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Development of a lifelong core outcome set for oesophageal atresia ± tracheoesophageal fistula: the OCELOT study

  • Rebecca Thursfield
  • , Sarah Gorst
  • , Nadine Teunisson
  • , Nick Lansdale
  • , Julia Faulkner
  • , Usha Krishnan
  • , Tom Kovesi
  • , Graham Slater
  • , Paul Cullis
  • , Lucy Bray
  • , A Donne
  • , Warwick Teague
  • , Paul D Losty
  • , Siobhan Carr
  • , Victoria Gray
  • , Lucia Gutierrez-Gammino
  • , Shireen Anne Nah
  • , Nigel J Hall
  • Aintree University Hospital
  • University of Liverpool
  • Royal Hospital for Children and Young People
  • Royal Manchester Children's Hospital
  • Yeovil District Hospital NHS Foundation Trust
  • Sydney Children's Hospital
  • Healthy Active Living and Obesity (HALO) Research Group, Children's Hospital of Eastern Ontario Research Institute, Ottawa, ON, Canada
  • TOFS Charity
  • Iuliu Hatieganu University of Medicine and Pharmacy
  • Alder Hey Children's NHS Foundation Trust
  • Mahidol University
  • Department of Paediatric Respiratory Medicine
  • Sor Maria Ludovia's Hospital
  • University of Malaya
  • Southampton General Hospital

Research output: Contribution to journalArticle (journal)peer-review

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Abstract

BackgroundDespite anatomical correction, people born with oesophageal atresia±tracheoesophageal fistula (OA-TOF) experience lifelong morbidity. Core outcome sets (COSs) are recognised as a means of improving research quality and, as a consequence, improving patient outcomes; one was not available for this population.ObjectiveThe scope of the study was to develop a COS for people born with OA-TOF that would be applicable regardless of age or geographic location.Study designPatient input was paramount to this study. For long-list generation, in addition to the systematic review (SR), patients and representatives were invited to participate in focus groups, interviews or complete activity packs to ascertain outcomes that matter most to them. International consensus was then sought using a two-step Delphi survey followed by an online consensus meeting.ResultsEight outcomes were identified through patient events that had not been picked up from SR. 175 people completed the Delphi survey from 26 countries and health care professionals from 13 different disciplines. 24 outcomes met predefined criteria for inclusion and following discussion and voting in the consensus meeting, and 14/24 outcomes were agreed for inclusion in the COS.Conclusion14 outcomes have been agreed on to form the COS. 12 of these outcomes are relevant to people of all ages, 1 to paediatric population and 1 to adult cohorts. The COS is, therefore, truly applicable lifelong, which was the scope of the project. This COS will help reduce research heterogeneity, enabling better quality research outcomes and more comparable data.
Original languageEnglish
Article numbere104771
Pages (from-to)1-8
Number of pages8
JournalBMJ Open
Volume16
Issue number3
Early online date4 Mar 2026
DOIs
Publication statusPublished - 4 Mar 2026

Keywords

  • Follow-up studies
  • Paediatrics
  • Neonatology
  • Oesophageal Disease
  • Thoracic Medicine
  • Paediatric Thoracic Surgery
  • Humans
  • Esophageal Atresia
  • Tracheoesophageal Fistula
  • Focus Groups
  • Consensus
  • Delphi Technique
  • Adult
  • Child
  • Female
  • Male
  • Outcome Assessment, Health Care
  • Paediatric thoracic surgery
  • Follow-Up Studies
  • PAEDIATRICS
  • Oesophageal disease
  • NEONATOLOGY
  • THORACIC MEDICINE
  • Tracheoesophageal Fistula/surgery
  • Esophageal Atresia/surgery

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