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The development of a faecal incontinence core outcome set: an international Delphi study protocol

PURPOSE: Faecal incontinence (FI) is estimated to affect around 7.7% of people. There is a lack of uniformity in outcome definitions, measurement and reporting in FI studies. Until now, there is no general consensus on which outcomes should be assessed and reported in FI research. This complicates c...

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Autores principales: Assmann, Sadé, Keszthelyi, Daniel, Kleijnen, Jos, Kimman, Merel, Anastasiou, Foteini, Bradshaw, Elissa, Carrington, Emma, Chiarioni, Giuseppe, Maeda, Yasuko, Muris, Jean, Pohl, Daniel, Rydningen, Mona, Vaizey, Carolynne, Breukink, Stephanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895769/
https://www.ncbi.nlm.nih.gov/pubmed/33532899
http://dx.doi.org/10.1007/s00384-021-03865-2
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author Assmann, Sadé
Keszthelyi, Daniel
Kleijnen, Jos
Kimman, Merel
Anastasiou, Foteini
Bradshaw, Elissa
Carrington, Emma
Chiarioni, Giuseppe
Maeda, Yasuko
Muris, Jean
Pohl, Daniel
Rydningen, Mona
Vaizey, Carolynne
Breukink, Stephanie
author_facet Assmann, Sadé
Keszthelyi, Daniel
Kleijnen, Jos
Kimman, Merel
Anastasiou, Foteini
Bradshaw, Elissa
Carrington, Emma
Chiarioni, Giuseppe
Maeda, Yasuko
Muris, Jean
Pohl, Daniel
Rydningen, Mona
Vaizey, Carolynne
Breukink, Stephanie
author_sort Assmann, Sadé
collection PubMed
description PURPOSE: Faecal incontinence (FI) is estimated to affect around 7.7% of people. There is a lack of uniformity in outcome definitions, measurement and reporting in FI studies. Until now, there is no general consensus on which outcomes should be assessed and reported in FI research. This complicates comparison between studies and evidence synthesis, potentially leading to recommendations not evidence-based enough to guide physicians in selecting an FI therapy. A solution for this lack of uniformity in reporting of outcomes is the development of a Core Outcome Set (COS) for FI. This paper describes the protocol for the development of a European COS for FI. METHODS: Patient interviews and a systematic review of the literature will be performed to identify patient-, physician- and researcher-oriented outcomes. The outcomes will be categorised using the COMET taxonomy and put forward to a group of patients, physicians (i.e. colorectal surgeons, gastroenterologists and general practitioners) and researchers in a Delphi consensus exercise. This exercise will consist of up to three web-based rounds in which participants will prioritise and condense the list of outcomes, which is expected to result in consensus. A consensus meeting with participants from all stakeholder groups will take place to reach a final agreement on the COS. DISCUSSION: This study protocol describes the development of a European COS to improve reliability and consistency of outcome reporting in FI studies, thereby improving evidence synthesis and patient care. TRIAL REGISTRATION: This project has been registered in the COMET database on the 1st of April 2020, available at http://www.comet-initiative.org/Studies/Details/1554. The systematic review has been registered on the PROSPERO database on the 31st of August 2020, available at https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=202020&VersionID=1381336.
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spelling pubmed-78957692021-03-19 The development of a faecal incontinence core outcome set: an international Delphi study protocol Assmann, Sadé Keszthelyi, Daniel Kleijnen, Jos Kimman, Merel Anastasiou, Foteini Bradshaw, Elissa Carrington, Emma Chiarioni, Giuseppe Maeda, Yasuko Muris, Jean Pohl, Daniel Rydningen, Mona Vaizey, Carolynne Breukink, Stephanie Int J Colorectal Dis Clinical Study Protocol PURPOSE: Faecal incontinence (FI) is estimated to affect around 7.7% of people. There is a lack of uniformity in outcome definitions, measurement and reporting in FI studies. Until now, there is no general consensus on which outcomes should be assessed and reported in FI research. This complicates comparison between studies and evidence synthesis, potentially leading to recommendations not evidence-based enough to guide physicians in selecting an FI therapy. A solution for this lack of uniformity in reporting of outcomes is the development of a Core Outcome Set (COS) for FI. This paper describes the protocol for the development of a European COS for FI. METHODS: Patient interviews and a systematic review of the literature will be performed to identify patient-, physician- and researcher-oriented outcomes. The outcomes will be categorised using the COMET taxonomy and put forward to a group of patients, physicians (i.e. colorectal surgeons, gastroenterologists and general practitioners) and researchers in a Delphi consensus exercise. This exercise will consist of up to three web-based rounds in which participants will prioritise and condense the list of outcomes, which is expected to result in consensus. A consensus meeting with participants from all stakeholder groups will take place to reach a final agreement on the COS. DISCUSSION: This study protocol describes the development of a European COS to improve reliability and consistency of outcome reporting in FI studies, thereby improving evidence synthesis and patient care. TRIAL REGISTRATION: This project has been registered in the COMET database on the 1st of April 2020, available at http://www.comet-initiative.org/Studies/Details/1554. The systematic review has been registered on the PROSPERO database on the 31st of August 2020, available at https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=202020&VersionID=1381336. Springer Berlin Heidelberg 2021-02-02 2021 /pmc/articles/PMC7895769/ /pubmed/33532899 http://dx.doi.org/10.1007/s00384-021-03865-2 Text en © The Author(s) 2021, corrected publication 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical Study Protocol
Assmann, Sadé
Keszthelyi, Daniel
Kleijnen, Jos
Kimman, Merel
Anastasiou, Foteini
Bradshaw, Elissa
Carrington, Emma
Chiarioni, Giuseppe
Maeda, Yasuko
Muris, Jean
Pohl, Daniel
Rydningen, Mona
Vaizey, Carolynne
Breukink, Stephanie
The development of a faecal incontinence core outcome set: an international Delphi study protocol
title The development of a faecal incontinence core outcome set: an international Delphi study protocol
title_full The development of a faecal incontinence core outcome set: an international Delphi study protocol
title_fullStr The development of a faecal incontinence core outcome set: an international Delphi study protocol
title_full_unstemmed The development of a faecal incontinence core outcome set: an international Delphi study protocol
title_short The development of a faecal incontinence core outcome set: an international Delphi study protocol
title_sort development of a faecal incontinence core outcome set: an international delphi study protocol
topic Clinical Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895769/
https://www.ncbi.nlm.nih.gov/pubmed/33532899
http://dx.doi.org/10.1007/s00384-021-03865-2
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