Cumulative illness severity and progression from moderate to severe retinopathy of prematurity

被引:22
作者
Hagadorn, J. I.
Richardson, D. K.
Schmid, C. H.
Cole, C. H.
机构
[1] Univ Connecticut, Sch Med, Connecticut Childrens Med Ctr, Div Neonatol,Dept Pediat, Hartford, CT 06106 USA
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Neonatol, Boston, MA USA
[3] Tufts Univ, Sch Med, Tufts New England Med Ctr, Inst Clin Res & Hlth Policy Studies, Boston, MA 02111 USA
关键词
retinopathy of prematurity; illness severity; predictive model;
D O I
10.1038/sj.jp.7211780
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To test cumulative neonatal illness severity ( IS) and IS fluctuation as predictors of progression from moderate to severe retinopathy of prematurity (ROP). Study Design: Data from research databases and medical record review were collected for infants from four neonatal intensive care unit (NICUs) admitted between 1995 and 2001 and diagnosed with prethreshold ROP. Cumulative neonatal IS measured using daily Scores for Neonatal Acute Physiology (SNAP) for the first 28 days of life, and IS fluctuation as assessed by summing changes between daily SNAP scores, were tested as predictors of progression to threshold ROP using logistic regression. Result: Infants progressing to threshold (n 79), compared to those not progressing to threshold (n 130), had significantly (P< 0.05) lower gestational ages (25.2 +/- 1.1 versus 25.8 +/- 1.4 weeks), higher cumulative neonatal SNAP (255 +/- 77 versus 224 +/- 63 weeks) and had more severe hospitalizations as indicated by diagnoses and medical management. In regression analysis, gestational age, chronological age and presence of plus disease at first diagnosis of prethreshold were associated with development of threshold. After adjusting for these factors, cumulative neonatal SNAP was significantly associated with progression to threshold. However, addition of cumulative SNAP to the model only increased receiver-operating characteristic curve area from 0.77 to 0.78 (NS). Other factors, including SNAP fluctuation, were not associated with progression to threshold after adjustment using this model. Conclusion: Cumulative neonatal IS, as measured by cumulative SNAP, is an independent risk factor for progression from moderate to severe ROP. However, cumulative IS does not enhance assessment of risk for ROP progression after adjusting for simpler clinical factors.
引用
收藏
页码:502 / 509
页数:8
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