Division of Neonatology, Department of Pediatrics, Hennepin County Medical Center and Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, USA.
J Matern Fetal Neonatal Med. 2021 Jan;34(2):195-200. doi: 10.1080/14767058.2019.1601698. Epub 2019 Apr 17.
Preterm infants <29 weeks of gestation are at risk for severe intraventricular hemorrhage (IVH). Lower gestational age, birth weight, severe illness, as indexed by higher Score for Neonatal Acute Physiology - Perinatal Extension II (SNAPPE-II) are associated with severe IVH. The role of coagulation abnormalities on the first day after birth in severe IVH remains controversial. The present study investigated factors that predict the risk of severe IVH, including SNAPPE-II at 12 h and coagulation parameters on the first day after birth. A retrospective chart review of infants < 29 weeks of gestation from January 2008 to December 2013 was performed. Prenatal and postnatal characteristics, SNAPPE-II at 12 h, coagulation parameters [prothrombin time (PT), INR, partial thromboplastin time (aPTT), thrombin time (TT), and fibrinogen] on the first day and cranial ultrasound examination records were collected. The association between clinical and laboratory variables and severe IVH was determined. A joint predictive model for the risk of severe IVH (grades 3 and 4) versus no-mild IVH (grades 0, 1, and 2) was developed using multiple regression analysis. Preterm infants of gestational age < 29 weeks were included ( = 101). Fifteen (15%) infants had severe IVH. Lower gestational age ( = .006), birth weight ( = .008), African American race ( = .031) and higher SNAPPE-II at 12 h ( = .001) were associated with severe IVH. Infants with severe IVH had longer PT ( = .004), higher INR ( = .004) and lower platelet count ( = .034) than those with no-mild IVH. Stepwise logistic regression showed that only SNAPPE-II at 12 h was an independent predictor of severe IVH. For each unit increase in SNAPPE-II, the log odds of severe IVH increased by 0.045 (95% CI: [0.017, 0.073]; = .002). A threshold of 55 on the SNAPPE-II yielded a sensitivity of 60% (9/15), a specificity of 91% (78/86), a positive predictive value (PPV) of 53% (9/17) and a negative predictive value (NPV) of 93% (78/84). All other demographic and clinical variables and coagulation abnormalities had an insignificant coefficient ( > .05) when included in a bivariate logistic model with SNAPPE-II. SNAPPE-II at 12 h after birth is an independent predictor of severe IVH in preterm infants with gestational age < 29 weeks.
29 周以下的早产儿有发生严重脑室出血(IVH)的风险。较低的胎龄、出生体重、严重疾病(以新生儿急性生理学-围产期扩展 II 评分(SNAPPE-II)较高为指标)与严重 IVH 相关。出生后第一天凝血异常在严重 IVH 中的作用仍存在争议。本研究旨在探讨预测严重 IVH 风险的因素,包括 12 小时的 SNAPPE-II 和出生后第一天的凝血参数。对 2008 年 1 月至 2013 年 12 月期间胎龄<29 周的早产儿进行了回顾性图表审查。收集了产前和产后特征、12 小时的 SNAPPE-II、凝血参数[凝血酶原时间(PT)、国际标准化比值(INR)、部分凝血活酶时间(aPTT)、凝血酶时间(TT)和纤维蛋白原]以及头颅超声检查记录。确定了临床和实验室变量与严重 IVH 之间的关联。使用多元回归分析建立了严重 IVH(3 级和 4 级)与无轻度 IVH(0 级、1 级和 2 级)风险的联合预测模型。纳入了胎龄<29 周的早产儿( = 101)。15 名(15%)婴儿发生严重 IVH。较低的胎龄( =.006)、出生体重( =.008)、非裔美国人种族( =.031)和较高的 12 小时 SNAPPE-II( =.001)与严重 IVH 相关。与无轻度 IVH 的婴儿相比,严重 IVH 患儿的 PT 更长( =.004)、INR 更高( =.004)和血小板计数更低( =.034)。逐步逻辑回归显示,只有 12 小时的 SNAPPE-II 是严重 IVH 的独立预测因子。SNAPPE-II 每增加 1 个单位,严重 IVH 的对数优势增加 0.045(95%CI:[0.017, 0.073]; =.002)。SNAPPE-II 阈值为 55 时,灵敏度为 60%(9/15),特异性为 91%(78/86),阳性预测值(PPV)为 53%(9/17),阴性预测值(NPV)为 93%(78/84)。当将 SNAPPE-II 与其他所有人口统计学和临床变量以及凝血异常一起纳入二元逻辑模型时,所有其他变量的系数均无统计学意义( >.05)。出生后 12 小时的 SNAPPE-II 是胎龄<29 周的早产儿发生严重 IVH 的独立预测因子。