Literature DB >> 18164341

Self-reported health status and quality of life in youth with cerebral palsy and typically developing youth.

Kristie F Bjornson1, Basia Belza, Deborah Kartin, Rebecca G Logsdon, John McLaughlin.   

Abstract

OBJECTIVE: To describe self-reported health status and quality of life (QOL) of ambulatory youths with cerebral palsy (CP) compared with sex- and age-matched typically developing youth (TDY).
DESIGN: Prospective cross-sectional cohort comparison.
SETTING: Community-based. PARTICIPANTS: A convenience sample of 81 youth with CP (age range, 10-13 y) with Gross Motor Function Classification System (GMFCS) levels I through III and 30 TDY participated. They were recruited from 2 regional children's hospitals and 1 regional military medical center.
INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: Participants completed the Child Health Questionnaire-Child Form (CHQ-CF87) for health status and the Youth Quality of Life for QOL.
RESULTS: Youth with CP reported significantly lower health status than age- and sex-matched TDY in the following CHQ-CF87 subscales: role/social behavioral physical, bodily pain, physical function, and general health (CP mean rank, 46.8-55.2; TDY mean rank, 62.2-80.9). There were significant differences across GMFCS levels. There were no significant differences in self-reported QOL.
CONCLUSIONS: Self-reported health status, but not QOL, appears sensitive to the functional health issues experienced by ambulatory youth with CP. Pain management and psychosocial support may be indicated for them.

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Mesh:

Year:  2008        PMID: 18164341      PMCID: PMC3653574          DOI: 10.1016/j.apmr.2007.09.016

Source DB:  PubMed          Journal:  Arch Phys Med Rehabil        ISSN: 0003-9993            Impact factor:   3.966


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