The roles and experiences of adolescents with cystic fibrosis and their parents during transition: A qualitative interview study.

Adolescents and young adults Cystic fibrosis Experiences Healthcare transition Parents Qualitative research

Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
13 Oct 2023
Historique:
received: 09 05 2023
revised: 19 07 2023
accepted: 03 10 2023
medline: 16 10 2023
pubmed: 16 10 2023
entrez: 15 10 2023
Statut: aheadofprint

Résumé

Inadequate participation of Adolescents and Young Adults (AYAs) and parents are well-established barriers of transition. Shifts in roles are mandatory with increasing responsibilities for AYAs and decreasing involvement of parents in care. This study explores the shifts in roles of AYAs and their parents and its association with the subjective experience of transition. We conducted in-depth semi-structured interviews with AYAs living with Cystic Fibrosis and parents. Participants were recruited through patient organizations via convenience sampling and questioned on which roles they assumed during transition. Three authors performed an interpretative phenomenological analysis, establishing separate code trees for AYAs and parents. Data saturation was achieved. 18 AYAs (age 21y±2.9) and 14 parents (age 50y±2.0) were included. We identified five common themes: (1) the reciprocal reliance between AYAs and parents, (2) the policies of physicians and hospitals, (3) the AYAs' changing appeal and need for support, (4) the identification of parents as co-patients, and (5) the enforced changes in the roles of parents. AYAs primarily addressed roles related to self-management, while parents discussed family functioning. This study identified motives underlying the assumption of roles by AYAs and parents. Both AYAs and parents addressed similar themes, highlighting their mutual challenges and needs. In contrast to AYAs, parents' desired roles were undefined and a latent sense of responsibility was identified as an important motive. Healthcare providers should acknowledge parents' challenging position and communicate transparently about changing roles. Additionally, healthcare providers should recognize that imposing restrictive roles may result in parental resistance, but can also foster AYAs' skill development. Future research should examine the short- and long-term impact of role-management interventions in AYAs and their parents.

Identifiants

pubmed: 37839982
pii: S1569-1993(23)00925-6
doi: 10.1016/j.jcf.2023.10.005
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Karsten Vanden Wyngaert (KV)

Pediatric Department, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent 9000, Belgium. Electronic address: Karsten.vandenwyngaert@uzgent.be.

Sara Debulpaep (S)

Pediatric Department, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent 9000, Belgium.

Wim Van Biesen (W)

Department of Internal Medicine, Renal Division, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent, Belgium.

Sabine Van Daele (S)

Pediatric Department, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent 9000, Belgium.

Sue Braun (S)

Department of Psychology, Universitair Ziekenhuis Brussel (UZ Brussel, Laarbeeklaan 101, Brussels 1090, Belgium; Department of Pediatrics, Pediatric Pulmonology, Cystic Fibrosis Clinic and Pediatric Infectious Diseases, Universitair Ziekenhuis Brussel (UZ Brussel), Laarbeeklaan 101, Brussels 1090, Belgium.

Kenneth Chambaere (K)

Department of Public Health and Primary Care, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium; End-of-life Care Research Group, University Brussels (VUB) and Ghent University, Ghent, Belgium.

Kim Beernaert (K)

Department of Public Health and Primary Care, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium; End-of-life Care Research Group, University Brussels (VUB) and Ghent University, Ghent, Belgium.

Classifications MeSH