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Sponsorship bias and quality of randomised controlled trials in veterinary medicine

BACKGROUND: Randomised controlled trials (RCTs) are considered the gold standard form of evidence for assessing treatment efficacy, but many factors can influence their reliability including methodological quality, reporting quality and funding source. The aim of this study was to examine the relati...

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Autores principales: Wareham, K. J., Hyde, R. M., Grindlay, D., Brennan, M. L., Dean, R. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557072/
https://www.ncbi.nlm.nih.gov/pubmed/28807033
http://dx.doi.org/10.1186/s12917-017-1146-9
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author Wareham, K. J.
Hyde, R. M.
Grindlay, D.
Brennan, M. L.
Dean, R. S.
author_facet Wareham, K. J.
Hyde, R. M.
Grindlay, D.
Brennan, M. L.
Dean, R. S.
author_sort Wareham, K. J.
collection PubMed
description BACKGROUND: Randomised controlled trials (RCTs) are considered the gold standard form of evidence for assessing treatment efficacy, but many factors can influence their reliability including methodological quality, reporting quality and funding source. The aim of this study was to examine the relationship between funding source and positive outcome reporting in veterinary RCTs published in 2011 and to assess the risk of bias in the RCTs identified. METHODS: A structured search of PubMed was used to identify feline, canine, equine, bovine and ovine clinical trials examining the efficacy of pharmaceutical interventions published in 2011. Funding source and outcomes were extracted from each RCT and an assessment of risk of bias made using the Cochrane risk of bias tool. RESULTS: Literature searches returned 972 papers, with 86 papers (comprising 126 individual RCTs) included in the analysis. There was found to be a significantly higher proportion of positive outcomes reported in the pharmaceutical funding group (P) compared to the non-pharmaceutical (NP) and ‘no funding source stated’ (NF) groups (P = 56.9%, NP = 34.9%, NF = 29.1%, p < 0.05). A high proportion of trials had an unclear risk of bias across the five criteria examined. CONCLUSIONS: We found evidence that veterinary RCTs were more likely to report positive outcomes if they have pharmaceutical industry funding or involvement. Consistently poor reporting of trials, including non-identification of funding source, was found which hinders the use of the available evidence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-017-1146-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-55570722017-08-16 Sponsorship bias and quality of randomised controlled trials in veterinary medicine Wareham, K. J. Hyde, R. M. Grindlay, D. Brennan, M. L. Dean, R. S. BMC Vet Res Research Article BACKGROUND: Randomised controlled trials (RCTs) are considered the gold standard form of evidence for assessing treatment efficacy, but many factors can influence their reliability including methodological quality, reporting quality and funding source. The aim of this study was to examine the relationship between funding source and positive outcome reporting in veterinary RCTs published in 2011 and to assess the risk of bias in the RCTs identified. METHODS: A structured search of PubMed was used to identify feline, canine, equine, bovine and ovine clinical trials examining the efficacy of pharmaceutical interventions published in 2011. Funding source and outcomes were extracted from each RCT and an assessment of risk of bias made using the Cochrane risk of bias tool. RESULTS: Literature searches returned 972 papers, with 86 papers (comprising 126 individual RCTs) included in the analysis. There was found to be a significantly higher proportion of positive outcomes reported in the pharmaceutical funding group (P) compared to the non-pharmaceutical (NP) and ‘no funding source stated’ (NF) groups (P = 56.9%, NP = 34.9%, NF = 29.1%, p < 0.05). A high proportion of trials had an unclear risk of bias across the five criteria examined. CONCLUSIONS: We found evidence that veterinary RCTs were more likely to report positive outcomes if they have pharmaceutical industry funding or involvement. Consistently poor reporting of trials, including non-identification of funding source, was found which hinders the use of the available evidence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-017-1146-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-14 /pmc/articles/PMC5557072/ /pubmed/28807033 http://dx.doi.org/10.1186/s12917-017-1146-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Wareham, K. J.
Hyde, R. M.
Grindlay, D.
Brennan, M. L.
Dean, R. S.
Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title_full Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title_fullStr Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title_full_unstemmed Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title_short Sponsorship bias and quality of randomised controlled trials in veterinary medicine
title_sort sponsorship bias and quality of randomised controlled trials in veterinary medicine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557072/
https://www.ncbi.nlm.nih.gov/pubmed/28807033
http://dx.doi.org/10.1186/s12917-017-1146-9
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