Our experience in developing and operating the Airway Intervention Registry for Recurrent Respiratory Papillomatosis (AIR-RRP): national data collection [version 2; peer review: 2 approved].
Recurrent respiratory papillomatosis (RRP) clinical registry development
Journal
NIHR open research
ISSN: 2633-4402
Titre abrégé: NIHR Open Res
Pays: England
ID NLM: 9918333281906676
Informations de publication
Date de publication:
12 Jan 2023
12 Jan 2023
Historique:
entrez:
1
3
2023
pubmed:
2
3
2023
medline:
2
3
2023
Statut:
ppublish
Résumé
Recurrent respiratory papillomatosis (RRP) is characterised by benign wart-like growths in the respiratory tract caused by the human papillomavirus (HPV). These warts vary in size and grow quickly, causing voice changes and airway obstruction. Whilst the condition is rare, RRP is more common and aggressive in children. There is currently no curative treatment for HPV, therefore RRP is managed by maintaining a safe airway and a serviceable voice by repeated surgery to remove the growths. A lack of specific diagnostic codes prevents reliable case ascertainment of RRP from routine administrative databases such as Hospital Episode Statistics. In 2017 a cross-sectional survey identified 918 RRP patients in the UK, half of whom had received surgical intervention for RRP in the previous 12 months with 16 different interventions. Randomised controlled trials for RRP interventions are difficult due to the rarity of the disease, variation in severity and progression and non-standard care across the NHS. Consequently, there is a lack of definitive efficacy and safety evidence. The only national guidance for RRP interventions is "Radiofrequency cold ablation for respiratory papillomatosis" (NICE IPG434, 2017) which recommended further data collection due to lack of evidence. However, due to the wide variation in RRP management across the NHS, clinical opinion favoured that any data collection should include a comparison of safety and efficacy of all RRP interventions in order to advise which improved patient outcomes and quality of life. To address lack of evidence, and inform the future care of RRP patients, we developed a registry and used it to collect real-world data from patients receiving treatment for RRP in NHS hospitals across the UK. The purpose of this paper is to share lessons learned from this national data collection exercise to inform future clinical registry development.
Identifiants
pubmed: 36855411
doi: 10.3310/nihropenres.13244.2
pmc: PMC7614251
mid: EMS167296
doi:
Types de publication
Journal Article
Langues
eng
Pagination
22Subventions
Organisme : Department of Health
ID : PB-PG-0416-20037
Pays : United Kingdom
Déclaration de conflit d'intérêts
Competing interests: AJS, KK, EB, AJ, SP and JB are employed by The Newcastle upon Tyne Hospitals NHS Foundation Trust which hosts an External Assessment Group funded by NICE. Competing interests: AJS, KK, EB, AJ, SP and JB are employed by The Newcastle upon Tyne Hospitals NHS Foundation Trust which hosts an External Assessment Group funded by NICE.
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