TY - JOUR T1 - Using individual participant data to improve network meta-analysis projects JF - BMJ Evidence-Based Medicine JO - BMJ EBM DO - 10.1136/bmjebm-2022-111931 SP - bmjebm-2022-111931 AU - Richard D Riley AU - Sofia Dias AU - Sarah Donegan AU - Jayne F Tierney AU - Lesley A Stewart AU - Orestis Efthimiou AU - David M Phillippo Y1 - 2022/08/10 UR - http://ebm.bmj.com/content/early/2022/08/10/bmjebm-2022-111931.abstract N2 - A network meta-analysis combines the evidence from existing randomised trials about the comparative efficacy of multiple treatments. It allows direct and indirect evidence about each comparison to be included in the same analysis, and provides a coherent framework to compare and rank treatments. A traditional network meta-analysis uses aggregate data (eg, treatment effect estimates and standard errors) obtained from publications or trial investigators. An alternative approach is to obtain, check, harmonise and meta-analyse the individual participant data (IPD) from each trial. In this article, we describe potential advantages of IPD for network meta-analysis projects, emphasising five key benefits: (1) improving the quality and scope of information available for inclusion in the meta-analysis, (2) examining and plotting distributions of covariates across trials (eg, for potential effect modifiers), (3) standardising and improving the analysis of each trial, (4) adjusting for prognostic factors to allow a network meta-analysis of conditional treatment effects and (5) including treatment–covariate interactions (effect modifiers) to allow relative treatment effects to vary by participant-level covariate values (eg, age, baseline depression score). A running theme of all these benefits is that they help examine and reduce heterogeneity (differences in the true treatment effect between trials) and inconsistency (differences in the true treatment effect between direct and indirect evidence) in the network. As a consequence, an IPD network meta-analysis has the potential for more precise, reliable and informative results for clinical practice and even allows treatment comparisons to be made for individual patients and targeted populations conditional on their particular characteristics.Data sharing not applicable as no datasets generated and/or analysed for this study. The work presented simply discusses and shares examples from published work, and therefore, no actual individual-level data are available for sharing. ER -