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A test for reporting bias in trial networks: simulation and case studies

BACKGROUND: Networks of trials assessing several treatment options available for the same condition are increasingly considered. Randomized trial evidence may be missing because of reporting bias. We propose a test for reporting bias in trial networks. METHODS: We test whether there is an excess of...

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Autores principales: Trinquart, Ludovic, Ioannidis, John PA, Chatellier, Gilles, Ravaud, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193287/
https://www.ncbi.nlm.nih.gov/pubmed/25262204
http://dx.doi.org/10.1186/1471-2288-14-112
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author Trinquart, Ludovic
Ioannidis, John PA
Chatellier, Gilles
Ravaud, Philippe
author_facet Trinquart, Ludovic
Ioannidis, John PA
Chatellier, Gilles
Ravaud, Philippe
author_sort Trinquart, Ludovic
collection PubMed
description BACKGROUND: Networks of trials assessing several treatment options available for the same condition are increasingly considered. Randomized trial evidence may be missing because of reporting bias. We propose a test for reporting bias in trial networks. METHODS: We test whether there is an excess of trials with statistically significant results across a network of trials. The observed number of trials with nominally statistically significant p-values across the network is compared with the expected number. The performance of the test (type I error rate and power) was assessed using simulation studies under different scenarios of selective reporting bias. Examples are provided for networks of antidepressant and antipsychotic trials, where reporting biases have been previously demonstrated by comparing published to Food and Drug Administration (FDA) data. RESULTS: In simulations, the test maintained the type I error rate and was moderately powerful after adjustment for type I error rate, except when the between-trial variance was substantial. In all, a positive test result increased moderately or markedly the probability of reporting bias being present, while a negative test result was not very informative. In the two examples, the test gave a signal for an excess of statistically significant results in the network of published data but not in the network of FDA data. CONCLUSION: The test could be useful to document an excess of significant findings in trial networks, providing a signal for potential publication bias or other selective analysis and outcome reporting biases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2288-14-112) contains supplementary material, which is available to authorized users.
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spelling pubmed-41932872014-10-11 A test for reporting bias in trial networks: simulation and case studies Trinquart, Ludovic Ioannidis, John PA Chatellier, Gilles Ravaud, Philippe BMC Med Res Methodol Research Article BACKGROUND: Networks of trials assessing several treatment options available for the same condition are increasingly considered. Randomized trial evidence may be missing because of reporting bias. We propose a test for reporting bias in trial networks. METHODS: We test whether there is an excess of trials with statistically significant results across a network of trials. The observed number of trials with nominally statistically significant p-values across the network is compared with the expected number. The performance of the test (type I error rate and power) was assessed using simulation studies under different scenarios of selective reporting bias. Examples are provided for networks of antidepressant and antipsychotic trials, where reporting biases have been previously demonstrated by comparing published to Food and Drug Administration (FDA) data. RESULTS: In simulations, the test maintained the type I error rate and was moderately powerful after adjustment for type I error rate, except when the between-trial variance was substantial. In all, a positive test result increased moderately or markedly the probability of reporting bias being present, while a negative test result was not very informative. In the two examples, the test gave a signal for an excess of statistically significant results in the network of published data but not in the network of FDA data. CONCLUSION: The test could be useful to document an excess of significant findings in trial networks, providing a signal for potential publication bias or other selective analysis and outcome reporting biases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2288-14-112) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-27 /pmc/articles/PMC4193287/ /pubmed/25262204 http://dx.doi.org/10.1186/1471-2288-14-112 Text en © Trinquart et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Trinquart, Ludovic
Ioannidis, John PA
Chatellier, Gilles
Ravaud, Philippe
A test for reporting bias in trial networks: simulation and case studies
title A test for reporting bias in trial networks: simulation and case studies
title_full A test for reporting bias in trial networks: simulation and case studies
title_fullStr A test for reporting bias in trial networks: simulation and case studies
title_full_unstemmed A test for reporting bias in trial networks: simulation and case studies
title_short A test for reporting bias in trial networks: simulation and case studies
title_sort test for reporting bias in trial networks: simulation and case studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193287/
https://www.ncbi.nlm.nih.gov/pubmed/25262204
http://dx.doi.org/10.1186/1471-2288-14-112
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