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Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice

An important question for clinicians appraising a meta‐analysis is: are the findings likely to be valid in their own practice—does the reported effect accurately represent the effect that would occur in their own clinical population? To this end we advance the concept of statistical validity—where t...

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Detalles Bibliográficos
Autores principales: Willis, Brian H., Riley, Richard D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575530/
https://www.ncbi.nlm.nih.gov/pubmed/28620945
http://dx.doi.org/10.1002/sim.7372
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author Willis, Brian H.
Riley, Richard D.
author_facet Willis, Brian H.
Riley, Richard D.
author_sort Willis, Brian H.
collection PubMed
description An important question for clinicians appraising a meta‐analysis is: are the findings likely to be valid in their own practice—does the reported effect accurately represent the effect that would occur in their own clinical population? To this end we advance the concept of statistical validity—where the parameter being estimated equals the corresponding parameter for a new independent study. Using a simple (‘leave‐one‐out’) cross‐validation technique, we demonstrate how we may test meta‐analysis estimates for statistical validity using a new validation statistic, Vn, and derive its distribution. We compare this with the usual approach of investigating heterogeneity in meta‐analyses and demonstrate the link between statistical validity and homogeneity. Using a simulation study, the properties of Vn and the Q statistic are compared for univariate random effects meta‐analysis and a tailored meta‐regression model, where information from the setting (included as model covariates) is used to calibrate the summary estimate to the setting of application. Their properties are found to be similar when there are 50 studies or more, but for fewer studies Vn has greater power but a higher type 1 error rate than Q. The power and type 1 error rate of Vn are also shown to depend on the within‐study variance, between‐study variance, study sample size, and the number of studies in the meta‐analysis. Finally, we apply Vn to two published meta‐analyses and conclude that it usefully augments standard methods when deciding upon the likely validity of summary meta‐analysis estimates in clinical practice. © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.
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spelling pubmed-55755302017-09-18 Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice Willis, Brian H. Riley, Richard D. Stat Med Research Articles An important question for clinicians appraising a meta‐analysis is: are the findings likely to be valid in their own practice—does the reported effect accurately represent the effect that would occur in their own clinical population? To this end we advance the concept of statistical validity—where the parameter being estimated equals the corresponding parameter for a new independent study. Using a simple (‘leave‐one‐out’) cross‐validation technique, we demonstrate how we may test meta‐analysis estimates for statistical validity using a new validation statistic, Vn, and derive its distribution. We compare this with the usual approach of investigating heterogeneity in meta‐analyses and demonstrate the link between statistical validity and homogeneity. Using a simulation study, the properties of Vn and the Q statistic are compared for univariate random effects meta‐analysis and a tailored meta‐regression model, where information from the setting (included as model covariates) is used to calibrate the summary estimate to the setting of application. Their properties are found to be similar when there are 50 studies or more, but for fewer studies Vn has greater power but a higher type 1 error rate than Q. The power and type 1 error rate of Vn are also shown to depend on the within‐study variance, between‐study variance, study sample size, and the number of studies in the meta‐analysis. Finally, we apply Vn to two published meta‐analyses and conclude that it usefully augments standard methods when deciding upon the likely validity of summary meta‐analysis estimates in clinical practice. © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2017-06-15 2017-09-20 /pmc/articles/PMC5575530/ /pubmed/28620945 http://dx.doi.org/10.1002/sim.7372 Text en © 2017 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Willis, Brian H.
Riley, Richard D.
Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title_full Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title_fullStr Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title_full_unstemmed Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title_short Measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
title_sort measuring the statistical validity of summary meta‐analysis and meta‐regression results for use in clinical practice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575530/
https://www.ncbi.nlm.nih.gov/pubmed/28620945
http://dx.doi.org/10.1002/sim.7372
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