TY - JOUR
T1 - Bivariate random effects models for meta-analysis of comparative studies with binary outcomes
T2 - Methods for the absolute risk difference and relative risk
AU - Chu, Haitao
AU - Nie, Lei
AU - Chen, Yong
AU - Huang, Yi
AU - Sun, Wei
PY - 2012/12
Y1 - 2012/12
N2 - Multivariate meta-analysis is increasingly utilised in biomedical research to combine data of multiple comparative clinical studies for evaluating drug efficacy and safety profile. When the probability of the event of interest is rare, or when the individual study sample sizes are small, a substantial proportion of studies may not have any event of interest. Conventional meta-analysis methods either exclude such studies or include them through ad hoc continuality correction by adding an arbitrary positive value to each cell of the corresponding 2-×-2 tables, which may result in less accurate conclusions. Furthermore, different continuity corrections may result in inconsistent conclusions. In this article, we discuss a bivariate Beta-binomial model derived from Sarmanov family of bivariate distributions and a bivariate generalised linear mixed effects model for binary clustered data to make valid inferences. These bivariate random effects models use all available data without ad hoc continuity corrections, and accounts for the potential correlation between treatment (or exposure) and control groups within studies naturally. We then utilise the bivariate random effects models to reanalyse two recent meta-analysis data sets.
AB - Multivariate meta-analysis is increasingly utilised in biomedical research to combine data of multiple comparative clinical studies for evaluating drug efficacy and safety profile. When the probability of the event of interest is rare, or when the individual study sample sizes are small, a substantial proportion of studies may not have any event of interest. Conventional meta-analysis methods either exclude such studies or include them through ad hoc continuality correction by adding an arbitrary positive value to each cell of the corresponding 2-×-2 tables, which may result in less accurate conclusions. Furthermore, different continuity corrections may result in inconsistent conclusions. In this article, we discuss a bivariate Beta-binomial model derived from Sarmanov family of bivariate distributions and a bivariate generalised linear mixed effects model for binary clustered data to make valid inferences. These bivariate random effects models use all available data without ad hoc continuity corrections, and accounts for the potential correlation between treatment (or exposure) and control groups within studies naturally. We then utilise the bivariate random effects models to reanalyse two recent meta-analysis data sets.
KW - beta-binomial distribution
KW - bivariate generalised linear mixed models
KW - bivariate random effects models
KW - clustered binary data
KW - meta-analysis
UR - http://www.scopus.com/inward/record.url?scp=84870014622&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84870014622&partnerID=8YFLogxK
U2 - 10.1177/0962280210393712
DO - 10.1177/0962280210393712
M3 - Article
C2 - 21177306
AN - SCOPUS:84870014622
SN - 0962-2802
VL - 21
SP - 621
EP - 633
JO - Statistical methods in medical research
JF - Statistical methods in medical research
IS - 6
ER -