Quality of Life in Children With Cerebral Palsy

Author:

Gilson Kim-Michelle1,Davis Elise1,Reddihough Dinah234,Graham Kerr5,Waters Elizabeth1

Affiliation:

1. The Jack Brockhoff Child Health and Wellbeing Program, Academic Centre for Health Equity, Melbourne School of Population and Global Health, University of Melbourne, Australia

2. Department of Developmental Medicine, Royal Children’s Hospital, Melbourne, Australia

3. Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia

4. Murdoch Children’s Research Institute, Melbourne, Victoria, Australia

5. Department of Orthopaedic Surgery, Royal Children’s Hospital, Melbourne, Australia

Abstract

The ability to assess the quality of life of children with cerebral palsy to inform and evaluate individual care plans, service planning, interventions, and policies is crucial. In this article, the recent evidence on quality of life in children with cerebral palsy is reviewed, with attention to the determinants of quality of life and role of this construct as a practical outcome indicator in clinical trials. Quality of life measurement advances for children with cerebral palsy are discussed with a focus on condition-specific quality of life measures, particularly, the Cerebral Palsy Quality of Life–Child, which is the first condition-specific quality of life measure for children with cerebral palsy. The article presents an overview for clinicians and researchers intending to use quality of life measures on children with cerebral palsy and provides recommendations for future research that will better inform practice in the field.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

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