Hearing loss, quality of life, and academic problems in long-term neuroblastoma survivors: Report from the Children's Oncology Group

被引:153
作者
Gurney, James G.
Tersak, Jean M.
Ness, Kirsten K.
Landier, Wendy
Matthay, Katherine K.
Schmidt, Mary Lou
机构
[1] Univ Michigan, Dept Pediat, Child Evalut & Res Unit, Ann Arbor, MI 48109 USA
[2] Univ Pittsburgh, Dept Pediat, Div Hematol Oncol, Pittsburgh, PA 15260 USA
[3] St Jude Childrens Res Hosp, Dept Epidemiol & Canc Control, Memphis, TN 38105 USA
[4] City Hope Natl Med Ctr, Div Populat Sci, Duarte, CA 91010 USA
[5] Univ Calif San Francisco, Dept Pediat, Pediat Hematol Oncol, San Francisco, CA 94143 USA
[6] Univ Illinois, Dept Pediat, Div Pediat Hematol Oncol, Chicago, IL USA
关键词
cancer; chemotherapy; cisplatin; education; psychosocial problems; treatment late effects; ototoxicity;
D O I
10.1542/peds.2007-0178
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVES. Among a cohort of long-term neuroblastoma survivors, our aims were to (1) assess the association between treatment intensity and parent-reported hearing loss in the child, (2) evaluate the strength of the association between hearing loss and parent-reported academic and psychosocial difficulties in the child, and (3) examine the association between parent-reported academic and psychosocial difficulties in the child and the child's self-reported quality of life. PATIENTS AND METHODS. Through a mailed survey that included the Pediatric Quality of Life Inventory 4.0 and an outcomes questionnaire for parents, we evaluated 137 children (aged 8-17 years) who were previously enrolled in 1 of 2 Children's Cancer Group neuroblastoma clinical studies. RESULTS. Childhood survivors of neuroblastoma who had prevalent hearing loss, as reported by their parents, had at least twice the risk of an identified problem with reading skills, math skills, and/or attention and a similarly higher risk of a general learning disability and/or special educational needs than did neuroblastoma survivors without hearing loss. Consistent with this finding, hearing loss was associated with a 10-point-lower mean score in the school-functioning scale of the Pediatric Quality of Life Inventory 4.0. We also observed a clear pattern of poorer self-reported quality-of-life scores among children with parent-reported academic and psychosocial problems compared with those without such problems, particularly with school functioning, even after controlling for reported hearing loss. CONCLUSIONS. We found evidence that long-term neuroblastoma survivors, especially those with hearing loss, are at elevated risk for academic learning problems and psychosocial difficulties. We also found strong concordance between parent-reported learning problems in the child and indications of distress in the child's self-reported quality of life.
引用
收藏
页码:E1229 / E1236
页数:8
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