Addressing continuous data for participants excluded from trial analysis: a guide for systematic reviewers

J Clin Epidemiol. 2013 Sep;66(9):1014-1021.e1. doi: 10.1016/j.jclinepi.2013.03.014. Epub 2013 Jun 15.

Abstract

Background: No methods directly address the impact of missing participant data for continuous outcomes in systematic reviews on risk of bias.

Methods: We conducted a consultative, iterative process to develop a framework for handling missing participant data for continuous outcomes. We considered sources reflecting real observed outcomes in participants followed-up in individual trials included in the systematic review, and developed a range of plausible strategies. We applied our approach to two systematic reviews.

Results: We used five sources of data for imputing the means for participants with missing data. To impute standard deviation (SD), we used the median SD from the control arms of all included trials. Using these sources, we developed four progressively more stringent imputation strategies. In the first example review, effect estimates diminished and lost significance as strategies became more stringent, suggesting rating down confidence in estimates of effect for risk of bias. In the second, effect estimates maintained statistical significance using even the most stringent strategy, suggesting missing data does not undermine confidence in results.

Conclusions: Our approach provides a useful, reasonable, and relatively simple, quantitative guidance for judging the impact of risk of bias as a result of missing participant data in systematic reviews of continuous outcomes.

Keywords: Continuous outcomes; Lost to follow-up; Meta-analysis; Missing participant data; Risk of bias; Systematic reviews.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bias
  • Data Interpretation, Statistical*
  • Humans
  • Lost to Follow-Up*
  • Meta-Analysis as Topic
  • Randomized Controlled Trials as Topic*
  • Review Literature as Topic*
  • Risk