Weiner Eran, Feldstein Ohad, Tamayev Liliya, Grinstein Ehud, Barber Elad, Bar Jacob, Schreiber Letizia, Kovo Michal
Department of Obstetrics & Gynecology, The Edith Wolfson Medical Center, Holon, Israel affiliated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Obstetrics & Gynecology, The Edith Wolfson Medical Center, Holon, Israel affiliated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Pregnancy Hypertens. 2018 Apr;12:6-10. doi: 10.1016/j.preghy.2018.02.001. Epub 2018 Feb 7.
We aimed to compare pregnancy outcome and placental histopathology in women with preeclampsia (PE) with and without severe features.
The medical records and placental pathology reports of all pregnancies complicated by PE during 2008-2016, were reviewed. Results were compared between those with and without severe features (severe PE vs. mild PE groups), according to current ACOG guidelines. Placental lesions were classified to maternal/fetal vascular supply lesions, and maternal/fetal inflammatory responses. Small for gestational age (SGA) was defined as neonatal birth-weight ≤10th%. Composite adverse neonatal outcome was defined as one or more of the following: sepsis, transfusion, phototherapy, respiratory morbidity, cerebral morbidity, NEC, or death.
The severe PE group (n = 284) was characterized by lower gestational age at delivery (p < 0.001), and higher rates of antenatal corticosteroid use (p = 0.003), and cesarean deliveries (p < 0.001) as compared to the mild PE group (n = 151). More placentas <10th% and more composite maternal vascular malperfusion (MVM) lesions were observed in the severe PE group as compared to the mild PE group (p < 0.001 for both). In multivariate analysis, composite placental MVM lesions were independently associated with severe PE (aOR = 1.75, 95%CI 1.4-4.9). Higher rates of SGA (p = 0.016), and composite adverse neonatal outcome (p = 0.002) characterized the severe PE group. In multivariate analysis, adverse neonatal outcome was independently associated with gestational age (aOR = 0.54, 95%CI 0.49-0.68), SGA (aOR = 1.75, 95%CI = 1.15-3.59), severe PE (aOR = 1.8, 95%CI = 1.13-3.54) and placental MVM lesions (aOR = 2.13, 95%CI = 1.05-4.39).
More pronounced placental pathology and higher rate of adverse neonatal outcome characterize preeclampsia with severe features as compared with the milder form of the disease.
我们旨在比较有和没有严重特征的子痫前期(PE)女性的妊娠结局和胎盘组织病理学。
回顾了2008年至2016年期间所有并发PE的妊娠的病历和胎盘病理报告。根据美国妇产科医师学会(ACOG)当前指南,对有和没有严重特征的患者(重度PE组与轻度PE组)的结果进行比较。胎盘病变分为母体/胎儿血管供应病变和母体/胎儿炎症反应。小于胎龄儿(SGA)定义为新生儿出生体重≤第10百分位数。复合不良新生儿结局定义为以下一项或多项:败血症、输血、光疗、呼吸系统疾病、脑部疾病、坏死性小肠结肠炎或死亡。
与轻度PE组(n = 151)相比,重度PE组(n = 284)的特点是分娩时孕周较小(p < 0.001),产前使用糖皮质激素的比例较高(p = 0.003),剖宫产率较高(p < 0.001)。与轻度PE组相比,重度PE组观察到更多<第10百分位数的胎盘和更多的复合母体血管灌注不良(MVM)病变(两者均p < 0.001)。在多变量分析中,复合胎盘MVM病变与重度PE独立相关(调整后比值比[aOR]=1.75,95%置信区间[CI] 1.4 - 4.9)。重度PE组的SGA发生率较高(p = 0.016)和复合不良新生儿结局发生率较高(p = 0.002)。在多变量分析中,不良新生儿结局与孕周(aOR = 0.54,95%CI 0.49 - 0.68)、SGA(aOR = 1.75,95%CI = 1.15 - 3.59)、重度PE(aOR = 1.8,95%CI = 1.13 - 3.54)和胎盘MVM病变(aOR = 2.13,95%CI = 1.05 - 4.39)独立相关。
与病情较轻的子痫前期相比,有严重特征的子痫前期具有更明显的胎盘病理学改变和更高的不良新生儿结局发生率。