Prenatal risk factors for severe retinopathy of prematurity among very preterm infants of the Australian and New Zealand Neonatal Network

被引:207
作者
Darlow, BA
Hutchinson, JL
Henderson-Smart, DJ
Donoghue, DA
Simpson, JM
Evans, NJ
机构
[1] Christchurch Sch Med & Hlth Sci, Dept Paediat, Christchurch, New Zealand
[2] Univ Sydney, Royal Prince Alfred Hosp, Ctr Perinatal Hlth Serv Res, Sydney, NSW 2006, Australia
[3] Univ Sydney, Royal Prince Alfred Hosp, Sch Publ Hlth, Sydney, NSW 2006, Australia
[4] Univ Sydney, Royal Prince Alfred Hosp, Dept Newborn Care, Sydney, NSW 2006, Australia
关键词
infant; premature; retinopathy of prematurity; gestational age; population based; small for gestational age;
D O I
10.1542/peds.2004-1309
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective. To identify prenatal and perinatal risk factors for clinically severe (stage 3 or 4) retinopathy of prematurity (ROP). Methods. Data were collected prospectively as part of the ongoing Australian and New Zealand Neonatal Network audit of high-risk infants (birth weight of <1500 g or gestational age [GA] of <32 weeks) admitted to a level III neonatal unit in Australia or New Zealand. Prenatal and perinatal factors to 1 minute of age were examined for the subset of infants with GA of <29 weeks who survived to 36 weeks' postmenstrual age and were examined for ROP (n = 2105). The factors significantly associated with stage 3 or 4 ROP were entered into a multivariate logistic regression model. Results. Two-hundred three infants (9.6%) had stage 3 or more ROP. Prematurity was the dominant risk factor, with infants with GA of <25 weeks having 20 times greater odds of severe ROP than infants with GA of 28 weeks. Birth weight for GA also had a "dose-response" effect; the more growth-restricted infants had greater risk, with infants below the 3rd percentile of weight for GA having 4 times greater odds of severe ROP than those between the 25th and 75th percentiles. Male gender was also a significant risk factor (odds ratio: 1.73; 95% confidence interval: 1.25-2.40). Conclusions. These data, for a large, essentially population-based cohort, suggest that factors related to the degree of immaturity, intrauterine growth restriction, and male gender contribute to severe ROP.
引用
收藏
页码:990 / 996
页数:7
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