How can we relieve gastrointestinal symptoms in people with cystic fibrosis? An international qualitative survey.


Journal

BMJ open respiratory research
ISSN: 2052-4439
Titre abrégé: BMJ Open Respir Res
Pays: England
ID NLM: 101638061

Informations de publication

Date de publication:
09 2020
Historique:
received: 20 04 2020
revised: 22 07 2020
accepted: 10 08 2020
entrez: 9 9 2020
pubmed: 10 9 2020
medline: 24 7 2021
Statut: ppublish

Résumé

Relieving gastrointestinal (GI) symptoms was identified as a 'top ten' priority by our James Lind Alliance Priority Setting Partnership in cystic fibrosis (CF). We conducted an online survey to find out more about the effect of GI symptoms in CF. We co-produced an online survey distributed to the CF community via web-based platforms. The survey consisted of open and closed questions designed to help us learn more about the effects of GI symptoms for people with CF (pwCF). We analysed the data using descriptive statistics and thematic analysis. We promoted the survey via social media and web-based platforms which allowed respondents from any country to take part. Our participants came from the CF community, including: adults and children with CF, parents and close family of pwCF and healthcare professionals (HCPs) working with pwCF. There were 276 respondents: 90 (33%) pwCF, 79 (29%) family, 107 (39%) HCPs. The most commonly reported symptoms by lay respondents were stomach cramps/pain, bloating and a 'combination of symptoms'. The top three symptoms that HCPs said were reported to them were reduced appetite, bloating and constipation. Almost all (94% (85/90)) HCPs thought medications helped to relieve GI symptoms but only 58% (82/141) of lay respondents agreed. Our survey has shown that GI symptoms among our participants are prevalent and intrude on daily lives of pwCF. There is a need for well-designed clinical studies to provide better evidence for management of GI symptoms and complications.

Identifiants

pubmed: 32900780
pii: 7/1/e000614
doi: 10.1136/bmjresp-2020-000614
pmc: PMC7478045
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 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.

Déclaration de conflit d'intérêts

Competing interests: GD reports personal fees from Chiesi, outside the submitted work. CN reports grants from Cystic Fibrosis Foundation, grants from Cystic Fibrosis Trust, grants and other from Vertex Pharmaceuticals, outside the submitted work. NR has given lectures at meetings sponsored by TEVA and has attended meetings sponsored by Vertex. AS reports a research grant and personal fees from Vertex. He has spoken at meetings supported by Teva and Novartis. These activities are outside the submitted work. In addition, AS has a patent for ‘Alkyl quinolones as biomarkers of Pseudomonas aeruginosa infection and uses thereof’ issued.

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Auteurs

Sherie Smith (S)

Child Health Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK sherie.smith@nottingham.ac.uk.

Nicola Rowbotham (N)

Child Health Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK.

Gwyneth Davies (G)

Institute of Child Health, UCL, London, UK.

Katie Gathercole (K)

Person with CF, University of Leeds, Leeds, West Yorkshire, UK.

Sarah J Collins (SJ)

CF Department, Royal Brompton and Harefield NHS Trust, London, UK.

Zoe Elliott (Z)

Mother of Children with CF, Nottingham, UK.

Sophie Herbert (S)

Child Health Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK.

Lorna Allen (L)

Cystic Fibrosis Trust, London, UK.

Christabella Ng (C)

Child Health Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK.

Alan Smyth (A)

Child Health Obstetrics and Gynaecology, University of Nottingham, Nottingham, UK.

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Classifications MeSH