记录临床伦理咨询

IF 0.3 Q4 MEDICAL ETHICS
A. Porter
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引用次数: 1

摘要

这个简短的透视片是关于加拿大临床伦理咨询的文件。它是在加拿大执业卫生保健伦理学家协会(CAPHE)努力制定加拿大临床伦理学实践标准的时候编写的。这篇简短的评论是根据我在三个不同省份从事临床伦理学工作的经验写成的,但它主要是为了引起人们对规范性问题的关注:临床伦理学文件中应该包括多少信息和什么样的信息?伦理咨询报告应该保存在哪里?谁应该可以访问这些报告?从根本上说,这些问题是关于我们应该如何平衡对隐私、保密、职业操守、问责制和促进信任的关注。它们还涉及临床伦理在更广泛的加拿大卫生系统中的地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Documenting Clinical Ethics Consultation
This short perspective piece is about the documentation of clinical ethics consultation in Canada. It is written at a time when the Canadian Association of Practicing Health Care Ethicists (CAPHE) is endeavoring to develop standards of practice for clinical ethics in Canada. This brief commentary is informed by my experience working in clinical ethics in three different provinces, but it is primarily an attempt to draw attention to the normative questions: How much and what kinds of information should be included in clinical ethics documentation? Where should ethics consultation reports be saved, and who should have access to them? These questions are, more fundamentally, about how we should balance concern for privacy, confidentiality, professional integrity, accountability and the promotion of trust. They are also about where clinical ethics fits within the broader Canadian health system.
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来源期刊
Canadian Journal of Bioethics
Canadian Journal of Bioethics Arts and Humanities-Philosophy
CiteScore
0.50
自引率
0.00%
发文量
46
审稿时长
35 weeks
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