Vora Niraj, Raju Muppala, Jackson Ineshia, Mallett Lea, Samson Shoji, Malhotra Sonal, Shetty Ashith, Beeram Madhava R, Bush Andrew, Sagar Malvika
Department of Pediatrics, Texas A&M Health Science Center, Baylor Scott & White Health, Temple, TX, USA.
Department of Pediatrics, Texas A&M Health Science Center, Baylor Scott & White Health, Temple, TX, USA -
Minerva Pediatr (Torino). 2025 Apr;77(2):111-116. doi: 10.23736/S2724-5276.22.07019-7. Epub 2022 Oct 14.
The aim of this study was to determine the effect of pre-eclampsia on the development of bronchopulmonary dysplasia (BPD) in preterm infants.
Retrospective cohort study of infants' ≤32 weeks' gestation admitted to a level-IV single center neonatal intensive care unit from 2014 to 2016. Infants with major congenital anomalies, death or transfer before 28 days were excluded. Infants were stratified by maternal pre-eclampsia status. Demographic, clinical, and laboratory data were reviewed. Logistic regression was used to examine predictors for BPD. Main Outcome measure: The primary outcome was BPD incidence.
Four hundred thirty-two infants met inclusion criteria; 22% developed BPD, of which, 16% had severe BPD. Thirty-eight percent of infants were born to preeclamptic mothers, with 23% of those infants developing BPD. Infants born to preeclamptic mothers were delivered by cesarean section (88% vs. 60%; P<0.0001) more often and had lower birthweight (median = 1265g, IQR 910-1555 vs. median = 1388g, IQR 959-1752; P=0.008) compared to infants born to non-preeclamptic mothers. Higher incidence of intrauterine growth restriction was noted in pre-eclampsia group, 24% vs. 8%, P=0.0001). Gestational age, length of stay and days on ventilator were all associated with the development of BPD. In multivariable logistic regression, pre-eclampsia was not a risk factor for development of BPD (OR 1.12 [0.68, 1.83]).
Pre-eclampsia was not a significant risk factor for development of BPD nor the severity of BPD in infants' ≤32 weeks' gestation. IUGR infants with or without pre-eclampsia mothers were at higher risk for BPD.
本研究旨在确定子痫前期对早产儿支气管肺发育不良(BPD)发生发展的影响。
对2014年至2016年入住四级单中心新生儿重症监护病房、孕周≤32周的婴儿进行回顾性队列研究。排除患有严重先天性畸形、在28天前死亡或转院的婴儿。根据母亲子痫前期状态对婴儿进行分层。回顾人口统计学、临床和实验室数据。采用逻辑回归分析来检验BPD的预测因素。主要结局指标:主要结局是BPD发病率。
432名婴儿符合纳入标准;22%发生了BPD,其中16%为重度BPD。38%的婴儿母亲患有子痫前期,这些婴儿中有23%发生了BPD。与非子痫前期母亲所生婴儿相比,子痫前期母亲所生婴儿剖宫产分娩的比例更高(88%对60%;P<0.0001),出生体重更低(中位数=1265g,四分位数间距910 - 1555对中位数=1388g,四分位数间距959 - 1752;P = 0.008)。子痫前期组宫内生长受限的发生率更高,为24%对8%,P = 0.0001)。胎龄、住院时间和机械通气天数均与BPD的发生发展相关。在多变量逻辑回归分析中,子痫前期不是BPD发生的危险因素(比值比1.12 [0.68, 1.83])。
子痫前期不是孕周≤32周婴儿发生BPD及其严重程度的重要危险因素。无论母亲是否患有子痫前期,宫内生长受限的婴儿发生BPD的风险更高。