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Random main effects of treatment: A case study with a network meta-analysis
Stephen Senn1,2, Susanne Schmitz3, Anna Schritz1
1Competence Centre for Methodology and Statistics, Luxembourg Institute of Health, Strassen, Luxembourg.
This study introduces a novel hierarchical random-effect model for network meta-analysis with many treatments. This approach provides more precise, shrunk treatment effect estimates and considers random within-trial variances.
Area of Science:
- Biostatistics
- Medical Research Methodology
- Evidence Synthesis
Background:
- Traditional network meta-analyses often assume fixed treatment effects.
- Large numbers of treatments in meta-analyses present analytical challenges.
- Existing random-effect models primarily address treatment-by-trial interactions or trial main effects.
Purpose of the Study:
- To propose and evaluate a hierarchical model for random main effects of treatments in network meta-analysis.
- To explore the utility of random-effect models for within-trial variances.
- To demonstrate the application of this approach using a real-world example.
Main Methods:
- Development of a hierarchical modeling framework to treat individual treatment effects as random realizations from a normal distribution.
- Application of the model to a network meta-analysis involving 44 treatments across 10 trials.
- Investigation of incorporating random-effect models for within-trial variances.
Main Results:
- The hierarchical model successfully produced shrunk (regressed toward the overall mean) estimates for individual treatment effects.
- This method offers improved precision for effect estimates when dealing with numerous treatments.
- Graphical representations of results were developed to aid interpretation.
Conclusions:
- Modeling the main effect of treatment as random is a viable and beneficial approach in network meta-analysis, especially with a large number of treatments.
- The proposed hierarchical method enhances the estimation of individual treatment effects.
- Further consideration of random-effect models for within-trial variances is warranted.
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