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Estimating required information size by quantifying diversity in random-effects model meta-analyses

BACKGROUND: There is increasing awareness that meta-analyses require a sufficiently large information size to detect or reject an anticipated intervention effect. The required information size in a meta-analysis may be calculated from an anticipated a priori intervention effect or from an interventi...

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Autores principales: Wetterslev, Jørn, Thorlund, Kristian, Brok, Jesper, Gluud, Christian
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809074/
https://www.ncbi.nlm.nih.gov/pubmed/20042080
http://dx.doi.org/10.1186/1471-2288-9-86
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author Wetterslev, Jørn
Thorlund, Kristian
Brok, Jesper
Gluud, Christian
author_facet Wetterslev, Jørn
Thorlund, Kristian
Brok, Jesper
Gluud, Christian
author_sort Wetterslev, Jørn
collection PubMed
description BACKGROUND: There is increasing awareness that meta-analyses require a sufficiently large information size to detect or reject an anticipated intervention effect. The required information size in a meta-analysis may be calculated from an anticipated a priori intervention effect or from an intervention effect suggested by trials with low-risk of bias. METHODS: Information size calculations need to consider the total model variance in a meta-analysis to control type I and type II errors. Here, we derive an adjusting factor for the required information size under any random-effects model meta-analysis. RESULTS: We devise a measure of diversity (D(2)) in a meta-analysis, which is the relative variance reduction when the meta-analysis model is changed from a random-effects into a fixed-effect model. D(2 )is the percentage that the between-trial variability constitutes of the sum of the between-trial variability and a sampling error estimate considering the required information size. D(2 )is different from the intuitively obvious adjusting factor based on the common quantification of heterogeneity, the inconsistency (I(2)), which may underestimate the required information size. Thus, D(2 )and I(2 )are compared and interpreted using several simulations and clinical examples. In addition we show mathematically that diversity is equal to or greater than inconsistency, that is D(2 )≥ I(2), for all meta-analyses. CONCLUSION: We conclude that D(2 )seems a better alternative than I(2 )to consider model variation in any random-effects meta-analysis despite the choice of the between trial variance estimator that constitutes the model. Furthermore, D(2 )can readily adjust the required information size in any random-effects model meta-analysis.
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spelling pubmed-28090742010-01-21 Estimating required information size by quantifying diversity in random-effects model meta-analyses Wetterslev, Jørn Thorlund, Kristian Brok, Jesper Gluud, Christian BMC Med Res Methodol Research article BACKGROUND: There is increasing awareness that meta-analyses require a sufficiently large information size to detect or reject an anticipated intervention effect. The required information size in a meta-analysis may be calculated from an anticipated a priori intervention effect or from an intervention effect suggested by trials with low-risk of bias. METHODS: Information size calculations need to consider the total model variance in a meta-analysis to control type I and type II errors. Here, we derive an adjusting factor for the required information size under any random-effects model meta-analysis. RESULTS: We devise a measure of diversity (D(2)) in a meta-analysis, which is the relative variance reduction when the meta-analysis model is changed from a random-effects into a fixed-effect model. D(2 )is the percentage that the between-trial variability constitutes of the sum of the between-trial variability and a sampling error estimate considering the required information size. D(2 )is different from the intuitively obvious adjusting factor based on the common quantification of heterogeneity, the inconsistency (I(2)), which may underestimate the required information size. Thus, D(2 )and I(2 )are compared and interpreted using several simulations and clinical examples. In addition we show mathematically that diversity is equal to or greater than inconsistency, that is D(2 )≥ I(2), for all meta-analyses. CONCLUSION: We conclude that D(2 )seems a better alternative than I(2 )to consider model variation in any random-effects meta-analysis despite the choice of the between trial variance estimator that constitutes the model. Furthermore, D(2 )can readily adjust the required information size in any random-effects model meta-analysis. BioMed Central 2009-12-30 /pmc/articles/PMC2809074/ /pubmed/20042080 http://dx.doi.org/10.1186/1471-2288-9-86 Text en Copyright ©2009 Wetterslev et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Wetterslev, Jørn
Thorlund, Kristian
Brok, Jesper
Gluud, Christian
Estimating required information size by quantifying diversity in random-effects model meta-analyses
title Estimating required information size by quantifying diversity in random-effects model meta-analyses
title_full Estimating required information size by quantifying diversity in random-effects model meta-analyses
title_fullStr Estimating required information size by quantifying diversity in random-effects model meta-analyses
title_full_unstemmed Estimating required information size by quantifying diversity in random-effects model meta-analyses
title_short Estimating required information size by quantifying diversity in random-effects model meta-analyses
title_sort estimating required information size by quantifying diversity in random-effects model meta-analyses
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809074/
https://www.ncbi.nlm.nih.gov/pubmed/20042080
http://dx.doi.org/10.1186/1471-2288-9-86
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