Destination unknown: Parents and healthcare professionals' perspectives on transition from paediatric to adult care in Down syndrome

Vincent Peters, Vinus Bok, Lieke de Beer, Joyce van Rooij, Bert Meijboom, J. E. H. Bunt

Research output: Contribution to journalArticleScientificpeer-review

4 Citations (Scopus)

Abstract

Background
Transitioning from paediatric medical care to adult care is a challenging process for children, parents and healthcare professionals. The aim of this study was to explore the experiences, concerns and needs of parents of children with Down syndrome and of professionals regarding this transition.

Method
A qualitative study was performed using semi-structured interviews with 20 parents of children with Down syndrome and six healthcare professionals.

Results
We showed that parents and professionals have concerns during each of the three distinct phases of transition (preparation, transfer and integration). Data disclose specific concerns regarding communication, continuity of care and rebuilding trust. We propose a framework for the transition to adult care.

Conclusions
The transition in medical care for children with Down syndrome should be flexible, patient-centred and coordinated together with patients and parents. Only in ensuring continuity of care will individuals with Down syndrome not get lost in transition.
Original languageEnglish
Pages (from-to)1208-1216
JournalJournal of Applied Research in Intellectual Disabilities
Volume35
Issue number5
Early online date5 Jun 2022
DOIs
Publication statusPublished - Sept 2022

Keywords

  • Down syndrome
  • adult care
  • paediatric care
  • qualitative research
  • service provision
  • transition

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