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临床试验中纳入、分析和报告性别及种族/民族:我们是否取得了进展?

Inclusion, analysis, and reporting of sex and race/ethnicity in clinical trials: have we made progress?

机构信息

Center for Research on Women and Gender, University of Illinois at Chicago, College of Medicine, 820 S. Wood Street, Chicago, IL 60612, USA.

出版信息

J Womens Health (Larchmt). 2011 Mar;20(3):315-20. doi: 10.1089/jwh.2010.2469. Epub 2011 Feb 25.

Abstract

BACKGROUND

The National Institutes of Health (NIH) Revitalization Act of 1993 requires that NIH-funded clinical trials include women and minorities as participants; other federal agencies have adopted similar guidelines. The objective of this study is to determine the current level of compliance with these guidelines for the inclusion, analysis, and reporting of sex and race/ethnicity in federally funded randomized controlled trials (RCTs) and to compare the current level of compliance with that from 2004, which was reported previously.

METHODS

RCTs published in nine prominent medical journals in 2009 were identified by PubMed search. Studies where individuals were not the unit of analysis, those begun before 1994, and those not receiving federal funding were excluded. PubMed search located 512 published articles. After exclusion of ineligible articles, 86 (17%) remained for analysis.

RESULTS

Thirty studies were sex specific. The median enrollment of women in the 56 studies that included both men and women was 37%. Seventy-five percent of the studies did not report any outcomes by sex, including 9 studies reporting <20% women enrolled. Among all 86 studies, 21% did not report sample sizes by racial and ethnic groups, and 64% did not provide any analysis by racial or ethnic groups. Only 3 studies indicated that the generalizability of their results may be limited by lack of diversity among those studied. There were no statistically significant changes in inclusion or reporting of sex or race/ethnicity when compared with 2004.

CONCLUSIONS

Ensuring enhanced inclusion, analysis, and reporting of sex and race/ethnicity entails the efforts of NIH, journal editors, and the researchers themselves.

摘要

背景

1993 年,美国国立卫生研究院(NIH)复兴法案要求 NIH 资助的临床试验将女性和少数族裔纳入参与者;其他联邦机构也通过了类似的指导方针。本研究的目的是确定目前在纳入、分析和报告联邦资助的随机对照试验(RCT)中的性别和种族/民族方面遵守这些指南的程度,并将当前的遵守程度与之前报告的 2004 年进行比较。

方法

通过 PubMed 搜索,确定了 2009 年九种著名医学期刊上发表的 RCT。排除了个体不是分析单位、研究开始于 1994 年之前且未获得联邦资金的研究。PubMed 搜索共找到了 512 篇已发表的文章。在排除不符合条件的文章后,仍有 86 篇(17%)可用于分析。

结果

有 30 项研究是专门针对性别的。在纳入男性和女性的 56 项研究中,女性的中位入组率为 37%。75%的研究没有按性别报告任何结果,其中包括 9 项报告女性入组率<20%的研究。在所有 86 项研究中,有 21%没有按种族和族裔报告样本量,64%没有提供任何种族或族裔的分析结果。只有 3 项研究表明,由于研究对象缺乏多样性,他们的研究结果可能具有一定的局限性。与 2004 年相比,在纳入或报告性别或种族/民族方面没有统计学上的显著变化。

结论

要确保增强纳入、分析和报告性别和种族/民族,需要 NIH、期刊编辑和研究人员自身的共同努力。

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