Meta-analysis refers to quantitative methods to combine results from independent studies so as to draw overall conclusions. Frequently, results from dissimilar studies are inappropriately combined, resulting in suspect inferential synthesis. We present a straightforward method to identify and addres
A basic introduction to fixed-effect and random-effects models for meta-analysis
β Scribed by Michael Borenstein; Larry V. Hedges; Julian P.T. Higgins; Hannah R. Rothstein
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 251 KB
- Volume
- 1
- Category
- Article
- ISSN
- 1759-2879
- DOI
- 10.1002/jrsm.12
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β¦ Synopsis
There are two popular statistical models for meta-analysis, the fixed-effect model and the random-effects model. The fact that these two models employ similar sets of formulas to compute statistics, and sometimes yield similar estimates for the various parameters, may lead people to believe that the models are interchangeable. In fact, though, the models represent fundamentally different assumptions about the data. The selection of the appropriate model is important to ensure that the various statistics are estimated correctly. Additionally, and more fundamentally, the model serves to place the analysis in context. It provides a framework for the goals of the analysis as well as for the interpretation of the statistics.In this paper we explain the key assumptions of each model, and then outline the differences between the models. We conclude with a discussion of factors to consider when choosing between the two models.
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**Praise for the First Edition** "This is a superb text from which to teach categorical data analysis, at a variety of levels. . . [t]his book can be very highly recommended." β*Short Book Reviews* "Of great interest to potential readers is the variety of fields that are represented in the examp
## SUMMARY Estimates of costβeffectiveness analyses are typically obtained either directly from βtrialβ based analyses or indirectly via surrogate endpoints in βmodelβ based analyses. Data from clinical trials that include both surrogate and final endpoints can be used in a joint analysis that comb