患者和家属参与临床指南的制定:囊性纤维化基金会的经验。

Q2 Medicine Journal of Participatory Medicine Pub Date : 2020-07-13 DOI:10.2196/17875
Sarah E Hempstead, Kelsey Fredkin, Cade Hovater, Edward T Naureckas
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引用次数: 4

摘要

尽管2011年美国医学研究所(Institute of Medicine)的《我们可以信任的指南》和指南国际网络(guide International Network)的GIN-Public Toolkit推荐了指南制定,但在指南制定界,患者和家属参与指南制定既不标准化,也不被统一接受。自2004年以来,囊性纤维化基金会已将患者和/或家属直接纳入指南制定中。随着时间的推移,实施了各种增加患者和家属参与的战略。最近对患者/家庭和临床指南委员会成员的调查显示,将囊性纤维化患者及其家庭成员纳入指南委员会,为临床医生提供了原本不可见的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Patient and Family Participation in Clinical Guidelines Development: The Cystic Fibrosis Foundation Experience.

Patient and family participation in guideline development is neither standardized nor uniformly accepted in the guideline development community, despite the 2011 Institute of Medicine's Guidelines We Can Trust and the Guideline International Network's GIN-Public Toolkit recommendations. The Cystic Fibrosis Foundation has included patients and/or family members directly in guideline development since 2004. Over time, various strategies for increasing patient and family member participation have been implemented. Surveys of recent patient/family and clinical guidelines committee members have shown that inclusion of individuals with cystic fibrosis and their family members on guidelines committees has provided insight otherwise invisible to clinicians.

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来源期刊
Journal of Participatory Medicine
Journal of Participatory Medicine Medicine-Medicine (miscellaneous)
CiteScore
3.20
自引率
0.00%
发文量
8
审稿时长
12 weeks
期刊最新文献
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