Nocturnal oxygen saturation and painful sickle cell crises in children

被引:125
作者
Hargrave, DR
Wade, A
Evans, JPM
Hewes, DKM
Kirkham, FJ
机构
[1] Royal Marsden Hosp, Paediat Oncol Unit, Sutton SM2 5PT, Surrey, England
[2] UCL Hosp, Dept Haematol, London, England
[3] Great Ormond St Hosp Sick Children, Inst Child Hlth, Neurosci Unit, London WC1N 3JH, England
[4] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
[5] Inst Child Hlth, Neurosci Unit, London, England
[6] Inst Child Hlth, Dept Paediat Epidemiol, London WC1N 1EH, England
[7] Inst Child Hlth, Dept Biostat, London WC1N 1EH, England
关键词
D O I
10.1182/blood-2002-05-1392
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The pathogenesis of acute painful crisis in children with sickle cell disease is poorly understood; suggested risk factors include sickle cell type, severity of anemia, fetal hemoglobin concentration, and hypoxemia from upper airway obstruction. In a cohort study of 95 patients the relationship between clinical, laboratory, and sleep study data and frequency of painful crisis was investigated. Both univariate and multiple regression modeling showed that low nocturnal oxygen saturation was highly significantly associated with a higher rate of painful crisis in childhood (P < .0001). Screening and treatment for hypoxemia may reduce the frequency of this and other complications of the disease. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:846 / 848
页数:3
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