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The Limits of Consent
A socio-ethical approach to human subject research in medicine
9780199231461
Dostawa
Wybierz Paczkomat Inpost, Orlen Paczkę, DPD lub Pocztę Polską. Kliknij po więcej szczegółów
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Opis
Since its inception as an international requirement to protect patients and healthy volunteers taking part in medical research, informed consent has become the primary consideration in research ethics. Despite the ubiquity of consent, however, scholars have begun to question its adequacy for contemporary biomedical research. The Limits of Consent explores this issue, reviewing the application of consent to genetic research, clinical trials, and research involving vulnerable populations. For example, in genetic research, information obtained from an autonomous research participant may have significant bearing on the interests of family members who have not consented to the study. This casts doubt on the adequacy of consent for such studies. The Limits of Consent also questions the assumptions that informed consent is essential and that it satisfactorily protects the principle of individual autonomy. It reviews recent empirical studies that challenge the possibility of truly informed consent and highlights the extent to which consent is governed by social norms and expectations. It also investigates how consent might be of secondary importance in some circumstances, for example when a research project appears to protect a publicor community interest. Building on these observations, the authors make bold attempts to outline constructive solutions to the problems identified with perspectives from medicine, law, philosophy and sociology. This fascinating and provocative exploration of the limits of informed consent will appeal to ethicists, social scientists, health lawyers, clinical researchers, research ethics committee members, policy makers, and others with an interest in bioethics.
Szczegóły produktu
84278
9780199231461
9780199231461
Opis
- Rok wydania
- 2009
- Numer wydania
- 1
- Oprawa
- twarda
- Liczba stron
- 248
- Wymiary (mm)
- 163 x 240
- Waga (g)
- 513
- Introduction; Informed consent in medical research - a procedure stretched beyond breaking point?; Beyond consent: the trust-based obligations of physicians to patients in clinical research; Consent and private liability in clinical research; The decision to refuse consent to participation in a clinical trial: does a double standard exist?; Beyond a rebarbative commitment to consent; The normative status of the requirement to gain an informed consent in clinical trials: comprehension, obligations and empirical evidence; Is there an obligation to participate in medical research?; Consent with older people: research as a virtuous relationship; Towards supported decision-making in biomedical research with cognitively vulnerable adults; Is consent sufficient? - a case study of qualitative research with men with intellectual disabilities; Consent to genetic testing: a family affair?; Cultural authority of informed consent: indigenous participation in biobanking and salmon genomics focus groups; Conclusion;
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