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审视风湿病学指南中基于种族的实践。

A Critical Look at Race-Based Practices in Rheumatology Guidelines.

机构信息

Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

Arthritis Care Res (Hoboken). 2022 Oct;74(10):1602-1607. doi: 10.1002/acr.24645. Epub 2022 Jul 7.

DOI:10.1002/acr.24645
PMID:33973416
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9169247/
Abstract

OBJECTIVE

To assess how race has been incorporated into rheumatology practice guidelines, including how race is defined and used in diagnostic and treatment recommendations.

METHODS

We searched race and ethnicity terms in all clinical practice guidelines from the American College of Rheumatology (ACR) and European Alliance of Associations for Rheumatology (EULAR) that were published between 2010 and 2020 and publicly available on professional society websites. Findings were summarized and assessed through standardized data abstraction forms. Key themes were identified through a thematic analysis approach.

RESULTS

A total of 23 ACR clinical practice guidelines and 42 EULAR recommendations were reviewed. In total, 16 of 65 (25%) of the guidelines used race terms in their text. No guideline clearly defined race, and race was often conflated with ethnicity and/or genetic ancestry. Reported racial categories varied substantially by guideline and often used classifications that oversimplified and excluded non-White races. Research with insufficient racial diversity was used to make race-based recommendations for Black patients that may not be generalizable. Additionally, recommendations using research on predominantly White populations reinforced data of White populations as normative and perpetuated race-based stereotypes, especially for rare diseases. Structural causes of identified racial disparities were not discussed in clinical guidelines.

CONCLUSION

There is an urgent need for standardized race reporting in rheumatology. Recommendations are provided to enhance consistency and accuracy of race and ethnicity terms, mitigate conflation of race with ethnicity or genetic ancestry, encourage a critical reanalysis of race-based diagnostic tools and treatment options, and better address the structural causes of racial disparities.

摘要

目的

评估种族在风湿病学实践指南中的纳入情况,包括种族在诊断和治疗建议中的定义和使用方式。

方法

我们在 2010 年至 2020 年间发布并在专业学会网站上公开的美国风湿病学会 (ACR) 和欧洲抗风湿病联盟 (EULAR) 的所有临床实践指南中搜索了种族和族裔术语。通过标准化数据提取表格总结和评估发现。通过主题分析方法确定主要主题。

结果

共审查了 23 项 ACR 临床实践指南和 42 项 EULAR 建议。总共,65 项指南中有 16 项(25%)在文本中使用了种族术语。没有指南明确定义种族,而且种族经常与族裔和/或遗传血统混淆。报告的种族类别因指南而异,并且经常使用过于简化和排除非白人种族的分类。基于种族的建议是基于对黑人患者的研究做出的,但可能不具有普遍性,这些研究的种族多样性不足。此外,使用主要为白人人群的研究为黑人患者提供的建议强化了白人人群的数据作为规范,并延续了基于种族的刻板印象,尤其是对于罕见疾病。临床指南中没有讨论已确定的种族差异的结构性原因。

结论

风湿病学中迫切需要标准化的种族报告。我们提供了一些建议,以提高种族和族裔术语的一致性和准确性,减轻种族与族裔或遗传血统混淆,鼓励对基于种族的诊断工具和治疗方案进行批判性重新分析,并更好地解决种族差异的结构性原因。

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本文引用的文献

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