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Health‐related quality of life in children with sickle cell disease: A report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium
Author(s) -
Dampier Carlton,
Lieff Susan,
LeBeau Petra,
Rhee Seungshin,
McMurray Marsha,
Rogers Zora,
SmithWhitley Kim,
Wang Winfred
Publication year - 2010
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.22497
Subject(s) - medicine , psychosocial , quality of life (healthcare) , physical therapy , avascular necrosis , disease , observational study , sickle cell anemia , clinical trial , asthma , pediatrics , shoulders , psychiatry , surgery , nursing , femoral head
Background Pediatric health‐related quality of life (HRQOL) questionnaires have been validated in children with sickle cell disease (SCD), but small sample sizes in these studies have limited clinical comparisons. We used the baseline clinical data from the Collaborative Data (C‐Data) Project of the Comprehensive Sickle Cell Centers (CSCC) Clinical Trial Consortium to perform a detailed, descriptive study of HRQOL using the PedsQL™ version 4.0 generic core and fatigue scales. Methods Retrospective clinical data were obtained via medical record abstraction. Staff‐administered health history, psychosocial, and health behavior interviews were completed by a parent or guardian. PedsQL™ forms were completed separately by the child and a parent/guardian. Results The study enrolled 1,772 subjects (53% boys) with a mean age of 9.6 years (SD 4.7). SS or Sβ 0 thalassemia occurred in 68% and 32% had SC or Sβ + thalassemia. The occurrences of pain, priapism, avascular necrosis of hips/shoulders (AVN), or asthma were the most common complications/conditions reported. Multiple regression models controlling for hemoglobinopathies, gender, and age suggested that parent reports of physical functioning and sleep/rest fatigue declined in response to pain or AVN, while school functioning scales declined in response to pain or asthma. Sickle pain, and to a lesser extent asthma, negatively influenced child reports on almost all functioning and fatigue scales. Conclusions While longitudinal studies will be necessary to determine sensitivity to change, the current study suggests the potential utility of several PedsQL™ HRQOL scales as patient‐reported outcome measures for observational or interventional treatment studies of children and adolescents with SCD. Pediatr Blood Cancer. 2010;55:485–494. © 2010 Wiley‐Liss, Inc.