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A comparison between two recommendations to conduct and report systematic reviews on drug’s safety

BACKGROUND: Several recommendations are available to conduct and report a systematic review of adverse drug reactions. This study is aimed at identifying and comparing the methodologies of the two most commonly used recommendations to conduct and report systematic reviews on drug’s safety. METHODS:...

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Autores principales: Penedones, Ana, Alves, Carlos, Batel Marques, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796334/
https://www.ncbi.nlm.nih.gov/pubmed/31619279
http://dx.doi.org/10.1186/s13643-019-1167-5
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author Penedones, Ana
Alves, Carlos
Batel Marques, Francisco
author_facet Penedones, Ana
Alves, Carlos
Batel Marques, Francisco
author_sort Penedones, Ana
collection PubMed
description BACKGROUND: Several recommendations are available to conduct and report a systematic review of adverse drug reactions. This study is aimed at identifying and comparing the methodologies of the two most commonly used recommendations to conduct and report systematic reviews on drug’s safety. METHODS: Two systematic reviews were conducted following the recommendations “Cochrane Handbook for Systematic Reviews of Interventions” and “Systematic Reviews’ Centre for Reviews and Dissemination guidance for undertaking reviews in healthcare.” The methods of each recommendation were characterized, and the results and the discussion of each systematic review were also evaluated. RESULTS: The methodologies of both recommendations are similar. The review question was structured. Both recommendations suggest to include pre- and post-marketing data. The recommended data sources differed and, consequently, the results of the systematic reviews (37 vs. 35 studies). Other aspects of search literature were identical. Different tools are suggested to evaluate the methodological quality of the included studies. For case reports, both recommendations only report some questions that may be helpful to assess risk of bias. The reporting of the results and discussion is also identical for both recommendations. CONCLUSIONS: Few methodological differences were observed between the analyzed recommendations to conduct a systematic review on drug’s safety. Combining their methods into a single and recognized recommendation could be of great value.
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spelling pubmed-67963342019-10-21 A comparison between two recommendations to conduct and report systematic reviews on drug’s safety Penedones, Ana Alves, Carlos Batel Marques, Francisco Syst Rev Methodology BACKGROUND: Several recommendations are available to conduct and report a systematic review of adverse drug reactions. This study is aimed at identifying and comparing the methodologies of the two most commonly used recommendations to conduct and report systematic reviews on drug’s safety. METHODS: Two systematic reviews were conducted following the recommendations “Cochrane Handbook for Systematic Reviews of Interventions” and “Systematic Reviews’ Centre for Reviews and Dissemination guidance for undertaking reviews in healthcare.” The methods of each recommendation were characterized, and the results and the discussion of each systematic review were also evaluated. RESULTS: The methodologies of both recommendations are similar. The review question was structured. Both recommendations suggest to include pre- and post-marketing data. The recommended data sources differed and, consequently, the results of the systematic reviews (37 vs. 35 studies). Other aspects of search literature were identical. Different tools are suggested to evaluate the methodological quality of the included studies. For case reports, both recommendations only report some questions that may be helpful to assess risk of bias. The reporting of the results and discussion is also identical for both recommendations. CONCLUSIONS: Few methodological differences were observed between the analyzed recommendations to conduct a systematic review on drug’s safety. Combining their methods into a single and recognized recommendation could be of great value. BioMed Central 2019-10-16 /pmc/articles/PMC6796334/ /pubmed/31619279 http://dx.doi.org/10.1186/s13643-019-1167-5 Text en © The Author(s). 2019 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 Methodology
Penedones, Ana
Alves, Carlos
Batel Marques, Francisco
A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title_full A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title_fullStr A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title_full_unstemmed A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title_short A comparison between two recommendations to conduct and report systematic reviews on drug’s safety
title_sort comparison between two recommendations to conduct and report systematic reviews on drug’s safety
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6796334/
https://www.ncbi.nlm.nih.gov/pubmed/31619279
http://dx.doi.org/10.1186/s13643-019-1167-5
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