Methodology of subgroup analyses used in individual patient data meta-analyses versus meta-analyses on published data

Laura Koopman, Geert JMG van der Heijden, Paul P Glasziou, Diederick E Grobbee, Maroeska M Rovers

Background:

A major advantage of meta-analyses using pooled raw individual patient data (IPD-MA) of randomised trials, compared to conventional meta-analysis of published data (MAP), are the possibilities for subgroup analysis. IPD-MA have greater power to carry out informative subgroup analyses allowing a more thorough assessment as to whether differences are spurious or not. Both the IPD-MA and MAP have never been compared with respect to the methodology used.

Objective:

To identify differences in the methodology of subgroup analyses between IPD-MA and MAP.

Methods:

An extended literature search was performed to identify all IPD-MA of randomized controlled trials, followed by a related article search to identify MAPs on the same research question. Data were extracted with special attention to the methodology of subgroup analysis.

Results:

We have identified 130 IPD-MA. To date, we have completed the search for 21 IPD-MA, these relate to 13 MAP. Fewer studies were included in the IPD-MA as compared to the MAP; median of 5 and 16 respectively. Subgroup analyses were performed in 12 IPD-MA (57%), and 9 MAPs (69%). In 8 of the 12 IPD-MA (67%) and in 4 of the 9 MAPs (44%) that performed subgroup analyses, the subgroups were defined a priori. In 7 IPD-MA (58%) and in 1 MAP (11%) an interaction test was performed, whereas 9 IPD-MA (75%) and 8 MAPs (89%) analysed their data stratified per trial.

Conclusion:

In spite of common objectives both IPD-MA and MAP use distinctly different strategies to perform subgroup analysis. The reasons and implications of these differences require further study. Final results will be presented at the Cochrane colloquium.

Melbourne 2005 O-07

Link to corresponding slides