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  1. Relationality and Consensus in Japan: Implications for Bioethics Policy.Michael C. Brannigan - 1999 - Health Care Analysis 7 (3):289-296.
    This paper examines the Japanese notion of relationality, that is, the idea that the individual is defined primarily within a web of relationships. Furthermore, it proposes that this relationality provides an ontological basis for morality, particularly the critical need for achieving consensus. This need for consensus is evident in the dispute over brain death. It was also conspicuous in the long-standing debate regarding heart transplantation. By reviewing key features of relationality, the study also demonstrates that the Japanese approach toward consensus (...)
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  • Medical decisions concerning the end of life: a discussion with Japanese physicians.A. Asai, S. Fukuhara, O. Inoshita, Y. Miura, N. Tanabe & K. Kurokawa - 1997 - Journal of Medical Ethics 23 (5):323-327.
    OBJECTIVES: Life-sustaining treatment at the end of life gives rise to many ethical problems in Japan. Recent surveys of Japanese physicians suggested that they tend to treat terminally ill patients aggressively. We studied why Japanese physicians were reluctant to withhold or withdraw life-support from terminally ill patients and what affected their decisions. DESIGN AND PARTICIPANTS: A qualitative study design was employed, using a focus group interview with seven physicians, to gain an in-depth understanding of attitudes and rationales in Japan regarding (...)
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  • (1 other version)Perspectives on advance directives in Japanese society: A population-based questionnaire survey. [REVIEW]Akira Akabayashi, Brian Taylor Slingsby & Ichiro Kai - 2003 - BMC Medical Ethics 4 (1):1-9.
    Background In Japan, discussion concerning advance directives (ADs) has been on the rise during the past decade. ADs are one method proposed to facilitate the process of communication among patients, families and health care providers regarding the plan of care of a patient who is no longer capable of communicating. In this paper, we report the results of the first in-depth survey on the general population concerning the preferences and use of ADs in Japan. Method A self-administered questionnaire was sent (...)
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  • (1 other version)Perspectives on advance directives in Japanese society: A population-based questionnaire survey.Akira Akabayashi, Brian Taylor Slingsby & Ichiro Kai - 2003 - BMC Medical Ethics 4 (1):1-9.
    In Japan, discussion concerning advance directives (ADs) has been on the rise during the past decade. ADs are one method proposed to facilitate the process of communication among patients, families and health care providers regarding the plan of care of a patient who is no longer capable of communicating. In this paper, we report the results of the first in-depth survey on the general population concerning the preferences and use of ADs in Japan. A self-administered questionnaire was sent via mail (...)
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  • Family consent, communication, and advance directives for cancer disclosure: a Japanese case and discussion.A. Akabayashi, M. D. Fetters & T. S. Elwyn - 1999 - Journal of Medical Ethics 25 (4):296-301.
    The dilemma of whether and how to disclose a diagnosis of cancer or of any other terminal illness continues to be a subject of worldwide interest. We present the case of a 62-year-old Japanese woman afflicted with advanced gall bladder cancer who had previously expressed a preference not to be told a diagnosis of cancer. The treating physician revealed the diagnosis to the family first, and then told the patient: "You don't have any cancer yet, but if we don't treat (...)
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  • The Family in Medical Decision Making: Japanese Perspectives.Michael D. Fetters - 1998 - Journal of Clinical Ethics 9 (2):132-146.
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  • Ethnicity and Advance Care Directives.Sheila T. Murphy, Joycelynne M. Palmer, Stanley Ken, Gelya Frank, Vicki Michel & Leslie J. Blackhall - 1996 - Journal of Law, Medicine and Ethics 24 (2):108-117.
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  • Ethnicity and Advance Care Directives.Sheila T. Murphy, Joycelynne M. Palmer, Stanley Azen, Gelya Frank, Vicki Michel & Leslie J. Blackhall - 1996 - Journal of Law, Medicine and Ethics 24 (2):108-117.
    Advance care directives for health care have been promoted as a way to improve end-of-life decision making. These documents allow a patient to state, in advance of incapacity, the types of medical treatments they would like to receive, to name a surrogate to make those decisions, or to do both. Although studies have shown that both physicians and patients generally have positive attitudes about the use of these documents, relatively few individuals have actually completed one.What underlies this discrepancy between attitudes (...)
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  • Medical Ethics the Japanese Way.Eric Feldman - 1985 - Hastings Center Report 15 (5):21-24.
    An American in Tokyo finds that the Japanese cultural values of consensus and deference to authority characterize their approach to ethical issues in health care.
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