Marginal structural models and other analyses allow multiple estimates of treatment effects in randomized clinical trials: Meta-epidemiological analysis

被引:10
作者
Ewald, Hannah [1 ,2 ,3 ]
Speich, Benjamin [1 ]
Ladanie, Aviv [1 ,2 ]
Bucher, Heiner C. [1 ]
Ioannidis, John P. A. [4 ,5 ,6 ,7 ,8 ]
Hemkens, Lars G. [1 ]
机构
[1] Univ Basel, Univ Hosp Basel, Basel Inst Clin Epidemiol & Biostat, Dept Clin Res, CH-4031 Basel, Switzerland
[2] Swiss Trop & Publ Hlth Inst, CH-4051 Basel, Switzerland
[3] Univ Basel, Univ Med Lib, CH-4051 Basel, Switzerland
[4] Stanford Univ, Sch Med, Stanford Prevent Res Ctr, Dept Med, Stanford, CA 94305 USA
[5] Stanford Univ, Meta Res Innovat Ctr Stanford METRICS, Palo Alto, CA 94305 USA
[6] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Dept Biomed Data Sci, Stanford, CA 94305 USA
[8] Stanford Univ, Sch Humanities & Sci, Dept Stat, Stanford, CA 94305 USA
关键词
Marginal structural models; Intention-to-treat; Randomized controlled trial; Reporting; Vibration of effects; Selective reporting; Prespecification; INTENTION-TO-TREAT; MEDICAL MALE CIRCUMCISION; ESTROGEN PLUS PROGESTIN; PER-PROTOCOL ANALYSES; CARDIOVASCULAR-DISEASE; PRIMARY PREVENTION; PHASE-III; MAINTENANCE BEVACIZUMAB; WOMENS HEALTH; STAGE IIIB;
D O I
10.1016/j.jclinepi.2018.11.001
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objectives: To determine how marginal structural models (MSMs), which are increasingly used to estimate causal effects, are used in randomized clinical trials (RCTs) and compare their results with those from intention-to-treat (ITT) or other analyses. Study Design and Setting: We searched PubMed, Scopus, citations of key references, and Clinicaltrials.gov. Eligible RCTs reported clinical effects based on MSMs and at least one other analysis. Results: We included 12 RCTs reporting 138 analyses for 24 clinical questions. In 19/24 (79%), MSM-based and other effect estimates were all in the same direction, 22/22 had overlapping 95% confidence intervals (CIs), and in 19/22 (86%), the MSM effect estimate lay within all 95% CIs of all other effects (in two cases no CIs were reported). For the same clinical question, the largest effect estimate from any analysis was 1.19-fold (median; interquartile range 1.13-1.34) larger than the smallest. All MSM and ITT effect estimates were in the same direction and had overlapping 95% Cis. In 71% (12/17), they also agreed on the presence of statistical significance. MSM-based effect estimates deviated more from the null than those based on ITT (P = 0.18). The effect estimates of both approaches differed 1.12-fold (median; interquartile range 1.02-1.22). Conclusions: MSMs provided largely similar effect estimates as other available analyses. Nevertheless, some of the differences in effect estimates or statistical significance may become important in clinical decision-making, and the multiple estimates require utmost attention of possible selective reporting bias. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 26
页数:15
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