Fratto Victoria M, Ananth Cande V, Gyamfi-Bannerman Cynthia
a Department of Reproductive Medicine, Division of Perinatology , University of California , San Diego, San Diego , CA , USA.
b Department of Obstetrics and Gynecology , College of Physicians and Surgeons, Columbia University , New York , NY , USA.
Hypertens Pregnancy. 2016 May;35(2):242-9. doi: 10.3109/10641955.2016.1139720. Epub 2016 Mar 1.
We estimated risks of late preterm (LP, 34°(/7)-36(6/7) weeks) delivery and neonatal respiratory and non-respiratory morbidity in women with mild and severe hypertension, in both low-risk and high-risk (history of chronic hypertension, preeclampsia (PE), or insulin-dependent diabetes in current pregnancy) cohorts.
This is a secondary analysis of two Maternal-Fetal Medicine Units Network randomized trials of aspirin to prevent PE. Women with non-anomalous singleton gestations delivered at ≥34 weeks were divided into three groups: normotensive, mild PE/gestational hypertension (GH), and severe PE/GH. Primary outcomes were respiratory (respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), or intubation) and non-respiratory (intraventricular hemorrhage, retinopathy of prematurity, small for gestational age (SGA) <10%, neonatal intensive care unit (NICU) admission, perinatal death, pulmonary hypertension, seizures, and 5 min Apgar <5) morbidity. Associations between LP delivery and risks of respiratory and non-respiratory morbidity were evaluated by fitting log-Binomial regression models before and after adjusting potential confounders.
Of 2781 women in the low-risk trial, mild and severe hypertension were diagnosed in 8.5% (n = 235) and 3.3% (n = 92), respectively. Respiratory morbidity was similar in all groups. Risks of non-respiratory morbidity were higher in the severe PE/GH group compared with normotensive women (28.3% vs. 16.8%, risk ratio 1.5, 95% confidence interval 1.1, 2.1). When restricting the analysis to late preterm infants, this risk was no longer present. Of the 1542 women in the high-risk trial, mild and severe hypertension were present in 16.6% (n = 256) and 11.9% (n = 184), respectively. Respiratory morbidity was again similar. Risks of non-respiratory morbidity were also not significantly increased in the high-risk cohort.
In both low- and high-risk women, mild PE/GH at ≥34 weeks is not associated with an increased risk of neonatal morbidity compared with normotensive women. Increased risk of composite neonatal morbidity related to severe PE/GH is confined to the subgroup of infants with non-respiratory morbidity, and disappears when including only late preterm infants.
我们评估了轻度和重度高血压女性发生晚期早产(LP,34⁰/₇ - 36⁶/₇周)以及新生儿呼吸和非呼吸性疾病的风险,这些女性来自低风险和高风险(有慢性高血压病史、子痫前期(PE)或本次妊娠为胰岛素依赖型糖尿病)队列。
这是两项母胎医学单位网络关于阿司匹林预防PE的随机试验的二次分析。孕周≥34周分娩的单胎妊娠无异常的女性被分为三组:血压正常、轻度PE/妊娠期高血压(GH)和重度PE/GH。主要结局为呼吸性(呼吸窘迫综合征(RDS)、支气管肺发育不良(BPD)或插管)和非呼吸性(脑室内出血、早产儿视网膜病变、小于胎龄儿(SGA)<10%、新生儿重症监护病房(NICU)入院、围产期死亡、肺动脉高压、惊厥和5分钟阿氏评分<5)疾病。通过拟合对数二项回归模型,在调整潜在混杂因素前后,评估晚期早产与呼吸和非呼吸性疾病风险之间的关联。
在低风险试验的2781名女性中,分别有8.5%(n = 235)和3.3%(n = 92)被诊断为轻度和重度高血压。所有组的呼吸性疾病发病率相似。与血压正常的女性相比,重度PE/GH组的非呼吸性疾病风险更高(28.3%对16.8%,风险比1.5,95%置信区间1.1,2.1)。当将分析限制在晚期早产儿时,这种风险不再存在。在高风险试验的1542名女性中,分别有16.6%(n = 256)和11.9%(n = 184)存在轻度和重度高血压。呼吸性疾病发病率再次相似。高风险队列中的非呼吸性疾病风险也没有显著增加。
在低风险和高风险女性中,孕周≥34周的轻度PE/GH与血压正常的女性相比,新生儿疾病风险并未增加。与重度PE/GH相关的复合新生儿疾病风险增加仅限于非呼吸性疾病的婴儿亚组,当仅纳入晚期早产儿时该风险消失。