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Multivariate meta-analysis of mixed outcomes: a Bayesian approach

Multivariate random effects meta-analysis (MRMA) is an appropriate way for synthesizing data from studies reporting multiple correlated outcomes. In a Bayesian framework, it has great potential for integrating evidence from a variety of sources. In this paper, we propose a Bayesian model for MRMA of...

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Autores principales: Bujkiewicz, Sylwia, Thompson, John R, Sutton, Alex J, Cooper, Nicola J, Harrison, Mark J, Symmons, Deborah PM, Abrams, Keith R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015389/
https://www.ncbi.nlm.nih.gov/pubmed/23630081
http://dx.doi.org/10.1002/sim.5831
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author Bujkiewicz, Sylwia
Thompson, John R
Sutton, Alex J
Cooper, Nicola J
Harrison, Mark J
Symmons, Deborah PM
Abrams, Keith R
author_facet Bujkiewicz, Sylwia
Thompson, John R
Sutton, Alex J
Cooper, Nicola J
Harrison, Mark J
Symmons, Deborah PM
Abrams, Keith R
author_sort Bujkiewicz, Sylwia
collection PubMed
description Multivariate random effects meta-analysis (MRMA) is an appropriate way for synthesizing data from studies reporting multiple correlated outcomes. In a Bayesian framework, it has great potential for integrating evidence from a variety of sources. In this paper, we propose a Bayesian model for MRMA of mixed outcomes, which extends previously developed bivariate models to the trivariate case and also allows for combination of multiple outcomes that are both continuous and binary. We have constructed informative prior distributions for the correlations by using external evidence. Prior distributions for the within-study correlations were constructed by employing external individual patent data and using a double bootstrap method to obtain the correlations between mixed outcomes. The between-study model of MRMA was parameterized in the form of a product of a series of univariate conditional normal distributions. This allowed us to place explicit prior distributions on the between-study correlations, which were constructed using external summary data. Traditionally, independent ‘vague’ prior distributions are placed on all parameters of the model. In contrast to this approach, we constructed prior distributions for the between-study model parameters in a way that takes into account the inter-relationship between them. This is a flexible method that can be extended to incorporate mixed outcomes other than continuous and binary and beyond the trivariate case. We have applied this model to a motivating example in rheumatoid arthritis with the aim of incorporating all available evidence in the synthesis and potentially reducing uncertainty around the estimate of interest. © 2013 The Authors. Statistics inMedicine Published by John Wiley & Sons, Ltd.
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spelling pubmed-40153892014-05-12 Multivariate meta-analysis of mixed outcomes: a Bayesian approach Bujkiewicz, Sylwia Thompson, John R Sutton, Alex J Cooper, Nicola J Harrison, Mark J Symmons, Deborah PM Abrams, Keith R Stat Med Research Articles Multivariate random effects meta-analysis (MRMA) is an appropriate way for synthesizing data from studies reporting multiple correlated outcomes. In a Bayesian framework, it has great potential for integrating evidence from a variety of sources. In this paper, we propose a Bayesian model for MRMA of mixed outcomes, which extends previously developed bivariate models to the trivariate case and also allows for combination of multiple outcomes that are both continuous and binary. We have constructed informative prior distributions for the correlations by using external evidence. Prior distributions for the within-study correlations were constructed by employing external individual patent data and using a double bootstrap method to obtain the correlations between mixed outcomes. The between-study model of MRMA was parameterized in the form of a product of a series of univariate conditional normal distributions. This allowed us to place explicit prior distributions on the between-study correlations, which were constructed using external summary data. Traditionally, independent ‘vague’ prior distributions are placed on all parameters of the model. In contrast to this approach, we constructed prior distributions for the between-study model parameters in a way that takes into account the inter-relationship between them. This is a flexible method that can be extended to incorporate mixed outcomes other than continuous and binary and beyond the trivariate case. We have applied this model to a motivating example in rheumatoid arthritis with the aim of incorporating all available evidence in the synthesis and potentially reducing uncertainty around the estimate of interest. © 2013 The Authors. Statistics inMedicine Published by John Wiley & Sons, Ltd. John Wiley & Sons 2013-09-30 2013-04-30 /pmc/articles/PMC4015389/ /pubmed/23630081 http://dx.doi.org/10.1002/sim.5831 Text en © 2013 The Authors. Statistics in Medicine Published by John Wiley & Sons, Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Bujkiewicz, Sylwia
Thompson, John R
Sutton, Alex J
Cooper, Nicola J
Harrison, Mark J
Symmons, Deborah PM
Abrams, Keith R
Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title_full Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title_fullStr Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title_full_unstemmed Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title_short Multivariate meta-analysis of mixed outcomes: a Bayesian approach
title_sort multivariate meta-analysis of mixed outcomes: a bayesian approach
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015389/
https://www.ncbi.nlm.nih.gov/pubmed/23630081
http://dx.doi.org/10.1002/sim.5831
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