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Adaptation, Translation, and Validation of a Patient-Reported Experience Measure for Children and Young People for the Canadian Context
Department of Surgical and Interventional Sciences, McGill University Faculty of Medicine and Health Sciences, Montreal, Quebec, Canada.
Harvey E. Beardmore Division of Pediatric Surgery, The Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Harvey E. Beardmore Division of Pediatric Surgery, The Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Great Ormond Street Hospital for Children (GOSH), London, United Kingdom.
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2024 (English)In: Journal of Pediatric Surgery, ISSN 0022-3468, E-ISSN 1531-5037, Vol. 59, no 5, p. 810-817Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Patient-reported experience measures (PREMs) evaluate children's and young people's (CYP) perceptions of care. An important PREM developed with and for children was created in London, UK. Given the absence of similar North American instruments, we aimed to adapt, translate, and linguistically validate this instrument for use in a Canadian pediatric outpatient setting.

METHODS: A qualitative design was used, involving CYP and their parents/caregivers. Phase 1 entailed the English survey adaptation using think-aloud testing, revision, and cognitive testing. Phase 2 involved translation into French, revision and back-translation, and cognitive testing. Phase 3 encompassed a cross-validation of the English and French versions of the adapted instrument.

RESULTS: Fifty-five children in 3 age groups (8-11y, 12-13y, 14-16y) participated in creating the Canadian PREM. In Phases 1 and 2, 41 children participated in reviewing and updating specific questions in the instrument, resulting in adjustments and revisions based on their feedback. In Phase 3, 14 bilingual children linguistically validated the PREM instrument.

CONCLUSIONS: This study reports the development of the first Canadian PREM specifically tailored to children. By incorporating the perspectives and preferences of CYP in clinical practice, this approach has the potential to amplify the delivery of patient-centered care for this vulnerable population and ensure that the needs and voices of CYP are acknowledged.

LEVEL OF EVIDENCE: V, Therapeutic.

Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 59, no 5, p. 810-817
Keywords [en]
Patient centered care, Perception of care, Qualitative design, Vulnerable populations
National Category
Nursing
Identifiers
URN: urn:nbn:se:oru:diva-111652DOI: 10.1016/j.jpedsurg.2024.01.030ISI: 001289163200001PubMedID: 38369398Scopus ID: 2-s2.0-85185579519OAI: oai:DiVA.org:oru-111652DiVA, id: diva2:1839470
Note

This work was supported by grants from the National Natural Science Foundation of China (82371429, 82071200, 82173599), National Ministry of Science and Technology (SQ2021AAA010157), Shanghai Municipal Science and Technology Major Project (2018SHZDZX01 and ZJ LAB).

Available from: 2024-02-21 Created: 2024-02-21 Last updated: 2024-08-21Bibliographically approved

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Anderzen-Carlsson, Agneta

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