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      Pitfalls of using the risk ratio in meta‐analysis

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          Abstract

          For meta‐analysis of studies that report outcomes as binomial proportions, the most popular measure of effect is the odds ratio (OR), usually analyzed as log(OR). Many meta‐analyses use the risk ratio (RR) and its logarithm because of its simpler interpretation. Although log(OR) and log(RR) are both unbounded, use of log(RR) must ensure that estimates are compatible with study‐level event rates in the interval (0, 1). These complications pose a particular challenge for random‐effects models, both in applications and in generating data for simulations. As background, we review the conventional random‐effects model and then binomial generalized linear mixed models (GLMMs) with the logit link function, which do not have these complications. We then focus on log‐binomial models and explore implications of using them; theoretical calculations and simulation show evidence of biases. The main competitors to the binomial GLMMs use the beta‐binomial (BB) distribution, either in BB regression or by maximizing a BB likelihood; a simulation produces mixed results. Two examples and an examination of Cochrane meta‐analyses that used RR suggest bias in the results from the conventional inverse‐variance–weighted approach. Finally, we comment on other measures of effect that have range restrictions, including risk difference, and outline further research.

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          Random effects meta-analysis of event outcome in the framework of the generalized linear mixed model with applications in sparse data.

          We consider random effects meta-analysis where the outcome variable is the occurrence of some event of interest. The data structures handled are where one has one or more groups in each study, and in each group either the number of subjects with and without the event, or the number of events and the total duration of follow-up is available. Traditionally, the meta-analysis follows the summary measures approach based on the estimates of the outcome measure(s) and the corresponding standard error(s). This approach assumes an approximate normal within-study likelihood and treats the standard errors as known. This approach has several potential disadvantages, such as not accounting for the standard errors being estimated, not accounting for correlation between the estimate and the standard error, the use of an (arbitrary) continuity correction in case of zero events, and the normal approximation being bad in studies with few events. We show that these problems can be overcome in most cases occurring in practice by replacing the approximate normal within-study likelihood by the appropriate exact likelihood. This leads to a generalized linear mixed model that can be fitted in standard statistical software. For instance, in the case of odds ratio meta-analysis, one can use the non-central hypergeometric distribution likelihood leading to mixed-effects conditional logistic regression. For incidence rate ratio meta-analysis, it leads to random effects logistic regression with an offset variable. We also present bivariate and multivariate extensions. We present a number of examples, especially with rare events, among which an example of network meta-analysis.
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            Conducting meta-analyses in R with the metaphor package

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              Issues in the selection of a summary statistic for meta-analysis of clinical trials with binary outcomes.

              Meta-analysis of binary data involves the computation of a weighted average of summary statistics calculated for each trial. The selection of the appropriate summary statistic is a subject of debate due to conflicts in the relative importance of mathematical properties and the ability to intuitively interpret results. This paper explores the process of identifying a summary statistic most likely to be consistent across trials when there is variation in control group event rates. Four summary statistics are considered: odds ratios (OR); risk differences (RD) and risk ratios of beneficial (RR(B)); and harmful outcomes (RR(H)). Each summary statistic corresponds to a different pattern of predicted absolute benefit of treatment with variation in baseline risk, the greatest difference in patterns of prediction being between RR(B) and RR(H). Selection of a summary statistic solely based on identification of the best-fitting model by comparing tests of heterogeneity is problematic, principally due to low numbers of trials. It is proposed that choice of a summary statistic should be guided by both empirical evidence and clinically informed debate as to which model is likely to be closest to the expected pattern of treatment benefit across baseline risks. Empirical investigations comparing the four summary statistics on a sample of 551 systematic reviews provide evidence that the RR and OR models are on average more consistent than RD, there being no difference on average between RR and OR. From a second sample of 114 meta-analyses evidence indicates that for interventions aimed at preventing an undesirable event, greatest absolute benefits are observed in trials with the highest baseline event rates, corresponding to the model of constant RR(H). The appropriate selection for a particular meta-analysis may depend on understanding reasons for variation in control group event rates; in some situations uncertainty about the choice of summary statistic will remain. Copyright 2002 John Wiley & Sons, Ltd.
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                Author and article information

                Contributors
                i.bakbergenuly@uea.ac.uk
                Journal
                Res Synth Methods
                Res Synth Methods
                10.1002/(ISSN)1759-2887
                JRSM
                Research Synthesis Methods
                John Wiley and Sons Inc. (Hoboken )
                1759-2879
                1759-2887
                11 April 2019
                September 2019
                : 10
                : 3 ( doiID: 10.1002/jrsm.v10.3 )
                : 398-419
                Affiliations
                [ 1 ] School of Computing Sciences University of East Anglia Norwich United Kingdom
                [ 2 ] University of Massachusetts Medical School Worcester Massachusetts
                Author notes
                [*] [* ] Correspondence

                Ilyas Bakbergenuly, School of Computing Sciences, University of East Anglia, Norwich NR4 7TJ, United Kingdom.

                Email: i.bakbergenuly@ 123456uea.ac.uk

                Author information
                https://orcid.org/0000-0001-7792-9051
                https://orcid.org/0000-0003-1336-181X
                Article
                JRSM1347 jrsm.1347
                10.1002/jrsm.1347
                6767076
                30854785
                ab712dcb-a86d-4d4f-817f-cc30285b1789
                © 2019 The Authors Research Synthesis Methods Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 02 November 2017
                : 28 November 2018
                : 11 February 2019
                Page count
                Figures: 9, Tables: 5, Pages: 22, Words: 15075
                Funding
                Funded by: Economic and Social Research Council
                Award ID: ES/L011859/1
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                jrsm1347
                jrsm1347-hdr-0001
                September 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.9 mode:remove_FC converted:30.09.2019

                beta‐binomial model,log‐binomial model,relative risk,response ratio,risk difference

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