Yang Chih-Chieh, Tang Pei-Ling, Liu Po-Yen, Huang Wei-Chun, Chen Ying-Yao, Wang Hsiao-Ping, Chang Jenn-Tzong, Lin Li-Te
Department of Pediatrics Research Center of Medical Informatics, Kaohsiung Veterans General Hospital, Kaohsiung Institute of Medicine, Chung Shan Medical University, Taichung Section of Critical Care and Cardiovascular Medical Center Department of Obstetrics and Gynecology, Kaohsiung Veterans General Hospital Department of Biological Science, National Sun Yat-sen University, Kaohsiung Department of Obstetrics and Gynecology, National Yang-Ming University School of Medicine, Taipei, Taiwan.
Medicine (Baltimore). 2018 Aug;97(31):e11739. doi: 10.1097/MD.0000000000011739.
The utero-placental ischemia induced by pregnancy-induced hypertension (PIH) could lead to fetal hypoxia and proinflammatory cytokine release, which are associated with the development of neonatal necrotizing enterocolitis (NEC). However, a few studies have investigated the relationship between PIH and neonatal NEC and have produced controversial results. Therefore, we attempted to assess the relationship between PIH and the subsequent neonatal NEC risk and identify predictive risk factors.Patients with newly diagnosed PIH were recruited from the Taiwan National Health Insurance Research Database (NHIRD). For each participant, 4 age- and delivery-year-matched participants without PIH were randomly selected. A multivariable logistic regression was performed for the identification of the predictive risk factors for neonatal NEC.Among the 23.3 million individuals registered in the NHIRD, 29,013 patients with PIH and 116,052 matched controls were identified. For the multivariable analysis, maternal PIH was associated with an increased risk of subsequent neonatal NEC development (odds ratio [OR] 1.86, 95% confidence interval [CI] 1.08-3.21, P = .026). Furthermore, single parity (OR 2.06, 95% CI 1.12-3.77, P = .019), preterm birth (OR 5.97, 95% CI 3.49-10.20, P < .001), multiple gestations (OR 2.25, 95% CI 1.22-4.14, P = .010), and intrauterine growth restriction (IUGR) (OR 3.59, 95% CI 2.06-6.24, P < .001) were independent risk factors for the development of subsequent neonatal NEC.Maternal PIH increases the risk for developing neonatal NEC. Furthermore, primiparity, preterm birth, multiple gestations, and IUGR were independent risk factors for neonatal NEC.
妊娠高血压综合征(PIH)引起的子宫胎盘缺血可导致胎儿缺氧和促炎细胞因子释放,这与新生儿坏死性小肠结肠炎(NEC)的发生有关。然而,少数研究调查了PIH与新生儿NEC之间的关系,结果存在争议。因此,我们试图评估PIH与随后发生的新生儿NEC风险之间的关系,并确定预测风险因素。
新诊断为PIH的患者来自台湾国民健康保险研究数据库(NHIRD)。对于每个参与者,随机选择4名年龄和分娩年份匹配的无PIH参与者。进行多变量逻辑回归以确定新生儿NEC的预测风险因素。
在NHIRD登记的2330万人中,确定了29013例PIH患者和116052例匹配对照。对于多变量分析,母亲患PIH与随后发生新生儿NEC的风险增加相关(优势比[OR]1.86,95%置信区间[CI]1.08 - 3.21,P = 0.026)。此外,初产(OR 2.06,95%CI 1.12 - 3.77,P = 0.019)、早产(OR 5.97,95%CI 3.49 - 10.20,P < 0.001)、多胎妊娠(OR 2.25,95%CI 1.22 - 4.14,P = 0.010)和宫内生长受限(IUGR)(OR 3.59,95%CI 2.06 - 6.24,P < 0.001)是随后发生新生儿NEC的独立风险因素。
母亲患PIH会增加发生新生儿NEC的风险。此外,初产、早产、多胎妊娠和IUGR是新生儿NEC的独立风险因素。