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How families in Japan view the disclosure of terminal illness: a study of iatrogenic HIV infection 

Authors: Yukiko Seki a;  Yoshihiko Yamazaki b;  Yuri Mizota c; Yoji Inoue d
Affiliations:   a Faculty of Education, Saitama University, Saitama, Japan
b Department of Health Sociology, The University of Tokyo, Tokyo, Japan
c Center for Cancer Control and Information Services, National Cancer Center, Tokyo, Japan
d The Open University of Japan, Chiba, Japan
DOI: 10.1080/09540120802282578
Publication Frequency: 12 issues per year
Published in: journal AIDS Care, Volume 21, Issue 4 April 2009 , pages 422 - 430
Formats available: HTML (English) : PDF (English)
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Abstract

Physicians in Japan typically do not disclose diagnoses of terminal illnesses to patients, in deference to the wishes of family members. Nonetheless, some evidence indicates that relatives of patients with iatrogenic HIV infection would prefer patient disclosure. We collected survey data from 314 family members in 225 households of hemophiliac patients who died from illnesses related to iatrogenic HIV infection in order to examine current attitudes toward patient disclosure in Japan. Family members reported that the diagnosis of iatrogenic HIV infection was disclosed to the patient by the primary physician in 32.8% of cases, by the family in 8.3% of cases, and not disclosed in 26.4% of cases. The majority of families indicated that the timing of the physician's disclosure occurred too late. Multivariate analysis indicated that families wished that patients had been informed of the diagnosis, despite the stigma associated with HIV in Japan. Furthermore, many families blamed the physician for the infection and fatality in those cases in which the physician did not convey feelings of regret. These results have important clinical ramifications to the practice of disclosing terminal diagnoses in Japan.
Keywords: HIV/AIDS; disclosure; bereavement; iatrogenic disease; Japan
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