Meta-analysis of continuous outcome data from individual patients

Stat Med. 2001 Aug 15;20(15):2219-41. doi: 10.1002/sim.918.

Abstract

Meta-analyses using individual patient data are becoming increasingly common and have several advantages over meta-analyses of summary statistics. We explore the use of multilevel or hierarchical models for the meta-analysis of continuous individual patient outcome data from clinical trials. A general framework is developed which encompasses traditional meta-analysis, as well as meta-regression and the inclusion of patient-level covariates for investigation of heterogeneity. Unexplained variation in treatment differences between trials is considered as random. We focus on models with fixed trial effects, although an extension to a random effect for trial is described. The methods are illustrated on an example in Alzheimer's disease in a classical framework using SAS PROC MIXED and MLwiN, and in a Bayesian framework using BUGS. Relative merits of the three software packages for such meta-analyses are discussed, as are the assessment of model assumptions and extensions to incorporate more than two treatments.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / drug therapy
  • Bayes Theorem
  • Cholinesterase Inhibitors / pharmacology
  • Cholinesterase Inhibitors / therapeutic use
  • Cognition / drug effects
  • Humans
  • Meta-Analysis as Topic*
  • Models, Biological*
  • Models, Statistical*
  • Randomized Controlled Trials as Topic / methods*
  • Regression Analysis
  • Tacrine / pharmacology
  • Tacrine / therapeutic use
  • Treatment Outcome*

Substances

  • Cholinesterase Inhibitors
  • Tacrine