日本医院的基因数据治理。

IF 1.3 Q3 ETHICS
Mizuho Yamazaki Suzuki, Yuko Ohnuki, Kei Takeshita
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引用次数: 0

摘要

基因检测结果的存储和获取对医疗记录有着独特的考虑。最初,基因检测仅限于患有单基因疾病的患者。基因医学和检测已经扩大,对适当处理基因信息的担忧也在扩大。在这项研究中,我们使用一份关于访问限制的问卷调查了日本综合医院的遗传信息管理情况。我们的问题包括是否以独特的方式管理任何其他医疗信息。我们确定了位于日本各地的1037家指定进行临床培训的医院,并收到了258家医院的回复,191家医院报告称,它们处理基因信息和基因检测结果。在191家处理基因信息的医院中,有112家医院实施了对基因信息的访问限制。71家医院,其中一家使用纸质医疗记录而非电子医疗记录,不执行访问限制。对于八家医院,尚不清楚是否实施了出入限制。这些医院的回复表明,访问限制和存储方法因机构类型(例如,普通医院与大学医院)、机构规模和临床遗传学部门的存在而有所不同。其他信息,如传染病诊断、心理咨询记录、虐待和犯罪史,也在42家医院受到访问限制。医疗机构处理敏感基因信息的方式存在差异,这表明医疗专业人员和公众需要就包括基因信息在内的敏感记录的存储进行讨论。补充信息:在线版本包含补充材料,请访问10.1007/s41649-023-00242-9。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genetic Data Governance in Japanese Hospitals

Genetic Data Governance in Japanese Hospitals

Abstract 

The storage and access of genetic testing results have unique considerations for medical records. Initially, genetic testing was limited to patients with single gene diseases. Genetic medicine and testing have expanded, as have concerns about appropriately handling genetic information. In this study, we surveyed the management of genetic information in general hospitals in Japan using a questionnaire on access restrictions. Our questions included whether any other medical information was managed in a unique way. We identified 1037 hospitals designated for clinical training located throughout Japan and received responses from 258 hospitals, and 191 reported that they handle genetic information and results of genetic tests. Of the 191 hospitals that handle genetic information, 112 hospitals implement access restrictions to genetic information. Seventy-one hospitals, one of which uses paper medical records rather than electrical medical records, do not enforce access restrictions. For eight hospitals, it was not known whether access restrictions were enforced or not. The responses from these hospitals indicated that access restrictions and storage methods varied across institution type (e.g., general vs. university hospitals), institution size, and the presence of a clinical genetics department. Other information, such as infectious disease diagnosis, psychological counseling records, abuse, and criminal history, was also subject to access restriction in 42 hospitals. The disparity in how medical facilities handle sensitive genetic information demonstrates a need for discussion between medical professionals and the general public on the storage of sensitive records, including genetic information.

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来源期刊
CiteScore
6.20
自引率
3.40%
发文量
32
期刊介绍: Asian Bioethics Review (ABR) is an international academic journal, based in Asia, providing a forum to express and exchange original ideas on all aspects of bioethics, especially those relevant to the region. Published quarterly, the journal seeks to promote collaborative research among scholars in Asia or with an interest in Asia, as well as multi-cultural and multi-disciplinary bioethical studies more generally. It will appeal to all working on bioethical issues in biomedicine, healthcare, caregiving and patient support, genetics, law and governance, health systems and policy, science studies and research. ABR provides analyses, perspectives and insights into new approaches in bioethics, recent changes in biomedical law and policy, developments in capacity building and professional training, and voices or essays from a student’s perspective. The journal includes articles, research studies, target articles, case evaluations and commentaries. It also publishes book reviews and correspondence to the editor. ABR welcomes original papers from all countries, particularly those that relate to Asia. ABR is the flagship publication of the Centre for Biomedical Ethics, Yong Loo Lin School of Medicine, National University of Singapore. The Centre for Biomedical Ethics is a collaborating centre on bioethics of the World Health Organization.
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