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Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction

INTRODUCTION: Velopharyngeal dysfunction (VPD) is present in up to 40% of patients following cleft palate repair. Children with VPD display hypernasal speech, nasal air emission and are at a high risk for developing articulation disorders. The overall result is decreased intelligibility and acceptab...

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Autores principales: de Blacam, Catherine, Baylis, Adriane L, Kirschner, Richard E, Smith, Susan M, Sell, Debbie, Sie, Kathleen C Y, Harris, Helen E, Orr, David J A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430341/
https://www.ncbi.nlm.nih.gov/pubmed/32792441
http://dx.doi.org/10.1136/bmjopen-2020-036824
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author de Blacam, Catherine
Baylis, Adriane L
Kirschner, Richard E
Smith, Susan M
Sell, Debbie
Sie, Kathleen C Y
Harris, Helen E
Orr, David J A
author_facet de Blacam, Catherine
Baylis, Adriane L
Kirschner, Richard E
Smith, Susan M
Sell, Debbie
Sie, Kathleen C Y
Harris, Helen E
Orr, David J A
author_sort de Blacam, Catherine
collection PubMed
description INTRODUCTION: Velopharyngeal dysfunction (VPD) is present in up to 40% of patients following cleft palate repair. Children with VPD display hypernasal speech, nasal air emission and are at a high risk for developing articulation disorders. The overall result is decreased intelligibility and acceptability of speech, as well as significant functional and social impairments. Although there are several surgical approaches for the management of children with VPD, standard treatment protocols have not been well defined. There is a need for a core outcome set (COS) to reduce outcome reporting bias and heterogeneity across studies of VPD. The COS-VPD Initiative is an international effort to establish a COS for the reporting of studies of the management of VPD. METHODS AND ANALYSIS: The study has been developed according to the Core Outcome Set-STAandards for Development standards for the design of a COS study and will be carried out according to the guidance of the Core Outcome Measures in Effectiveness Trials (COMET) initiative. A long list of clinical and patient-reported outcomes will be identified from a systematic review of the literature. A two-stage Delphi consensus process will be used to refine this list into a COS. An international panel of key stakeholders including patients, parents and multidisciplinary clinical and academic experts will be invited to participate in this process. Consensus criteria will be specified a priori and the steering group will ratify the final COS. ETHICS AND DISSEMINATION: The study has ethical approval through Children’s Health Ireland at Crumlin Research and Ethics Committee, Ref: GEN/683/18. The study is registered with the COMET Initiative (http://www.cometinitiative.org/studies/details/1146?result=true). The COS will be disseminated by publication in the peer-reviewed literature, presentation at international research meetings and distribution to patient-representative organisations. This will facilitate the application of the COS in future studies of the management of VPD.
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spelling pubmed-74303412020-08-24 Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction de Blacam, Catherine Baylis, Adriane L Kirschner, Richard E Smith, Susan M Sell, Debbie Sie, Kathleen C Y Harris, Helen E Orr, David J A BMJ Open Surgery INTRODUCTION: Velopharyngeal dysfunction (VPD) is present in up to 40% of patients following cleft palate repair. Children with VPD display hypernasal speech, nasal air emission and are at a high risk for developing articulation disorders. The overall result is decreased intelligibility and acceptability of speech, as well as significant functional and social impairments. Although there are several surgical approaches for the management of children with VPD, standard treatment protocols have not been well defined. There is a need for a core outcome set (COS) to reduce outcome reporting bias and heterogeneity across studies of VPD. The COS-VPD Initiative is an international effort to establish a COS for the reporting of studies of the management of VPD. METHODS AND ANALYSIS: The study has been developed according to the Core Outcome Set-STAandards for Development standards for the design of a COS study and will be carried out according to the guidance of the Core Outcome Measures in Effectiveness Trials (COMET) initiative. A long list of clinical and patient-reported outcomes will be identified from a systematic review of the literature. A two-stage Delphi consensus process will be used to refine this list into a COS. An international panel of key stakeholders including patients, parents and multidisciplinary clinical and academic experts will be invited to participate in this process. Consensus criteria will be specified a priori and the steering group will ratify the final COS. ETHICS AND DISSEMINATION: The study has ethical approval through Children’s Health Ireland at Crumlin Research and Ethics Committee, Ref: GEN/683/18. The study is registered with the COMET Initiative (http://www.cometinitiative.org/studies/details/1146?result=true). The COS will be disseminated by publication in the peer-reviewed literature, presentation at international research meetings and distribution to patient-representative organisations. This will facilitate the application of the COS in future studies of the management of VPD. BMJ Publishing Group 2020-08-13 /pmc/articles/PMC7430341/ /pubmed/32792441 http://dx.doi.org/10.1136/bmjopen-2020-036824 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Surgery
de Blacam, Catherine
Baylis, Adriane L
Kirschner, Richard E
Smith, Susan M
Sell, Debbie
Sie, Kathleen C Y
Harris, Helen E
Orr, David J A
Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title_full Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title_fullStr Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title_full_unstemmed Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title_short Protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
title_sort protocol for the development of a core outcome set for reporting outcomes of management of velopharyngeal dysfunction
topic Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430341/
https://www.ncbi.nlm.nih.gov/pubmed/32792441
http://dx.doi.org/10.1136/bmjopen-2020-036824
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