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Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study

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...

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Autores principales: Ryan, Jennifer M., Walsh, Michael, Owens, Mary, Byrne, Michael, Kroll, Thilo, Hensey, Owen, Kerr, Claire, Norris, Meriel, Walsh, Aisling, Lavelle, Grace, Fortune, Jennifer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084269/
https://www.ncbi.nlm.nih.gov/pubmed/35729753
http://dx.doi.org/10.1111/dmcn.15317
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author Ryan, Jennifer M.
Walsh, Michael
Owens, Mary
Byrne, Michael
Kroll, Thilo
Hensey, Owen
Kerr, Claire
Norris, Meriel
Walsh, Aisling
Lavelle, Grace
Fortune, Jennifer
author_facet Ryan, Jennifer M.
Walsh, Michael
Owens, Mary
Byrne, Michael
Kroll, Thilo
Hensey, Owen
Kerr, Claire
Norris, Meriel
Walsh, Aisling
Lavelle, Grace
Fortune, Jennifer
author_sort Ryan, Jennifer M.
collection PubMed
description 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.
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spelling pubmed-100842692023-04-11 Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study Ryan, Jennifer M. Walsh, Michael Owens, Mary Byrne, Michael Kroll, Thilo Hensey, Owen Kerr, Claire Norris, Meriel Walsh, Aisling Lavelle, Grace Fortune, Jennifer Dev Med Child Neurol Original Articles 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. John Wiley and Sons Inc. 2022-06-21 2023-02 /pmc/articles/PMC10084269/ /pubmed/35729753 http://dx.doi.org/10.1111/dmcn.15317 Text en © 2022 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Ryan, Jennifer M.
Walsh, Michael
Owens, Mary
Byrne, Michael
Kroll, Thilo
Hensey, Owen
Kerr, Claire
Norris, Meriel
Walsh, Aisling
Lavelle, Grace
Fortune, Jennifer
Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title_full Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title_fullStr Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title_full_unstemmed Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title_short Transition to adult services experienced by young people with cerebral palsy: A cross‐sectional study
title_sort transition to adult services experienced by young people with cerebral palsy: a cross‐sectional study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084269/
https://www.ncbi.nlm.nih.gov/pubmed/35729753
http://dx.doi.org/10.1111/dmcn.15317
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