Enrollment in clinical trials according to patients race: experience from the VA Cooperative Studies Program (1975–2000)

Eugene Z Oddone , Maren K Olsen , Jennifer Hoff Lindquist , Melinda Orr , Ronnie Horner , Domenic Reda , Philip Lavori , Gary Johnson , Joseph Collins , John R Feussner
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引用次数: 26

Abstract

Background: Racial distribution of clinical trial participants is important because results from these studies serve to define evidence-based practice. This report summarizes the experience of the VA Cooperative Studies Program (CSP) in enrolling white, black and Hispanic patients. Methods: An analysis of enrollment in randomized controlled trials conducted by VA CSP between 1975 and 2000. A standardized enrollment ratio for each trial was calculated by dividing the observed number of enrolled white patients in the trial by the expected number of eligible white patients based on the proportion of white patients hospitalized at the enrolling VA Medical Centers. Results: 138 VA CSP clinical trials were initiated between 1975 and 2000, 83 contained information on race for 71,463 patients. Overall, 76% of enrolled patients were white, 20% were black, and 4% were Hispanic. Based on standardized enrollment ratios, 60 of the 83 trials had 95% confidence intervals that excluded 1.0. Of these, 32 studies enrolled more white patients than expected and 28 enrolled more Black and/or Hispanic patients than expected based on the racial distribution of patients hospitalized at sites involved in the trials. When trials were separated by intervention type, 13 of the 19 trials that had an invasive arm enrolled fewer minority patients than expected. In trials that targeted diseases that affect minority populations to a greater degree than whites (diabetes, hypertension and end stage renal disease), 11 of the 14 trials enrolled more minority patients than expected. Conclusions: There were several trials that enrolled either more or less minority patients than expected based on patients hospitalized at study sites. Trials that included an invasive arm enrolled fewer minority participants than expected. Trials that involve invasive therapies may wish to adopt special recruitment strategies to reach minority populations.

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根据患者种族登记临床试验:来自退伍军人管理局合作研究项目的经验(1975-2000)
背景:临床试验参与者的种族分布很重要,因为这些研究的结果有助于定义循证实践。本报告总结了退伍军人事务部合作研究项目(CSP)在招募白人、黑人和西班牙裔患者方面的经验。方法:分析VA CSP在1975年至2000年间进行的随机对照试验的入组情况。每个试验的标准化入组比例是通过将试验中观察到的入组白人患者的数量除以根据入组VA医疗中心住院的白人患者比例计算的符合条件的白人患者的预期数量来计算的。结果:在1975年至2000年间,有138项VA CSP临床试验启动,其中83项包含71463例患者的种族信息。总的来说,76%的入组患者是白人,20%是黑人,4%是西班牙裔。基于标准化入组比,83项试验中有60项的95%置信区间不包括1.0。其中,32项研究招募了比预期更多的白人患者,28项研究招募了比预期更多的黑人和/或西班牙裔患者,这是基于在参与试验的地点住院的患者的种族分布。当试验按干预类型分开时,19项具有侵入性臂的试验中有13项招募的少数民族患者比预期的要少。在针对对少数族裔人群的影响大于白人的疾病(糖尿病、高血压和终末期肾病)的试验中,14项试验中有11项招募的少数族裔患者比预期的要多。结论:有几项试验入组的少数民族患者多于或少于基于研究地点住院患者的预期。包括侵入性手臂的试验招募的少数民族参与者比预期的要少。涉及侵入性治疗的试验可能希望采用特殊的招募策略来覆盖少数民族人群。
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