Franklin Jessica M, Dejene Sara, Huybrechts Krista F, Wang Shirley V, Kulldorff Martin, Rothman Kenneth J
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Research Triangle Institute, Research Triangle Park, NC, USA.
Epidemiol Methods. 2017 Apr;6(1). doi: 10.1515/em-2016-0018. Epub 2017 Apr 22.
In a recent article, the authors conducted a meta-analysis to compare estimated treatment effects from randomized trials with those derived from observational studies based on routinely collected data (RCD). They calculated a pooled relative odds ratio (ROR) of 1.31 (95% confidence interval [CI]: 1.03-1.65) and concluded that RCD studies systematically over-estimated protective effects. However, their meta-analysis inverted results for some clinical questions to force all estimates from RCD to be below 1. We evaluated the statistical properties of this pooled ROR, and found that the selective inversion rule employed in the original meta-analysis can positively bias the estimate of the ROR. We then repeated the random effects meta-analysis using a different inversion rule and found an estimated ROR of 0.98 (0.78-1.23), indicating the ROR is highly dependent on the direction of comparisons. As an alternative to the ROR, we calculated the observed proportion of clinical questions where the RCD and trial CIs overlap, as well as the expected proportion assuming no systematic difference between the studies. Out of 16 clinical questions, 50% CIs overlapped for 8 (50%; 25 to 75%) compared with an expected overlap of 60% assuming no systematic difference between RCD studies and trials. Thus, there was little evidence of a systematic difference in effect estimates between RCD and RCTs. Estimates of pooled RORs across distinct clinical questions are generally not interpretable and may be misleading.
在最近的一篇文章中,作者进行了一项荟萃分析,以比较随机试验得出的估计治疗效果与基于常规收集数据(RCD)的观察性研究得出的效果。他们计算出合并相对比值比(ROR)为1.31(95%置信区间[CI]:1.03 - 1.65),并得出结论,RCD研究系统性地高估了保护效果。然而,他们的荟萃分析颠倒了一些临床问题的结果,以使RCD的所有估计值都低于1。我们评估了这个合并ROR的统计特性,发现原始荟萃分析中采用的选择性颠倒规则会使ROR的估计产生正向偏差。然后,我们使用不同的颠倒规则重复了随机效应荟萃分析,发现估计的ROR为0.98(0.78 - 1.23),这表明ROR高度依赖于比较的方向。作为ROR的替代方法,我们计算了RCD和试验CI重叠的临床问题的观察比例,以及假设研究之间无系统差异时的预期比例。在16个临床问题中,8个(50%;25%至75%)的95%CI重叠,而假设RCD研究和试验之间无系统差异时的预期重叠率为60%。因此,几乎没有证据表明RCD和随机对照试验(RCT)在效应估计上存在系统差异。跨不同临床问题的合并ROR估计通常无法解释,可能会产生误导。