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Individual participant data meta-analyses should not ignore clustering
OBJECTIVES: Individual participant data (IPD) meta-analyses often analyze their IPD as if coming from a single study. We compare this approach with analyses that rather account for clustering of patients within studies. STUDY DESIGN AND SETTING: Comparison of effect estimates from logistic regressio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717206/ https://www.ncbi.nlm.nih.gov/pubmed/23651765 http://dx.doi.org/10.1016/j.jclinepi.2012.12.017 |
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author | Abo-Zaid, Ghada Guo, Boliang Deeks, Jonathan J. Debray, Thomas P.A. Steyerberg, Ewout W. Moons, Karel G.M. Riley, Richard David |
author_facet | Abo-Zaid, Ghada Guo, Boliang Deeks, Jonathan J. Debray, Thomas P.A. Steyerberg, Ewout W. Moons, Karel G.M. Riley, Richard David |
author_sort | Abo-Zaid, Ghada |
collection | PubMed |
description | OBJECTIVES: Individual participant data (IPD) meta-analyses often analyze their IPD as if coming from a single study. We compare this approach with analyses that rather account for clustering of patients within studies. STUDY DESIGN AND SETTING: Comparison of effect estimates from logistic regression models in real and simulated examples. RESULTS: The estimated prognostic effect of age in patients with traumatic brain injury is similar, regardless of whether clustering is accounted for. However, a family history of thrombophilia is found to be a diagnostic marker of deep vein thrombosis [odds ratio, 1.30; 95% confidence interval (CI): 1.00, 1.70; P = 0.05] when clustering is accounted for but not when it is ignored (odds ratio, 1.06; 95% CI: 0.83, 1.37; P = 0.64). Similarly, the treatment effect of nicotine gum on smoking cessation is severely attenuated when clustering is ignored (odds ratio, 1.40; 95% CI: 1.02, 1.92) rather than accounted for (odds ratio, 1.80; 95% CI: 1.29, 2.52). Simulations show models accounting for clustering perform consistently well, but downwardly biased effect estimates and low coverage can occur when ignoring clustering. CONCLUSION: Researchers must routinely account for clustering in IPD meta-analyses; otherwise, misleading effect estimates and conclusions may arise. |
format | Online Article Text |
id | pubmed-3717206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37172062013-08-01 Individual participant data meta-analyses should not ignore clustering Abo-Zaid, Ghada Guo, Boliang Deeks, Jonathan J. Debray, Thomas P.A. Steyerberg, Ewout W. Moons, Karel G.M. Riley, Richard David J Clin Epidemiol Original Article OBJECTIVES: Individual participant data (IPD) meta-analyses often analyze their IPD as if coming from a single study. We compare this approach with analyses that rather account for clustering of patients within studies. STUDY DESIGN AND SETTING: Comparison of effect estimates from logistic regression models in real and simulated examples. RESULTS: The estimated prognostic effect of age in patients with traumatic brain injury is similar, regardless of whether clustering is accounted for. However, a family history of thrombophilia is found to be a diagnostic marker of deep vein thrombosis [odds ratio, 1.30; 95% confidence interval (CI): 1.00, 1.70; P = 0.05] when clustering is accounted for but not when it is ignored (odds ratio, 1.06; 95% CI: 0.83, 1.37; P = 0.64). Similarly, the treatment effect of nicotine gum on smoking cessation is severely attenuated when clustering is ignored (odds ratio, 1.40; 95% CI: 1.02, 1.92) rather than accounted for (odds ratio, 1.80; 95% CI: 1.29, 2.52). Simulations show models accounting for clustering perform consistently well, but downwardly biased effect estimates and low coverage can occur when ignoring clustering. CONCLUSION: Researchers must routinely account for clustering in IPD meta-analyses; otherwise, misleading effect estimates and conclusions may arise. Elsevier 2013-08 /pmc/articles/PMC3717206/ /pubmed/23651765 http://dx.doi.org/10.1016/j.jclinepi.2012.12.017 Text en © 2013 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Original Article Abo-Zaid, Ghada Guo, Boliang Deeks, Jonathan J. Debray, Thomas P.A. Steyerberg, Ewout W. Moons, Karel G.M. Riley, Richard David Individual participant data meta-analyses should not ignore clustering |
title | Individual participant data meta-analyses should not ignore clustering |
title_full | Individual participant data meta-analyses should not ignore clustering |
title_fullStr | Individual participant data meta-analyses should not ignore clustering |
title_full_unstemmed | Individual participant data meta-analyses should not ignore clustering |
title_short | Individual participant data meta-analyses should not ignore clustering |
title_sort | individual participant data meta-analyses should not ignore clustering |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717206/ https://www.ncbi.nlm.nih.gov/pubmed/23651765 http://dx.doi.org/10.1016/j.jclinepi.2012.12.017 |
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