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Titlebook: Making Sense of Advance Directives; Nancy M. P. King Book 1991 Springer Science+Business Media Dordrecht 1991 concept.consciousness.ethics

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书目名称Making Sense of Advance Directives
编辑Nancy M. P. King
视频video
丛书名称Clinical Medical Ethics
图书封面Titlebook: Making Sense of Advance Directives;  Nancy M. P. King Book 1991 Springer Science+Business Media Dordrecht 1991 concept.consciousness.ethics
描述The first time I read the medical consent and authorization. it had registered in my mind simply as a legal document. Now I began to understand what it meant. It was a letter of ultimate love and trust. (Schucking. 1985. p. 268) Ever since Karen Ann Quinlan slipped into permanent unconsciousness in 1975 and her father agonized publicly over whether she should remain indefinitely on a respirator (In re Quinlan, 1976), the desires of patients, their families, and their friends to limit the application of apparently limitless medical technology have been a pressing concern for ethics, law, and public policy. Ms. Quinlan‘s case contained nearly all the elements of the problems we still face: vague, general, but sincere prior oral statements suggesting that she would not want continued treatment; a family attempting to do what they saw as best for her; and physicians uncertain whether to use medical judgment alone (and if so, what the "right" medical decision was), to preserve her life at all costs, or to honor the family‘s interpretation of their daughter‘s choice. Most ironically, once she was removed from her respirator, she did not die. Karen Quinlan - like dozens of other names mad
出版日期Book 1991
关键词concept; consciousness; ethics; foundation; history; history of literature; interpret; love; mind; morality; p
版次1
doihttps://doi.org/10.1007/978-94-011-3380-7
isbn_softcover978-94-010-5495-9
isbn_ebook978-94-011-3380-7Series ISSN 0926-969X
issn_series 0926-969X
copyrightSpringer Science+Business Media Dordrecht 1991
The information of publication is updating

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When Choices Fail,In a handbook that is about advance directives — written statements directly expressing patients’ treatment choices — it may seem superfluous to spend time discussing what happens to patients without written directives. There are two good reasons to do so, however.
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Introduction,ly on a respirator (., 1976), the desires of patients, their families, and their friends to limit the application of apparently limitless medical technology have been a pressing concern for ethics, law, and public policy. Ms. Quinlan’s case contained nearly all the elements of the problems we still
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,Treatment Refusal and the Patient’s Choice: Foundations in History, Law, and Ethics,s of health care decisions should patients be permitted to make? The chapter provides a general foundation in the moral and legal basis for informed consent and refusal of treatment, a brief look at the impact of technology upon how patients’ choices are regarded, and an examination of what it means
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Advance Directives: Current Forms, Legal Fears, Moral Goals,s: directives that give caregivers instructions about the patient’s choices, and directives that name a proxy to make choices on the patient’s behalf and convey them to caregivers (President’s Commission, 1982, pp. 156–166). Many directives combine these forms in various ways. In this chapter, we ex
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The Forecast For Advance Directives: Indispensable or Superfluous?,moting them to patients and providers as useful and even indispensable documents. Advocacy groups send subscribers wallet-size laminated “living will” cards containing toll-free numbers for a central registry that can supply callers with the full text of the patient’s directive in emergencies. “Medi
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