insurance products, and employers and individuals choose whether to purchase health insurance—and, if so, what type. Indeed, insurance carriers have had wide latitude to determine the indi- viduals or groups that may join a plan, employers have had broad discretion to determine whether to offer

coverage and what type to offer, and individuals have had the choice whether to purchase health insurance coverage, although this choice was often illusory due to the high cost of health care. The ACA attempts to change these choices and incentives. For example, many insurance plans will have to meet new require- ments, such as offering a package of “essential health benefits”; most employers will have to provide health insurance coverage or pay a penalty; and most indi- viduals will have to purchase health insurance or pay a penalty. For each choice, the question is: What policy goal (e.g., equity, universal coverage, fiscal restraint, market efficiency) should drive the design and regu- lation of health insurance?

This chapter begins with a short history of health insurance in the United States and then reviews the health insurance concepts key to understanding the structure and operation of health insurance. It con- cludes with an overview of managed care, a particular form of health insurance dominant in today’s market.

▸ A Brief History of the Rise of Health Insurance in the United States

Although about 88% of people in this country were insured in 2017, health insurance was not always an integral part of our society (Auter, 2018). The initial movement to bring health insurance to the United States was modeled after activities in Europe. In the late 1800s and early 1900s, the European social insur- ance movement resulted in the creation of “sickness” insurance throughout many countries: Germany in 1883, Austria in 1888, Hungary in 1891, Britain in 1911, and Russia in 1912, to name just a few exam- ples. These programs varied in scope and structure, from a compulsory national system in Germany, to industry-based requirements in France and Italy, to extensive state aid in Sweden and Switzerland. Although the Socialist and Progressive parties advo- cated for the adoption of similar social insurance systems in the United States in the early 1900s, their efforts were unsuccessful (Starr, 1982).

In the absence of government-sponsored health insurance plans, the private sector insurance industry flourished with the growth of Blue Cross, Blue Shield, and commercial insurance carriers. Blue Cross estab- lished its first hospital insurance plan at Baylor Uni- versity in 1929 by agreeing to provide 1,500 teachers with 21 days of hospital care per year for the price of $6 per person (Starr, 1982, p. 295). The hospital

BOX 8-1 Vignette

William owns a small business that sells all kinds of wheels and gears. He has nine employees and has always made it a priority to offer competitive benefits, including health insurance. Unfortunately, last year one of his employees was diagnosed with cancer, which he continues to fight. Due to the sharp increase in use of health services by his employee group, the insurance company doubled his group premiums for the upcoming year. When William contacted other carriers, several of them would not consider insuring his group, and most of the others gave him quotes as expensive as his current carrier. One company gave him a lower quote, but it covered only catastrophic care; his employees would have to pay for the first $5,000 of care out of their own pockets. After reviewing his company’s finances, William is left with several unattractive options: stop offering health insurance; offer comprehensive health insurance but pass on the cost increase to his employees, which would make it unaffordable for most of them; offer the bare-bones catastrophic plan only; or significantly lower wages and other benefits to defray the rising health insurance costs. In addition to wanting to offer competitive benefits, William is concerned that adopting any of these options will cause his employees to leave and make it hard to attract others, threatening the sustainability of his company.

The 2010 health reform law, the Patient Protection and Affordable Care Act (ACA), attempts to help small businesses like William’s by creating state health insurance exchanges. Starting in 2014, these exchanges were intended to offer a variety of plans to individuals and small businesses that otherwise might not be able to afford health insurance coverage. By creating large groups of purchasers through the exchanges, it is possible to pool risk and keep prices lower than if individuals or small businesses were attempting to purchase insurance coverage on their own.

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industry supported the growth of private insurance as a way to secure payment for services during the Depression. Blue Shield, the physician-based insur- ance plan, began in 1939 as a way to forestall renewed efforts to enact compulsory national health insurance and to avoid growth in consumer-controlled prepaid health plans, both of which would have reduced the type of physician autonomy endemic at that time (Starr, 1982, p. 307).

World War II led to rapid growth in employer- sponsored health insurance. With employees scarce and a general wage freeze in effect, a 1942 War Labor Board ruling that employee fringe benefits of up to 5% of wages did not violate the wage freeze created a strong incentive for employers to provide health bene- fits to attract new workers and keep their current ones. After the war, labor unions gained the right to bargain collectively, leading to another expansion of employee health plans. In 1954, the Internal Revenue Service declared that employers could pay health insurance premiums for their employees with pre-tax dollars, further increasing the value of the fringe benefit to employers.a By 1949, 28 million people had commer- cial hospital insurance, 22 million had commercial physician insurance, and 4 million had independent hospital plans. At that time, over 31 million had Blue Cross hospital coverage and 12  million had Blue Shield coverage (Starr, 1982, p. 327). Employer-sponsored health insurance, not national health insurance, was well on its way to becoming entrenched as the primary form of health insurance.

The federal government first became a major player in health insurance with the passage of Med- icaid and Medicare in 1965. These programs were created, in part, to fill in coverage gaps left by the private insurance market—namely, coverage for the elderly, disabled, and low-income populations who had too little income and too high health risks to be viable candidates for insurance coverage from the insurance carriers’ point of view. Like many major policy changes, the passage of these programs was a multilayered compromise. Before the final design of these programs was established, several proposals were considered: the American Medical Association (AMA) supported a combination federal–state pro- gram to subsidize private insurance policies for older adults to cover hospital care, physician care, and pre- scription drugs; Representative John Byrnes (R-WI), ranking Republican on the House Ways and Means Committee, endorsed an AMA-like proposal but with federal, instead of federal–state, administration; the Johnson administration supported hospital insurance for older adults through Social Security; and Senator

Jacob Javitz (R-NY) supported federal payments to state programs to provide health care to poor, elderly individuals (Stevens & Stevens, 2003, pp. 46–48). In the end, the Medicare and Medicaid programs were passed in one bill with features from all of these pro- posals. For example, Medicare was established as a federally funded program with two parts, one for hos- pital insurance and one for physician insurance, and Medicaid as a state–federal program for the poor.

By the 1970s a number of factors converged to place rising healthcare costs on the national agenda: advances had been made in medical technology, hos- pitals expanded and became more involved in high- tech care, physician specialties became more common, hospitals and physicians had a large new pool of pay- ing patients due to Medicaid and Medicare, wages for medical staff increased, and an aging population required an increasing amount of services (Starr, 1982, pp. 383–384). In addition, the prevailing fee-for- service (FFS) insurance system rewarded healthcare professionals for providing a high quantity of services. As the name suggests, fee-for-service reimbursement means the providers are paid for each service they provide—the more services (and the more expensive the services) rendered, the more reimbursement the provider receives. From 1960 to 1970, hospital care expenditures tripled from $9.3 billion to $28 billion, and physician service expenditures almost matched that growth rate, increasing from $5.3 billion to $13.6 billion (Sultz & Young, 2001, pp. 257–258). Federal and state governments were also feeling the burden of high healthcare costs. From 1965 to 1970, federal and state governments collectively experienced a 21% annual rate of increase in their healthcare expendi- tures (Starr, 1982, p. 384).

BOX 8-2 Discussion Questions

Most people in this country obtain health insurance through employer-sponsored plans. Although the historical background you just read explains how this system came about, it does not discuss whether it is a good or bad thing. Is our reliance on employer- sponsored health insurance ideal for individuals? Providers? Employers? Society? What are the benefits and drawbacks to having employers as the primary source of health insurance? How different are the benefits and drawbacks when considered from various stakeholder perspectives? Would it be better to have more federal government involvement in providing health insurance? What primary policy goal would you use to decide how to answer these questions?

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As is discussed in more detail later in this chap- ter, managed care moves away from the FFS sys- tem by integrating the payment for services and the delivery of services into one place in an attempt to rein in healthcare costs and utilization. The federal Health Maintenance Organization Act of 1973 was intended to spur the growth of managed care by pro- viding incentives to increase the use of health main- tenance organizations (HMOs). The act relied on federal loans and grants and a mandate that employ- ers with 25 or more employees offer an HMO option if one was available in their area (Sultz & Young, 2001, pp. 262–263). Even so, managed care did not flourish due to opposition by patients who did not want their provider and service choices restricted, and by providers who did not want to lose control over their practices.

As healthcare cost and quality concerns remained a national priority, the managed care industry eventu- ally found a foothold in the health insurance market. Indeed, enrollment in managed care doubled during the 1990s, with almost 80 million enrollees by 1998. In 2017, only 1% of workers were in conventional, non-managed-care arrangements (Kaiser Family Foundation [KFF], 2017). Although only about 33% of Medicare enrollees choose managed care arrange- ments (Jacobson, Damico, & Neuman, 2017), some 65% of Medicaid beneficiaries receive some or all of their services through managed care, though for many of them it is mandatory that they receive ser- vices through a managed care arrangement (Rudowitz & Garfield, 2018).

▸ How Health Insurance Operates

This section provides an overview of the purpose and structure of health insurance. It begins with a review of basic health insurance terminology, considers the role of uncertainty and risk in insurance, and con- cludes with a discussion of how insurance companies set their premium rates.

Basic Terminology As you read earlier, the health insurance industry first developed when the FFS system was standard. Under this system, not only do providers have incen- tive to conduct more and more expensive services, but patients are unbridled in their use of the health- care system because FFS does not limit the use of ser- vices or accessibility to providers. As we will discuss

later in this chapter, managed care developed as a response to the incentives created by the FFS system. However, even though there are numerous differ- ences between FFS and managed care, many of the fundamental principles of how insurance operates are applicable to any type of health insurance con- tract. The following discussion reviews how health insurance works generally, regardless of the type of insurance arrangement.

The health insurance consumer (also known as the beneficiary or insured) buys health insurance in advance for an annual fee, usually paid in monthly installments, called a premium. In return, the health insurance carrier (or company) pays for all or part of the beneficiary’s healthcare costs if she or he becomes ill or injured and has a covered medical need. (A cov- ered need is a medical good or service that the insurer is obligated to pay for because it is covered based on the terms of the insurance contract or policy. As dis- cussed in detail elsewhere, the ACA requires many plans to cover all “essential health benefits.”) Insurance contracts cannot identify every conceivable healthcare need of beneficiaries, so they are generally structured to include categories of care (e.g., outpatient, inpatient, vision, maternity) to be provided if deemed medically necessary. Definitions of the term medically necessary vary by contract and are important when determining whether a procedure is covered.

Even if the beneficiary never needs healthcare ser- vices covered by the insurance policy, he or she still pays for the policy through premiums. The consumer benefits by having financial security in case of illness or injury, and the insurance company benefits by mak- ing money selling health insurance.

In addition to premiums, the beneficiary typically pays other costs under most health insurance policies. Many policies have deductibles, which is the amount of money the beneficiary must pay on his or her own for healthcare needs each year before the insurance carrier starts to help with the costs. For example, if a policyholder has a $500 deductible, the beneficiary must pay 100% of the first $500 of healthcare costs each year. The insurance carrier is not liable to cover any costs until the individual’s healthcare bill reaches $501 in a given year. If the individual does not need more than $500 worth of health care in a specific year, the insurance carrier generally will not help that indi- vidual pay his or her healthcare costs.

Furthermore, a beneficiary generally contin- ues to incur some costs in addition to the premiums even after the deductible has been met. Insurance carriers often impose cost sharing on the beneficiary through co-payment or co-insurance requirements.

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A co-payment is a set dollar amount the beneficiary pays when receiving a service from a provider. For example, many HMOs charge their beneficiaries $15 every time a beneficiary sees a primary care provider. Co-insurance refers to a percentage of the healthcare cost the individual must cover. For example, 20% is a common co-insurance amount. This arrangement means the beneficiary pays 20% of all healthcare costs after the deductible has been met, with the insurance carrier paying the other 80%.

Uncertainty From a traditional economic perspective, insurance exists because of two basic concepts—risk and uncer- tainty. The world is full of risks—auto theft, house fires, physical disabilities—and uncertainty about whether any such events might affect a particular individual. As a result, people buy various forms of insurance (e.g., automobile insurance, home insurance, life or disability insurance) to protect themselves and their

families against the financial consequences of these unfortunate and unforeseen events.

Although genetic predisposition or behavioral choices such as smoking or working a high-risk job may increase the chances that an individual will suf- fer from a health-related problem, in general there is a high level of uncertainty as to whether a particular person will become sick or injured and need medical assistance. Health insurance protects the consumer from medical costs associated with both expensive and unforeseen events. Even if the consumer does not experience a negative event, a benefit exists from the peace of mind and reduced uncertainty of financial exposure that insurance provides.

In terms of health status and wise use of resources, when insurance allows consumers to purchase nec- essary services they would not otherwise be able to afford, it functions in a positive manner. Conversely, when insurance leads consumers to purchase unnec- essary healthcare goods or services of low value because the consumer is not paying full cost, it works in a negative manner. The difficult task is trying to fig- ure out how to set the consumer’s share of the burden at just the right point to encourage and make avail- able the proper use of health care, while discouraging improper usage.

BOX 8-3 Discussion Questions

As a general matter, all types of insurance under traditional economic models cover expensive and unforeseen events, not events that have small financial risk or little uncertainty (Council of Economic Advisors, 2004, p. 195). For example, auto insurance does not cover regular maintenance such as an oil change, and home insurance does not protect against normal wear and tear, such as the need to replace an old carpet. Accordingly, many economists argue that health insurance should not cover regular, foreseeable events such as physical exams or low-cost occurrences such as vaccinations. Other economists support a different school of thought. An alternative economic view is that health insurance should insure one’s health, not just offer protection against the financial consequences of major adverse health events. Because people without health insurance are less likely to obtain preventive care such as physical exams or vaccinations, these economists believe it is in everyone’s best interest, ethically and financially, to promote preventive care. Therefore, it is appropriate for insurance to cover both unpredictable and expensive events as well as predictable and less expensive events. Which theory do you support? What do you think is the best use of insurance? If insurance does not cover low-cost and predictable events, should another resource be available to assist individuals, or should people pay out of their own pockets for these healthcare needs? BOX 8-4 Discussion Questions

As discussed earlier, risk and uncertainty are important concepts in health insurance. Individuals purchase health insurance policies to protect themselves financially against healthcare costs, and insurance carriers try to set premiums that will cover the cost of the services used by their beneficiaries. Currently (when allowed by law), insurance carriers may consider factors such as medical history, demographics, type of occupation, size of the beneficiary pool, and similar criteria when setting the terms of an insurance policy. Should health insurance carriers also have access to and be able to use genetic testing results when deciding whether to insure an individual, what premiums to charge, or which services to cover? If you think the answer to that question should be “no,” why is genetic information different from all of the other kinds of information insurance carriers may take into account when making those decisions? Conversely, what is the strongest argument you can make in favor of allowing insurance carriers to consider an applicant’s genetic information? How would allowing genetic testing alter an individual’s or a provider’s diagnosis and treatment decisions? What is the primary policy goal that affects your view?

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Risk Risk is a central concern in insurance. Consumers buy insurance to protect themselves against the risk of unforeseen and costly events. But health insurers are also concerned about risk—the risk that their benefi- ciaries will experience a covered medical event.

Individuals purchase health insurance to protect themselves against the risk of financial consequences of healthcare needs. Because of differences in risk level, individuals who are generally healthy or otherwise do not anticipate having health expenses may place a lower value on insurance than individuals who are unhealthy or those who are healthy but expect to have medical expenses, such as pregnant women. Therefore, healthy individuals tend to seek out lower-cost insurance plans or refrain from obtaining insurance altogether if it is not, in their view, cost effective. Unhealthy individu- als or healthy individuals who often use the healthcare system would obviously prefer a low-cost insurance plan (with comprehensive benefits) but are generally more willing to pay higher premiums because of the value they place on having insurance.

Health insurance carriers are businesses that need to cover their expenditures, including the cost of accessing capital needed to run their company, to stay in the market.b They earn money by collecting premi- ums from their beneficiaries, and they pay out money to cover their beneficiaries’ healthcare costs above the deductible amount and to cover the costs of running a business (e.g., overhead, marketing, taxes). One way health insurance companies survive is to make sure the premiums charged to beneficiaries cover these costs. From the insurance carrier’s perspective, it would be ideal to be able to charge lower premiums to attract healthy individuals who are less likely to use their ben- efits, and higher premiums to unhealthy individuals who are more likely to need medical care.

However, insurance companies have difficulty matching healthy people with low-cost plans and unhealthy people with high-cost plans because of the problem of asymmetric information. This is the term used by economists when one party to a transaction has more information than the other party. In the case of insurance, the imbalance often favors the consumer because insurance carriers generally do not know as much as the individual does about the individu- al’s healthcare needs and personal habits. Although relatively healthy low-cost individuals want to make their status known because insurance carriers might be willing to sell them an insurance product for a lower price, relatively unhealthy individuals do not want their status known because insurance companies might charge them higher premiums. For this reason,

when an insurance carrier lacks complete informa- tion, it is more beneficial to unhealthy beneficiaries than to healthy ones.

Together, uncertainty about risk and the pres- ence of asymmetric information lead to the problem of adverse selection. In terms of health insurance, adverse selection is when unhealthy people overse- lect (that is, select beyond a random distribution) a particular plan. This occurs because people at risk for having high healthcare costs choose a particular plan because of that plan’s attractive coverage rules (Pen- ner, 2004, pp. 12–13). The consumer who knows he is a high risk for needing services will be more likely to choose a more comprehensive plan because it cov- ers more services, even though it is probably a more expensive option. This overselection leaves the insurer that offers the comprehensive plan with a dispropor- tionate number of high-risk beneficiaries. As a result of the relatively high-risk pool, beneficiaries will have high service utilization rates, requiring the insurance carrier to raise premiums to pay for the increased cost of covering services for beneficiaries. In turn, some of the healthier individuals might choose to leave the plan because of the higher premiums, resulting in an even riskier beneficiary pool and even higher premi- ums, and the cycle continues. The healthier consumers may find a lower-cost plan or may choose to go with- out health insurance (especially since the Tax Cut and Jobs Act of 2017 repealed, as of 2019, the penalty asso- ciated with violating the ACA’s individual mandate, as described in more detail in a subsequent chapter), while the insurance plan is left with an increasingly higher percentage of relatively unhealthy people. This is the problem of adverse selection.

One instance where adverse selection is a key concern is with an increasingly popular type of health plan, the high-deductible health plan (HDHP). As the name suggests, these plans have very high deductibles (usually defined as at least $1,000 for an individual or $2,000 for a family). In 2017, annual premiums for the average HDHP were $6,024 for individuals and $17,581 for families (KFF, 2017). As with other insurance plans, consumers pay most of their health- care expenses out-of-pocket until they reach the deductible. HDHPs are often used in conjunction with health reimbursement arrangements (HRAs) or health savings accounts (HSAs), which allow individ- uals to set aside money for future healthcare needs. Health reimbursement arrangements are funded solely by employers, who usually commit to making a specified amount of money available for healthcare expenses incurred by employees or their dependents, while HSAs are created by individuals, but employers may also contribute to HSAs if the employers offer a

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4%

40%

30%

20%

10%

0% 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017

6%

3% 3%

7%* 3%

6% 6%

9% 7%*

9%* 12% 11%

8%

8% 9%

20% 21%

7%

14% 15%

9%

24%

28% 28%

9% 9%

19%19%*

13%*

17%*

20%

3%2% 2% 4%*

* Estimate is statistically different from estimate for the previous year shown (p < 0.05). Note: Covered workers enrolled in an HDHP/SO are enrolled in either an HDHP/HRA or a HSA-Qualified HDHP.

HDHP/HRA HSA-qualified HDHP

70%

60%

50%

40%

30%

20%

10%

0%

2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017

8%

16%* 18%

21%

26%*

32%

41%* 40% 43%

45%

52%*

57% 58%

5%

13%*

18%

26%

39% 38% 38%

49%* 52%

33%

21%

15%

4%

7% 10%

22%

27% 25%

27% 23%

31%

23%

15% 11%

13%

* Estimate is statistically different from estimate for the previous year shown (p < 0.05).

3–199 Workers 1,000 or more workers

200–999 Workers

Source: Reproduced from: Kaiser/HRET Survey of Employer-Sponsored Health Benefits, 2017 https://www.kff.org/report-section/ehbs-2017-section-8-high-deductible-health-plans-with-savings-option/

Source: Reproduced from: Kaiser/HRET Survey of Employer-Sponsored Health Benefits, 2017. https://www.kff.org/report-section/ehbs-2017-section-8-high-deductible-health-plans-with-savings-option/

qualified HDHP. Individual contributions to HSAs are made with pre-income tax dollars, and withdrawals to pay for qualified healthcare expenses are also not taxed. As shown in FIGURES 8-1 and 8-2, HDHPs are increasingly popular with employers and employees.

Those who support HDHPs assert that plans with high deductibles promote personal responsi- bility because enrollees have a financial incentive to avoid overusing the healthcare system and to choose

cost-effective treatment options. As a result, HDHPs are favored by employers and others as a cost-cutting strategy. Others are concerned that HDHPs will have a negative effect on enrollees’ health because individuals cannot or will not price shop and are more likely to save money by simply avoiding needed care. As discussed in BOX 8-5, researchers continue to evaluate these questions.

An enrollee’s experience with a HDHP may depend, in part, on income level. Individuals who are

FIGURE 8-1 Percentage of Covered Workers Enrolled in a High-Deductible Health Plan (HDHP) or Health Reimbursement Arrangement, or in a Health Savings Account–Qualified HDHP, 2006–2017

FIGURE 8-2 Among Firms Offering Health Benefits, Percentage That Offer a High-Deductible Health Plan With a Savings Option, 2005–2017

How Health Insurance Operates 159

 

 

wealthier and healthier are likely to have funds to place in a savings account, can afford high out-of-pocket expenses, and are less likely to use the healthcare sys- tem (Davis, 2004). As a result, critics contend that the lower service utilization associated with HDHP enrollees is likely due to their better health status, not price sensitivity, undermining one of the main argu- ments in support of these plans (Davis, 2004). Poorer individuals who may be drawn to the lower premium cost of HDHPs may not be able to afford care when they need it. In fact, a 2018 study found that HDHP enrollees without a savings account were less likely to obtain primary care, preventive services, or specialty care and more likely to be in poor or fair health as compared to enrollees with a savings account (Jetty, Petterson, Rabin, & Liaw, 2018). Finally, if healthier and wealthier individuals flock to HDHPs, poorer individuals in a comprehensive group plan (assuming one is available and affordable), face the possibility of adverse selection due to being part of a relatively high- risk insurance pool (Davis, 2004).

Setting Premiums Assuming that insurance companies make their decisions in the context of asymmetric information, they cannot determine with certainty the appropri- ate amount of premium to charge each individual.

Instead, insurance companies rely on making edu- cated guesses about the risk each individual or group of individuals has of needing healthcare services. The two main methods of setting premiums are experience rating and community rating.

When insurance companies use experience rating to make an educated guess about the risk of someone’s needing healthcare services, they are relying on how much a beneficiary or group of beneficiaries spent on medical services previously to determine the amount of the premium for each member or group. Thus, if an individual or group had very high medical costs in a given year, premiums are likely to rise the following year. Conversely, community rating does not take into account health status or claims history when setting premiums. In “pure” community rating, insurers use only geography and family composition to set rates; in “modified” community rating, insurers may be allowed to consider other characteristics, such as age and sex.

Which rating system makes more sense from a policy perspective as a basis for setting premiums may depend on whether you evaluate the insurance market based on efficiency or equity (think back to discussions of competing conceptual frameworks). If the market is judged based on efficiency, then the key issue is whether the optimal amount of risk has shifted from consumers to insurers. If there are individuals willing to pay a higher amount for greater coverage

BOX 8-5 Discussion Questions

A literature review of studies relating to consumer behavior with HDHPs found that these plans reduced the use of both appropriate care, such as preventive screenings, and inappropriate care, such as unnecessary emergency department visits (Argwal, Mazurenko, & Menachemi, 2017). To date, research generally has not focused on health outcomes of HDHP users. Some recent studies have shown consumers rarely engaging in price-conscious behavior, instead achieving savings through use of fewer services (Kullgren, Cliff, & Krenz, 2018; Sinaiko, Mehrotra, & Sood, 2016; Sood, Wagner, Huckfeldt, & Haviland, 2013).

Do HDHPs achieve the right balance of providing insurance coverage while incentivizing consumers to use resources prudently? Or are they simply a way to lower employer healthcare costs while making it unaffordable for many consumers to obtain the health care they need? How easy is it for consumers to compare costs for healthcare providers and services? What additional challenges might an HDHP present for individuals who are low-income, live in rural areas, speak a primary language other than English, or have low health literacy?

BOX 8-6 Discussion Questions

In general, people with low incomes or no health insurance (or both) tend to be less healthy than those who are financially better off or insured (or both). As a result, policy proposals that suggest including poor, uninsured individuals in already-existing insurance plans are met with resistance by individuals in those plans and by carriers or employers who operate them. Yet, if an insurance plan is created that subscribes only a less-healthy, poor, or uninsured population, it is likely to be an unattractive business opportunity because beneficiaries are likely to need a high quantity of health care that will be costly to provide. Given what you know about adverse selection and risk, what, in your opinion, is the best way to provide insurance coverage to the poor and uninsured? Should they be included in current plans? Should the government provide financial incentives for private carriers to insure them? Should a separate plan or program be created to serve them? In these various scenarios, what incentives are created for plans, current plan members, government, and so on?

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and insurers willing to provide greater coverage for the higher amount, but something in the market pre- vents this transaction from occurring, then the opti- mal amount of risk shifting has not occurred. Or, if individuals value a certain level of insurance coverage at a price that is less than the price at which insurers are willing to provide that coverage, but individuals buy coverage anyway at the higher price, the market is not optimally efficient (due to excess coverage).

Conversely, the market may be judged based on equity or fairness. Even the most efficient market may result in some inequities. Some individuals may be uninsured, some may have to pay more than other individuals for the same level of insurance, some may not be able to purchase the level of coverage they desire, and some individuals may not be able to join a particular plan. These inequities are often a concern in the context of the uninsured, especially as uninsur- ance relates to low-income individuals or those with high health needs due to random events, such as an accident or genetic condition.

Regardless of the underwriting methodology used, premiums are cheaper for people purchasing insurance as part of a large group rather than buy- ing health insurance individually or as part of a small group. Due to the law of averages, larger groups of people are more likely to have an average risk rate. When people join a group for reasons unrelated to health status, such as working for the same com- pany, it is also more likely that the group will have an average risk rate. Groups with average risk rates are attractive to insurers because the cost of insuring a few unhealthy people will probably be offset by sav- ings from insuring many healthy ones. Conversely, in smaller groups it is more likely that the group will have a relatively high risk rate and less likely that the cost of insuring an unhealthy person can be offset by the savings of insuring a few other healthy people. This is the problem faced by William, the small business owner described at the outset of the chapter who has one high-cost employee. Even though he would like to offer health insurance coverage to his employees, William and other small business owners like him often are able to offer only expensive or limited cov- erage, if they can offer any health insurance benefit at all. To help individuals and small business owners like William, some states require insurers to use a commu- nity rating system to set premiums for these groups and in the state health insurance exchanges that were created by the ACA.

Carriers also prefer to insure large groups because most of the administrative costs associated with insur- ance are the same whether the carrier is covering a few

people or a few thousand (Phelps, 2003, pp. 342–344). In fact, group coverage has traditionally required fewer marketing resources than individual cover- age, which targets customers one at a time. However, the proliferation of information on the Internet may change this equation.

Medical Underwriting The prior discussion about rate setting assumed asymmetric information (i.e., where the insurer has little information about the consumer’s health status and the consumer has substantial information about his or her own healthcare needs). Of course, there are ways for insurers to gain information about the medical needs of a consumer looking to join a health plan: physical exams, questionnaires, medical records, occupation, and demographics all provide clues about the health status of the consumer. Although it is much more difficult to accomplish, insurers may also try to predict an individual’s future costs through question- naires that ask, for example, whether an individual engages in risky activities (e.g., riding a motorcycle) or through genetic testing (which is itself an emerging health policy and law issue).

Whether companies are allowed to consider an applicant’s medical history or other personal information to help assess risk of healthcare needs in the future—a practice referred to as medical underwriting—is a somewhat complicated legal question that involves both federal and state law. The Health Insurance Portability and Accountability Act of 1996 (HIPAA) includes an important protection for consumers by prohibiting group health plans from excluding or limiting otherwise qualified individuals due to preexisting conditions (a preexisting condition is a medical condition, such as cancer or diabetes, that is present at the time an individual applies to enroll in an insurance plan). The ACA expands this protection

BOX 8-7 Discussion Questions

What populations or types of people pay more under experience rating? Does experience rating create any incentives for individuals to act in a certain way? What populations or types of people pay more under community rating? Does community rating create any incentives for individuals to act in a certain way? Which rating system seems preferable to you? What trade-offs are most important to you? Should the focus be on the good of the individual or the good of the community? Are these mutually exclusive concerns?

How Health Insurance Operates 161

 

 

by requiring all health insurers to sell policies to all applicants, regardless of preexisting conditions. This requirement was in effect for children shortly after the ACA was signed into law, and took effect for adults in 2014 (as discussed in the Health Reform in the United States chapter, attempts are being made to chip away at this protection).

Prior to HIPAA, many individuals with pre- existing conditions were denied insurance altogether, denied coverage for particular medical care, or charged very high premiums if they sought to purchase a pol- icy. These practices led to a problem referred to as “job lock.” Because most Americans receive insurance cov- erage through their employers, many employees with preexisting conditions could not switch jobs for fear that their new company’s insurance policy would be denied to them on account of their preexisting condi- tion. One study estimated that job lock resulted in a 4% reduction in voluntary turnover (Phelps, 2003, p. 341).

Although HIPAA and the ACA do not regulate the amount of premiums that may be charged, all members of a group generally pay the same premium due to the laws’ nondiscrimination provisions. In HIPAA, these provisions prohibit plans or insurance carriers from requiring any individual to pay a higher premium or contribution than another “similarly situated” indi- vidual (Nondiscrimination in health coverage, 2001, p.  1382) in the plan based on eight health factors: health status, physical or mental medical conditions, claims experience (i.e., the individual has a history of high health claims), receipt of health care, medical history, genetic information, evidence of insurability, and disability (Nondiscrimination in health coverage, 2001, pp. 1378–1384, 1396–1403). However, because those who purchase individual health insurance plans are not covered by HIPAA’s protections, the ACA pro- tections were needed as well. The ACA also prohibits plans from charging individuals higher premiums due to their preexisting conditions.

▸ Managed Care The prior sections reviewed the history, basic struc- ture, and purpose of health insurance generally. In this section, we discuss a specific kind of health insurance structure that has come to dominate the American mar- ket: managed care. We will describe why managed care emerged, some of the frequent cost-containment strate- gies used by managed care organizations, and the most common managed care structures in the market today.

Managed care became the predominant health- care financing and delivery arrangement in the United

States because healthcare costs had risen to alarming levels and there were few mechanisms for containing costs under the FFS system. As mentioned earlier, FFS does not create incentives for providers or patients to utilize healthcare services sparingly. Providers have an incentive under FFS to provide more services and more expensive services (but not necessarily higher-quality services) because their income rises with each procedure or office visit and fees are higher for more expensive services. As long as providers are accessible, insured patients can request services and assume their insurance company will pay most or all of the costs to the extent that the services are covered by the health plan and medically necessary.

In addition, the FFS system does not create incen- tives for providers or patients to use the lowest-cost quality care available. Many people believe specialists provide higher-quality care and turn to them even for minor needs that do not truly require expensive spe- cialty services, and the FFS system does not discour- age this behavior. Furthermore, because traditional insurance coverage requires a specific diagnosis for reimbursement, patients are discouraged from seek- ing preventive services when they are symptom-free under FFS. At the same time, traditional insurance companies do not have the ability to control costs or quality of care under FFS. Their job is limited to deter- mining whether a service is covered and medically necessary and providing the agreed-upon reimburse- ment. They have little ability to measure or improve the quality of care provided by healthcare profession- als and cannot control costs by limiting the amount or type of services received; instead, they can only raise premiums and other rates in the future to cover increasing costs.

To alter the inherent incentives under FFS and to grant insurers some ability to control the quality and utilization of services, managed care integrates the provision of and payment for healthcare services. Through various strategies discussed in the following sections, managed care organizations (MCOs) and managed care plans create incentives to provide fewer services and less expensive care, while still maintain- ing the appropriate level of healthcare quality. MCOs also attempt to alter patients’ decision making through cost-sharing requirements, cost containment tools, utilization restrictions, and free or low-cost coverage for preventive care.

MCOs take various forms, but certain general features apply to all of them to varying degrees. All MCOs provide a comprehensive, defined package of benefits to the purchaser/member for a preset fee (including both monthly premium and cost-sharing

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requirements). Services are offered to members through a network of providers, all of whom have a contractual relationship with the MCO. The MCOs choose which providers to include in their networks and what services are rendered by network providers. Most notably, they also use financial incentives and other mechanisms to control the delivery, use, quality, and cost of services in ways that are not present in FFS insurance systems (Sultz & Young, 2001, p. 260).

Cost Containment and Utilization Tools Managed care introduced a variety of tools in its attempt to contain costs and control healthcare ser- vice utilization. The cost containment strategies of performance-based salary bonuses or withholdings, discounted fee schedules, and capitated payments shift financial risk or limit payments to providers who, in turn, have an incentive to choose the least costly, but still effective, treatment option. The utilization control strategies of gatekeeping and utilization review focus on ensuring that only appropriate and necessary care is provided to patients. Another type of strategy, case management, is designed to ensure that necessary care is provided in the most coordinated and cost-effective way possible.

Provider Payment Tools Depending on the structure of the MCO, provider salaries are based on a discounted fee schedule or capitation rate and include incentives to act or not act in certain ways. Providers in what are called staff- model MCOs are employees of the MCO and are paid an annual salary. The salary structure often includes

bonuses or salary withholdings that are paid (or with- held) upon meeting (or not meeting) utilization or performance goals, thus shifting some financial risk from the MCO to the provider. A discounted fee schedule is a service-specific fee system, as is used in FFS. However, an MCO-style fee schedule pays lower reimbursement rates than is true in FFS systems; pro- viders agree to accept less than their usual fee in return for the large volume of patients available to them by being a part of the MCO provider network. The MCO retains the financial risk in a discounted fee system, but the costs are lower for the company due to the discounted rate paid to providers. Finally, a capitated payment rate is a fixed monthly sum per member that the MCO uses to determine the provider salary. The capitation rate does not vary regardless of the number or type of services provided to patients. The physician receiving a salary based on a capitated rate is respon- sible for providing all of the care needed by his or her MCO patients, within the provider’s scope of practice. As a result, the financial risk in the case of capitated arrangements is shifted entirely from the MCO to the provider. Depending on the contract between the pro- vider and the MCO, the insurance company may or may not guarantee the provider a minimum number of patients in exchange for accepting a capitated rate. These provider-focused cost containment strategies are summarized in TABLE 8-1.

These payment methods lead to very different incentives for providers than is the case under the FFS system. Instead of being paid more for doing more, HMO providers are paid the same amount regardless of the number or type of services they provide. Given the use of bonuses and withholdings,

TABLE 8-1 Provider Payment Cost Containment Strategies

Strategy Provider Payment Method How Costs Are Controlled Who Assumes Financial Risk

Salary and bonuses/ withholdings

Provider receives a salary as an employee of an MCO

Incentive for provider to perform fewer and/or less-costly services

MCO and provider

Discounted fee schedule

Provider receives a lower fee than under FFS for each service to members

Pays provider less per service rendered than under FFS

MCO (but also has lower costs)

Capitation Provider receives a set payment per month for each member regardless of services provided

Incentive for provider to perform fewer and/or less-costly services

Provider

Abbreviations: FFS = fee for service; MCO = managed care organization.

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salaried providers may be paid more if they make treatment decisions deemed favorable by an MCO. By using these incentives, MCOs encourage provid- ers to render the fewest and most cost-effective ser- vices necessary.

Critics of managed care payment methodologies argue that MCO plan members will not receive all necessary care if providers are incentivized to provide fewer services and less-costly care. Instead of treating patients using both the most cost-efficient and medi- cally necessary services, critics claim MCOs encourage providers to save money by providing fewer ser- vices and less specialized care than necessary; MCOs counter that their own incentive is to keep their mem- bers healthy so they do not need expensive services in the future. In addition, MCOs point to their ability to impose quality control measures on providers as a way to ensure that patients are properly treated. In response, critics argue that because members switch health plans relatively frequently, MCOs do not have an incentive to keep their members healthy because the MCOs will not realize the long-term savings as members come and go.

Which side has the better argument? There is no definitive answer. On the one hand, studies have found that treatment decisions under MCO arrange- ments are mostly influenced by clinical factors (not economic ones), that there is little or no measurable difference in the health outcomes of patients in FFS versus managed care plans, and that the quality of care provided under FFS and managed care plans is basi- cally equal (Shi & Singh, 2017, p. 235; Shi & Singh, 2019, p. 382). In fact, patients in areas with a high market share of HMOs are more likely to engage in preventive care, receive diabetes care, and give high provider satisfaction ratings than are patients in areas with low HMO market share (Shi & Singh, 2017, p.  235). Researchers also have not found disparities based on race, ethnicity, and socioeconomic status in MCO versus FFS settings (Shi & Singh, 2017, p. 235; Shi & Singh, 2019, p.  382). While previous studies found that mental health patients did not fare as well in MCOs as in FFS plans, more recent research refutes that conclusion (Shi & Singh, 2019, p. 383).

On the other hand, nonprofit HMOs (a type of MCO) score better on quality measures than do for-profit ones, and HMO enrollees indicate lower patient satisfaction than do non-HMO patients (Shi & Singh, 2017, pp. 235–262; Shi & Singh, 2019, p. 382). Also, due to low reimbursement rates, access is a particular concern for Medicaid MCO enrollees, who appear to have more limited access to certain services, higher emergency department use, and

more unmet prescription drug needs (Shi & Singh, 2019, p. 381).

Utilization Control Tools MCOs also employ other techniques, not related to provider payment methods, to control use of health- care services. Once again, the goal in using these tools is to reduce the use of unnecessary and costly services. We review three common utilization control tools: gatekeeping, utilization review, and case management.

Gatekeepers monitor and control the services a patient receives. Members of managed care plans are often required to select a primary care provider from the MCO network upon enrollment. This provider acts as the member’s “gatekeeper” and is responsible for providing primary care, referring patients for addi- tional care, and generally coordinating the patient’s care. Having a gatekeeper allows the MCO, not the patient or specialty provider, to determine when a patient needs additional or specialty services, diagnos- tic tests, hospital admissions, and the like. As with the cost containment strategies discussed earlier, there are critics who contend that utilization-based bonuses or salary withholdings give gatekeepers financial incen- tive not to provide specialty referrals even when it is in the best interest of the patient.

Utilization review (UR) allows an MCO to evalu- ate the appropriateness of the services provided and to deny payment for unnecessary services. MCO person- nel review and approve or deny the services performed or recommended by network providers. UR specialists are often healthcare professionals, and MCOs gener- ally use existing clinical care guidelines to determine whether services are appropriate.

UR may occur prospectively, concurrently, or retrospectively. Prospective UR means that an MCO reviews the appropriateness of treatment before a ser- vice is rendered. A request for a recommended service is sent to a UR panel for approval or denial. A denial does not mean a patient cannot move forward with his preferred treatment plan; however, it does mean that the patient will have to pay for the treatment out of his own pocket. Prospective UR is distinguished from concurrent UR, which is when the MCO review of the appropriateness of treatment occurs while treatment is being rendered. For example, a patient may need a procedure that requires hospitalization. Even though the procedure is performed and covered, a UR spe- cialist might still determine the number of days the patient may remain in the hospital or whether certain services, such as home care or physical therapy, will be covered upon discharge from the hospital. Finally,

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retrospective review means the MCO reviews the appropriateness of treatment (and therefore its cover- age) after a service is rendered. In this case, a patient’s medical records are reviewed to determine whether the care provided was appropriate and billed accu- rately; MCOs will not provide reimbursement for ser- vices deemed inappropriate or unnecessary. This latter type of review may also be used to uncover provider practice patterns and determine incentive compensa- tion (Shi & Singh, 2019, pp. 373–374). Regardless of when the review occurs, the use of UR is controver- sial because it may interfere with the patient–provider relationship and allow for second-guessing of provider treatment decisions by a third party who is not part of the diagnosis and treatment discussions.

Case management is a service utilization approach that uses trained personnel to manage and coordinate patient care. Although gatekeeping serves as a basic form of case management for all members, many patients with complex or chronic conditions, such as HIV/AIDS or spinal cord injuries, may benefit from more intensive case management. These patients may have frequent need for care from various specialists and thus benefit from assistance by personnel who are familiar with the many resources available to care for the patient and who are able to provide information and assistance to patients and their families. A case manager works with providers to determine what care is necessary and to help arrange for patients to receive that care in the most appropriate and cost-effective settings (Shi & Singh, 2019, p. 370). Although the general idea of case management is not controversial, some people believe it can be implemented in a man- ner that acts more as a barrier than an asset to care because additional approval is needed before a patient

receives care and because another layer of bureau- cracy is placed between the patient and the provider. TABLE  8-2 summarizes the three service utilization control strategies just discussed.

As you might imagine, managed care’s use of ser- vice utilization control mechanisms frequently leads to disputes between patients and their managed care company over whether the company is improperly affecting the provider–patient relationship (and nega- tively impacting the quality of care provided) by mak- ing decisions as to the type or quantity of care a patient should receive. This is both a highly charged health policy issue and a complicated legal issue, and one that is discussed in more detail in a review of individual rights in health care. For purposes of this chapter, it is enough to note that MCOs must have a grievance and appeal process to at least initially handle these sorts of disputes. Although companies’ processes differ in their specifics, they generally allow members to appeal a coverage decision, provide evidence to support the appeal, and receive an expedited resolution when medically necessary. The ACA included a number of provisions relating to the appeals process required of insurance plans; these provisions establish a federal standard for state external appeals laws governing products in the individual and group markets and cre- ate a new federal appeals process for self-insured plans (the provisions do not affect Medicaid and Medicare, which have their own appeals processes) (National Conference of State Legislatures, 2018). The need for adequate grievance and appeal procedures can be particularly acute for patients with special healthcare needs, such as those with physical or mental disabil- ities, and patients who otherwise use the healthcare system more frequently than most people.

TABLE 8-2 Service Utilization Control Strategies

Strategy Description Potential Concerns

Gatekeeper Uses a primary care provider to make sure only necessary and appropriate care is provided

Gatekeepers may have financial incentive to approve fewer services or less-costly care

Utilization review

Uses MCO personnel to review and approve or deny services requested by a provider to make sure only necessary and appropriate care is provided

Interferes with patient–provider relationship; someone other than the patient’s provider decides whether treatment is appropriate

Case management

Uses MCO personnel to manage and coordinate patient care to make sure care is provided in the most cost-effective manner

May act as a barrier to receiving care if the case manager does not approve a desired service or service provider

Abbreviation: MCO = managed care organization.

Managed Care 165

 

 

Source: Reproduced from: Kaiser/HRET Employer Health Benefits Survey, 2017. Retrieved from https://www.kff.org/health-costs/report/2017-employer-health-benefits-survey/

Common Managed Care Structures There are three managed care structures common in the market today: health maintenance organizations (HMOs), preferred provider organizations (PPOs), and point-of-service (POS) plans. All three provide preventive and specialty care, but the rules relating to accessing care differ for each. In general, HMOs have the most restrictive rules pertaining to patients and providers, PPOs have the least restrictive rules, and POS plans fall in the middle.

As shown in FIGURE 8-3, PPOs are the most popu- lar type of managed care plan, while very few people are still insured by a conventional FFS plan. In general, the more control an MCO has over its providers and

members, the easier it is to control utilization of ser- vices and, therefore, healthcare costs and quality. Con- versely, providers and patients prefer to have as much autonomy as possible, so the more restrictive MCO structures may be less desirable in that respect. How- ever, the distinctions among managed care structures have become blurred recently because of the consumer and provider backlash against MCO restrictions.

Health Maintenance Organizations When managed care first became prominent in the 1970s, HMOs were the most common type of MCO. There are several characteristics shared by all HMOs:

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Note: Information was not obtained for POS plans in 1988 or for HDHP/SO plans until 2006. A portion of the change in plan type enrollment for 2005

is likely attributable to incorporating more recent Census Bureau estimates of the number of state and local government workers and removing federal

workers from the weights. See the Survey Design and Methods section from the 2005 Kaiser/HRET Survey of Employer-Sponsored Health Benefits for

additional information.

Conventional POSHMO PPO HDHP/SO

FIGURE 8-3 Distribution of Health Plan Enrollment for Covered Workers by Plan Type, 1988–2017

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■ They pay providers a salary to cover the cost of any and all services that beneficiaries need within a provider’s scope of practice.

■ They negotiate a capitated rate with plan purchas- ers (e.g., employers) that prices the plan based on a per-member, per-month amount for each type of provider.

■ They coordinate and control receipt of services. ■ They arrange for care using only their network

providers. ■ They are responsible for providing care according

to established quality standards.

Despite these commonalities, HMOs may be structured through a variety of models, including

the staff model/closed-panel model, group model, network model, individual practice association, and direct-contract model (Shi & Singh, 2019, pp. 374– 377). Each model has advantages and disadvantages from the perspective of the HMO, its providers, and its members, as shown in TABLE 8-3.

Preferred Provider Organizations As is evident from Table 8-3, every form of HMO is fairly restrictive. In all models, the HMO provides coverage only if members seek care from network providers, and providers may or may not be limited to serving only HMO members. As both patients and providers began rebelling over these restrictions, new

TABLE 8-3 Key Characteristics of Common HMO Models

HMO Model

HMO-Provider Relationship and Payment Type

Provider Employment Arrangement

Must Members Seek Care From Network?

May Providers Care for Nonmembers? General Comments

Staff model/ closed-panel

HMO employs providers and pays a salary that often includes bonuses or withholdings.

Employed by HMO.

Yes No Provides services only in HMO’s office and affiliated hospitals. Relatively speaking, HMO has the most control over providers and service utilization, but has fixed costs of building and staff. HMO may contract with outside providers if necessary. Providers and consumers often do not like restrictions imposed by HMO. Providers do not need to solicit patients. Consumers may find it to be the most cost- effective option.

Group HMO contracts with one multispecialty group for a capitated rate.

Employed by own provider group.

Yes Depends on terms of contract

HMO has less control over utilization. HMO contracts for hospital care on a prepaid or FFS basis. Providers may prefer this model because they remain independent as opposed to becoming an employee of the HMO and because they may serve nonmembers if their contract permits.

(continues)

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HMO Model

HMO-Provider Relationship and Payment Type

Provider Employment Arrangement

Must Members Seek Care From Network?

May Providers Care for Nonmembers? General Comments

Network HMO contracts with several group practices (often primary care practices) for a capitated rate.

Employed by own provider group.

Yes Depends on terms of contract

The group practices may make referrals but are financially responsible for reimbursing outside providers. HMO has less control over utilization due to greater number of contracts and ability of providers to subcontract. Providers may prefer additional autonomy, but also take on financial risk of providing primary and specialty care. Members may have a relatively greater choice of providers.

IPA HMO contracts with IPA for a capitated rate.

IPA is intermediary between HMO and solo practitioners and groups. IPA pays providers a capitated rate.

Yes Depends on terms of contract

HMO has reduced control over providers but may have less malpractice liability because IPA is an intermediary. HMO may contract with specialty physicians as needed and for hospital care on a prepaid or FFS basis. Providers may prefer contracting with IPA instead of HMO to retain more autonomy. Members may have greater choice of providers.

Direct- contract

HMO contracts directly with individual providers for a capitated rate.

Self- employed.

Yes Depends on terms of contract

HMO has more leverage over providers because it contracts with them as individuals, but its administrative costs are much higher than having one contract or a few contracts with groups. Providers have less leverage regarding practice restrictions when contracting on an individual basis.

Abbreviations: fee for service = FFS; HMO = health maintenance organization; IPA = individual practice association.

TABLE 8-3 Key Characteristics of Common HMO Models (continued)

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forms of MCOs emerged, often formed by providers and hospitals themselves.

Like HMOs, PPOs have a provider network, referred to as preferred providers. Unlike HMOs, how- ever, PPOs provide coverage to patients seeking care from any provider, regardless of whether the provider is part of the member’s PPO preferred provider network. However, the amount of the service price that the PPO will cover is greater for an in-network provider than an out-of-network provider. For example, a PPO may agree to cover 80% of the cost for an in-network physi- cian visit, but only 70% of the cost for a similar, but out- of-network, physician visit. PPO patients thus have the option of paying more but choosing among a greater number of providers or paying less but choosing among a more limited number of (in-network) providers. In addition, a PPO member’s cost-sharing responsibilities are often higher than is the case for HMO members.

In exchange for being in the network, providers agree to accept a discounted rate for their services, often 25–35% below their usual rates (Shi & Singh, 2019, p. 378). Because PPO members have a financial incentive to seek providers who are in-network, these healthcare professionals find it worthwhile to accept a reduced rate from the PPO in exchange for the higher likelihood that PPO members will select them over non-network providers. Furthermore, unlike the cap- itation system found in HMOs, PPO providers do not assume financial risk for providing services. Depend- ing on the terms of their contract with the PPO, pre- ferred providers may or may not agree to limit their practice to PPO members. Although it is rare, PPOs may choose to guarantee preferred providers a mini- mum number of patients.

Even though an MCO has much less control over service utilization in the PPO model than in the HMO

model, PPOs still provide more incentives to use care judiciously than is the case in an FFS system. For exam- ple, in-network PPO providers are paid less than their customary rate by the company when they provide care to PPO members and often agree to abide by quality control and UR strategies used by the PPO. In addition, PPO patients have an incentive to use certain providers who will cost them less and have cost-sharing require- ments unlike anything found under FFS. The PPO model attempts to locate a middle ground between the very restrictive HMO models and the FFS structure that resulted in very high healthcare utilization and costs.

Point-of-Service Plans In another effort to contain costs while still provid- ing patients the freedom to choose their provider, POS plans combine features of HMOs and PPOs. Like an HMO, POS plans have a provider network, use a capitated or other payment system that shares financial risk with providers, and require members to use a gatekeeper to help control service utilization. However, designated services may be obtained from out-of- network providers who are paid on an FFS basis, but use of these providers costs the member more money, as with the PPO model. A POS gate- keeper must approve all in- network care and may also have some control over out-of- network care, depend- ing on the terms of the plan. The call by many con- sumers for increased choice in providers has become forceful enough that some HMOs are now offering POS plans, which they may refer to as open-ended (as opposed to closed-panel) models.

The Future of Managed Care Managed care is likely to remain an integral part of the health system despite its drawbacks. Patients chafe at utilization restrictions, as is evident by the increase

BOX 8-8 Discussion Questions

Cost containment strategies embraced by MCOs were a direct result of the FFS experience with ever-increasing utilization and healthcare costs. However, many consumers and providers chafe at the restrictions imposed by MCOs and are concerned that someone other than the provider is making treatment decisions. Are these restrictions appropriate and necessary? Do you favor some of the restrictions over others? Is it appropriate for one entity to be responsible for both paying for and providing care? Should someone other than an MCO—say the federal or state governments—have primary responsibility for making determinations about service utilization?

BOX 8-9 Discussion Questions

In terms of containing healthcare costs and improving healthcare quality, do you think healthcare consumers and professionals need even more restrictions than are currently used in managed care? Are there any reasons to revert back to the FFS system, even knowing its inflationary qualities? If you think that managed care is not the answer to our still-rising healthcare costs and quality concerns, what other tools might help lower costs and improve the quality of care? Should any tools be imposed by government regulation or agreed to voluntarily by insurers and the insured?

Managed Care 169

 

 

in PPO popularity and the emergence of the hybrid HMO/POS plan. Accurate or not, there is a widespread perception that managed care plans deny necessary care and provide lower-quality care (Shi & Singh, 2017, pp. 218, 235). Providers also complain that managed care interferes with their ability to practice medicine in a manner of their choosing, placing them in ethi- cal dilemmas due to the use of financial incentives and possibly lowering the quality of care they provide due to limits on tests and procedures they order. Yet, the key circumstance that led to the creation of managed care—high healthcare expenditures—has not abated. While the country struggles with ever-growing health- care costs, even under managed care, the willingness to experiment with various cost and utilization con- tainment strategies is likely to endure.

▸ Conclusion This introduction to health insurance serves as a building block for additional study, which expands upon many of the key health policy and law themes mentioned here. It should be clear to readers that health policy analysts and decision makers must be particularly attuned to health insurance issues; with- out knowing both the basic structure of health insur- ance and how various incentives impact the actions of healthcare consumers, professionals, and insur- ance carriers, they cannot make informed recom- mendations and policies addressing the key health issues of the day.

References Argwal, R., Mazurenko, O., & Menachemi, N. (2017). Health

deductible health plans reduce health care costs and utilization, including use of needed preventive services. Health Affairs, 36(10), 1762–1768. doi:10.1377/hlthaff.2017.0610

Auter, Z. (2018, January 16). U.S. uninsured rate steady at 12.2% in fourth quarter of 2017. Retrieved from https://news.gallup .com/poll/225383/uninsured-rate-steady-fourth-quarter-2017 . aspx ? g _ s ou rc e = Wel l – B e i ng & g _ me d iu m = ne w s fe e d & g _campaign=tiles

Council of Economic Advisors. (2004). Economic report of the President. Washington, DC: U.S. Government Printing Office.

Davis, K. (2004). Consumer-directed health care: Will it improve system performance? Health Services Research, 39, 1219–1233.

Health Insurance Portability and Accountability Act of 1996, 42 U.S.C. §§ 18, 26, & 29.

Jacobson, G., Damico, A., & Neuman, T. (2017, June 6). Medicare Advantage 2017 spotlight: Enrollment market update. Retrieved from https://www.kff.org/medicare/issue-brief/medicare -advantage-2017-spotlight-enrollment-market-update/

Jetty, A., Petterson, S., Rabin, D. L., & Liaw, W. (2018). Privately insured adults in HDHP with higher deductibles reduce rates of primary care and preventive services. Translational Behavioral Medicine, 8(3), 375–385. doi:10.1093/tbm/ibx076

Kaiser Family Foundation. (2017, September 19). 2017 Employer health benefits survey. Retrieved from https://www.kff.org /health-costs/report/2017-employer-health-benefits-survey/

Kullgren, J. T., Cliff, E. Q., & Krenz, C. (2018). Consumer behaviors among individuals enrolled in high deductible health plans in the United States. JAMA Internal Medicine, 178(3), 424–426. doi:10.1001/jamainternmed.2017.6622

National Conference of State Legislatures. (2018). Right to health insurance appeals process. Retrieved from http://www.ncsl.org /research/health/right-to-health-insurance-appeals-in-aca .aspx

Nondiscrimination in health coverage in the group market: Interim final rules and proposed rules, 66 Fed. Reg, 1378, 1382 (January, 2001) (codified in 29 C.F.R. pt. 2590.702).

Patient Protection and Affordable Care Act of 2010, Pub. L. No. 111-148 (2010).

Penner, S. (2004). Introduction to health care economics and financial management: Fundamental concepts with practical application. Philadelphia, PA: Lippincott, Williams, and Wilkins.

Phelps, C. E. (2003). Health economics (3rd ed.). Boston, MA: Addison-Wesley.

Rudowitz, R., & Garfield, R. (2018, April 12). Ten things to know about Medicaid: Setting the facts straight. Retrieved from https://www.kff.org/medicaid/issue-brief/10-things-to-know -about-medicaid-setting-the-facts-straight/

Shi, L., & Singh, D. A. (2019). Delivering health care in America: A  systems approach (7th ed.). Burlington, MA: Jones and Bartlett Learning.

Shi, L., & Singh, D. A. (2017). Essentials of the U.S. health care system (4th ed.). Burlington, MA: Jones and Bartlett Learning.

Sinaiko, A. D., Mehrotra, A., & Sood, N. (2016). Cost-sharing obligations, high-deductible health plan growth, and shopping for health care: Enrollees with skin in the game. JAMA Internal Medicine, 176(3), 395–397. doi:10.1001 /jamainternmed.2015.7554

Sood, N., Wagner, Z., Huckfeldt, P., & Haviland, A. (2013). Price-shopping in consumer-directed health plans. Forum of Health Economics and Policy, 16(1), 1–19. doi:10.1515 /thep-2012-0028

Starr, P. (1982). The social transformation of American medicine: The rise of a sovereign profession and the making of a vast industry. New York, NY: Basic Books, Inc.

Stevens, R., & Stevens, R. (2003). Welfare medicine in America: A case study of Medicaid. New Brunswick, NJ: Transaction Publishers.

Sultz, H. A., & Young, K. M. (2001). Healthcare USA: Understanding its organization and delivery (3rd ed.). Gaithersburg, MD: Aspen Publishers.

Tax Cut and Jobs Act of 2017, Pub. L. No. 115-97 (2017).

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▸ Endnotes a. Section 106 of the IRS Code of 1954 states that

employers who pay a share of premiums for employees’ hospital and medical insurance may exclude that amount from the gross income of employees.

b. There are both for-profit and not-for-profit insurance companies. Both types of companies

seek to earn enough revenues to cover expenses and the cost of accessing capital. However, for-profit companies return excess revenue to their investors whereas not-for-profit compa- nies put excess revenue back into the company.

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CHAPTER 9

Health Economics in a Health Policy Context

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Understand why it is important for health policymakers to be familiar with basic economic concepts ■ Understand how economists view decision making and options analysis ■ Describe the basic tenets of supply, demand, and markets ■ Understand how health insurance affects economic conditions ■ Apply economic concepts to health policy problems

▸ Introduction

There are several disciplines that may be used to assist you in analyzing health policy prob-lems; these include frameworks such as topi- cal domains, historically dominant perspectives, and key stakeholder perspectives, along with political and legal analysis. Furthermore, throughout the text, issues are viewed through a social framework by ask- ing you to consider what policies guide your decision making—in other words, what do you think should happen? This chapter informs you about yet another discipline—economics—that is useful when conduct- ing health policy analysis.

Students just beginning their health policy studies often question why it is necessary to study econom- ics. Most would rather think about and discuss what policies they support and what values should govern decision making, not about competitive markets,

equilibriums, and externalities. What may not be clear initially to students is that economic theory provides one of the fundamental building blocks for making policy choices, both generally and in the context of health care and public health. For instance, economic tools help policymakers predict how consumers and producers will react if they implement certain policies. Knowing this may help policymakers choose the most effective and efficient policy to achieve their goals. The governor’s request to Jaia in BOX 9-1 provides one example of how economic knowledge would prove helpful in health policy decision making. Other exam- ples include the following:

■ When federal officials decide which communi- ties should receive grants to support primary care clinics, they need to know if appropriate providers are available to staff clinics. Economic theory can help explain why some providers prefer to locate in urban or suburban Maryland instead of rural

 

 

174 Chapter 9 Health Economics in a Health Policy Context

West Virginia, why there is a shortage of qualified nurses but an abundance of cardiologists, and how to change this situation and help a rural primary care clinic remain viable.

■ In the face of a flu vaccine shortage, the president considers launching an initiative to ensure that every American can be vaccinated against the flu in the case of an epidemic. Economic theory sheds light on why there are so few vaccine producers supplying the United States currently and what could be done to entice manufacturers to partici- pate in the flu vaccine market.

Entire books and courses are devoted to the con- cept of health economics, and this chapter is not an attempt to distill all the theories and lessons of those texts and courses. Instead, our goal is to introduce you to the basic concepts of health economics, because understanding how economists view health-related problems is one essential component of being a good health policy analyst and decision maker. This chapter

begins with an overview of what health economics is, how economists view health care, and how individu- als determine whether obtaining health insurance is a priority in their lives. It then moves to a review of the basic economic principles of supply, demand, and mar- ket structure. As part of this discussion, you will learn what factors make supply and demand increase or decrease, how the presence of health insurance affects supply and demand, how different market structures function, and what interventions are available when the market fails to achieve desired policy goals.

▸ Health Economics Defined Economics is concerned with the allocation of scarce resources, as well as the production, distribution, and consumption of goods and services. Macroeconomics studies these areas on a broad level, such as how they relate to national production or national unemployment levels, while microeconomics studies the distribution and production of resources on a smaller level, including individual decisions to purchase a good or a firm’s deci- sion to hire an employee. Microeconomics also consid- ers how smaller economic units, such as firms, combine to form larger units, such as industries or markets (Pin- dyck & Rubinfeld, 2003, p. 3). Health economics, then, is the study of economics as it relates to the health field.

How Economists View Decision Making Economists assume that people, given adequate infor- mation, are rational decision makers. Rational deci- sion making requires that people have the ability to rank their preferences (whichever preferences are rel- evant when any sort of decision is being made) and assumes that people will never purposely choose to make themselves worse off. Instead, individuals will make the decision that gives them the most satisfac- tion, by whatever criteria the individual uses to rate his level of satisfaction. This satisfaction, referred to as utility by economists, may be achieved in many ways, including volunteering time or giving money to char- ities. Utility in a health context takes into account that individuals have different needs for and find different value in obtaining healthcare goods and services, and that whether they purchase health resources—and, if so, which ones they purchase—will depend on the individual’s preferences and resources.

Utility Analysis What does utility mean in terms of health care? Most people do not enjoy going to the doctor or taking medicine. It seems strange to think of individuals as

BOX 9-1 Vignette

Jaia is Governor Jara’s chief health policy analyst. Governor Jara is interested in improving the health status of residents in the state but is concerned about the impact any new initiative will have on the state’s economy. She asks Jaia to compare the economic consequences of three options: tax incentives for individuals to purchase exercise equipment or gym memberships, tax incentives for employers to offer wellness programs, and a mandate requiring that all stores selling food in the state provide fresh food and other healthy options. Fortunately, Jaia has a background in economics and knows that she needs to be concerned with basic principles of supply, demand, and market functions to help her governor make the best choice. This knowledge will lead her to ask questions such as: How big of a tax incentive is necessary to compel individuals or employers to act? Will tax incentives encourage behaviors, such as people joining a gym or employers offering wellness programs, that would not occur otherwise, or will the government simply be subsidizing transactions that would take place anyway? Is the problem that exercise options and healthy foods are not available and affordable, or are individuals simply making the choice not to engage in healthy behavior because they prefer to spend their time and money on other goods and activities? Will a mandate lead to the proliferation of healthy food stores or encourage stores to leave the state? The answers to these questions will help Jaia supply the governor with informed policy recommendations.

 

 

Health Economics Defined 175

being “happy” as a result of, for example, receiving weekly allergy shots or getting chemotherapy treat- ments. Likewise, it seems odd to think of individuals as undergoing such regimens to “maximize the utility” of the interventions. However, health care can be dis- cussed in terms of utility because most people enjoy being healthy.

Everyone has a different level of health, some due to their status at birth (e.g., infants born prematurely may have problems with their lungs or mental devel- opment) and others due to incidents that occur during their lives (e.g., an individual who was in a serious car crash may suffer from back pain). In addition, peo- ple have various tolerance levels for being unhealthy. In other words, the willingness to pay for a particular healthcare good or service will vary among individu- als based on their circumstances and preferences.

Furthermore, at some point, obtaining additional “units” of a particular good will bring less satisfaction than the previous units did. For example, although icing a sore knee for 20 minutes may reduce swelling, icing the same knee for 40 minutes will not reduce swelling twice as much, or, although buying one pair of glasses may bring high satisfaction, buying two pairs of glasses will not double the consumer’s satis- faction, because the second pair of glasses cannot do more than the first. This concept is called diminishing marginal utility, and it also affects what goods and ser- vices a consumer purchases.

In addition, consumers must consider the oppor- tunity costs of their decisions. Opportunity costs refer to the cost associated with the options that are not chosen. For example, if a consumer decides not to purchase any medication to ease his or her back pain, there is zero accounting or monetary cost; that is, it did not cost the consumer any money because he or she did not purchase the medication. However, there may be opportunity costs, monetary or otherwise, because the consumer is not pain-free. The consumer may endure a monetary loss if he or she has to take time off from work due to the injury. Or, the consumer may endure a nonmonetary loss because he or she can- not enjoy walking or exercising due to the back pain. Opportunity costs are the hidden costs associated with every decision, and in order to fully assess the cost and benefits of any decision, these hidden costs must be included in the calculation.

In terms of healthcare goods only, utility can be thought of as a function of individuals’ health and the healthcare goods and services they desire. Utility maximization in health care is the ideal set of health- related goods and services that an individual pur- chases. However, people need to purchase a variety of goods and services, not just those relating to health

care. Overall, consumers maximize their utility by purchasing what they consider to be an ideal bundle of healthcare goods and services, as well as other goods and services, based on their desire for each good and service and subject to the income they have available to make these purchases.

Scarce Resources In the healthcare arena, consumers have to make choices about the production, distribution, and con- sumption of healthcare resources. There are many types of healthcare resources. Healthcare goods include items such as eyeglasses, prescription drugs, and hos- pital beds; healthcare personnel include providers such as physicians, nurses, and midwives, as well as lab technicians, home healthcare workers, and count- less others; and healthcare capital inputs (resources used in a production process) include items such as nursing homes, hospitals, and diagnostic equipment (such as an X-ray machine). All of these things (and others) are considered healthcare resources.

If there were unlimited healthcare resources and an unlimited ability to pay for goods and services, the questions confronted by health policy analysts about what healthcare items should be produced and who should have access to them would still exist, but the answers would be less dire because there would be enough health care available for everyone. In reality, however, there is a finite amount of healthcare goods, personnel, and capital inputs. The financial resources are not available to provide all of the health care demanded by the entire population and still provide other goods and services that are demanded. As  a result of this scarcity of resources, choices and very apparent trade-offs must be made.

In general, consumer choices are based on indi- vidual preference, as discussed earlier, and the con- cept of efficiency. In economic terms, an efficient distribution of resources occurs when the resource distribution cannot be changed to make someone bet- ter off without making someone else worse off. This notion of efficiency in exchange is also referred to as Pareto-efficient, named after the Italian economist Vilfredo Pareto, who developed the concept. There are several types of efficiency, such as allocative effi- ciency, production efficiency, and technical efficiency (Penner, 2004, pp. 9–10; Santerre & Neun, 2004, p. 5). Allocative efficiency focuses on providing the most value or benefit with goods and services. Production efficiency focuses on reducing the cost of the inputs used to produce goods and services. Technical effi- ciency focuses on using the least amount of inputs to create goods or services.

 

 

176 Chapter 9 Health Economics in a Health Policy Context

The notion of efficiency raises many questions because there are always trade-offs to be made when producing goods and services. For example, should the production be more automated or more labor- intensive? Should the production sites be located in the United States or overseas? Can a service be pro- vided in a less costly setting? Is there any additional or different service or product that will enhance the benefits of the goods or services consumers receive?

Although they may not use this technical eco- nomic jargon, public and private policymakers often consider concepts of efficiency when they answer these types of questions. The answers, in turn, help identify which goods and services should be produced over- all in society and which of those goods and services should be related to health care. Because there is a finite amount of resources available, the choice to pro- duce more healthcare goods and services would result in the production of fewer non-healthcare goods and services, and vice versa. Similarly, the choice to pro- duce more of one kind of healthcare good or service will lead to the production of fewer healthcare goods and services of other types.

Finally, policymakers must also decide whether equity or fairness concerns should be taken into account, and in response alter their production and distribution decisions in ways that may make some people better off at the expense of others. For example, when a U.S. flu vaccine shortage occurred, some states required that vaccines be given only to individuals in high-risk groups. Individuals who had access to the vaccine, but were not in those high-risk groups, were made worse off by this decision because they were no longer allowed to receive the inoculation. On the other hand, some individuals in the high-risk group who otherwise would not have been able to obtain the vaccine were made better off under the new pol- icy. The point is not that efficiency is more import- ant than equity or vice versa. However, it is important to understand that these are distinct and not always complementary concerns, and whether and how one decides to influence the market will depend, in part, on how much the decision maker values efficiency and equity. In a world of limited resources, balancing con- sumer preferences, efficiency, and equity concerns can be a very difficult task for policymakers.

How Economists View Health Care Health economics helps explain how health-related choices are made, what choices should be made, and the ramifications of those choices. Evaluating the con- sequences of these choices is referred to as positive

economics. Positive economics identifies, predicts, and evaluates who receives a benefit and who pays for a public policy choice. Positive economics answers the questions, “What is the current situation?” and “What already happened?” Normative economics discusses what public policy should be implemented based on the decision maker’s values. It answers the question, “What should be?” (Feldstein, 2005, p. 5; Senterre & Neun, 2004, p. 14). For example:

A positive statement: In 2016 approximately 28  million people in the United States did not have health insurance for the entire year.

A normative statement: All people living in the United States should have health insurance.

As shown by the concepts of positive and nor- mative economics, health economists, like other ana- lysts, cannot avoid discussing how health care should be perceived. Is health care a good or service like any other good or service such as food, shelter, or clothing that consumers obtain or refrain from obtaining based on availability, price, resources, and preference? Or is health care a special and unique commodity for rea- sons such as its importance to individuals’ quality of life or how the healthcare market is structured? Bear in mind that health policymakers take their own view of health care’s place in the market into account when they argue for or against a policy.

The following sections identify two theories of how to view health care. Many economists’ views fall some- where in the middle of these two theories or combine aspects of the two theories to create a hybrid theory. These theories were not presented to be an either/or choice, but to illustrate that even within the field of economics there is a fundamental debate about how to view health care.

▸ Economic Basics: Demand Consumers, whether an individual, firm, or country, purchase goods and services. Demand is the quan- tity of goods and services that a consumer is willing and able to purchase over a specified time. In the case of health care, for example, demand equals the total demand for healthcare goods and services by all the consumers in a given market.

Demand Changers In general, as the price of a good or service increases, demand for that good or service will fall. Conversely, as the price of goods or services decreases, demand for those goods or services will rise.

 

 

Economic Basics: Demand 177

Various factors in addition to price also increase or decrease the demand for a product. Insurance is an important factor relating to demand that is discussed separately later in this chapter. A few of the other fac- tors that may change the demand for a product include the following:

■ Consumer’s income: As a consumer’s income increases, demand for a product may increase. For example, a consumer may desire a new pair of eyeglasses but cannot afford it. Once the consum- er’s income increases, the consumer can purchase the eyeglasses.

■ Quality: Consumers have preferences based on quality, both actual and perceived. In addition, a change in quality will likely result in a change in demand. A decrease in the quality of a product may result in a decrease in demand because con- sumers decide the product is no longer worth the price charged. For example, a consumer may discover that the eyeglasses he or she wants fall apart easily, thus may decide not to buy the product.

■ Price of substitutes: A substitute is a differ- ent product that satisfies the same demand. For example, contact lenses may be a substitute for eyeglasses. As the price of contact lenses drops, a consumer may decide he or she prefers contact lenses to eyeglasses.

■ Price of complements: A complement is a prod- uct associated with another product. For exam- ple, cleaning solution is a complement to contact lenses. The price and quality of cleaning solution (the complement) may be an important factor when a consumer is debating whether to keep wearing glasses (the original product) or switch to contact lenses (the alternative product). If the price of cleaning solution increases, even though the price of contact lenses stays the same, the consumer may decide to purchase eyeglasses instead of contact lenses. In other words, demand for complements and alternative products shifts in opposite ways, so an increase in the price of a complement will decrease the demand for the alternative product, and vice versa.

BOX 9-2 Discussion Questions

Consider each of the following issues and discuss whether you support Theory X, Theory Y, neither theory, or some combination of them.

Issue Theory X Theory Y

Your view about how an individual’s health is determined

Whether a person is healthy or sick is determined randomly.

Whether a person is healthy or sick depends on lifestyle choices such as whether a person smokes, drinks, or wears a seatbelt.

Your view of medical practice

Medicine is a science, and experts will ultimately discover the best means for treating every illness.

Medicine is an art and there will never be one best way to treat every illness because illnesses are often patient-specific and because there will always be a demand for lower-cost and less painful treatments.

Your view of medical care

Medical care is a unique commodity. Medical care is similar to any other good or service.

Your view of the government’s role in health care

Government regulations are necessary to protect this unique commodity, to control profiteering at the cost of patient care, to control resources spent on health care, and to improve information sharing.

Government regulations are not necessary, technological advances and more services are desirable, and competition, not regulation, should drive the market.

Source: From Musgrave, GL. Health economics outlook: two theories of health economics. Bus Econ. 1995;30:7–13.

 

 

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The physical profile of a consumer has an impact on demand for healthcare services in some predict- able ways. Women generally demand more healthcare services than men do before reaching 65 years of age, primarily due to health needs related to childbearing, whereas men older than 65 years use more care than do women in the same age group. In addition, many diseases are more prevalent in women than in men, resulting in an expected increase in demand for health services by women. Some of these diseases include cardiovascular disease, osteoporosis, and immuno- logic diseases (Phelps, 2003, pp. 149–150; Senterre & Neun, 2004, p. 111). Regardless of sex, an individual who is born with a medical problem, or who devel- ops one at a relatively young age, can be expected to have a higher than average demand for healthcare ser- vices. Aging consumers are more likely to have higher healthcare needs than younger consumers. Of course, any factor that usually leads to increases in demand for healthcare services may be offset by lack of finan- cial resources or lack of access to providers.

In addition to the physical profile of a consumer, interesting research is being conducted in relation to consumers’ level of education and their demand for services. Although there is no consensus on the direct impact of general education on demand for health services, some studies show a positive relationship between medical knowledge and demand for health- care services; that is, the more the consumer knows about medicine, the higher the level of consumption of healthcare services. This association may indicate that consumers without as much medical knowledge underestimate the appropriate amount of health ser- vices they need, or it may mean that consumers with more medical education have a greater ability to pur- chase medical care. Other explanations are possible as well (Agency for Healthcare Research and Quality, n.d.; Cutler & Lleras-Muney, 2006; Senterre & Neun, 2004, p. 127).

Elasticity Two of the demand changers discussed previously are shifts in price and shifts in income. Elasticity is the term used to describe how responsive the change in demand or supply is when there is either a change in price or a change in income. The concept of elasticity is important to understand as a policy analyst because it is essential to know whether changes in consumers’ incomes (say, through a tax credit) or changes in the price of a product (perhaps through incentives given to producers) will result in the desired outcome. The desired outcome may be increased consumption,

which might be the case if the service is well-child checkups. Conversely, the desired outcome may be decreased consumption, which might be the case if cigarettes are the product being consumed.

Price Elasticity of Demand Price elasticity of demand is based on the percentage change in the quantity demanded resulting from a 1% change in price. In other words, does consumer demand for a product, such as a vaccination, increase as the price of a product decreases by 1%, or vice- versa? Elasticity is calculated as follows:

=Demand elasticity % change in quantity demanded

% change in price

(Economists often use the midpoint method which averages the percentage change in quantity and price. This results in the same answer whether there is a price increase or decrease. Price elasticities are always negative because price and demand are inversely related. Even so, elasticities are reported in absolute values, not negative numbers).

Demand for a product is considered elastic if the sum is greater than 1 and inelastic if the sum is less than 1. An elasticity of 0 is perfectly inelastic, meaning the demand does not change in response to a change in price.

For example, suppose a vaccine costs $20 per dose and at that price a family buys four doses, for a total of $80. The next year the price increases 20% to $24 per dose and the family buys only three doses for a total of $72. The mid-point of the two prices is $22 and the mid-point of the two quantities demanded is 3.5. Using the mid-point method, the calculation is as follows

− = −

1/3.5 2/22

3.14 or 3.14

Because elasticity equals 3.14, the product is con- sidered elastic (because the result of the elasticity cal- culation is greater than1). In this example, for every 1% increase in vaccine price, demand decreases by 3.14%. If the price decreases, the quantity demanded would be expected to increase.

Of course, goods may also be inelastic, which means the demand for the good is not as sensitive to a change in price. As a result, when price increases, the quantity demanded will not decrease at the same rate as the price increases. For example, some people will not reduce their consumption of cigarettes even

 

 

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if the price of cigarettes increases. However, at some point the price could become high enough that con- sumer behavior will change, resulting in a decrease in demand.

Supply elasticity works in much the same way as the price elasticity of demand and uses the same formula, except it refers to the relationship between the quantity of goods supplied and the price of the goods. Supply elasticity is often defined as the percent- age change in quantity supplied resulting from a 1% increase in the price of buying the good. The change is usually positive because producers have an incen- tive to increase output as the price they will receive for the good rises. However, if supply elasticity refers to variables other than the price of the good, such as the cost of raw materials or wages, then the supply elastic- ity will be negative; that is, as prices of labor or other inputs rise, the quantity supplied will fall (all other things being equal).

Income Elasticity of Demand Elasticity works in the opposite way in the case of inferior goods. An inferior good, as the name suggests, is less desirable than a normal good. As a result, as a consumer’s income increases, demand for the infe- rior good will decrease. Instead of buying more of the inferior good, the consumer will prefer to buy the normal good. For example, suppose a generic over-the-counter pain medication is cheaper than a particular prescription pain medication, but the prescription pain medication is more effective. Con- sumers with low income may choose to purchase the over-the-counter medicine, the inferior good. If their income increases, they will not buy more of the infe- rior good, but instead will switch to the prescription pain medicine because it is a better good, for their purposes, than the inferior good.

Health Insurance and Demand In addition to the general economic rules of demand for health services, the presence of health insurance affects demand for healthcare goods and services. Health insurance acts as a buffer between consum- ers and the cost of healthcare goods and services. In an insured consumer’s view, healthcare goods or ser- vices cost less because instead of paying full price, the consumer may only have to pay, for example, a co- insurance rate of 20% (after satisfying the deduct- ible). For example, if a surgical procedure normally costs $10,000, the insured consumer may have to pay only $2,000 for the benefit of the surgery because his

or her insurance company pays for the remainder. In this way, the presence of health insurance can have an effect on the consumer—to increase demand—in the same way that an increase in the consumer’s income can increase demand.

In general, insured consumers are less sensitive to the cost of healthcare goods and services than unin- sured consumers (Penner, 2004, p. 38). Thus, the pres- ence of health insurance creates the problem of moral hazard. Moral hazard can occur in a variety of eco- nomic situations when consumers buy more goods or services than necessary because they do not have to pay the full cost of acquiring the good or service. In relation to health insurance, moral hazard results when an insured consumer uses more services than he or she would otherwise because part of the cost is covered by insurance.

For example, if a consumer has a $500 health insurance deductible, the consumer pays 100% of the first $500 of health care received. If there is a 20% co-insurance charge after that, the consumer pays only $.20 per dollar for every dollar spent after $500. If the consumer values a particular healthcare service, such as a preventive dental exam, at $50 but the ser- vice costs $100, the consumer will not purchase the service before meeting the deductible. However, after the deductible has been met, the dental exam (assum- ing it is a covered benefit) will cost the consumer $20 (20% of $100), so the consumer will purchase the service because it is under the consumer’s $50 value threshold.

As the portion of the healthcare cost that a con- sumer pays based on co-payments or co-insurance decreases, the consumer becomes less sensitive to changes in the price of the product. Say a consumer decides he or she is unwilling to pay more than $2,500 for surgery. If the consumer owes a 10% co-insurance charge, the consumer will be willing to pay for sur- gery as long as it is not priced at more than $25,000. At $25,000, the consumer would pay $2,500 and the insurance company would pay $22,500. However, if the same consumer has a 20% co-insurance rate, he or she will not elect surgery once the price rises above $12,500 because the cost to the consumer would be more than the consumer’s $2,500 limit; for example, if the surgery costs $15,000, the consumer would owe $3,000 and the insurance company would cover the other $12,000.

The problem of moral hazard is particularly rel- evant in health care because consumers have an incentive to seek out more medical care: they think it will make them feel better. And, as noted earlier, an insured consumer is more likely to purchase a

 

 

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desirable healthcare good or service because the pres- ence of insurance reduces his or her cost. The same cannot be said of owning a home or auto insurance; although consumers may be a little less careful because of the protection fire or car insurance affords them, it is unlikely that a person will allow an automotive cen- ter to replace a working fuel pump on his or her car just because he or she has car insurance.

▸ Economic Basics: Supply Supply is the amount of goods and services that pro- ducers are able and willing to sell at a given price over a given period of time. As with demand, the price of a product is a key factor in determining the level of supply. However, unlike demand, where there is often an inverse relationship between price and demand, an increase in the price a good is sold for usually leads to an increase in quantity supplied. Conversely, as the price consumers will pay for a product decreases, sup- ply will often decrease as well. As with demand, there are many factors that affect the quantity of a good or service being supplied.

Costs Costs are a key factor in determining the level of sup- ply. Costs refer to what inputs are needed to produce a good or service. For example, the price of cotton may impact the cost of producing medical scrubs or bed linens made out of cotton, or the price of steel may affect the cost of producing an autoclave or X-ray machine made with steel. As the cost of these inputs increases, the cost of producing the final good increases as well. If the price for a good or service does not increase as the cost of inputs increases, the quantity supplied is likely to decrease. Thus, if it costs a manufacturer $100 more to build an X-ray machine because the cost of steel has risen, it is likely that the manufacturer will pass that production cost increase on to the consumer by raising the purchase price of the X-ray machine. Alternately, the manufacturer may choose to absorb the $100 cost increase and not raise the purchase price, which will lead the manufacturer to supply fewer X-ray machines, find a way to produce the good more cheaply using the same method, or find a different way to produce the good.

Costs are counted in many different ways. We focus here on average costs and marginal costs.

■ Average cost: The cost of producing one product over a specific period of time. For example, if it costs a manufacturer $2 million to produce 2,000

hospital beds in 1 year, the average cost is $1,000 per bed during that year.

= = =

Average cost Total cost/Quantity $2,000,000/2,000 hospital beds $1,000 per hospital bed

■ Marginal cost: The price of producing one more unit of the output—in our example, one more hos- pital bed. Whatever additional labor, equipment, and supplies are needed to produce one more hospital bed is the marginal cost of production. As a general matter, the marginal cost increases as output increases.

Supply Changers Other factors in addition to sale price and cost can increase or decrease the supply of a product. Two common factors are number of sellers and changes in technology:

■ Number of sellers: As the number of sellers of a good increases, the supply of the good will increase as well because there are more compa- nies producing the good. As long as the market is profitable, new sellers will be enticed to enter the market. This occurs until the market reaches equilibrium, where the quantity demanded equals the quantity supplied.

■ Change in technology: New technology may mean a new way to produce a desired outcome, which may alter the supply of a good or service. For example, fiberglass has replaced plaster in most casts and the production of each material has shifted accordingly (fiberglass up, plaster down). New technology can also make a product more accessible than before. For example, many surgeries once handled on an inpatient basis may now be performed on an outpatient basis or in a physician’s office due to new technology, such as arthroscopy. In addition, evolving technology has led to brand new fields, such as robotic sur- gery. Technological improvements can increase demand for some services and reduce it for oth- ers, leading to a change in the production of these goods and services.

Profit Maximization Although consumers are driven by the desire to max- imize their satisfaction, suppliers are driven by their desire to maximize revenues. For-profit companies

 

 

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seek to make profits to pass on to their sharehold- ers, while not-for-profit companies face a variety of requirements regarding disposing of the revenue they generate in excess of expenses and the cost of acquiring capital to run the company. For ease of explanation, the term profit will be used here to discuss supplier incentives, even though the healthcare field includes a large share of not-for-profit companies.

Profit is the price per unit sold less the produc- tion cost per unit. In a competitive market, profit is maximized at the level of output where the marginal cost equals the price. If a hospital bed costs $1,000 to produce and is sold for $1,500, the profit per bed is $500. If the marginal cost of producing one more bed is $1,400, the producer will make that additional bed because it can be sold for $1,500, a $100 profit; how- ever, if the marginal cost of producing an additional bed is $1,600, the producer has no incentive to pro- duce that additional bed because it can only be sold at a loss of $100. Due to the profit maximization goal, if the price of a product increases and a competitive market exists for the product, manufacturers will increase production of the product until the output level again reaches the point where the marginal cost equals the price.

When a profitable market exists, new produc- ers will be drawn into the market so they can reap financial benefits. The new producer may price its hospital bed for less than $1,500 to attract consum- ers, or the new producer may think there is a niche for a higher-priced bed that has additional features. Assume the new producer chooses to market a similar bed as the $1,500 bed but sells it for $1,250. If a con- sumer can purchase the bed from the competing com- pany for $1,250 with no additional opportunity costs, demand for the $1,500 hospital bed is likely to fall. The manufacturer of the $1,500 bed will have to lower its price or improve the product (or the perception of the product) to increase demand for a higher-priced bed. At the point where there is a balance between the quantity supplied and the quantity demanded and the price is set to the marginal cost of production, there is equilibrium in the market.

If such a balance does not occur, there is disequi- librium in the market. The disequilibrium could repre- sent a surplus of a good or service due to excess supply or sudden drop in demand, or it could result from a product shortage due to inadequate supply or a sharp increase in demand. Surpluses occur when the market price in a competitive market is higher than the mar- ginal cost of production; as a result, producers lower their prices to increase sales of their product. These price reductions will keep happening until market

equilibrium is reached. For example, there could be a sudden drop in demand for a food product due to a news report that eating the product more than three times a week may put people’s health at risk. Due to the sudden drop in demand, excess product will be available. Producers will, in turn, lower the price of the product until equilibrium is reached. Shortages occur when the market price is lower than the marginal cost of production. As a result of the shortage, consum- ers might be willing to pay more for the product, so producers increase their prices until demand stops increasing and market equilibrium is reached. If an opposite news story appeared, hailing the food product as improving health if eaten at least four times a week, there may be a sudden surge in demand. As a result, consumers will likely be willing to pay more for the product and producers will raise the price until equi- librium is reached. Because producers often cannot make significant changes to their production schedule or products in a short amount of time, market equilib- rium positions may take some time to achieve.

Health Insurance and Supply Just as the presence of health insurance affects a con- sumer’s demand for medical goods and services, it also may impact a healthcare provider’s willingness to supply goods and services. This is a complicated issue because, on the one hand, a provider is expected to act as the patient’s agent and thus should act in the patient’s best interests. If providers encourage only appropriate care, insurance is working in a positive way.

On the other hand, providers may have a financial incentive to encourage or discourage the consumption of healthcare goods and services. Providers could rec- ommend against treatment because of financial incen- tives resulting from the presence or absence of health insurance. For example, financial incentives found in managed care may discourage providers from rec- ommending a particular treatment. Additionally, if a patient is both uninsured and unable to pay for ser- vices out-of-pocket, providers have a financial incen- tive not to provide potentially necessary services due to their inability to receive payment. Similarly, a provider may seek to increase his or her income by encourag- ing inappropriate or excessive care. This problem—the provider version of moral hazard—is referred to as supplier- induced demand. Supplier-induced demand is the level of demand that exists beyond what a well- informed consumer would have chosen. The theory behind supplier-induced demand is that instead of consumer demand leading to an increase in suppliers (healthcare providers), the suppliers create demand

 

 

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in the consumers (patients), often by relying on infor- mation only available to the supplier. However, econ- omists debate whether supplier-induced demand actually exists because it is difficult to study empirically and because behavior consistent with supplier-induced demand may also be consistent with appropriate med- ical treatment (Phelps, 2003, pp. 237–242).

▸ Economic Basics: Markets To this point, we have reviewed many basic aspects of economic theory—how consumers behave, how sup- pliers behave, what drives and shifts demand, and what drives and shifts supply. To understand how these the- ories work in the healthcare industry, it is necessary to explore how health insurance affects markets, what kind of market exists for health care, how market structure relates to the production and distribution of goods and services, and why markets fail and what can be done to alleviate the problems associated with market failure.

Health Insurance and Markets Before delving into the basics of economic markets, it is necessary to highlight how the presence of health insurance alters the dynamics of a standard economic transaction. In a typical market transaction, such as buying food at the grocery store, there are only two parties involved—the consumer who buys the food and the supplier who sells the food. The cost to the consumer is the cost of the food; the consumer bears full responsibility for paying that cost and pays that cost directly to the supplier, the grocery store.

The typical medical transaction, however, does not follow these rules, both because of the types of events that lead to a medical transaction and because of the presence of health insurance. In health care, there are both routine and expected events (e.g., an annual physical) and unanticipated needs due to an unpredictable illness or injury. The exact diagnosis and treatment are often unknown initially and the patient’s response to treatment is not guaranteed, resulting in an inability to predict exactly what resources will be needed. Without knowing what goods and services are required, it is impossible to estimate the cost to be incurred. This makes it very difficult for consumers to weigh their preferences for medical care as compared to other goods and services, and makes it difficult for suppliers to know which goods and services will be demanded and at what price they can sell their goods and services.

Another reason healthcare transactions often do not follow the typical market exchange is because the

presence of health insurance means healthcare trans- actions involve three players, instead of two; these three players are (1) patients (the consumer), (2) healthcare providers (the supplier), and (3) insurers (who are often proxies for employers). Insurers are also known as “third-party payers” because they are the third party involved in addition to the two customary parties. In the public insurance system, the third-party payer is the government, and in the private sector, the third- party payers are private health insurance companies. Having the health insurance carrier as a third party means consumers do not pay the full cost of health- care resources used and therefore may be less likely to choose the most cost-effective treatment option, to reduce the information gap between themselves and providers, or be as vigilant against supplier-induced demand as they might in other circumstances.

Market Structure Understanding markets begins with the notion of a perfectly competitive market, because in economic theory a perfectly competitive market serves society by efficiently allocating the finite resources available. Due to specific market conditions that make up a per- fectly competitive market, a competitive equilibrium is reached once quantities supplied equal the quanti- ties demanded.

There are numerous types of market structures, ranging from perfectly competitive markets with many buyers and sellers to monopolistic markets with a single seller controlling the market. Other common market structures include oligopolies, which have a few domi- nant firms and substantial but not complete barriers to entry, and monopsonies, which have a limited number of consumers who control the price paid to suppliers. Based on the market structure, consumers and pro- ducers have varying degrees of power in terms of set- ting prices, choosing among products, and deciding whether to participate in the market. TABLE 9-1 reviews the characteristics of three market structures that are most useful to understanding healthcare markets: per- fectly competitive markets, monopolistic markets, and monopolistically competitive markets.

You know from the discussion of supply and demand that the healthcare market cannot be perfectly competitive based on the description in Table 9-1. (In fact, no markets are truly perfectly competitive.) Some consumers, such as the federal government, may have extensive market power as well as the ability to set prices. Producers of patent-protected healthcare products are provided with supply power for a limited period of time, which gives them an ability to control

 

 

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prices. Consumers do not have perfect information regarding healthcare needs and healthcare costs, and providers and insurers do not have perfect informa- tion regarding patient illnesses. Given the presence of health insurance, consumers do not bear all the cost of using healthcare services. With these characteristics, the healthcare market is monopolistically competitive. In many areas of the healthcare market, there are a few dominant firms with a lot of market power and many smaller firms who participate in the market, but the smaller firms do not have the power to shape market conditions.

Market Failure A market failure means resources are not produced or allocated efficiently. As you recall, we defined effi- ciency generally as the state of least cost production where the resource distribution cannot be changed to make someone better off without making someone else worse off, and we also described a few specific types of efficiency. When something about the structure of the

market prohibits it from being efficient, it is referred to as market failure; the question then becomes what interventions in the market, if any, should occur in an attempt to alleviate the market failure.

Before we turn to why markets fail, we must address one additional issue: Does an inequitable distribution of resources constitute a market failure? Under the tra- ditional economic school of thought, the answer is no; a market failure refers to inefficiency, and concerns about equity are not part of the efficiency calculation. How- ever, some economists consider equity a valid factor when evaluating the functioning of a market. Regard- less, whether an inequitable distribution of resources fits under the economic designation of “market failure” is not as important as whether policymakers choose to intervene in a market based on equity concerns.

Some of the most salient reasons that market fail- ures occur in health care include concentration of market power, imperfect information (producers or consumer not having complete and accurate infor- mation), the consumption of public goods, and the presence of externalities. We have already discussed

TABLE 9-1 Characteristics of Key Market Structures

Perfectly Competitive Monopoly Monopolistically Competitive

Number of firms Many One (in a pure monopoly) Many

Market share No dominant firms One firm has all market share and price and output.

There may be many firms with market share and or a few dominant firms. Firms can set price because of product differentiation.

Barriers to entry for new firms into market

No Yes—absolute barriers; no new firms may enter market.

Some barriers, due to differentiation of product, licensure, etc.

Product differentiation

No. Products are for each other.

No. Only one product; no substitutes are available.

Yes. Many products; they are not substitutes for each other (brand loyalty).

Access to information and resources

Consumers and producers have perfect information.

One firm controls all information (asymmetric information).

All firms have equal access to resources and technology unless there are a few dominant firms with more access to resources.

Cost of transaction

Consumers bear cost of consumption, and producers bear cost of production.

Higher price to consumer because firm has ability to reduce quantity, retain excess profits.

Blend of costs in perfectly competitive market and monopoly market.

 

 

184 Chapter 9 Health Economics in a Health Policy Context

concentration of market power and imperfect infor- mation; the next sections focus on public goods and externalities.

Public Goods Public goods have two main features. First, public goods are nonrival, meaning that more than one per- son can enjoy the good simultaneously. An example of a rival private good would be a single pen, as two people may not use the same pen at the same time. Second, a public good is nonexclusive, because it is too costly to try to exclude nonpaying individuals from enjoying public goods (Senterre & Neun, 2004, p. 230).

Classic examples of public goods are national defense measures and lighthouses. Everyone simulta- neously benefits from national defense, and it is not economically feasible to exclude nonpaying individ- uals (e.g., tax evaders) from enjoying the benefits. In the same way, multiple ships may benefit at the same time from a warning provided by a lighthouse, and it would be very difficult to exclude a particular ship from enjoying the benefit. In the health field, examples of local public goods include clean water in a free pub- lic swimming area or a public health awareness cam- paign on city streets. Everyone enjoys the clean water (at least until it is overcrowded), and it would be costly to exclude nonpayers. Similarly, multiple people can benefit from a public health campaign simultaneously, and exclusion of nonpayers would be impossible or quite costly.

Public goods can be transformed into other types of goods. For example, a public good could be made exclusive by charging a fee; these are called toll goods (Weimer & Vining, 1999, p. 81). The public swimming water could be fenced off and a fee charged for admis- sion, or the public health campaign could be placed in the subway, which would exclude those who could not afford the fare. Once public goods are transformed into toll goods, concerns arise about whether the price is set at the most efficient level. Toll goods may still lead to market failure if the cost of using the good excludes users who would gain more from enjoying the good than they would cost society by consuming the good (Weimer & Vining, 1999, pp. 81–82).

In addition, goods provided by local, state, and federal governments may be, but are not necessarily, public goods in the economic sense. For example, if a state funds a free healthcare clinic, it is not funding a public good. Even though nonpayers are, by defini- tion, included, the benefits generally inure to the indi- vidual and, in most cases, more than one individual cannot enjoy the same healthcare good or service. It is

possible, however, that other people will benefit from a healthcare service they do not receive; for example, if your neighbor receives a service that helps him quit smoking, you will receive the benefit of no longer being exposed to your neighbor’s secondhand smoke.

Public goods also create the free rider problem, making it unprofitable for private firms to produce and sell goods due to the high cost of excluding non- payers (Santerre & Neun, 2004, p. 230). The free rider is one who enjoys the benefit of the good without paying for the cost of producing the good. Because it is impossible to exclude users or force consumers to reveal their true demand for the public good, they do not have incentive to pay for the units of the good they use (Weimer & Vining, 1999, p. 86). For example, an individual cannot be prevented from gaining knowl- edge from a public health awareness campaign, so if a private company were responsible for providing the education campaign, it could not force a consumer to pay for it. Eventually, even though many people would like to take advantage of clean air or health educa- tion, the lack of people paying for it would result in an underproduction of these services unless some action were taken to alter the market dynamics.

Externalities Externalities are much more common than pub- lic goods in the healthcare market. An externality is “any valued impact (positive or negative) resulting from any action (whether related to production or consumption) that affects someone who did not fully consent to it through participation in a voluntary exchange” (Weimer & Vining, 1999, p. 94). In a typi- cal economic transaction, the costs and benefits asso- ciated with a transaction impact only those involved in the transaction. For example, remember our con- sumer buying food at the grocery store? The only two people affected by that transaction are the consumer, who pays money and receives food, and the grocer, who provides food and receives money. Situations with externalities, however, are different. Externalities exist when the action of one party impacts another party who is not part of the transaction; in other words, the parties to the transaction will find there is an “unpriced by-product” of producing or consuming a good or service (Santerre & Neun, 2004, p. 231).

Externalities may be positive or negative. An exam- ple of a positive externality is when one person gets vaccinated against the chicken pox and other people benefit because chicken pox is less likely to be transmit- ted in that community. If enough people get vacci- nated, “herd immunity” will exist in the community.a

 

 

Economic Basics: Markets 185

In this case, the positive unpriced by-product is the additional protection received by others who were not vaccinated. An example of a negative externality is represented by illegal hazardous waste disposal. Say a hospital dumps biologic waste such as blood, syringes, gauze with infected material on it, and the like into a public water source. The unpriced by-product is paid by the general public, who face an increased risk of illness from using the contaminated water source. The costs to the general public may not have been included in the hospital’s cost–benefit analysis when it decided to dump the biologic waste.

With both positive and negative externalities, the cost and benefits of production or consumption are borne by individuals who do not participate in the transaction. Due to the unpriced by-products, there are external costs and benefits that are not considered when deciding whether to make the transaction, lead- ing to an under- or overproduction of the resource from society’s perspective.

Government Intervention When market failures occur, the government may intervene to promote efficiency or to promote equity (of course, it may also choose not to intervene at all). Some examples of government interventions include financing or directly providing public goods, creating incentives through tax breaks and subsidies, imposing mandates through regulation, prohibiting activities, and redistributing income. We discuss these options in the following sections.

Government Finances or Directly Provides Public Goods. When market failure occurs, the government may choose to finance or provide a good or service directly instead of attempting to influence the actions of private producers. For example, if the government wanted to increase access to health care, it could cre- ate new government-run health centers or provide financing to privately run health centers.

These are two different paths—direct provision or financing—with different sets of issues. The main dif- ference when the government provides or finances care instead of a private sector is the lack of profit motive on the part of the government (Santerre & Neun, 2004, p. 252). Instead of focusing on the financial bottom line, public providers may focus on other goals, such as equity or assuring the presence of a particular good or service for everyone or for specific populations.

When the government creates or expands a public program, there is concern that crowd-out may occur. Whenever a program is established or expanded, the

program has a particular goal and targets a particu- lar audience. For example, the government may try to reduce the number of people without insurance by expanding an existing public program such as the Children’s Health Insurance Program. Crowd- out occurs when instead of reaching only the target audience (in this case, the uninsured), the public pro- gram also creates an incentive for other individuals (in this case, privately insured people) to participate in the public program. Because the program has a finite amount of resources, some of the target audi- ence (the uninsured) may be crowded out from par- ticipating in the program by the presence of the other, nontargeted individuals (the privately insured). This unintended development prevents programs from maximizing cost-effectiveness because instead of obtaining the largest change (in this case, the reduc- tion in the number of uninsured) for the public dollar, some of the change is simply a result of a cost shift from a private payer (the privately insured) to a public payer (the expanded program). Crowd-out may also change incentives for other providers of services. In this example, the presence of the new or expanded government program may reduce the incentive for private employers to provide the same good or service (in this case, health insurance).

Government Increases Taxes, Tax Deductions, or Subsidies. Taxes and subsidies can be used to alter the price, production, or consumption of goods in an effort to fix a market failure. For example, increasing a tax on a good raises the price of that good and dis- courages consumption; this strategy is often employed to discourage consumption of harmful products, such as cigarettes. Similarly, the government could choose to tax cigarette producers as a way to encourage them to produce less of the harmful product or leave the market altogether.

Conversely, the government could subsidize a good, directly or through a tax deduction, when it wants to encourage the consumption and production of the good. For example, if the government wanted more low-income individuals to purchase healthy foods, it could choose to subsidize their purchase of fruits and vegetables by allowing individuals who use public ben- efits, such as food stamps, to purchase more fruits and vegetables than would normally be allowed by the face value of the food stamps (for example, $1 in food stamps would allow for the purchase of $2 of fruits or vegeta- bles). Similarly, if the government wanted to encourage vaccine manufacturers to produce more vaccine doses, it could accomplish this goal through direct subsidies to or tax deductions for the manufacturers.

 

 

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Note that the government has an economic incen- tive to tax goods that are price inelastic. This incentive exists because the amount purchased declines by a smaller percentage than the price increase. For exam- ple, if cigarettes are price inelastic, a 10% cigarette tax increase will result in less than a 10% decrease in cig- arette consumption, meaning the cigarette tax will be a good revenue producer for the government because consumers will continue to purchase cigarettes despite the tax. However, taxing price-inelastic goods is less effective as a public health tool for the same reason. If the government desires a 10% reduction in cigarette consumption, the tax must be much higher than 10% if cigarettes are price inelastic. Of course, the govern- ment may choose to impose a higher cigarette tax, but it is likely that, for political reasons, a higher tax increase will be harder to obtain than a smaller one.

Government Issues Regulatory Mandates. Regula- tions may be used to fix a market failure by controlling the price, quantity, or quality of goods and services, or the entry of new firms into the market (Santerre & Neun, 2004, p. 241). For example, healthcare consum- ers often have imperfect information when making their healthcare decisions. As a result, the government may choose to create a requirement that a type of pro- vider, such as nursing homes, supply information to the public about the quality of care in their facilities to aid in consumers’ decision making. The government may also promulgate regulations that restrict entry of new firms into a market and regulate prices because it is cheaper for one or a few firms to produce a high level of output. Of course, government regulations could also be used to achieve a policy goal like reducing carbon emissions by mandating that public transportation sys- tems use alternative fuels that result in lower emissions.

The government could also set a cap on the price of a good and prohibit producers from selling that good above the set price. This will keep the good at a price the government deems socially acceptable. How- ever, if the price is set below the market price, some unfavorable market consequences may occur because it is no longer profitable for the producer to supply the product. Possible consequences include the following:

■ Suppliers exiting the market or reducing the quan- tity of the good supplied, resulting in a shortage

■ Suppliers reducing the quality of the good by making cheaper products or providing less care

■ Suppliers shifting cost from one product to another

■ Suppliers engaging in unethical behavior because some consumers will be willing to pay more than the government price ceiling

Furthermore, regulations aimed at increasing the quality of a good or service will likely impose additional costs on producers of the good. As the cost of inputs rise, the price charged to consumers is likely to rise as well. As a result, some consum- ers will be priced out of the market for that good or service.

Government Prohibits Goods or Services. Pro- hibiting the production of goods and services often is ineffective and leads to a “black market” for such products. Because the prohibited goods or services are not available legally, consumers may be tempted to purchase goods or services that are not protected by price or quality controls. This situation may occur with the use of drugs or supplements not approved by the Food and Drug Administration, including unapproved drugs from other countries entering the United States via the Internet or other sources. In addition, because other countries are producing the good or service, the United States may be at a competitive disadvantage. For example, if stem cell research is permitted abroad but not in this country, some scientists may leave the United States to work abroad and domestic companies may not remain competitive in certain fields.

Redistribution of Income In the case of market failure, the government may also act to redistribute income. Remember, efficient allocation of resources is not the same as equitable allocation of resources. A government may decide that every member of society should obtain a cer- tain minimum level of income or resources or health status. Redistributing income may occur by taxing

BOX 9-3 Discussion Questions

Some people argue that the government should not intervene in the case of a market failure because the government itself is inefficient and will simply create new problems to replace the ones it is trying to fix. In addition, critics contend that the government is usually less efficient than private sectors. Do you think the government is less efficient than the private sector? Does it depend on the issue involved? If you think it is inefficient in a particular area, does that lead you to recommend against government intervention, or is there a reason that you would still support government intervention? If you think the government should intervene, which intervention options do you prefer and why?

 

 

187Endnotes

the wealthier members of society and using the reve- nue to provide resources to poorer members of soci- ety. If the government sought to create more market equity through voluntary donations, it is likely that a free rider problem would exist because some citi- zens would volunteer to contribute resources while others would not, but the latter would still receive a benefit from the redistribution. For example, wealth- ier citizens who should be in the “donor group” but do not contribute may benefit from the donations given by other wealthy citizens that lead to increased productivity and welfare of those in the recipient group. Both the notion of income redistribution and the decisions as to who should be providing versus receiving resources is open to debate. In addition, it is important to remember that income redistribu- tion may reduce efficiency or have other undesirable market effects.

▸ Conclusion This introduction to economic concepts illustrates why health policy analysts and decision makers must under- stand how economists analyze healthcare problems. We have taken a broad look at the issues of supply, demand, and market structure with a focus on concerns that are relevant in the health policy field. In particular, it is essential to understand how health insurance affects both consumer and producer decisions. Although we only scratched the surface of healthcare economics in this chapter, you should now realize that without an understanding of the economic ramifications of a pol- icy decision, a health policy analyst cannot know, for example, whether to recommend addressing a problem through a government-run program, subsidy, or the like, or if it would be better to let the free market set the production level and price of a resource.

References Agency for Healthcare Research and Quality. (n.d.). Population

health: Behavioral and social science insights. Retrieved from https://www.ahrq.gov/professionals/education/curriculum -tools/population-health/zimmerman.html

Cutler, D., & Lleras-Muney, A. (2006). Education and health: Evaluating theories and evidence (National Bureau of Economic Research Working Paper 12352). Retrieved from http://www .nber.org/papers/w12352.pdf

Feldstein, P. (2005). Health care economics (6th ed.). Clifton Park, NY: Thomas Delmar Learning.

Gordis, L. (2000). Epidemiology (2nd ed., p. 19). Philadelphia, PA: WB Saunders.

Penner, S. J. (2004). Introduction to health care economics and financial management: Fundamental concepts with practical applications. Philadelphia, PA: Lippincott, Williams, & Wilkins.

Phelps, C. E. (2003). Health economics (3rd ed.). Boston, MA: Addison-Wesley.

Pindyck, R. S., & Rubinfeld, D. L. (2003). Microeconomics (5th ed.). Upper Saddle River, NJ: Prentice Hall.

Senterre, R. E., & Neun, S. P. (2004). Health economics: Theories, insights, and industry studies (3rd ed.). Mason, OH: Thomas South-Western.

Weimer, D., & Vining, A. (1999). Policy analysis: Concepts and practice (3rd ed.). Upper Saddle River, NJ: Prentice-Hall.

▸ Endnotes a. Herd immunity is “the resistance of a group to

an attack by a disease to which a large propor- tion of the members of the group are immune” (Gordis, 2000). Once a certain portion of

the group is immune, there is only a small chance that an infected person will find a sus- ceptible person to whom the disease may be transmitted.

 

 

 

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© Mary Terriberry/Shutterstock

CHAPTER 10

Health Reform in the United States

LEARNING OBJECTIVES

By the end of this chapter you will be able to:

■ Describe previous national health reform attempts ■ Understand why national health reform has been difficult to achieve in the United States ■ Analyze why national health reform succeeded in 2010 when so many previous attempts had failed ■ Understand the key components of the Patient Protection and Affordable Care Act ■ Understand the core rulings of multiple U.S. Supreme Court decisions related to the Affordable Care Act ■ Evaluate the political climate regarding repealing and replacing the Affordable Care Act, and understand the

main features of legislation drafted toward that end ■ Describe key issues going forward related to implementation of the Affordable Care Act

▸ Introduction

The Patient Protection and Affordable Care Act of 2010 (generally referred to as the Affordable Care Act, or ACA) is the most monumental piece of U.S. federal health policymaking in nearly 50  years. It reorders not only many aspects of the health insurance and healthcare delivery systems but also longstanding relationships that underpin those systems. Yet beyond the sheer scope and content of the ACA and the policy trade-offs that led to its passage lies another story: its implementation and subsequent effect on the lives of tens of millions of Americans. Implementation of the ACA is an ongoing, dynamic process for the federal government, states, employers, insurers, providers, patients, and others. In addition,

there have been and, no doubt, will continue to be state and federal court decisions across the country that alter the trajectory of the law and its implementation.

The vignette in BOX 10-1 describes just a few of the competing viewpoints about the ACA and its role in creating a new and potentially more equitable health insurance system. As ACA implementation moves forward, bear in mind the many different ways that this round of health reform can be perceived and how it affects people differently.

Furthermore, the future of the ACA was made even more uncertain by the monumental election cycle in 2016. Unexpectedly, Donald Trump was elected president in November of that year, and the Repub- licans maintained control of both the U.S. House of Representatives and the Senate. Having control of

 

 

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Congress and the White House gives Republicans a chance to fulfill a promise they have campaigned on for years—to repeal and replace the ACA. Even if they are not successful in passing a repeal and replacement bill, President Trump can use his executive powers to rewrite existing regulations and implement new poli- cies. Indeed, he has already started to do so, as will be discussed in this chapter.

The interplay between legal and political decisions makes it difficult to discern how implementation of the law will be carried out, assuming it is not repealed entirely. By way of example, the U.S. Supreme Court’s landmark 2012 decision upholding the constitutional- ity of the ACA and 2015 decision upholding subsidies provided through the ACA to the federal insurance exchange are described in the pages that follow, and there are currently dozens of lawsuits challenging the ACA’s coverage mandate related to contraceptive and

other family planning services. The practical conse- quences and legal rulings that actually manifest as a result of ACA implementation—not just the changes to American health care contemplated by Congress when they put pen to paper with the ACA—will, for years to come, need to be studied and understood by students across a range of disciplines, not just for aca- demic purposes, but for healthcare and public health job market purposes as well.

Although there has been general agreement about the problems facing the U.S. healthcare system— high costs, high uninsured rates, health disparities, quality concerns—politicians and voters have dis- agreed about the best solutions. As a result, numerous attempts to pass national health reform legislation did not succeed. What was different in 2010? Why was the Obama administration successful when several pre- vious attempts had failed? This chapter begins with a discussion of why it has been so difficult to achieve broad health reform in this country and then exam- ines the numerous failed attempts at national health reform over the last century. It then analyzes how health reform was enacted in 2010, provides an over- view of the law that eventually emerged, and covers the U.S. Supreme Court decision upholding its consti- tutionality. Finally, the discussion turns to the current political climate and what it means for health reform going forward, including a discussion of key political and implementation issues. Throughout this chapter we examine several key themes: choosing between state flexibility and national uniformity; determining the appropriate role for government, the private sec- tor, and the healthcare financing and delivery entities; defining a primary decision-making goal (e.g., fiscal restraint, equity/social justice, improved health out- comes, uniformity); and settling on the appropriate scope of coverage to offer beneficiaries.

▸ Difficulty Achieving Health Reform in the United States

The array of problems facing the healthcare system has led to numerous health reform proposals and implemented policies. The concept of health reform can have several different meanings. Given the patch- work health insurance system, health reform often refers to changes that seek to reduce the number of uninsured. Due to the high and increasing cost of healthcare services, health reform might also include changes that seek to contain costs and control utiliza- tion. The notion of health reform could also address other shortcomings, such as trying to reduce medical

BOX 10-1 Vignette

A group of friends were talking about the ACA, illustrating the wide-ranging viewpoints about the law. Katherine, whose friend Sophia is struggling to make a living as an artist, is pleased that Sophia has health insurance for the first time since graduating from college. Although Sophia cannot stay on her parents’ insurance because she just turned 27 years old, she can now afford a good health insurance plan that she found on her state’s health exchange. While Katherine has not noticed much of a change in her own health insurance coverage, which she obtains through her government employer, her cousin Mia is upset about health reform. She does not want the government forcing her to purchase health insurance (although she always chose to be insured in the past), and she recently found out that her old plan was cancelled because it did not meet the law’s requirements. Mia found several new plan options to choose from, but none had her former plan’s exact combination of benefits, providers, and price. In addition, Katherine’s uncle, Ethan, is 55 years old and self-employed. He purchases his health insurance on his state’s exchange and because he has preexisting conditions, he is grateful to be able to find a plan. Even so, Ethan’s premiums will increase by 15% this year and his deductible is $5,000, making health care difficult to afford even with insurance. Katherine’s husband, Calvin, thinks we should all be willing to pay a little more or change some aspects of our plans to help the millions of people who can now afford insurance for the first time as a result of the ACA. After witnessing her uncle’s experience, however, Katherine is doubtful that the government will be able to keep its promises.

 

 

Difficulty Achieving Health Reform in the United States 191

errors, strengthening patient rights, building the pub- lic health infrastructure, and confronting the rising cost of medical malpractice insurance. Unsurpris- ingly, the ACA touches on many of these issues.

We begin with a discussion about why health reform is difficult to achieve in the United States and then introduce some of the reforms that have been attempted, with varying degrees of success, on a national level. Numerous authors have addressed the main factors that deter significant social reform in this country, including health reform (Blake & Ado- lino, 2001; Gordon, 2003; Jost, 2004). Factors that are prominently discussed include the country’s culture, the nature of U.S. political institutions, the power of interest groups, and path dependency (i.e., the notion that people are generally opposed to change).

Culture This country’s culture and lack of consensus about health reform have impeded attempts to create uni- versal coverage health plans. The twin concepts of entrepreneurialism and individualism have had a real impact on health policy decisions: Americans gen- erally oppose government solutions to social welfare problems (Jost, 2004, p. 238). In addition, there is no agreement about the overall scope of the healthcare problems we face (Kaiser Family Foundation [KFF], 2008). Prior to the passage of the ACA, most Amer- icans believed the extant health system needed major changes, yet 22% believed only minor changes were required and another 17% thought the system should basically stay the same (KFF, 2009b).

Americans have a complicated and partisan view of the proper role of the federal government in the healthcare arena. On one hand, 60% of respondents to a 2017 survey felt that the federal government has a responsibility to ensure healthcare coverage for all Americans (Kiley, 2017). This is much higher than the 47% who shared that view in 2010, at the height of the health reform debate (Newport, 2010). Of those who supported federal intervention in the 2017 sur- vey, 33% reported they would like to see a single-payer system developed (Kiley, 2017).

At the same time, there was a stark difference of opinion based on the respondents’ political views. While 85% of Democrats and Democrat-leaning independents believed the federal government was responsible for ensuring healthcare coverage, only 32% of Republicans and Republican-leaning indepen- dents agreed (Kiley, 2017). Even so, over half (57%) of Republican/Republican-leaners supported the contin- uation of Medicaid and Medicare, the country’s largest public health insurance programs. Furthermore, only

5% of respondents thought the federal government should not have any role in ensuring healthcare cover- age (Kiley, 2017).

It is accepted political dogma that it is difficult to take away benefits once they are established, and this has proven to be true with healthcare coverage (Steinhauer, 2017). The popularity of the ACA has increased since the Republicans gained power in the 2016 elections and the threat of repealing the ACA became a realistic possibility. A June 2017 Kaiser Tracking poll showed the ACA’s favorability ratings above 50% for the first time since the poll began in 2010 (KFF, 2017b), and a separate poll taken a cou- ple months later showed 64% of respondents pre- ferred to either keep the ACA as it is or make fixes to it that would shore up problems and weaknesses (Kahn & Erman, 2017). Furthermore, the public is clearly opposed to the proposed Republican replace- ment plans. A majority of respondents opposed both the House (56% opposed) (Magness, 2017) and Sen- ate (55% opposed) (Wynn, 2017) bills. Even though many Republicans also opposed the replacement options (only 21% have a very favorable view) (KFF, 2017b), most Republicans (about 75%) would still like to see the ACA repealed and replaced at some point (Kahn & Erman, 2017).

U.S. Political System The country’s system of government also has made it difficult to achieve universal coverage. Traditionally, social welfare programs—including the provision of health care—have been the responsibility of the states. Initially, there was almost no federal involvement in the provision of health care, and when the federal gov- ernment became more heavily involved in 1965, Med- icaid continued to keep the locus of decision making at the state level. Of course, there are select popula- tions, such as older adults (Medicare) and veterans (Veterans Health Administration), who have a feder- alized health insurance system. However, support for federal involvement in health care depends on what language is used to describe the change. For example, “single-payer” or “socialized” health care was backed by less than half of the public in a 2017 poll, while “universal health coverage” and “Medicare-for-all” was supported by over 60% (KFF, 2017c).

Although states are generally home to social wel- fare changes, it is difficult to provide universal health care on a state-by-state basis. If state health reform efforts lead the way, the country could have a patch- work of programs and policies that vary from state to state, with the potential to make health coverage even more complex and inefficient than it is currently.

 

 

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In  addition, states must consider whether they are making policy decisions that will give employers an incentive to choose to locate in another state with fewer or less onerous legal requirements. If employers leave the state, it could result in loss of jobs and have downstream effects on the state’s economy.

The federal government also has resource advan- tages over states, making it easier for the federal level to be the engine for health reform. Individual states have a much smaller tax and revenue base than the federal government to draw from to implement health reform plans. In addition, once the federal government decides to tax a good or service, a state’s ability to tax that same good or service is constrained by the indi- vidual’s willingness and ability to pay a higher price. Unlike the federal government, most states have some type of balanced budget requirement (Garrett, 2011). While state legislatures may use accounting gim- micks and other maneuvers to avoid balanced budget requirements, states more often must make difficult choices about resource allocation that federal policy- makers often avoid (and thus generate enormous defi- cits). These restrictions, however, also may help with reform efforts by forcing states to a crisis point where a decision must be made to avoid an untenable situ- ation. The federal government rarely reaches such a crisis point, which means tough decisions are often left for the next Congress, executive branch adminis- tration, or generation.

State reform efforts are also constrained by the Employee Retirement Income Security Act of 1974 (ERISA). ERISA is a federal law that regulates “welfare benefit programs,” including health plans, operated by private employers. ERISA limits ability of states to reform because it broadly preempts state laws that “relate to” employer-sponsored plans and because it applies to nearly all individuals who receive health benefits through a private employer. One effect of the law, for example, is that states have little regulatory con- trol over the benefits covered in employer- sponsored health plans, because ERISA accords employers near-total discretion over the design of their benefit packages (Weissert & Weissert, 2002, p. 237).

Despite these hurdles, it is also important to rec- ognize that a health reform strategy focusing on states has benefits as well. At its best, reform at the state level can be accomplished more rapidly and with more innovation than at the federal level. State legislatures may have an easier time convincing a narrower band of constituents important to the state than Congress has in accommodating the varied needs of stakehold- ers nationwide. Along the same lines, states are able to target reforms to meet the particular needs of their

population, instead of covering more diverse needs across the entire country. Additionally, through the use of “direct democracy” (e.g., referenda, ballot ini- tiatives), it is easier for citizens to have an impact on decisions by state-level policymakers than by federal legislators. Finally, because the healthcare delivery system is run primarily on the state level, states have the expertise and ability to implement many parts of healthcare reform.

Other aspects of the U.S. political system also make it difficult to institute sweeping reform. For example, although presidents have significant influence on set- ting policy agenda and proposing budgets, they have limited power to make changes without the assistance of Congress. The federal government is often politi- cally divided, with different parties holding power in the executive and legislative branches. This division often results in partisanship and policy inaction due to different policy priorities and views.

Furthermore, although members of Congress may ride the coattails of a popular president from their own party, they are not reliant on the president to keep their jobs. The issues and views their constituents care about most may not align with the president’s priori- ties. In those cases, members of Congress have a strong incentive to adhere to the wishes of those who vote for them, instead of simply following the president’s lead. Barring an overwhelming wave of discontent, as occurred in the 2010 midterm elections when Dem- ocrats suffered historic losses in Congress, it is usu- ally difficult to unseat incumbents. Even when there is a historic level of turnover, reelection rates remain very high. For example, 97% of House incumbents successfully defended their seats in 2016; even in the Senate, where turnover is relatively more common, 93% of incumbents won reelection in 2016 (Kondick & Skelley, 2016). As a result, legislators in Congress may have confidence in focusing on their district’s or state’s needs before those of the entire nation.

Federal legislative rules also support inaction or incremental reform over sweeping changes. In the Senate, 60 (of 100) votes are needed to break a fili- buster in most cases. Thus, even the political party in the majority can have difficulty effecting change. One exception to the filibuster rule is the “reconciliation” process, which allows bills to pass with only 51 votes. Reconciliation is used as part of the budgetary pro- cess, and bills passed via reconciliation may not be fil- ibustered (so can pass with 51 votes), can pertain only to federal revenue and spending issues, must comply with spending and revenue targets set forth in the budget resolution, and must adhere to other budget- ary rules (Tax Policy Center, n.d.). The reconciliation

 

 

Difficulty Achieving Health Reform in the United States 193

process is being increasingly used when one party maintains a slim majority and that party cannot find 60 votes to pass a bill. For example, the Democrats used a reconciliation bill to pass the ACA in 2010 after they lost their filibuster-proof majority, and like- wise, the Republicans attempted to use a reconcilia- tion bill to pass their ACA repeal-and-replace bills. Also, because both the House and the Senate have to pass bills containing the same policies and language to have any chance at becoming law, a large political majority in one chamber or the other does not guar- antee the ability to enact a policy. As a result, in many cases members of Congress have to work together, at least to some degree, to devise a consensus policy that satisfies enough members to pass a bill. This need to build consensus makes radical change unlikely.

Interest Groups Interest groups often influence the decisions of pol- iticians. The role of interest groups is to represent their members’ interests in policy decisions. These groups can be corporate for-profit entities or non- profit consumer-oriented organizations. They lobby politicians and the general public about the virtues or vices of specific proposals, work to improve proposals on the policy agenda, and attempt to defeat proposals they believe are not in the best interest of their group. By contributing to political campaigns or by helping to draw supportive voters out on Election Day, interest groups gain the ear, and often the influence, of poli- ticians who vote on issues that are important to the group.

In terms of health reform, interest groups rep- resenting various providers, businesses, employer groups, insurance companies, and managed care orga- nizations often have been opposed to comprehensive health reform (Jost, 2004, pp. 438–439). There are numerous points along the path—from developing a policy idea to voting for or against a bill—when inter- est groups can attempt to affect politicians’ views. The more radical the policy proposal, the more interest groups are likely to become engaged in the political decision-making process, making it difficult to pass a bill that includes comprehensive reform.

In general, it is easier to oppose a proposal than to develop one and pass a bill. Opponents of propos- als are not required to provide a better alternative to whatever is on the table. Instead, they can simply point to aspects of the policy idea that are unpopular and call for the proposal to be rejected. This was the tactic used by the Health Insurance Association of America in their well-known “Harry and Louise” television ads

that opposed the Clinton administration’s compre- hensive health reform bill in 1993, the Health Security Act. In the ad, Harry and Louise, two “average” Amer- icans, are seen discussing the healthcare system over breakfast. Although they both agree the system needs to be improved, they highlight certain aspects of the Clinton plan that were particularly controversial, such as an overall cap on funds for healthcare needs and restrictions on provider choice. The tag line for the ad was, “There’s got to be a better way” (West, Heith, & Goodwin, 1996). Similarly, before the 2016 elections, many Republicans promised to “repeal and replace” the health reform bill without specifying their favored replacement option. To be effective in opposing health reform, opponents did not have to propose an alter- native that was scrutinized and compar