Muutke küpsiste eelistusi

Making Medical Decisions for the Profoundly Mentally Disabled [Pehme köide]

  • Formaat: Paperback / softback, 320 pages, kõrgus x laius x paksus: 229x152x19 mm, kaal: 454 g
  • Sari: Basic Bioethics
  • Ilmumisaeg: 01-Aug-2009
  • Kirjastus: MIT Press
  • ISBN-10: 0262513277
  • ISBN-13: 9780262513272
Teised raamatud teemal:
  • Formaat: Paperback / softback, 320 pages, kõrgus x laius x paksus: 229x152x19 mm, kaal: 454 g
  • Sari: Basic Bioethics
  • Ilmumisaeg: 01-Aug-2009
  • Kirjastus: MIT Press
  • ISBN-10: 0262513277
  • ISBN-13: 9780262513272
Teised raamatud teemal:
A legal and moral analysis of medical decision making on behalf of those with such severe cognitive impairments that they cannot exercise self-determination.

In this book, Norman Cantor analyzes the legal and moral status of people with profound mental disabilities—those with extreme cognitive impairments that prevent their exercise of medical self-determination. He proposes a legal and moral framework for surrogate medical decision making on their behalf. The issues Cantor explores will be of interest to professionals in law, medicine, psychology, philosophy, and ethics, as well as to parents, guardians, and health care providers who face perplexing issues in the context of surrogate medical decision making.

The profoundly mentally disabled are thought by some moral philosophers to lack the minimum cognitive ability for personhood. Countering this position, Cantor advances both theoretical and practical arguments for according them full legal and moral status. He also argues that the concept of intrinsic human dignity should have an integral role in shaping the bounds of surrogate decision making. Thus, he claims, while profoundly mentally disabled persons are not entitled to make their own medical decisions, respect for intrinsic human dignity dictates their right to have a conscientious surrogate make medical decisions on their behalf. Cantor discusses the criteria that bind such surrogates. He asserts, contrary to popular wisdom, that the best interests of the disabled person are not always the determinative standard: the interests of family or others can sometimes be considered. Surrogates may even, consistent with the intrinsic human dignity standard, sometimes authorize tissue donation or participation in nontherapeutic medical research by profoundly disabled persons. Intrinsic human dignity limits the occasions for such decisions and dictates close attention to the preferences and feelings of the profoundly disabled persons themselves. Cantor also analyzes the underlying philosophical rationale that makes these decision-making criteria consistent with law and morals.

Basic Bioethics series
Series Foreword vii
Acknowledgments ix
Introduction 1(12)
The Moral Status of the Profoundly Disabled: Persons or Something Less?
13(20)
The Concepts of Personhood and Full Moral Status
13(4)
Criteria of Personhood
17(3)
The Legal and Moral Status of the Profoundly Disabled
20(6)
The Role of Intrinsic Human Dignity
26(7)
The Profoundly Disabled as Rights Holders: No Rights, the Same Rights as the Fully Capacitated, or Some Rights?
33(36)
Attributing the ``Same Rights'' to the Profoundly Disabled
33(8)
A Constitutional Claim to Appropriate Medical Options
41(2)
A Constitutional Right to Some Surrogate Decision on Behalf of the Disabled Person?
43(26)
Who Decides for the Profoundly Disabled?
69(32)
Minors Living with Their Parents
70(24)
Disabled Persons Living in Institutions
94(7)
Defining the Best Interests of Profoundly Disabled Persons
101(48)
The Focus on a Never Competent Patient's Well-Being
103(3)
The Problematic of Assessing Well-Being
106(7)
Quality of Life, Dignity, and Never Competent Persons
113(14)
Must Medical Decisions Be in the Best Interests of a Profoundly Disabled Person?
127(9)
Can the Interests of Others Be Included within a Patient's Best Interests?
136(13)
Forced Altruism
149(54)
The Problematic of Surrogate Consent to Nontherapeutic Medical Procedures
149(10)
Reliance on the Best Interests of the Profoundly Disabled Patient
151(3)
Discrimination against the Disabled
154(2)
The Kantian Imperative
156(3)
Existing Jurisprudence
159(10)
The Decided Cases on the Donation of Bodily Resources
159(5)
The Legal and Moral Frameworks Governing Nontherapeutic Medical Research
164(5)
Justifications for Seeking Sacrifice from Profoundly Disabled Persons
169(34)
Utilitarianism as a Rationale for Exploitation
169(4)
Ascribing Altruism to Never Competent Persons
173(5)
Parental Child-Rearing Prerogatives
178(8)
Social Fairness as a Justification for Using the Profoundly Disabled
186(5)
The Limits of a Surrogate's Imposition of Sacrifice
191(12)
The Voice of the Profoundly Disabled Person
203(12)
The Connection between Consultation and Well-Being
204(2)
Dignity-Based Reasons for Soliciting Input
206(1)
Limited Self-Determination
207(4)
Ambiguity of Expressions
211(4)
Notes 215(60)
References 275(18)
Index of Cases and Statutes 293(2)
Subject Index 295