Abstract
This paper examines two topics in Japanese medical ethics: non-disclosure of medical information by Japanese physicians, and the history of human rights abuses by Japanese physicians during World War II. These contrasting issues show how culture shapes our view of ethically appropriate behavior in medicine. An understanding of cultural context reveals that certain practices, such as withholding diagnostic information from patients, may represent ethical behavior in that context. In contrast, nonconsensual human experimentation designed to harm the patient is inherently unethical irrespective of cultural context. Attempts to define moral consensus in bioethics, and to distinguish between acceptable and unacceptable variation across different cultural contexts, remain central challenges in articulating international, culturally sensitive norms in medical ethics
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DOI 10.1186/1747-5341-1-4
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Paying for Informed Consent.A. Akabayashi - 2000 - Journal of Medical Ethics 26 (3):212-213.
Patients' Rights in Japan: Progress and Resistance.Isao Morikawa - 1994 - Kennedy Institute of Ethics Journal 4 (4):337-343.

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