figshare
Browse
Develop Med Child Neuro - 2022 - Ryan - Transition to adult services experienced by young people with cerebral palsy A (1).pdf (507.49 kB)

Transition to adult services experienced by young people with cerebral palsy: a cross-sectional study

Download (507.49 kB)
journal contribution
posted on 2023-12-01, 16:37 authored by Jennifer RyanJennifer Ryan, Michael Walsh, Mary Owens, Michael Byrne, Thilo Kroll, Owen Hensey, Claire Kerr, Meriel Norris, Aisling WalshAisling Walsh, Grace Lavelle, Jennifer FortuneJennifer Fortune

Aim: To assess if young people with cerebral palsy experience and health professionals provide practices that may improve transition from child to adult health services.

Method: Seventy-five young people (31 females, 44 males; mean age 18 years 5 months [standard deviation 2 years 2 months]) and/or parents and 108 health professionals completed a questionnaire describing their experience or the provision of nine transition practices.

Results: The percentage of young people reporting each practice was: appropriate parent involvement (90%); promotion of health self-efficacy (37%); named worker who supports the transition process (36%); self-management support for physical health (36%); self-management support for mental health (17%); information about the transition process (24%); meeting the adult team (16%); and life skills training (16%). Post-discharge, 10% of young people reported that their general practitioner (GP) received a discharge letter. The percentage of health professionals reporting each practice was: promotion of health self-efficacy (73.2%); self-management support (73.2%); information (69%); consulting the parent and young person about parent involvement (63% and 66%); discharge letter to a GP (55%); life skills training (36%); named worker (35%); meeting the adult team (30%); and senior manager (20%).

Interpretation: Many young people did not experience practices that may improve the experience and outcomes of transition. Young people should be involved in the development and delivery of transition to ensure it meets their needs.

What this paper adds: Many young people with cerebral palsy (CP) do not receive support that may improve the experience of transition. Appropriate protocols and training for health professionals may improve the provision of transition and reduce inconsistency in care between and within organizations. Young people and their families should be involved in service design, delivery, and evaluation related to the transition to ensure it meets their needs.

Funding

Improving transition from children’s to adults' services for young people with cerebral palsy living in Ireland. | Funder: Health Research Board / HRB | Grant ID: APA-2019-004

Improving transition from children’s to adults' services for young people with cerebral palsy living in Ireland. | Funder: Central Remedial Clinic | Grant ID: APA-2019-004

Open access funding provided by IReL.

History

Data Availability Statement

The data that support the findings of this study are openly available in Zenodo at http://doi.org/10.5281/zenodo.6636481

Comments

The original article is available at https://onlinelibrary.wiley.com/

Published Citation

Ryan JM, et al. Transition to adult services experienced by young people with cerebral palsy: a cross-sectional study. Dev Med Child Neurol. 2022;65(2):285-293.

Publication Date

21 June 2022

PubMed ID

35729753

Department/Unit

  • Public Health and Epidemiology
  • School of Population Health

Research Area

  • Population Health and Health Services

Publisher

Wiley

Version

  • Published Version (Version of Record)