Deciding for Others

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Format: Paperback
Pub. Date: 1990-02-01
Publisher(s): Cambridge Univ Pr
List Price: $67.19

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Summary

This book is the most comprehensive treatment available of one of the most urgent - and yet in some respects most neglected - problems in bioethics: decision-making for incompetents. Part I develops a general theory for making treatment and care decisions for patients who are not competent to decide for themselves. It provides an in-depth analysis of competence, articulates and defends a coherent set of principles to specify suitable surrogate decisionmakers and to guide their choices, examines the value of advance directives, and investigates the role that considerations of cost ought to play in decisions concerning incompetents. Part II applies this theoretical framework to the distinctive problems of three important classes of individuals, many of whom are incompetent: minors, the elderly and psychiatric patients. The authors' approach combines a probing analysis of fundamental issues in ethical theory with a sensitive awareness of the concrete realities of health care institutions and the highly personal and individual character of difficult practical problems. Its broad scope will appeal to health professionals, moral philosophers and lawyers alike.

Table of Contents

Preface xi
Introduction 1(1)
The question
1(1)
The history of the problem
2(2)
Ethics and the law
4(1)
Ethics and public policy analysis
5(2)
The method
7(2)
The plan
9(6)
Part one Theory 15(198)
Competence and incompetence
17(70)
The concept of competence
18(5)
Competence as decision-relative
18(2)
Global conceptions of competence
20(3)
Capacities needed for competence
23(3)
Competence as a threshold concept, not a comparative one
26(3)
Standads of competence: Underlying values
29(12)
Promotion of individual well-being
29(7)
Respect for individual self-determination
36(4)
Conflict between the values of self-determination and well-being
40(1)
Contrast with a single value foundation - individual self-determination as sovereign
41(6)
Deciding on standards of competence
47(1)
Different standards of competence
48(3)
A minimal standards of competence
49(1)
An outcome standard of competence
49(1)
A process standard of decision-making competence
50(1)
Relation of the process standard of competence to expected harms and benefits
51(6)
Table 1.1: Decision-making competence and patient well-being
53(4)
Relation of refusal of treatment to determination of incompetence
57(2)
Contrast with a fixed minimum threshold conception of competence
59(6)
A two-step model of patient decision-making authority - the competence of the decision-maker and the rationality of his or her choice
65(5)
Operational measures in the medical setting
70(5)
Use of formal tests to determine competence
71(2)
Importance of informal evaluations of competence
73(2)
Competence determination in nonmedical settings
75(2)
Varying standards of competence
77(3)
Difficulties raised by determinations regarding the incompetent's finances
78(2)
The need for institutional policies for the determination of competence
80(4)
Summary of conclusions concerning competence
84(3)
The primary ethical framework: patient-centered principles
87(65)
The need for an ethical framework
87(2)
Underlying ethical values
89(4)
The scope of the competent patient's right to refuse treatment
90(2)
Limitations on the competent person's right to refuse care or treatment
92(1)
Guidance principles
93(3)
Conflicts among guidance principles
96(2)
The advance directive principles
98(14)
The case against always giving priority to advance dirctives
101(1)
Practical problems
101(2)
Moral objections
103(7)
Conclusions: The scope and limits of the moral authority of advance directives
110(2)
The substituted judgment standard
112(5)
Scope and limits of the moral authority of substituted judgment
117(5)
The best interest principle
122(12)
Beyond the scope of the best interest principle: Permanently unconscious patients
126(6)
The individual's interest in the good of others
132(1)
The dependence of the patient's well-being on institutional options and others' interest in the patient
133(1)
Authority principles: Who should decide?
134(8)
The family as decision-maker
136(2)
Disagreements within the family
138(1)
Physicians and judges as decision-makers
139(3)
Intervention principles: Attempts to specify conditions that rebut the presumptive authority of the family
142(10)
Challenges to the family as decision-maker
147(1)
The institutional ethics committee
148(4)
Advance directives, personhood, and personal identity
152(38)
The value of advance directives
152(1)
The moral authority of advance directives
152(2)
Loss of personal identity
154(5)
How much psychological continuity is enough?
159(3)
Surviving interests
162(3)
The distinction between the surviving interests of a self that no longer exists and the surviving interests in the persisting self
165(4)
Attempts to raise the threshold for psychological continuity
169(9)
A compromise position
178(6)
Conclusions concerning personal identity
184(6)
Distributive justice and the incompetent
190(23)
The need to qualify the patient-centered approach
190(1)
The relevance of guidance principles to questions of distributive justice
191(9)
Incompetence, moral status, and rights of distributive justice
193(1)
The permanently unconscious: Minimal interests
194(2)
The severely and permanetly demanted: Truncated interests
196(4)
Rationing health care: The role of physicians and surrogates deciding for incompetents
200(7)
The moral responsibility of families toward elderly incomptent individuals
207(6)
Part two Application 213(153)
Minors
215(52)
Noninfant minors
216(30)
The current legal presumption of incompetence
216(1)
The concept of competence
217(1)
The developmental evidence about children's decision-making capacities
218(6)
Determining a standard of competence
224(1)
The values at state in the competence determination
225(1)
The child's well-being
226(3)
The child's self-determination
229(3)
The parents' interest in making decisions concerning their children
232(2)
Children's competence and children's decisional authority
234(1)
The legitimate interests of parents and the best interest principle
235(2)
The variable standard of competence
237(3)
Implications for medical practice and legal policy regarding children's competence
240(6)
Newborns
246(21)
The correct guidance principle: Best interest, not substituted judgment
246(1)
The nature of the infant's interests
247(12)
The interests of others
259(1)
The fundamental moral status of infants: A radical challenge to the decision-making framework
260(7)
The elderly
267(44)
The magnitude of the problem
267(4)
Table 6.1: Share of U.S. population over 64 years of age, 1900, 1940, 1960, 1975, and 2000
269(1)
Table 6.2: Distribution of U.S. elderly population by age-group, 1950, 1975 and 2000
269(2)
How incompetence is determined, formally and informally, and by whom, in varioius settings
271(18)
Determinaing competence to make medical decisions
272(8)
Formal determinations of incompetence for decisions concerning finances and places of residence
280(9)
How surrogates actually decide for those elderly individuals who are considered to be incompetent
289(1)
Some important trends in recent case law
290(5)
Advance directives and other planning approaches: Who uses them and how effective are they?
295(11)
Living wills
296(1)
Durable powers of attorney
297(1)
General durable power of attorney
297(1)
Durable power of attorney for health care
298(8)
Summary
306(5)
The mentally ill
311(55)
Decisions about involuntary hospitalization or commitment
312(20)
The historical context of involuntary commitment
312(5)
Patient-centered commitment - danger to self versus need for care and treatment
317(8)
Society-centered commitment - dangerousness to others
325(7)
Decisions to refuse treatment by involuntary committed patients
332(15)
The historical context of treatment refusal by involvuntarily committed patients
332(4)
An ethical framework for treatment refusal by involuntarily committed mental patients
336(1)
Persons dangerous to others
336(6)
Persons dangerous to themselves or in need of care and treatment
342(5)
Some residual issues in decisions for the mentally ill
347(19)
The least restrictive alternative condition
347(3)
Advance directives by the mentally ill
350(8)
Involuntary outpatient commitment
358(3)
Special limits on surrogate consent for ``inhumane'' treatments
361(5)
Looking forward 366(4)
Appendix one: Living trust and nomination of conservatorship 370(4)
Appendix two: Durable power of attoreny for health care 374(13)
Notes 387(26)
Index 413

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