索引于
  • 打开 J 门
  • Genamics 期刊搜索
  • 期刊目录
  • 乌尔里希的期刊目录
  • 参考搜索
  • 哈姆达大学
  • 亚利桑那州EBSCO
  • OCLC-WorldCat
  • 普罗奎斯特传票
  • 普布隆斯
  • 日内瓦医学教育与研究基金会
  • 欧洲酒吧
  • 谷歌学术
分享此页面
期刊传单
Flyer image

抽象的

Health-Related Quality of Life is Associated with Hemoglobin Level in Children with Sickle Cell Anemia

Ruth Williams-Hooker, Stacie Olivi, Matthew P Smeltzer and Winfred C Wang

Purpose: Pediatric health quality of life (HQOL) refers to a child’s physical, emotional, and social well being. HQOL is often compromised in persons with sickle cell anemia (SCA). The purpose of this study was to compare HQOL with hemoglobin in children with SCA. Methods: In a pilot study looking at energy expenditure in children with SCA, we measured subjects’ QOL using the PedsQL survey and compared it to their hemoglobin (Hb) levels at baseline. Results: Twenty-five subjects, all with HbSS, completed the instrument. Their mean age (standard deviation) was 11.4 (3.25) years and 52% were male. Their mean Hb level was 8.4 (1.2) g/dL. Higher scores in social functioning (R=0.63, p=0.0001) and school functioning (R=0.40, p=0.05) were significantly associated with higher Hb levels. Conclusions: We conclude that Hb level is related to HQOL and that treatments aimed at improving Hb may help to improve overall HQOL.