Health-related quality of life in sickle cell disease: Past, present, and future

被引:123
|
作者
Panepinto, Julie A. [1 ]
Bonner, Melanie [2 ]
机构
[1] Med Coll Wisconsin, Childrens Hosp Wisconsin, Dept Pediat, Childrens Res Inst, Milwaukee, WI 53226 USA
[2] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA
关键词
health-related quality of life; sickle cell disease; well being; CLINICAL-TRIAL CONSORTIUM; PISCES PROJECT; CARE UTILIZATION; ORGAN DAMAGE; CHILDREN; PAIN; HYDROXYUREA; ADULTS; ADOLESCENTS; ANEMIA;
D O I
10.1002/pbc.24176
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Health-related quality of life (HRQL) is defined as the patient's appraisal of how his/her well being and level of functioning, compared to the perceived ideal, are affected by individual health. The study of HRQL in children and adults with sickle cell disease (SCD) has begun to flourish. Given the devastating complications of the disease and other co-morbid factors patients experience that influence HRQL, it is increasingly important to understand HRQL. The focus of this critical review was to examine past and current research in HRQL in SCD where a validated instrument was used. In addition, future directions for HRQL in SCD are explored. Pediatr Blood Cancer 2012;59:377385. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:377 / 385
页数:9
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