Health-related quality of life in childhood cancer: Discrepancy in parent-child reports
- 1 January 1999
- journal article
- research article
- Published by Wiley in International Journal of Cancer
- Vol. 83 (S12) , 58-64
- https://doi.org/10.1002/(sici)1097-0215(1999)83:12+<58::aid-ijc11>3.0.co;2-a
Abstract
The purpose of our study was to describe reports of parents and of children with cancer on items taken from 4 domains of health-related quality of life (HRQL), bodily pain/distress, general health perceptions, physical functioning and limitations in role/social functioning as a result of physical health, and to examine whether differences in parent–child reports varied as a function of the child's health condition (cancer vs. healthy). Twenty-seven child–parent dyads with cancer and 27 child–parent dyads who were healthy (child ages 8 to 18 inclusive) completed measures of child HRQL [Child Health Questionnaire-Parent Form (CHQ-PF50) and Child Health Questionnaire (CHQ-CF87)] and demographic information at a scheduled out-patient general pediatric or pediatric oncology clinic appointment. Sixteen items included on both the CHQ-CF87 and CHQ-PF50 were examined to compare parent and child reports of child HRQL. As hypothesized, greater discrepancies were evident in the reports of parents of children with cancer than parents of children who are healthy [F(16,31) = 3.98, p < 0.0001]. Statistically significant discrepancies emerged in parent and child responses on 50% of the items in the sample of children with cancer, with parents reporting that their children experience more limitations in their lives than did the children themselves. In the healthy group, statistically significant discrepancies emerged on only 1 of the 16 items (6.3%). Int. J. Cancer Suppl. 12:58–64, 1999. ©1999 Wiley-Liss, Inc.Keywords
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