Sangam: A Confluence of Knowledge Streams

Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures

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dc.creator Morris, Christopher
dc.creator Janssens, A.
dc.creator Shilling, V.
dc.creator Allard, A.
dc.creator Fellowes, A.
dc.creator Tomlinson, Richard
dc.creator Williams, J.
dc.creator Thompson Coon, J.
dc.creator Rogers, M.
dc.creator Beresford, B.
dc.creator Green, C.
dc.creator Jenkinson, C.
dc.creator Tennant, A.
dc.creator Logan, Stuart
dc.date 2016-01-19T12:38:36Z
dc.date 2016-01-19T12:38:36Z
dc.date 2015-06-25
dc.date.accessioned 2023-02-17T19:47:55Z
dc.date.available 2023-02-17T19:47:55Z
dc.identifier Health Qual Life Outcomes. 2015 Jun 25;13:87.
dc.identifier 1477-7525
dc.identifier 26108625
dc.identifier 10.1186/s12955-015-0284-7
dc.identifier http://hdl.handle.net/11287/594014
dc.identifier Health and quality of life outcomes
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/241993
dc.description BACKGROUND: Health services are increasingly focused on measuring and monitoring outcomes, particularly those that reflect patients' priorities. To be meaningful, outcomes measured should be valued by patients and carers, be consistent with what health professionals seek to achieve, and be robust in terms of measurement properties. The aim of this study was (i) to seek a shared vision between families and clinicians regarding key aspects of health as outcomes, beyond mortality and morbidity, for children with neurodisability, and (ii) to appraise which multidimensional patient reported outcome measures (PROMs) could be used to assess salient health domains. METHODS: Relevant outcomes were identified from (i) qualitative research with children and young people with neurodisability and parent carers, (ii) Delphi survey with health professionals, and (iii) systematic review of PROMs. The International Classification of Functioning Disability and Health provided a common language to code aspects of health. A subset of stakeholders participated in a prioritisation meeting incorporating a Q-sorting task to discuss and rank aspects of health. RESULTS: A total of 33 pertinent aspects of health were identified. Fifteen stakeholders from the qualitative and Delphi studies participated in the prioritisation meeting: 3 young people, 5 parent carers, and 7 health professionals. Aspects of health that emerged as more important for families and targets for health professionals were: communication, emotional wellbeing, pain, sleep, mobility, self-care, independence, mental health, community and social life, behaviour, toileting and safety. Whilst available PROMs measure many aspects of health in the ICF, no single PROM captures all the key domains prioritised as for children and young people with neurodisability. The paucity of scales for assessing communication was notable. CONCLUSIONS: We propose a core suite of key outcome domains for children with neurodisability that could be used in evaluative research, audit and as health service performance indicators. Future work could appraise domain-specific PROMs for these aspects of health; a single measure assessing the key aspects of health that could be applied across paediatric neurodisability remains to be developed.
dc.description This article is available via Open Access. Please click on the 'Additional Link' above to access the full-text.
dc.language eng
dc.publisher BioMed Central
dc.relation http://hqlo.biomedcentral.com/articles/10.1186/s12955-015-0284-7
dc.title Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures
dc.type Journal Article
dc.type Research Support, Non-U.S. Gov't


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