Tolsma Kristi Washburn, Allred Elizabeth N, Chen Minghua L, Duker Jay, Leviton Alan, Dammann Olaf
Division of Newborn Medicine, Floating Hospital for Children, Tufts Medical Center, 800 Washington St, PO Box 854, Boston, MA 02111-1526, USA.
Arch Ophthalmol. 2011 Dec;129(12):1555-63. doi: 10.1001/archophthalmol.2011.319.
To explore whether early or late and presumed or definite neonatal bacteremia are associated with an increased risk of severe retinopathy of prematurity (ROP).
We evaluated 1059 infants born before week 28 of gestation for ROP. Infants were classified as having early (postnatal week 1) or late (weeks 2-4) definite (culture-proven) or presumed (antibiotics taken for >72 hours despite negative blood culture results) bacteremia. Severe ROP was defined as stage 3 to 5, zone 1, prethreshold/threshold, or plus disease. We used time-oriented risk models to adjust for confounders.
In univariable, but not multivariable, analysis, newborns with presumed early bacteremia were at increased risk for plus disease (odds ratio [OR], 1.7; 95% CI, 1.1-2.7), and those with definite early bacteremia were at increased risk for stage 3 to 5 disease (1.9; 1.1-3.2). Infants who had presumed or definite late bacteremia were at increased risk for all 4 indicators of severe ROP in univariable analysis. In multivariable analysis, newborns with presumed late bacteremia were at increased risk for prethreshold/threshold ROP (OR, 1.8; 95% CI, 1.02-3.2), and those with definite late bacteremia were at increased risk for prethreshold/threshold ROP (1.8; 1.1-2.9) and plus disease (1.8; 1.05-2.9).
Definite late neonatal bacteremia seems to be an independent risk factor for prethreshold/threshold ROP and plus disease, and presumed late bacteremia seems to be related to prethreshold/threshold ROP.
探讨早发型或晚发型以及疑似或确诊的新生儿菌血症是否与早产儿严重视网膜病变(ROP)风险增加相关。
我们评估了1059例孕周小于28周出生的婴儿的ROP情况。婴儿被分类为患有早发型(出生后第1周)或晚发型(第2 - 4周)确诊(血培养证实)或疑似(尽管血培养结果为阴性但已使用抗生素超过72小时)菌血症。严重ROP定义为3至5期、1区、阈值前/阈值或附加病变。我们使用时间导向风险模型来调整混杂因素。
在单变量分析而非多变量分析中,疑似早发型菌血症的新生儿发生附加病变的风险增加(优势比[OR],1.7;95%置信区间[CI],1.1 - 2.7),确诊早发型菌血症的新生儿发生3至5期病变的风险增加(1.9;1.1 - 3.2)。在单变量分析中,疑似或确诊晚发型菌血症的婴儿发生所有4项严重ROP指标的风险均增加。在多变量分析中,疑似晚发型菌血症的新生儿发生阈值前/阈值ROP的风险增加(OR,1.8;95% CI,1.02 - 3.2),确诊晚发型菌血症的新生儿发生阈值前/阈值ROP(1.8;1.1 - 2.9)和附加病变(1.8;1.05 - 2.9)的风险增加。
确诊的晚发型新生儿菌血症似乎是阈值前/阈值ROP和附加病变的独立危险因素,疑似晚发型菌血症似乎与阈值前/阈值ROP有关。