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Rethinking informed consent in bioethics / Neil C. Manson, Onora O'Neill.

Van Pelt Library K3611.I5 M36 2007
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Format:
Book
Author/Creator:
Manson, Neil C.
Contributor:
O'Neill, Onora, 1941-
Language:
English
Subjects (All):
Informed consent (Medical law).
Bioethics.
Medicine--Research--Moral and ethical aspects.
Medicine.
Medicine--Research.
Physical Description:
xiv, 212 pages ; 23 cm
Place of Publication:
Cambridge ; New York : Cambridge University Press, 2007.
Summary:
Informed consent is a central topic in contemporary biomedical ethics. Yet attempts to set defensible and feasible standards for consenting have led to persistent difficulties. In Rethinking Informed Consent in Bioethics, Neil Manson and Onora O'Neill set debates about informed consent in medicine and research in a fresh light. They show why informed consent cannot be fully specific or fully explicit, and why more specific consent is not always ethically better. They argue that consent needs distinctive communicative-transactions, by which other obligations, prohibitions, and rights can be waived or set aside in controlled and specific ways. Their book offers a coherent, wide-ranging and practical account of the role of consent in biomedicine which will be valuable to readers working in a range of areas in bioethics, medicine and law.
Contents:
1 Consent: Nuremberg, Helsinki and beyond 1
Beginning at Nuremberg 2
Extending scope: from research ethics to clinical ethics 4
Raising standards: explicit and specific consent 6
Improving justifications: the quest for autonomy 16
Regulatory reinforcement: consent requirements 22
2 Information and communication: the drift from agency 26
Framing informed consent 27
Two layers of distortion 34
Information and the drift from agency 34
What the conduit and container metaphors hide 38
3 Informing and communicating: back to agency 50
Agency 50
Communicative actions 54
Communicative norms 57
Two 'models' of information and communication 64
4 How to rethink informed consent 68
Introduction: two models of informed consent 68
Why consent transactions matter: beyond autonomy 69
Justifying consent transactions: consent as waiver 72
Scope and standards 77
Consent transactions: standards for communication 84
Consent transactions: commitments 90
Conclusion: consent in practice 94
5 Informational privacy and data protection 97
Informational privacy 100
Informational rights and obligations 101
Informational privacy as a right over content 105
Data protection legislation: second-order informational obligations 111
Rethinking informational privacy 121
Confidentiality: regulating communicative action rather than information content 123
6 Genetic information and genetic exceptionalism 130
Questions about genetic information 131
Genetic privacy and genetic exceptionalism 133
Is Genetic information contained within DNA? 145
7 Trust, accountability and transparency 154
Consent, paternalism and trust 154
Placing and refusing trust intelligently 159
Accountability and trustworthiness 167
Accountability, trustworthiness and trust in biomedicine 169
Accountability with transparency 177
Appendix The structure of accountability 181
Some conclusions and proposals 183
Informed consent and epistemic norms 184
Informed consent and individual autonomy 185
Informed consent as waiver 187
Practices and policies for informed consent 189
After rethinking: the possibility of change 198
Institutional sources and documents 207.
Notes:
Includes bibliographical references (pages 201-206) and index.
ISBN:
9780521874588
0521874580
9780521697477
0521697476
OCLC:
77540852

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