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  1. For the patient's good: the restoration of beneficence in health care.Edmund D. Pellegrino - 1988 - New York: Oxford University Press. Edited by David C. Thomasma.
    In this companion volume to their 1981 work, A Philosophical Basis of Medical Practice, Pellegrino and Thomasma examine the principle of beneficence and its role in the practice of medicine. Their analysis, which is grounded in a thorough-going philosophy of medicine, addresses a wide array of practical and ethical concerns that are a part of health care decision-making today. Among these issues are the withdrawing and withholding of nutrition and hydration, competency assessment, the requirements for valid surrogate decision-making, quality-of-life determinations, (...)
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  • Incompetent Persons as Research Subjects and the Ethics of Minimal Risk.Kathleen Cranley Glass & Marc Speyer-Ofenberg - 1996 - Cambridge Quarterly of Healthcare Ethics 5 (3):362.
    The voluntary and informed consent of subjects has been the central focus of concern in research reviews, overshadowing the importance of all other considerations. The Nuremberg Code, with its rights-based protection of the subject's autonomy above all else, made it difficult to justify research with no intended benefit when subjects are incompetent to make a valid informed choice to participate. Subsequent codes providing for research with incompetent subjects followed the lead of Nuremberg, substituting the informed authorization of a proxy for (...)
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  • Consent to clinical research--adequately voluntary or substantially influenced?S. Hewlett - 1996 - Journal of Medical Ethics 22 (4):232-237.
    In clinical research the giving of consent by the patient often lies within the context of illness or the doctor/patient relationship. On exploration of these issues it would appear unlikely that the patient's consent is free of substantial influences, some of which may be strong enough to be controlling. Five categories of consent are suggested: voluntary, involuntary, coerced, enforced and partially voluntary. It is argued that consent in clinical research is substantially influenced and thus only partially voluntary. Several practical strategies (...)
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  • Our Brothers' Keepers. [REVIEW]R. E. GOODIN - 2012 - Hastings Center Report 15 (6):46-47.
    Book reviewed in this article: Protecting The Vulnerable: A Reanalysis of Our Social Responsibilities. By Robert E. Goodin. Chicago: University of Chicago Press.
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  • Beyond voluntary consent: Hans Jonas on the moral requirements of human experimentation.C. Fethe - 1993 - Journal of Medical Ethics 19 (2):99-103.
    In his essay, Philosophical Reflections on Experimenting with Human Subjects, Hans Jonas contends that except in cases of widespread medical emergencies, people do not have a moral or social obligation to volunteer to be subjects in medical experiments. He further argues that any appeal for volunteer subjects in medical experiments should whenever possible give priority to those who can identify with the project and offer a strong sense of commitment to its goals. The first of these claims is given support (...)
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  • A philosophical basis of medical practice: toward a philosophy and ethic of the healing professions.Edmund D. Pellegrino - 1981 - New York: Oxford University Press. Edited by David C. Thomasma.
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  • Suffering Presence: Theological Reflections on Medicine, the Mentally Handicapped and the Church.Stanley Hauerwas - 1988 - Burns & Oates.
    This work examines contemporary views on medical ethics, such as preventing death, defining family relations, and reproductive and disabled issues.
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