Medical Research Centre Oulu, PEDEGO Research Unit, University of Oulu, Oulu, Finland.
Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland.
J Matern Fetal Neonatal Med. 2021 Aug;34(15):2506-2512. doi: 10.1080/14767058.2019.1668925. Epub 2019 Sep 26.
This study aimed to analyze the mortality of extremely preterm infants (ELGA born alive before 28 weeks) until the postconceptional age of 42 weeks, death, or home discharge, whichever came first. It was focused especially on studying the relationship between antenatal risk factors, the time of death, and the postnatal morbidities associated with mortality.
The original data obtained from the nationwide Finnish medical birth register of extremely preterm and low birthweight infants born during 2005-2013 were analyzed. The total population consisted of 1353 ELGA infants after the exclusion of 18 infants born with lethal congenital anomalies or genetic defects. Mortality risks were adjusted according to the length of gestation, the administration of antenatal steroids, and the delivery hospital.
During the first 48 hours, extreme immaturity was seen to be the prominent cause of death, and intrauterine growth did not influence mortality. The ELGA population surviving for at least 48 hours ( = 1135) was submitted for mortality risk analysis. After the adjustments, small-for-gestational-age (SGA) (birth weight below -2 SD) was found to be the factor with the highest risk for demise [OR 6.2; 95% CI (3.9-10.0) < .001]. Multiple deliveries were associated with increased risk for death [OR 1.5; 95% CI (1.0-2.1), = .048] to a lesser extent. The main neonatal morbidities associated with the risk of mortality after 48 postnatal hours of life were severe intraventricular hemorrhage (IVH) [OR 4.4; 95% CI (3.0-6.7), < .001], respiratory distress syndrome (RDS) [OR 2.6; 95% CI (1.3-5.0), = .006], and necrotizing enterocolitis (NEC) [OR 2.3; 95% CI (1.5-3.4), < .001]. The major morbidities associated with deaths among non-SGA infants were severe IVH (32.1% of all deaths), NEC (19.1%), and sepsis (8.4%). In SGA infants, severe respiratory disease (RDS, severe bronchopulmonary dysplasia, pulmonary hemorrhage, or pulmonary hypertension) was the main cause of death (60.9% of all deaths). Medical or surgical PDA treatment was not found to be associated with increased risk of death [OR 0.4; 95% CI (0.2-0.5), < .001] compared to infants who had survived for more than 2 days. Severe preeclampsia was found to be associated with 42% of all ELGA-SGA births. After the adjustments, ELGA infants from pregnancies complicated by preeclampsia of the mother exhibited a significantly lower risk of severe IVH [OR 0.3; 95% CI (0.2-0.5), < .001] compared to the non-preeclamptic mothers' infants. The low incidence of severe IVH was evident regardless of fetal growth in this patient group.
SGA infants with less than 28 gestational weeks, who had survived for at least 2 days, had excessively high mortality due to severe pulmonary disease. Intrauterine growth had no influence on the risk of death, other than pulmonary causes. The infants of preeclamptic mothers exhibited an increased risk of intrauterine growth retardation; however, despite this serious complication, these infants exhibited a significant decrease in the risk for severe IVH.
本研究旨在分析直到孕龄 42 周或死亡或出院的极低出生体重儿(ELGA,28 周前活产)的死亡率,重点研究产前危险因素、死亡时间和与死亡率相关的围生期合并症之间的关系。
分析了 2005 年至 2013 年芬兰全国极低出生体重儿和早产儿医疗出生登记处获得的原始数据。总人群包括在排除了 18 名患有致死性先天性异常或遗传缺陷的婴儿后存活的 1353 名 ELGA 婴儿。根据胎龄、产前类固醇的使用和分娩医院调整死亡率风险。
在最初的 48 小时内,极度不成熟是导致死亡的主要原因,宫内生长情况对死亡率没有影响。至少存活 48 小时的 ELGA 存活人口(n=1135)进行了死亡率风险分析。调整后,小于胎龄儿(SGA)(出生体重低于-2 SD)是死亡风险最高的因素[比值比(OR)6.2;95%置信区间(CI)(3.9-10.0)<0.001]。多胎分娩与死亡风险增加相关[OR 1.5;95% CI(1.0-2.1),P=0.048],但程度较轻。与出生后 48 小时生命风险相关的主要新生儿合并症是严重颅内出血(IVH)[OR 4.4;95% CI(3.0-6.7),P<0.001]、呼吸窘迫综合征(RDS)[OR 2.6;95% CI(1.3-5.0),P=0.006]和坏死性小肠结肠炎(NEC)[OR 2.3;95% CI(1.5-3.4),P<0.001]。非 SGA 婴儿死亡的主要合并症是严重 IVH(所有死亡的 32.1%)、NEC(19.1%)和败血症(8.4%)。在 SGA 婴儿中,严重呼吸系统疾病(RDS、严重支气管肺发育不良、肺出血或肺动脉高压)是主要死亡原因(所有死亡的 60.9%)。与存活超过 2 天的婴儿相比,接受药物或手术治疗的 PDA 治疗并不增加死亡风险[OR 0.4;95% CI(0.2-0.5),P<0.001]。严重子痫前期导致所有 ELGA-SGA 分娩的 42%。调整后,母亲患有子痫前期的 ELGA 婴儿发生严重 IVH 的风险显著降低[OR 0.3;95% CI(0.2-0.5),P<0.001]。在该患者组中,无论胎儿生长情况如何,严重 IVH 的发生率均较低。
胎龄小于 28 周且至少存活 2 天的 SGA 婴儿,由于严重肺部疾病,死亡率极高。除了肺部原因外,宫内生长情况对死亡风险没有影响。子痫前期母亲的婴儿发生宫内生长迟缓的风险增加;然而,尽管存在这种严重并发症,这些婴儿发生严重 IVH 的风险显著降低。