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  1. Communicating with the dying.J. M. Wilson - 1975 - Journal of Medical Ethics 1 (1):18-21.
    Telling a patient that the outcome of his illness is not good, or even hopeless, requires sensitivity and the ability to communicate with him in the setting of a hospital which is an unnatural environment divorced from family and friends. It is a task which must be taught and learned by doctors and nurses.
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  • Communicating with the dying.Michael Wilson - 1975 - Journal of Medical Ethics 1 (1):18.
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  • Metaphysics and medical ethics.C. Parkin - 1995 - Journal of Medical Ethics 21 (2):106-111.
    I take issue with Frank Leavitt's sketch of a pragmatic criterion for the relevance of metaphysics to medical ethics. I argue that appeal to the potential for confusion generated by metaphysical subtlety establishes a need for better communication rather than shows philosophical insight beside the point. I demonstrate that the proposed Criterion of Relevance has absurd consequences, and I claim that the relevance of philosophical doctrines, whether ethical or metaphysical, is best accounted for in terms of improved understanding.
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  • Moral Personhood. [REVIEW]William J. Mohan - 1993 - International Studies in Philosophy 25 (3):147-149.
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  • Facilitating Medical Ethics Case Review: What Ethics Committees Can Learn from Mediation and Facilitation Techniques.Mary Beth West & Joan McIver Gibson - 1992 - Cambridge Quarterly of Healthcare Ethics 1 (1):63.
    Medical ethics committees are increasingly called on to assist doctors, patients, and families in resolving difficult ethics issues. Although committees are becoming more sophisticated in the substance of medical ethics, little attention has been given to the processes these committees use to facilitate decision-making. In 1990, the National Institute for Dispute Resolution in Washington, D.C., provided a planning grant from its Innovation Fund to the Institute of Public Law of the University of New Mexico School of Law to look at (...)
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  • Whose will is it, anyway? A discussion of advance directives, personal identity, and consensus in medical ethics.Mark G. Kuczewski - 1994 - Bioethics 8 (1):27–48.
    ABSTRACTI consider objections to the use of living wills based upon the discontinuity of personal identity between the time of the execution of the directive anbd the time the person becomes incompetent. Recent authors, following Derek Parfit's “Complex View” of personal identity, have argued that there is often not sufficient identity interests between the competent person who executes the living will and the incompetent patient to warrant the use of the advance directive. I argue that such critics err by seeking (...)
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  • The medicalization of life.I. Illich - 1975 - Journal of Medical Ethics 1 (2):73-77.
    Two contributions from Dr Ivan Illich follow. The first, in which he sets out his primary thesis of the medicalization of life, is a section from Dr Illich's book `Medical Nemesis'. (It is reprinted with the permission of the author and his publishers, Messrs Calder and Boyars.) The second is a transcript of the paper which Dr Illich read at the conference organized by the London Medical Group on iatrogenic disease. Both are ultimately addressed to the recipients of medical care, (...)
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  • The Oxford Practice Skills Project: teaching ethics, law and communication skills to clinical medical students.T. Hope & K. W. Fulford - 1994 - Journal of Medical Ethics 20 (4):229-234.
    We describe the teaching programme in ethics, law and communication skills for clinical medical students which is being developed as part of the Oxford Practice Skills Project. These three elements of practice are approached in an integrated teaching programme which aims to address everyday clinical practice. The role of a central value of patient-centred health care in guiding the teaching is described. Although the final aim of the teaching is to improve actual practice, we have found three 'sub-aims' helpful in (...)
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  • Ethics in an Aging Society.Martin J. Gorbien - 1998 - Perspectives in Biology and Medicine 41 (3):452.
  • Twenty years of the JME--reflections. Journal of Medical Ethics.R. Gillon - 1995 - Journal of Medical Ethics 21 (1):3-4.
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  • Review of Allen E. Buchanan and Dan W. Brock: Deciding for Others: The Ethics of Surrogate Decision Making[REVIEW]Jonathan D. Moreno - 1992 - Ethics 103 (1):172-175.
  • Deciding for Others: The Ethics of Surrogate Decision Making, by Allan E. Buchanan and Dan W. Brock. [REVIEW]Donald Vandeveer - 1992 - Philosophy and Phenomenological Research 52 (1):232-237.
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  • Doing what the patient orders: Maintaining integrity in the doctor‐patient relationship.Jeffrey Blustein - 1993 - Bioethics 7 (4):289-314.
    No profession has undergone as much scrutiny in the past several decades as that of medicine. Indeed, one might well argue that no profession has ever undergone so much change in so short a time. An essential part of this change has been the growing insistence that competent, adult patients have the right to decide about the course of their own medical treatment. However, the familiar and widely accepted principle of patient self-determination entails a corollary that has received little attention (...)
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  • No longer patient: feminist ethics and health care.Susan Sherwin - 1992 - Philadelphia: Temple University Press.
    Her careful building of positions, her unique approaches to analyzing problems, and her excellent insights make this an important work for feminists, those ...
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  • Contemporary Issues in Bioethics.Tom L. Beauchamp - 1982 - Cengage Learning.
    This anthology represents all of the most important points of view on the most pressing topics in bioethics. Containing current essays and actual medical and legal cases written by outstanding scholars from around the globe, this book provides readers with diverse range of standpoints, including those of medical researchers and practitioners, legal exerts, and philosophers.
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  • Deciding for Others: The Ethics of Surrogate Decision Making.Allen E. Buchanan & Dan W. Brock - 1989 - New York: Cambridge University Press. Edited by Dan W. Brock.
    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 (...)
     
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