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Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment
Flaws in the conduct of randomized trials can lead to biased estimation of the intervention effect. Methods for adjustment of within‐trial biases in meta‐analysis include the use of empirical evidence from an external collection of meta‐analyses, and the use of expert opinion informed by the assessm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916311/ https://www.ncbi.nlm.nih.gov/pubmed/31857745 http://dx.doi.org/10.1111/rssa.12485 |
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author | Rhodes, K. M. Savović, J. Elbers, R. Jones, H. E. Higgins, J. P. T. Sterne, J. A. C. Welton, N. J. Turner, R. M. |
author_facet | Rhodes, K. M. Savović, J. Elbers, R. Jones, H. E. Higgins, J. P. T. Sterne, J. A. C. Welton, N. J. Turner, R. M. |
author_sort | Rhodes, K. M. |
collection | PubMed |
description | Flaws in the conduct of randomized trials can lead to biased estimation of the intervention effect. Methods for adjustment of within‐trial biases in meta‐analysis include the use of empirical evidence from an external collection of meta‐analyses, and the use of expert opinion informed by the assessment of detailed trial information. Our aim is to present methods to combine these two approaches to gain the advantages of both. We make use of the risk of bias information that is routinely available in Cochrane reviews, by obtaining empirical distributions for the bias associated with particular bias profiles (combinations of risk of bias judgements). We propose three methods: a formal combination of empirical evidence and opinion in a Bayesian analysis; asking experts to give an opinion on bias informed by both summary trial information and a bias distribution from the empirical evidence, either numerically or by selecting areas of the empirical distribution. The methods are demonstrated through application to two example binary outcome meta‐analyses. Bias distributions based on opinion informed by trial information alone were most dispersed on average, and those based on opinions obtained by selecting areas of the empirical distribution were narrowest. Although the three methods for combining empirical evidence with opinion vary in ease and speed of implementation, they yielded similar results in the two examples. |
format | Online Article Text |
id | pubmed-6916311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69163112019-12-17 Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment Rhodes, K. M. Savović, J. Elbers, R. Jones, H. E. Higgins, J. P. T. Sterne, J. A. C. Welton, N. J. Turner, R. M. J R Stat Soc Ser A Stat Soc Original Articles Flaws in the conduct of randomized trials can lead to biased estimation of the intervention effect. Methods for adjustment of within‐trial biases in meta‐analysis include the use of empirical evidence from an external collection of meta‐analyses, and the use of expert opinion informed by the assessment of detailed trial information. Our aim is to present methods to combine these two approaches to gain the advantages of both. We make use of the risk of bias information that is routinely available in Cochrane reviews, by obtaining empirical distributions for the bias associated with particular bias profiles (combinations of risk of bias judgements). We propose three methods: a formal combination of empirical evidence and opinion in a Bayesian analysis; asking experts to give an opinion on bias informed by both summary trial information and a bias distribution from the empirical evidence, either numerically or by selecting areas of the empirical distribution. The methods are demonstrated through application to two example binary outcome meta‐analyses. Bias distributions based on opinion informed by trial information alone were most dispersed on average, and those based on opinions obtained by selecting areas of the empirical distribution were narrowest. Although the three methods for combining empirical evidence with opinion vary in ease and speed of implementation, they yielded similar results in the two examples. John Wiley and Sons Inc. 2019-07-01 2020-01 /pmc/articles/PMC6916311/ /pubmed/31857745 http://dx.doi.org/10.1111/rssa.12485 Text en © 2019 The Authors Journal of the Royal Statistical Society: Series A (Statistics in Society) Published by John Wiley & Sons Ltd on behalf of the Royal Statistical Society. 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. |
spellingShingle | Original Articles Rhodes, K. M. Savović, J. Elbers, R. Jones, H. E. Higgins, J. P. T. Sterne, J. A. C. Welton, N. J. Turner, R. M. Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title | Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title_full | Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title_fullStr | Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title_full_unstemmed | Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title_short | Adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
title_sort | adjusting trial results for biases in meta‐analysis: combining data‐based evidence on bias with detailed trial assessment |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916311/ https://www.ncbi.nlm.nih.gov/pubmed/31857745 http://dx.doi.org/10.1111/rssa.12485 |
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