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  1. Principles of biomedical ethics.Tom L. Beauchamp - 1989 - New York: Oxford University Press. Edited by James F. Childress.
    Over the course of its first seven editions, Principles of Biomedical Ethics has proved to be, globally, the most widely used, authored work in biomedical ethics. It is unique in being a book in bioethics used in numerous disciplines for purposes of instruction in bioethics. Its framework of moral principles is authoritative for many professional associations and biomedical institutions-for instruction in both clinical ethics and research ethics. It has been widely used in several disciplines for purposes of teaching in the (...)
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  • (1 other version)Principles of Biomedical Ethics.Ezekiel J. Emanuel, Tom L. Beauchamp & James F. Childress - 1995 - Hastings Center Report 25 (4):37.
    Book reviewed in this article: Principles of Biomedical Ethics. By Tom L. Beauchamp and James F. Childress.
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  • More information, broader dissent on informed consent.William R. LaFleur - 2006 - American Journal of Bioethics 6 (1):15 – 16.
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  • (1 other version)‘Bioethics’ is Subordinate to Morality in Japan.Noritoshi Tanida - 1996 - Bioethics 10 (3):201-211.
    Disputes over brain death and euthanasia are used to illuminate the question whether there really is a Japanese way of thinking in bioethics. In Japanese thought, a person does not exist as an individual but as a member of the family, community or society. I describe these features of Japanese society as ‘mutual dependency’. In this society, an act is ‘good’ and ‘right’ when it is commonly done, and it is ‘bad’ and ‘wrong’ when nobody else does it. Thus, outsiders (...)
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  • The family-facilitated approach could be dangerous if there is pressure by family dynamics.Chieko Tamura - 2006 - American Journal of Bioethics 6 (1):16 – 18.
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  • (1 other version)‘Bioethics’ is Subordinate to Morality in Japan.Noritoshi Tanida - 1996 - Bioethics 10 (3):201–211.
    Disputes over brain death and euthanasia are used to illuminate the question whether there really is a Japanese way of thinking in bioethics. In Japanese thought, a person does not exist as an individual but as a member of the family, community or society. I describe these features of Japanese society as ‘mutual dependency’. In this society, an act is ‘good’ and ‘right’ when it is commonly done, and it is ‘bad’ and ‘wrong’ when nobody else does it. Thus, outsiders (...)
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  • Informed consent revisited: Japan and the U.s.Akira Akabayashi & Brian Taylor Slingsby - 2006 - American Journal of Bioethics 6 (1):9 – 14.
    Informed consent, decision-making styles and the role of patient-physician relationships are imperative aspects of clinical medicine worldwide. We present the case of a 74-year-old woman afflicted with advanced liver cancer whose attending physician, per request of the family, did not inform her of her true diagnosis. In our analysis, we explore the differences in informed-consent styles between patients who hold an "independent" and "interdependent" construal of the self and then highlight the possible implications maintained by this position in the context (...)
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  • Self-Determination of Death in Japan: A Review & Discussion.Atsushi Asai & Sayaka Sakamoto - 2007 - Eubios Journal of Asian and International Bioethics 17 (2):35-40.
    Self-determination is a central concept in the field of bioethics and the most critical decision among the myriad of decisions concerning medical care is the decision to choose to die; “self-determination of death.” The purpose of this paper is to clarify the basic positions on self-determination of death held by present Japanese people and we tentatively sorted these positions into 10 arguments. We discuss the problems and implications of these positions revealed within our present review and conclude that a society (...)
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  • Death with dignity is impossible in contemporary Japan: Considering patient peace of mind in end-of-life care.A. Asai, K. Aizawa, Y. Kadooka & N. Tanida - 2012 - Eubios Journal of Asian and International Bioethics 22 (2):49-52.
    Currently in Japan, it is extremely difficult to realize the basic wish of protecting personal dignity at the end of life. A patient’s right to refuse life-sustaining treatment has not been substantially warranted, and advance directives have not been legally enforceable. Unfortunately, it is not until the patient is moribund that all concerned parties start to deliberate on whether or not death with dignity should be pursued. Medical intervention is often perceived as a worthwhile goal to not only preserve life, (...)
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