[麻风病与人权:日本与世界的趋势]。

Q4 Medicine
Japanese Journal of Leprosy Pub Date : 2014-12-01
Yozo Yokota
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引用次数: 0

摘要

麻风病,或称汉森病,长期以来一直被认为是一种无法治愈的可怕传染病。病人被强行送入医院,并被剥夺了许多基本人权。他们的家庭成员往往因与这种疾病有关的耻辱而受到歧视。第二次世界大战后不久,一种被称为“多药治疗”(MDT)的特殊疗法被发现,麻风病成为一种相对容易治愈的疾病。尽管取得了这一医疗发展,但改变强制麻风病患者住院的政策和立法需要时间。围绕麻风病的污名和随之而来的歧视仍在继续。在日本,直到1996年才废除了强制麻风病患者住院的立法。政府决定向因这项政策而受害的前病人提供补救办法。在联合国,大会通过了一项决议,以消除对麻风病患者及其家庭成员的歧视。希望所有有关方面,特别是这一疾病的专家医生和护士的努力将很快消除与汉森病有关的歧视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Leprosy and human rights: trends in Japan and in the world].

Leprosy, or Hansen's disease, has long been regarded as an incurable and dreadful contagious disease. The patients have been forcefully hospitalized and deprived of many basic human rights. Their family members have often been discriminated against due to stigma associated with this disease. Soon after the Second World War, a specific remedy called "multi-drug therapy" (MDT) was discovered and leprosy became a relatively easily curable disease. Despite this medical development, it took time to change the policy and legislation of forceful hospitalization of leprosy patients. The stigma surrounding leprosy and consequent discrimination have continued. In Japan, it was only in 1996 that the legislation requiring forceful hospitalization of leprosy patients was repealed. The Government decided to provide remedies to the former patients who had suffered from this policy. At the United Nations, the General Assembly adopted a resolution to eradicate discrimination against persons affected by leprosy and their family members. It is hoped that discrimination associated with Hansen's disease will soon be overcome by the efforts of all concerned, particularly doctors and nurses who are specialists of this disease.

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来源期刊
Japanese Journal of Leprosy
Japanese Journal of Leprosy Medicine-Dermatology
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