Literature DB >> 18166557

Parent-reported quality of life of children with cerebral palsy in Europe.

Catherine Arnaud1, Melanie White-Koning, Susan Ishoy Michelsen, Jackie Parkes, Kathryn Parkinson, Ute Thyen, Eva Beckung, Heather O Dickinson, Jerome Fauconnier, Marco Marcelli, Vicki McManus, Allan Colver.   

Abstract

OBJECTIVE: The goal was to determine whether the type and severity of the child's impairments and the family's psychosocial, social, and economic characteristics influence parent-reported child quality of life across the spectrum of severity of cerebral palsy.
METHODS: Our population-based, cross-sectional survey conducted in 2004 to 2005 involved 818 children with cerebral palsy, 8 to 12 years of age, from 7 countries (9 regions) in Europe. Child quality of life was assessed through parent reports by using the Kidscreen questionnaire, and data were analyzed separately for each of its 10 domains.
RESULTS: The parental response rates were >93% for all domains except one. Gross motor function and IQ level were found to be associated independently with quality of life in most domains. However, greater severity of impairment was not always associated with poorer quality of life; in the moods and emotions, self-perception, social acceptance, and school environment domains, less severely impaired children were more likely to have poor quality of life. Pain was associated with poor quality of life in the physical and psychological well-being and self-perception domains. Parents with higher levels of stress were more likely to report poor quality of life in all domains, which suggests that factors other than the severity of the child's impairment may influence the way in which parents report quality of life.
CONCLUSIONS: The parent-reported quality of life for children with cerebral palsy is associated strongly with impairment. However, depending on the areas of life, the most severely impaired children (in terms of motor functioning or intellectual ability) do not always have the poorest quality of life.

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Year:  2008        PMID: 18166557     DOI: 10.1542/peds.2007-0854

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  36 in total

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Review 2.  Pain in cognitively impaired children: a focus for general pediatricians.

Authors:  M Massaro; S Pastore; A Ventura; E Barbi
Journal:  Eur J Pediatr       Date:  2012-03-20       Impact factor: 3.183

3.  Mental health problems in children with neuromotor disabilities.

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Journal:  Paediatr Child Health       Date:  2016-03       Impact factor: 2.253

4.  Diverse Brains.

Authors:  Morton Ann Gernsbacher
Journal:  Gen Psychol       Date:  2015-04

5.  Racial disparities in health-related quality of life in a cohort of very low birthweight 2- and 3-year-olds with and without cerebral palsy.

Authors:  Beth Marie McManus; Stephanie A Robert; Aggie Albanese; Mona Sadek-Badawi; Mari Palta
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7.  Neonatal Magnetic Resonance Imaging Pattern of Brain Injury as a Biomarker of Childhood Outcomes following a Trial of Hypothermia for Neonatal Hypoxic-Ischemic Encephalopathy.

Authors:  Seetha Shankaran; Scott A McDonald; Abbot R Laptook; Susan R Hintz; Patrick D Barnes; Abhik Das; Athina Pappas; Rosemary D Higgins
Journal:  J Pediatr       Date:  2015-09-16       Impact factor: 4.406

8.  Study protocol: determinants of participation and quality of life of adolescents with cerebral palsy: a longitudinal study (SPARCLE2).

Authors:  Allan F Colver; Heather O Dickinson
Journal:  BMC Public Health       Date:  2010-05-26       Impact factor: 3.295

9.  The quality of life of a multidiagnosis group of special needs children: associations and costs.

Authors:  Sandy Thurston; Louise Paul; Patricia Loney; Maria Wong; Gina Browne
Journal:  Int J Pediatr       Date:  2010-04-18

10.  Interactions among Ecological Factors That Explain the Psychosocial Quality of Life of Children with Complex Needs.

Authors:  Sandy Thurston; Louise Paul; Chenglin Ye; Patricia Loney; Gina Browne; Lehana Thabane; Peter Rosenbaum
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