Addressing Dichotomous Data for Participants Excluded from Trial Analysis: A Guide for Systematic Reviewers

被引:118
作者
Akl, Elie A. [1 ,2 ,3 ]
Johnston, Bradley C. [3 ,4 ,5 ]
Alonso-Coello, Pablo [6 ]
Neumann, Ignacio [3 ]
Ebrahim, Shanil [3 ]
Briel, Matthias [3 ,7 ]
Cook, Deborah J. [3 ,8 ]
Guyatt, Gordon H. [3 ,8 ]
机构
[1] Amer Univ Beirut, Dept Internal Med, Beirut, Lebanon
[2] SUNY Buffalo, Dept Med, Buffalo, NY 14260 USA
[3] McMaster Univ, Dept Clin Epidemiol & Biostat, Hamilton, ON, Canada
[4] Hosp Sick Children, Dept Anesthesia & Pain Med, Toronto, ON M5G 1X8, Canada
[5] SickKids Res Inst, Toronto, ON, Canada
[6] CIBERESP IIB St Pau, Iberoamer Cochrane Ctr, Barcelona, Spain
[7] Univ Basel Hosp, Basel Inst Clin Epidemiol & Biostat, CH-4031 Basel, Switzerland
[8] McMaster Univ, Dept Med, Hamilton, ON, Canada
来源
PLOS ONE | 2013年 / 8卷 / 02期
基金
加拿大健康研究院;
关键词
FOLLOW-UP INFORMATION; CLINICAL-TRIALS; INTENTION; OUTCOMES; TREAT; LOST;
D O I
10.1371/journal.pone.0057132
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Systematic reviewer authors intending to include all randomized participants in their meta-analyses need to make assumptions about the outcomes of participants with missing data. Objective: The objective of this paper is to provide systematic reviewer authors with a relatively simple guidance for addressing dichotomous data for participants excluded from analyses of randomized trials. Methods: This guide is based on a review of the Cochrane handbook and published methodological research. The guide deals with participants excluded from the analysis who were considered 'non-adherent to the protocol' but for whom data are available, and participants with missing data. Results: Systematic reviewer authors should include data from 'non-adherent' participants excluded from the primary study authors' analysis but for whom data are available. For missing, unavailable participant data, authors may conduct a complete case analysis (excluding those with missing data) as the primary analysis. Alternatively, they may conduct a primary analysis that makes plausible assumptions about the outcomes of participants with missing data. When the primary analysis suggests important benefit, sensitivity meta-analyses using relatively extreme assumptions that may vary in plausibility can inform the extent to which risk of bias impacts the confidence in the results of the primary analysis. The more plausible assumptions draw on the outcome event rates within the trial or in all trials included in the meta-analysis. The proposed guide does not take into account the uncertainty associated with assumed events. Conclusions: This guide proposes methods for handling participants excluded from analyses of randomized trials. These methods can help in establishing the extent to which risk of bias impacts meta-analysis results.
引用
收藏
页数:7
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