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Meta-analysis of continuous outcomes combining individual patient data and aggregate data
Richard D Riley1, Paul C Lambert, Jan A Staessen
1Centre for Medical Statistics and Health Evaluation, Faculty of Medicine, University of Liverpool, Shelley's Cottage, Brownlow Street, Liverpool, U.K. richard.riley@liv.ac.uk
Combining individual patient data (IPD) and aggregate data (AD) in meta-analysis enhances evidence synthesis. New statistical methods allow for the integration of both IPD and AD, improving the utilization of all available clinical trial information.
Area of Science:
- Biostatistics
- Clinical Epidemiology
- Health Research Synthesis
Background:
- Meta-analysis of individual patient data (IPD) is the gold standard for evidence synthesis.
- Aggregate data (AD) meta-analysis is used when IPD is unavailable, potentially leading to incomplete evidence utilization.
Purpose of the Study:
- To develop and assess statistical methods for combining IPD and AD in meta-analysis of continuous outcomes.
- To improve the comprehensive synthesis of evidence from randomized controlled trials.
Main Methods:
- Development of one-step and two-step statistical approaches for IPD and AD meta-analysis.
- Utilizing dummy variables in a one-step approach to differentiate IPD and AD trials and constrain parameter estimation.
- Developing models to separate within-trial and across-trials treatment-covariate interactions to avoid ecological bias.
Main Results:
- The one-step approach provides a flexible framework for integrating patient-level and trial-level parameters.
- Models effectively separate within-trial and across-trials treatment-covariate interactions, addressing confounding.
- Demonstrated benefits of utilizing AD alongside IPD in a hypertension meta-analysis.
Conclusions:
- Statistical methods for combining IPD and AD are crucial for maximizing evidence from clinical studies.
- The developed methods offer a robust framework for meta-analysis involving mixed data types.
- Integrating AD with IPD enhances the accuracy and completeness of meta-analytic findings.
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