Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, Connecticut, USA.
Department of Veterinary Pathobiology, Texas A&M University, College Station, Texas, USA.
Clin Infect Dis. 2024 Jul 19;79(1):141-147. doi: 10.1093/cid/ciae049.
Equitable representation of members from historically marginalized groups is important in clinical trials, which inform standards of care. The goal of this study was to characterize the demographics and proportional subgroup reporting and representation of participants enrolled in randomized controlled trials (RCTs) of antibacterials used to treat Staphylococcus aureus infections.
We examined randomized controlled registrational and strategy trials published from 2000 to 2021 to determine the sex, race, and ethnicity of participants. Participant to incidence ratios (PIRs) were calculated by dividing the percentage of study participants in each demographic group by the percentage of the disease population in each group. Underrepresentation was defined as a PIR < 0.8.
Of the 87 included studies, 82 (94.2%) reported participant sex, 69 (79.3%) reported participant race, and 20 (23.0%) included ethnicity data. Only 17 (19.5%) studies enrolled American Indian/Alaskan Native participants. Median PIRs indicated that Asian and Black participants were underrepresented in RCTs compared with the incidence of methicillin-resistant S. aureus infections in these subgroups. Underrepresentation of Black participants was associated with a larger study size, international sites, industry sponsorship, and phase 2/3 trials compared with phase 4 trials (P < .05 for each). Black participants had more than 4 times the odds of being underrepresented in phase 2/3 trials compared with phase 4 trials (odds ratio, 4.57; 95% confidence interval: 1.14-18.3).
Standardized reporting methods for race and ethnicity and efforts to increase recruitment of marginalized groups would help ensure equity, rigor, and generalizability in RCTs of antibacterial agents and reduce health inequities.
在临床试验中,代表历史上处于边缘地位的群体的成员具有公平代表性非常重要,因为临床试验为护理标准提供了信息。本研究的目的是描述纳入用于治疗金黄色葡萄球菌感染的抗菌药物的随机对照试验(RCT)参与者的人口统计学和亚组报告及代表性特征。
我们检查了 2000 年至 2021 年期间发表的随机对照注册和策略试验,以确定参与者的性别、种族和民族。通过将每个群体中研究参与者的百分比除以每个群体中疾病人群的百分比来计算参与者与发病率的比值(PIR)。代表性不足定义为 PIR < 0.8。
在纳入的 87 项研究中,82 项(94.2%)报告了参与者的性别,69 项(79.3%)报告了参与者的种族,20 项(23.0%)包括了种族数据。只有 17 项(19.5%)研究纳入了美洲印第安人/阿拉斯加原住民参与者。中位数 PIR 表明,与这些亚组中耐甲氧西林金黄色葡萄球菌感染的发病率相比,亚洲和黑人参与者在 RCT 中代表性不足。与 4 期试验相比,黑人参与者在 RCT 中代表性不足与研究规模较大、国际站点、工业赞助和 2/3 期试验有关,而与 4 期试验无关(每种情况 P <.05)。与 4 期试验相比,黑人参与者在 2/3 期试验中代表性不足的可能性是其 4 倍以上(比值比,4.57;95%置信区间:1.14-18.3)。
标准化报告种族和民族的方法以及努力增加边缘群体的招募将有助于确保抗菌药物 RCT 的公平性、严谨性和普遍性,并减少健康不平等。