Literature DB >> 25131769

Patient-reported outcome measures in pediatric epilepsy: a content analysis using World Health Organization definitions.

Salva Sadeghi1, Nora Fayed, Gabriel M Ronen.   

Abstract

OBJECTIVE: Patient-reported outcome (PRO) measures that assess the effect of epilepsy on children's lives include the concepts of health, health-related quality of life (HRQOL), and quality of life (QOL). They also contain varied health and health-related content. Our objectives were to identify what generic and epilepsy-specific PRO instruments are used in childhood epilepsy research and to make explicit their conceptual approach and biopsychosocial content.
METHODS: MEDLINE, EMBASE, and PsycINFO were searched from 2001 to 2011 for PRO measures used in pediatric epilepsy. Measures were analyzed on an item-by-item basis according to World Health Organization (WHO) definitions of QOL and the International Classification of Functioning, Disability and Health for Children and Youth (ICF-CY) biopsychosocial health framework to distinguish the conceptual approach within each measure. The health content analysis coded each item according to specific ICF-CY components of body function, activity and participation, environment, or personal factors to determine the health content for each measure.
RESULTS: Three generic and 13 epilepsy-specific PRO measures were identified; 10 of 16 measures utilized a biopsychosocial health approach rather than an HRQOL or QOL approach. Content analysis showed that in 11 of 16 measures, >25% of the items represented participation and activity components of the ICF-CY, whereas a high proportion of environment items were found in only one epilepsy-specific measure. SIGNIFICANCE: This comprehensive review provides information aiding clinicians and researchers in the selection of the appropriate PRO instruments for children with epilepsy on the basis of content. Most epilepsy-specific and generic PROs use a biopsychosocial health approach as opposed to a subjective HRQOL/QOL approach to measurement. Clinicians and researchers must be aware of these concepts and content when intending to measure outcomes validly. Wiley Periodicals, Inc.
© 2014 International League Against Epilepsy.

Entities:  

Keywords:  Biopsychosocial health; Children; Epilepsy; ICF-CY; Quality of life; World Health Organization

Mesh:

Year:  2014        PMID: 25131769     DOI: 10.1111/epi.12740

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  6 in total

1.  Children's perspective of quality of life in epilepsy.

Authors:  Nora Fayed; Aileen M Davis; David L Streiner; Peter L Rosenbaum; Charles E Cunningham; Lucyna M Lach; Michael H Boyle; Gabriel M Ronen
Journal:  Neurology       Date:  2015-04-03       Impact factor: 9.910

2.  A systematic review of patient-reported outcome measures in paediatric endocrinology.

Authors:  Richard G McGee; Edward Y B Zhang; Jennifer J G Tan; Aiden C K Cheung; Matthew P Garvey
Journal:  BMC Endocr Disord       Date:  2022-07-15       Impact factor: 3.263

Review 3.  Core Health Outcomes In Childhood Epilepsy (CHOICE): protocol for the selection of a core outcome set.

Authors:  Christopher Morris; Colin Dunkley; Frances M Gibbon; Janet Currier; Deborah Roberts; Morwenna Rogers; Holly Crudgington; Lucy Bray; Bernie Carter; Dyfrig Hughes; Catrin Tudur Smith; Paula R Williamson; Paul Gringras; Deb K Pal
Journal:  Trials       Date:  2017-11-28       Impact factor: 2.279

4.  Parents' Assessments of Disability in Their Children Using World Health Organization International Classification of Functioning, Disability and Health, Child and Youth Version Joined Body Functions and Activity Codes Related to Everyday Life.

Authors:  Niels Ove Illum; Kim Oren Gradel
Journal:  Clin Med Insights Pediatr       Date:  2017-06-19

Review 5.  Measurement properties of multidimensional patient-reported outcome measures in neurodisability: a systematic review of evaluation studies.

Authors:  Astrid Janssens; Morwenna Rogers; Rebecca Gumm; Crispin Jenkinson; Alan Tennant; Stuart Logan; Christopher Morris
Journal:  Dev Med Child Neurol       Date:  2015-12-11       Impact factor: 5.449

6.  Epilepsy-specific patient-reported outcome measures of children's health-related quality of life: A systematic review of measurement properties.

Authors:  Holly Crudgington; Morwenna Rogers; Hannah Morris; Paul Gringras; Deb K Pal; Christopher Morris
Journal:  Epilepsia       Date:  2020-01-17       Impact factor: 5.864

  6 in total

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