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尿石症临床试验中的多样性、公平性和包容性:按种族、族裔和性别代表性入组。

Diversity, Equity, and Inclusion in Urolithiasis Clinical Trials: Representative Enrollment by Race, Ethnicity, and Sex.

机构信息

Department of Urology, Vanderbilt University Medical Center, Nashville, Tennessee.

出版信息

Urol Pract. 2024 Jul;11(4):685-691. doi: 10.1097/UPJ.0000000000000595. Epub 2024 May 8.

Abstract

INTRODUCTION

We sought to assess whether participant enrollment is appropriately representative of the overall urolithiasis population in published urolithiasis clinical trials.

METHODS

PubMed was queried for urolithiasis US clinical trials published from 2000 to 2022. Trials were evaluated for reporting patient race/ethnicity and sex data. These were then compared to the stone prevalence reported by the National Health and Nutrition Examination Survey from 2015 to 2018. We calculated a representation quotient (RQ) to describe enrollment of patients and then stratified by geographic location, study type, and funding source.

RESULTS

Of the 180 urolithiasis trials performed in the US, we identified 40 trials (22%) reporting race or ethnicity and 104 trials (58%) reporting sex. Male and female participants are well represented (RQ 0.97 and 1.02, respectively). Overall, the RQ of Black, Asian American and Pacific Islander, White, Hispanic, and mixed/other participants is 1.84, 1.06, 1.04, 0.46, and 0.34, respectively. Trials completed in the Western Section and multi-institutional trials have the most proportional enrollment, while trials in the South Central and Southeastern Sections have underrepresentation of mixed/other and Hispanic patients. Enrollment was similar among all trial subtypes. Government- and industry-funded trials had more diverse enrollment than academic-funded trials.

CONCLUSIONS

Only 1 in 4 published US urolithiasis trials report race or ethnicity enrollment. Mixed race and Hispanic participants are consistently underrepresented, while Black participants are overrepresented. Government- and industry-sponsored multi-institutional trials have the most proportional representation. Investigators should prioritize inclusive recruitment and improve reporting practices to accurately reflect the diversity of the urolithiasis population.

摘要

介绍

我们旨在评估发表的尿石症临床试验中参与者的入组是否能恰当地代表整体尿石症人群。

方法

在 PubMed 上检索了 2000 年至 2022 年发表的美国尿石症临床试验。评估了试验报告患者种族/族裔和性别的数据。然后将这些数据与 2015 年至 2018 年全国健康和营养检查调查报告的结石患病率进行比较。我们计算了一个代表商(RQ)来描述患者的入组情况,然后按地理位置、研究类型和资金来源进行分层。

结果

在美国进行的 180 项尿石症试验中,我们确定了 40 项(22%)报告种族或族裔的试验和 104 项(58%)报告性别的试验。男性和女性参与者的代表性很好(RQ 分别为 0.97 和 1.02)。总体而言,黑种人、亚裔美国人/太平洋岛民、白种人、西班牙裔和混合/其他参与者的 RQ 分别为 1.84、1.06、1.04、0.46 和 0.34。在西部和多机构完成的试验入组比例最合理,而在中南部和东南部完成的试验中,混合/其他和西班牙裔患者的代表性不足。所有试验亚型的入组情况相似。政府和行业资助的试验比学术资助的试验入组更加多样化。

结论

只有 1/4 的发表的美国尿石症试验报告种族或族裔入组情况。混合种族和西班牙裔参与者一直代表性不足,而黑种人参与者则代表性过高。政府和行业资助的多机构试验具有最合理的代表性。研究人员应优先考虑包容性招募,并改善报告实践,以准确反映尿石症人群的多样性。

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