Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.authorWright, Alice Elisabeth
dc.contributor.authorRobb, James
dc.contributor.authorShearer, Morven Caroline
dc.date.accessioned2016-02-29T10:40:04Z
dc.date.available2016-02-29T10:40:04Z
dc.date.issued2016-06
dc.identifier.citationWright , A E , Robb , J & Shearer , M C 2016 , ' Transition from paediatric to adult health services in Scotland for young people with cerebral palsy ' , Journal of Child Health Care , vol. 20 , no. 2 , pp. 205-213 . https://doi.org/10.1177/1367493514564632en
dc.identifier.otherPURE: 214270685
dc.identifier.otherPURE UUID: ad0f733f-1a37-4deb-817b-6f3ad661bf05
dc.identifier.otherScopus: 84966728304
dc.identifier.otherORCID: /0000-0002-9180-6928/work/60195511
dc.identifier.otherWOS: 000376306500009
dc.identifier.urihttp://hdl.handle.net/10023/8331
dc.descriptionA.E.W. was funded by a grant from Tayside Health Fund.en
dc.description.abstractTransition from paediatric to adult health-care services has been characterized as being poorly planned and coordinated, resulting in a reduction in services and may be distressing for families. This study aimed to establish what provisions are currently available in Scotland for transition of young people with cerebral palsy and what some clinicians believe future provisions should involve. Semi-structured interviews were conducted with 13 community paediatricians (or equivalents in health boards without community paediatricians) from 12 different Scottish health boards. Interviews were audio recorded, transcribed and analysed thematically using framework analysis. Both current transition provision and the areas that the clinicians felt needed improvement varied greatly between health boards. Key areas in need of improvement were coordination and communication within health services and also between health services and educational, social services and adult health services to which young people were transitioning. Transition remains problematic and variable. For transition to be improved, further research is needed to explore the effect this variation is having on young people and their families.
dc.format.extent9
dc.language.isoeng
dc.relation.ispartofJournal of Child Health Careen
dc.rights© 2016, Publisher / the Author(s). This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at chc.sagepub.com / https://dx.doi.org/10.1177/1367493514564632en
dc.subjectCare pathwaysen
dc.subjectCerebral palsyen
dc.subjectChild healthen
dc.subjectTransitionen
dc.subjectRA Public aspects of medicineen
dc.subjectRJ Pediatricsen
dc.subjectNDASen
dc.subject.lccRAen
dc.subject.lccRJen
dc.titleTransition from paediatric to adult health services in Scotland for young people with cerebral palsyen
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews.School of Medicineen
dc.contributor.institutionUniversity of St Andrews.Institute of Behavioural and Neural Sciencesen
dc.contributor.institutionUniversity of St Andrews.St Andrews Sustainability Instituteen
dc.identifier.doihttps://doi.org/10.1177/1367493514564632
dc.description.statusPeer revieweden


This item appears in the following Collection(s)

Show simple item record