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

Authors
  • de Blacam, Catherine1, 2
  • Baylis, Adriane L3, 4
  • Kirschner, Richard E3, 4
  • Smith, Susan M5
  • Sell, Debbie6
  • Sie, Kathleen C Y7
  • Harris, Helen E8
  • Orr, David J A9, 10
  • 1 Department of Plastic Surgery, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland catherinede[email protected] , (Ireland)
  • 2 Department of Surgical Affairs, Royal College of Surgeons in Ireland, Dublin, Ireland. , (Ireland)
  • 3 Department of Plastic and Reconstructive Surgery, Nationwide Children's Hospital, Columbus, Ohio, USA.
  • 4 Ohio State University College of Medicine, Columbus, Ohio, USA.
  • 5 Department of General Practice, RCSI, Dublin, Ireland. , (Ireland)
  • 6 Centre for Outcomes and Experience Research in Children's Health, Illness and Disability (ORCHID), Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • 7 Division of Pediatric Otolaryngology, Seattle Children's Hospital, Seattle, Washington, USA.
  • 8 London, UK.
  • 9 Department of Plastic Surgery, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland. , (Ireland)
  • 10 School of Medicine, Trinity College Dublin, Dublin, Ireland. , (Ireland)
Type
Published Article
Journal
BMJ Open
Publisher
BMJ
Publication Date
Aug 13, 2020
Volume
10
Issue
8
Identifiers
DOI: 10.1136/bmjopen-2020-036824
PMID: 32792441
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

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. 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. 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. © 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.

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