Multivariate meta-analysis of mixed outcomes: a Bayesian approach

被引:47
作者
Bujkiewicz, Sylwia [1 ]
Thompson, John R. [2 ]
Sutton, Alex J. [1 ]
Cooper, Nicola J. [1 ]
Harrison, Mark J. [3 ]
Symmons, Deborah P. M. [4 ]
Abrams, Keith R. [1 ]
机构
[1] Univ Leicester, Dept Hlth Sci, Biostat Res Grp, Leicester LE1 7RH, Leics, England
[2] Univ Leicester, Dept Hlth Sci, Genet Epidemiol Grp, Leicester LE1 7RH, Leics, England
[3] Univ Manchester, Hth Econ Hlth Sci Methodol Res Grp, Sch Community Based Med, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, NIHR Manchester Musculoskeletal Biomed Res Unit, Arthrit Res UK Epidemiol Unit, Sch Translat Med, Manchester M13 9PT, Lancs, England
基金
英国医学研究理事会;
关键词
Bayesian analysis; multivariate meta-analysis; multiple outcomes; rheumatoid arthritis; BIAS;
D O I
10.1002/sim.5831
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:3926 / 3943
页数:18
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