ArticleBMC medical research methodology2025
Random-effects meta-analysis models for pooling rare events data: a comparison between frequentist and bayesian methods.
Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Quantifying uncertainty: a practical comparison of Bayesian and frequentist meta-analytic frameworks applied to lead exposure and children's IQ.BMC medical research methodology · 2026Pooled it
- Review
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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
backgroundStandard random-effects meta-analysis models for rare events exhibit significant limitations, particularly when synthesizing studies with double-zero events. While methodological advances in both frequentist and Bayesian frameworks now offer robust alternatives that bypass continuity corrections, the comparative performance of these approaches-especially between Bayesian and frequentist paradigms-remains understudied.
methodsThis study evaluates the performance of ten widely used meta-analysis models for binary outcomes, using the odds ratio as the effect measure. The evaluated models comprise seven frequentist and three Bayesian approaches. Simulations systematically varied key parameters, including control event rates, treatment effects, study numbers, and heterogeneity levels, to compare model performance across four metrics: percentage bias, 95% confidence/credible interval width, root mean square error, and coverage. The methods were further illustrated through applications to two published rare events meta-analyses.
resultsThe results show that the beta-binomial model proposed by Kuss generally performed well, while the generalised estimating equations did not. In cases where heterogeneity is not large, all models tended to have a good performance except for the generalised estimating equations. When the heterogeneity is large, none of the compared models produced good performance. The Bayesian model incorporating the Beta-Hyperprior proposed by Hong et al. performed well, followed by the binomial-normal hierarchical model proposed by Bhaumik.
conclusionsIn summary, the beta-binomial model proposed by Kuss is recommended for rare events meta-analyses, and the Bayesian model is a promising method for pooling rare events data.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.