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This book examines the implications of Confucian moral and ontological understandings for medical decision-making, human embryonic stem cell research, and health care financing.
Questions concerning the notion of quality of life, its definition, and its ap plications for purposes of assessment and measurement in social and medical contexts, have been widely discussed in Scandinavia during the last ten years.
Michael Ryan's Writings on Medical Ethics offers both an annotated reprint of his key ethical writings, and an extensive introductory essay that fills in many previously unknown details of Ryan's life, analyzes the significance of his ethical works, and places him within the historical trajectory of the field of medical ethics.
This book aims to give an account, called Variabilism, of the moral significance of merely possible persons and to use Variabilism to illuminate abortion. In doing so it lays the groundwork for a more productive discussion on abortion.
Michael Ryan's Writings on Medical Ethics offers both an annotated reprint of his key ethical writings, and an extensive introductory essay that fills in many previously unknown details of Ryan's life, analyzes the significance of his ethical works, and places him within the historical trajectory of the field of medical ethics.
Contributors examine the nature and plausibility of moral expertise, the relationship between character and expertise, the nature and limits of moral authority, how one might become a moral expert, and the trustworthiness of moral testimony.
Medical practice is practiced morality, and clinical research belongs to normative ethics. Fuzzy medical deontics, fuzzy medical ontology, fuzzy medical concept formation, fuzzy medical decision-making and biomedicine and many other techniques of fuzzification in medicine are introduced for the first time.
Contributors examine the nature and plausibility of moral expertise, the relationship between character and expertise, the nature and limits of moral authority, how one might become a moral expert, and the trustworthiness of moral testimony.
This book brings together the debate concerning personal identity (in metaphysics) and central topics in biomedical ethics (conception of birth and death;
The idea of preparing a new critical edition of Elisha Bartlett's Essay on the Philosophy of Medical Science was suggested to me several years ago by Dr. H. I was able to find many of Bartlett's published works and other nineteenth-century medical literature there, and the entire library staff provided quick and able research assistance.
This work provides a phenomenological account of the experience of illness and the manner in which meaning is constituted by the patient and the physician. The author provides a detailed account of the way in which illness and body are apprehended differently by doctor and patient.
This volume offers a collection of writings on ethical issues regarding retarded persons. Of course, many people have been very concerned with practical matters concerning the care of retarded persons such as what liberties, entitlements or advocacy they should have.
The contributions to this volume grew out of papers presented at an international conference Individual, Community & Society: Bioethics in the Third Millennium, held in Hong Kong, Special Administrative Region of the People's Republic of China, between 25-28 May 1999.
It may be unnecessary to some to publish a text on sexuality in 1986 since the popular press speaks of the sexual revolution as if it were over and was possibly a mistake. Indeed, we are experiencing something of a backlash against open sexuality and sexual liberation.
Features essays that demonstrate that because phenomenology provides extraordinary insights into many of the issues that are directly addressed within the world of medicine. This title is suitable for those who are interested in the philosophy of medicine, but for all healthcare professionals who are actively engaged in the care of the sick.
of UB's medical school, that UB developed its School of Arts and Sciences, and thus, assumed its place among the other institutions of higher education.
This collection provides a philosophical and historical analysis of the development and current situation of managed care. Its special feature is its depth of analysis as the philosophical, social, and economic issues of managed care are developed.
This book reprints Human Guinea Pigs, by Kenneth Mellanby, a seminal work in the history of medical ethics and human subject research that has been nearly unavailable for over 40 years.
Medical practice is practiced morality, and clinical research belongs to normative ethics. Fuzzy medical deontics, fuzzy medical ontology, fuzzy medical concept formation, fuzzy medical decision-making and biomedicine and many other techniques of fuzzification in medicine are introduced for the first time.
The media have catapulted the dilemmas of bioethics out of the laboratory and library into public view arid discussion with a steady report of the so-called 'mira cles of modern medicine' and the moral perplexities which frequently accom pany them.
This volume addresses the proper character of patient informed consent to medical treatment and clinical research. In contrast to that individually oriented approach, this volume explores the importance of family-oriented approaches to informed consent for medical treatment and clinical research.
The contributions to this volume grew out of papers presented at an international conference Individual, Community & Society: Bioethics in the Third Millennium, held in Hong Kong, Special Administrative Region of the People's Republic of China, between 25-28 May 1999.
This volume explores the plurality of moral perspectives shaping bioethics. It offers a rich perspective of the range of approaches to bioethics and brings into question whether there is unambiguously one ethics for bioethics to apply.
lt is with great pleasure that I write this preface for Or Li's book, wh ich addresses the venerable and vexing issues surrounding the problem of whether death can be a harm to the person who dies.
This is the first book in healthcare ethics addressing the moral issues regarding ownership of the human body. In the final section of the book, different theoretical perspectives on the human body are analyzed: libertarian, personalist, deontological and utilitarian theories of body ownership.
The principle of respecting the free and informed consent of the person is clearly stressed. The issue of interventions on persons unable to provide an informed consent has been controversial for a long time;
Positions for or against a market in human organs are nested within moral intuitions, ontological or political theoretical premises, or understandings of special moral concerns, such as permissible uses of the body, which have a long history of analysis.
When confronted by the concerns of human sexual function or dys function, American medicine finds itself well impaled on the horns of a dilemma.
It may be unnecessary to some to publish a text on sexuality in 1986 since the popular press speaks of the sexual revolution as if it were over and was possibly a mistake. Indeed, we are experiencing something of a backlash against open sexuality and sexual liberation.
This volume addresses the nature of health care organizational ethics, including such issues as corporate fraud and institutional moral integrity, and covers the broad range of issues that must be addressed for a coherent discussion of organizational moral responsibility.
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