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Göteborgs universitets publikationer

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

Författare och institution:
Catherine Arnaud (-); Melanie White-Koning (-); Susan Ishoy Michelsen (-); Jackie Parkes (-); Kathryn Parkinson (-); Ute Thyen (-); Eva Beckung (Institutionen för neurovetenskap och fysiologi, sektionen för arbetsterapi, audiologi och fysioterapi & Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa); Heather O Dickinson (-); Jerome Fauconnier (-); Marco Marcelli (-); Vicki McManus (-); Allan Colver (-)
Publicerad i:
Pediatrics, 121 ( 1 ) s. 54-64
Artikel, refereegranskad vetenskaplig
Sammanfattning (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.
Ämne (baseras på Högskoleverkets indelning av forskningsämnen):
Annan samhällsvetenskap ->
Övrig annan samhällsvetenskap ->
Adaptation, Physiological, Adaptation, Psychological, Cerebral Palsy, diagnosis, psychology, rehabilitation, Child, Cross-Sectional Studies, Developmental Disabilities, epidemiology, psychology, Disabled Children, psychology, rehabilitation, Europe, Female, Humans, Linear Models, Logistic Models, Male, Parent-Child Relations, Quality of Life, Questionnaires, Severity of Illness Index, Sickness Impact Profile, Social Desirability, Social Support
Postens nummer:
Posten skapad:
2009-01-05 17:24
Posten ändrad:
2011-01-20 09:58

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