Bateman Brian T, Patorno Elisabetta, Desai Rishi J, Seely Ellen W, Mogun Helen, Maeda Ayumi, Fischer Michael A, Hernandez-Diaz Sonia, Huybrechts Krista F
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, and Department of Anesthesiology, Critical Care, and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; and
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, and.
Pediatrics. 2016 Sep;138(3). doi: 10.1542/peds.2016-0731.
β blockers are widely used in the treatment of hypertensive disorders during pregnancy. These medications cross the placenta and may cause physiologic changes in neonates exposed in utero. We sought to define the risks of neonatal hypoglycemia and bradycardia associated with maternal exposure to β blockers at the time of delivery in a large, nationwide cohort of Medicaid beneficiaries.
We used a cohort of 2 292 116 completed pregnancies linked to liveborn infants of Medicaid-enrolled women from 2003 to 2007. We examined the risks of neonatal hypoglycemia and neonatal bradycardia associated with maternal exposure to β blockers at the time of delivery. Propensity score matching was used to control for potential confounders including maternal demographics, obstetric and medical conditions, and exposure to other medications.
There were 10 585 (0.5%) pregnancies exposed to β blockers at the time of delivery. The risk of neonatal hypoglycemia was 4.3% in the β blocker-exposed neonates versus 1.2% in the unexposed; the risk of neonatal bradycardia was 1.6% in the exposed versus 0.5% in the unexposed. After controlling for confounders, risk remained elevated for both neonatal hypoglycemia and bradycardia among exposed pregnancies versus unexposed (adjusted odds ratio, 1.68, 95% confidence interval, 1.50-1.89 and adjusted odds ratio, 1.29, 95% confidence interval, 1.07-1.55, respectively).
Our findings suggest that neonates born to mothers exposed to β blockers in late pregnancy, including labetalol, are at elevated risk for neonatal hypoglycemia and bradycardia.
β受体阻滞剂广泛用于治疗妊娠期高血压疾病。这些药物可穿过胎盘,可能导致子宫内暴露的新生儿发生生理变化。我们试图在一个大型的全国医疗补助受益人群队列中,确定分娩时母亲暴露于β受体阻滞剂与新生儿低血糖和心动过缓风险之间的关系。
我们使用了一个队列,该队列包含2003年至2007年期间与医疗补助参保妇女的活产婴儿相关的2292116例完整妊娠。我们研究了分娩时母亲暴露于β受体阻滞剂与新生儿低血糖和新生儿心动过缓风险之间的关系。倾向评分匹配用于控制潜在混杂因素,包括母亲的人口统计学特征、产科和医疗状况以及其他药物暴露情况。
分娩时暴露于β受体阻滞剂的妊娠有10585例(0.5%)。暴露于β受体阻滞剂的新生儿发生低血糖的风险为4.3%,未暴露的新生儿为1.2%;暴露的新生儿发生心动过缓的风险为1.6%,未暴露的新生儿为0.5%。在控制混杂因素后,暴露妊娠的新生儿低血糖和心动过缓风险与未暴露妊娠相比仍然升高(调整后的优势比分别为1.68,95%置信区间为1.50 - 1.89;调整后的优势比为1.29,95%置信区间为1.07 - 1.55)。
我们的研究结果表明,妊娠晚期暴露于β受体阻滞剂(包括拉贝洛尔)的母亲所生的新生儿发生新生儿低血糖和心动过缓的风险升高。