Prediction of adverse outcomes in children with sickle cell anemia: a study of the Dallas Newborn Cohort

被引:59
|
作者
Quinn, Charles T. [1 ,3 ]
Lee, Nancy J. [2 ,3 ]
Shull, Elizabeth P. [2 ,3 ]
Ahmad, Naveed [3 ]
Rogers, Zora R. [1 ,3 ]
Buchanan, George R. [1 ,3 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Div Hematol Oncol, Dept Pediat, Dallas, TX 75390 USA
[2] SW Comprehens Sickle Cell Ctr, Dallas, TX USA
[3] Childrens Med Ctr, Dallas, TX 75235 USA
关键词
D O I
10.1182/blood-2007-07-100719
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Cooperative Study of Sickle Cell Disease reported that dactylitis, severe anemia, and leukocytosis in very young children with sickle cell disease (SCD) increased the risk of later adverse outcomes, including death, stroke, frequent pain, and recurrent acute chest syndrome. This model has not been validated in other cohorts. We evaluated its performance in the Dallas Newborn Cohort, a newborn inception cohort of children with SCD. We studied 168 children (55% male, 97% sickle cell anemia) with a mean follow-up of 7.1 years who provided 1188 patient-years of observation. Of the 23 (13.7%) subjects who experienced adverse events, 2 (1.2%) died, 14 (8.3%) had a stroke, 4 (2.4%) had frequent pain, and 3 (1.8%) had recurrent acute chest syndrome. No relationship existed between early clinical predictors and later adverse outcomes, with the possible exception of leukocyte count. Most subjects who experienced adverse events were predicted to be at low risk for those events. No subject who was predicted to be at high risk actually experienced an adverse outcome. The sensitivity of the model did not rise above 20% until specificity fell below 60%. We suggest that this model not be used as a criterion to initiate early interventions for SCD.
引用
收藏
页码:544 / 548
页数:5
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