Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Obstetrics and Gynaecology, Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Int J Cardiol. 2024 Sep 1;410:132234. doi: 10.1016/j.ijcard.2024.132234. Epub 2024 Jun 4.
Beta-blockers are commonly used drugs during pregnancy, especially in women with heart disease, and are regarded as relatively safe although evidence is sparse. Differences between beta-blockers are not well-studied.
In the Registry of Pregnancy And Cardiac disease (ROPAC, n = 5739), a prospective global registry of pregnancies in women with structural heart disease, perinatal outcomes (small for gestational age (SGA), birth weight, neonatal congenital heart disease (nCHD) and perinatal mortality) were compared between women with and without beta-blocker exposure, and between different beta-blockers. Multivariable regression analysis was used for the effect of beta-blockers on birth weight, SGA and nCHD (after adjustment for maternal and perinatal confounders).
Beta-blockers were used in 875 (15.2%) ROPAC pregnancies, with metoprolol (n = 323, 37%) and bisoprolol (n = 261, 30%) being the most frequent. Women with beta-blocker exposure had more SGA infants (15.3% vs 9.3%, p < 0.001) and nCHD (4.7% vs 2.7%, p = 0.001). Perinatal mortality rates were not different (1.4% vs 1.9%, p = 0.272). The adjusted mean difference in birth weight was -177 g (-5.8%), the adjusted OR for SGA was 1.7 (95% CI 1.3-2.1) and for nCHD 2.3 (1.6-3.5). With metoprolol as reference, labetalol (0.2, 0.1-0.4) was the least likely to cause SGA, and atenolol (2.3, 1.1-4.9) the most.
In women with heart disease an association was found between maternal beta-blocker use and perinatal outcomes. Labetalol seems to be associated with the lowest risk of developing SGA, while atenolol should be avoided.
β受体阻滞剂是妊娠期间常用的药物,特别是在患有心脏病的女性中,尽管证据较少,但被认为相对安全。β受体阻滞剂之间的差异尚未得到充分研究。
在妊娠和心脏病注册研究(ROPAC,n=5739)中,对结构性心脏病女性的妊娠进行了前瞻性全球注册,比较了有和无β受体阻滞剂暴露的女性以及不同β受体阻滞剂之间的围产期结局(胎儿生长受限(SGA)、出生体重、新生儿先天性心脏病(nCHD)和围产儿死亡率)。多变量回归分析用于研究β受体阻滞剂对出生体重、SGA 和 nCHD 的影响(在调整了母体和围产期混杂因素后)。
ROPAC 妊娠中有 875 例(15.2%)使用了β受体阻滞剂,其中美托洛尔(n=323,37%)和比索洛尔(n=261,30%)最为常见。有β受体阻滞剂暴露的女性中 SGA 婴儿(15.3%比 9.3%,p<0.001)和 nCHD(4.7%比 2.7%,p=0.001)的发生率更高。围产儿死亡率无差异(1.4%比 1.9%,p=0.272)。出生体重的调整平均差值为-177g(-5.8%),SGA 的调整 OR 为 1.7(95%CI 1.3-2.1),nCHD 为 2.3(1.6-3.5)。以美托洛尔为参照,拉贝洛尔(0.2,0.1-0.4)最不可能导致 SGA,而阿替洛尔(2.3,1.1-4.9)则最有可能。
在患有心脏病的女性中,母体使用β受体阻滞剂与围产期结局之间存在关联。拉贝洛尔似乎与 SGA 风险最低相关,而阿替洛尔应避免使用。