Martins Pedro Nascimento, Lourenço Mateus Henrique Toledo, Mota Gabriel Paz Souza, Cavalcanti Alexandre Biasi, Peçanha Antonio Ana Carolina, Diaz-Quijano Fredi Alexander
Federal University of Juiz de Fora, Juiz de Fora, Brazil.
Department of Epidemiology, School of Public Health, University of São Paulo, São Paulo, Brazil.
Clin Trials. 2025 Feb;22(1):77-87. doi: 10.1177/17407745241276130. Epub 2024 Oct 10.
BACKGROUND/AIMS: This study aimed to determine the prevalence of ordinal, binary, and numerical composite endpoints among coronavirus disease 2019 trials and the potential bias attributable to their use.
We systematically reviewed the Cochrane COVID-19 Study Register to assess the prevalence, characteristics, and bias associated with using composite endpoints in coronavirus disease 2019 randomized clinical trials. We compared the effect measure (relative risk) of composite outcomes and that of its most critical component (i.e. death) by estimating the Bias Attributable to Composite Outcomes index [ln(relative risk for the composite outcome)/ln(relative risk for death)].
Composite endpoints accounted for 152 out of 417 primary endpoints in coronavirus disease 2019 randomized trials, being more frequent among studies published in high-impact journals. Ordinal endpoints were the most common (54% of all composites), followed by binary or time-to-event (34%), numerical (11%), and hierarchical (1%). Composites predominated among trials enrolling patients with severe disease when compared to trials with a mild or moderate case mix (odds ratio = 1.72). Adaptations of the seven-point World Health Organization scale occurred in 40% of the ordinal primary endpoints, which frequently underwent dichotomization for the statistical analyses. Mortality accounted for a median of 24% (interquartile range: 6%-48%) of all events when included in the composite. The median point estimate of the Bias Attributable to Composite Outcomes index was 0.3 (interquartile range: -0.1 to 0.7), being significantly lower than 1 in 5 of 24 comparisons.
Composite endpoints were used in a significant proportion of coronavirus disease 2019 trials, especially those involving severely ill patients. This is likely due to the higher anticipated rates of competing events, such as death, in such studies. Ordinal composites were common but often not fully appreciated, reducing the potential gains in information and statistical efficiency. For studies with binary composites, death was the most frequent component, and, unexpectedly, composite outcome estimates were often closer to the null when compared to those for mortality death. Numerical composites were less common, and only two trials used hierarchical endpoints. These newer approaches may offer advantages over traditional binary and ordinal composites; however, their potential benefits warrant further scrutiny.
Composite endpoints accounted for more than a third of coronavirus disease 2019 trials' primary endpoints; their use was more common among studies that included patients with severe disease and their point effect estimates tended to underestimate those for mortality.
背景/目的:本研究旨在确定2019冠状病毒病试验中有序、二元和数值复合终点的患病率,以及使用这些终点可能导致的偏差。
我们系统检索了Cochrane COVID-19研究注册库,以评估2019冠状病毒病随机临床试验中使用复合终点的患病率、特征和偏差。我们通过估计复合终点归因偏差指数[ln(复合结局的相对风险)/ln(死亡的相对风险)],比较了复合结局的效应量(相对风险)与其最关键组成部分(即死亡)的效应量。
在2019冠状病毒病随机试验的417个主要终点中,复合终点占152个,在高影响力期刊发表的研究中更为常见。有序终点最为常见(占所有复合终点的54%),其次是二元或事件发生时间终点(34%)、数值终点(11%)和分层终点(1%)。与纳入轻、中度病例的试验相比,在纳入重症患者的试验中复合终点更为常见(优势比=1.72)。40%的有序主要终点采用了七点世界卫生组织量表的改编版,这些终点在统计分析中经常进行二分法处理。当死亡作为复合终点的一部分时,所有事件中死亡的中位数占比为24%(四分位间距:6%-48%)。复合终点归因偏差指数的中位数点估计值为0.3(四分位间距:-0.1至0.7),在24项比较中有5项显著低于1。
在相当比例的2019冠状病毒病试验中使用了复合终点,尤其是那些涉及重症患者的试验。这可能是由于在此类研究中预期的竞争事件(如死亡)发生率较高。有序复合终点很常见,但往往未得到充分认识,降低了信息和统计效率方面的潜在收益。对于二元复合终点的研究,死亡是最常见的组成部分,而且出乎意料的是,与死亡率相比,复合结局估计值往往更接近无效值。数值复合终点不太常见,只有两项试验使用了分层终点。这些新方法可能比传统的二元和有序复合终点具有优势;然而,它们的潜在益处值得进一步审视。
复合终点占2019冠状病毒病试验主要终点的三分之一以上;在纳入重症患者的研究中其使用更为常见,且其点效应估计往往低估死亡率。