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Characteristics of young people with long term conditions close to transfer to adult health services

BACKGROUND: For many young people with long term conditions (LTC), transferring from paediatric to adult health services can be difficult and outcomes are often reported to be poor. We report the characteristics and representativeness of three groups of young people with LTCs as they approach transf...

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Autores principales: Merrick, Hannah, McConachie, Helen, Le Couteur, Ann, Mann, Kay, Parr, Jeremy R., Pearce, Mark S., Colver, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589084/
https://www.ncbi.nlm.nih.gov/pubmed/26424085
http://dx.doi.org/10.1186/s12913-015-1095-6
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author Merrick, Hannah
McConachie, Helen
Le Couteur, Ann
Mann, Kay
Parr, Jeremy R.
Pearce, Mark S.
Colver, Allan
author_facet Merrick, Hannah
McConachie, Helen
Le Couteur, Ann
Mann, Kay
Parr, Jeremy R.
Pearce, Mark S.
Colver, Allan
author_sort Merrick, Hannah
collection PubMed
description BACKGROUND: For many young people with long term conditions (LTC), transferring from paediatric to adult health services can be difficult and outcomes are often reported to be poor. We report the characteristics and representativeness of three groups of young people with LTCs as they approach transfer to adult services: those with autism spectrum disorder with additional mental health problems (ASD); cerebral palsy (CP); or diabetes. METHODS: Young people aged 14 years-18 years 11 months with ASD, or those with diabetes were identified from children’s services and those with CP from population databases. Questionnaires, completed by the young person and a parent, included the ‘Mind the Gap’ Scale, the Rotterdam Transition Profile, and the Warwick and Edinburgh Mental Wellbeing Scale. RESULTS: Three hundred seventy four young people joined the study; 118 with ASD, 106 with CP, and 150 with diabetes. Participants had a significant (p < 0.001) but not substantial difference in socio-economic status (less deprived) compared to those who declined to take part or did not respond. Condition-specific severity of participants was similar to that of population data. Satisfaction with services was good as the ‘gap’ scores (the difference between their ideal and current care) reported by parents and young people were small. Parents’ satisfaction was significantly lower than their children’s (p < 0.001). On every domain of the Rotterdam Transition Profile, except for education and employment, significant differences were found between the three groups. A larger proportion of young people with diabetes were in a more independent phase of participation than those with ASD or CP. The wellbeing scores of those with diabetes (median = 53, IQR: 47–58) and CP (median = 53, IQR: 48–60) were similar, and significantly higher than for those with ASD (median = 47, IQR: 41–52; p < 0.001). CONCLUSIONS: Having established that our sample of young people with one of three LTCs recruited close to transfer to adult services was representative, we have described aspects of their satisfaction with services, participation and wellbeing, noting similarities and differences by LTC. This information about levels of current functioning is important for subsequent evaluation of the impact of service features on the health and wellbeing of young people with LTCs following transfer from child services to adult services.
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spelling pubmed-45890842015-10-01 Characteristics of young people with long term conditions close to transfer to adult health services Merrick, Hannah McConachie, Helen Le Couteur, Ann Mann, Kay Parr, Jeremy R. Pearce, Mark S. Colver, Allan BMC Health Serv Res Research Article BACKGROUND: For many young people with long term conditions (LTC), transferring from paediatric to adult health services can be difficult and outcomes are often reported to be poor. We report the characteristics and representativeness of three groups of young people with LTCs as they approach transfer to adult services: those with autism spectrum disorder with additional mental health problems (ASD); cerebral palsy (CP); or diabetes. METHODS: Young people aged 14 years-18 years 11 months with ASD, or those with diabetes were identified from children’s services and those with CP from population databases. Questionnaires, completed by the young person and a parent, included the ‘Mind the Gap’ Scale, the Rotterdam Transition Profile, and the Warwick and Edinburgh Mental Wellbeing Scale. RESULTS: Three hundred seventy four young people joined the study; 118 with ASD, 106 with CP, and 150 with diabetes. Participants had a significant (p < 0.001) but not substantial difference in socio-economic status (less deprived) compared to those who declined to take part or did not respond. Condition-specific severity of participants was similar to that of population data. Satisfaction with services was good as the ‘gap’ scores (the difference between their ideal and current care) reported by parents and young people were small. Parents’ satisfaction was significantly lower than their children’s (p < 0.001). On every domain of the Rotterdam Transition Profile, except for education and employment, significant differences were found between the three groups. A larger proportion of young people with diabetes were in a more independent phase of participation than those with ASD or CP. The wellbeing scores of those with diabetes (median = 53, IQR: 47–58) and CP (median = 53, IQR: 48–60) were similar, and significantly higher than for those with ASD (median = 47, IQR: 41–52; p < 0.001). CONCLUSIONS: Having established that our sample of young people with one of three LTCs recruited close to transfer to adult services was representative, we have described aspects of their satisfaction with services, participation and wellbeing, noting similarities and differences by LTC. This information about levels of current functioning is important for subsequent evaluation of the impact of service features on the health and wellbeing of young people with LTCs following transfer from child services to adult services. BioMed Central 2015-09-30 /pmc/articles/PMC4589084/ /pubmed/26424085 http://dx.doi.org/10.1186/s12913-015-1095-6 Text en © Merrick et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Merrick, Hannah
McConachie, Helen
Le Couteur, Ann
Mann, Kay
Parr, Jeremy R.
Pearce, Mark S.
Colver, Allan
Characteristics of young people with long term conditions close to transfer to adult health services
title Characteristics of young people with long term conditions close to transfer to adult health services
title_full Characteristics of young people with long term conditions close to transfer to adult health services
title_fullStr Characteristics of young people with long term conditions close to transfer to adult health services
title_full_unstemmed Characteristics of young people with long term conditions close to transfer to adult health services
title_short Characteristics of young people with long term conditions close to transfer to adult health services
title_sort characteristics of young people with long term conditions close to transfer to adult health services
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589084/
https://www.ncbi.nlm.nih.gov/pubmed/26424085
http://dx.doi.org/10.1186/s12913-015-1095-6
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