Health-related quality of life in boys with Duchenne muscular dystrophy: Agreement between parents and their sons | DuchenneXchange

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Scientific Articles

Health-related quality of life in boys with Duchenne muscular dystrophy: Agreement between parents and their sons

key information

source: Journal of Child Neurology

year: 2010

authors: Bray P, Bundy AC, Ryan MM, North KN, Everett A.

summary/abstract:

This study investigated agreement between boys and their parents when reporting on health-related quality of life and the effects of steroid use, age, and physical functioning on self-reported health-related quality of life in boys with Duchenne muscular dystrophy. The Pediatric Quality of Life Inventory™ and brief functional measures were administered to 35 parent-son dyads.

We found that agreement between parents and their sons was moderate (intraclass correlation coefficient [ICC](2,1) = 0.66; 95% confidence interval [CI], 0.40-0.80) to poor (ICC(2,1) = 0.64; 95% CI, 0.43-0.64). The boys’ self-reports revealed a relationship between disease progression and physical functioning (r = -.75; P = .01); however, disease stage was not related to psychosocial functioning (r = -.27; NS). Parents and boys affected by Duchenne muscular dystrophy have a moderate to poor agreement on health-related quality of life measures, with parents reporting lower overall health-related quality of life when compared with their sons.

organisation: The University of Sydney, Australia; The Children's Hospital at Westmead, Australia; Royal Children's Hospital, Australia; Sydney Children's Hospital, Australia

DOI: 10.1177/0883073809357624

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