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α/β- and β-Blocker Exposure in Pregnancy and the Risk of Neonatal Hypoglycemia and Small for Gestational Age
Kana Kubota1,2, Kei Inai1, Eriko Shimada1
1Department of Pediatric Cardiology and Adult Congenital Cardiology, Tokyo Women's Medical University.
Insights
Maternal use of carvedilol during pregnancy increased neonatal hypoglycemia risk. Beta-blockers were linked to more frequent small for gestational age (SGA) infants. Careful monitoring of newborns exposed to these heart medications is crucial.
Area of Science:
- Cardiology
- Maternal-Fetal Medicine
- Pharmacology
Background:
- Congenital heart disease management in pregnant women often involves alpha/beta-blockers and beta-blockers.
- Limited data exists on the fetal and maternal effects of these medications during pregnancy.
- This study investigates the risks of neonatal hypoglycemia and small for gestational age (SGA) associated with maternal exposure.
Purpose of the Study:
- To assess the risks of neonatal hypoglycemia and SGA in infants born to mothers using alpha/beta-blockers or beta-blockers.
- To compare these risks with a control group of pregnant women with heart disease not on these medications.
Main Methods:
- A retrospective study included 306 pregnancies (267 women) with heart disease from January 2014 to October 2020.
- Participants were divided into an alpha/beta-blocker group (carvedilol, n=32), a beta-blocker group (n=11), and a control group (n=263).
- Outcomes analyzed included neonatal hypoglycemia and SGA.
Main Results:
- Neonatal hypoglycemia occurred more frequently in the carvedilol group compared to controls (P=0.025).
- Small for gestational age (SGA) was significantly more common in the beta-blocker group than in the carvedilol and control groups (P<0.001).
- Carvedilol-associated hypoglycemia was not time- or dose-dependent.
Conclusions:
- Maternal carvedilol use during pregnancy is associated with an increased risk of neonatal hypoglycemia.
- Beta-blocker use in pregnancy is linked to a higher incidence of SGA infants.
- Routine blood glucose monitoring for newborns exposed to alpha/beta-blockers and beta-blockers is recommended.
Background:
α/β- and β-blockers are essential in pregnant women's perinatal congenital heart disease management. Nevertheless, data on the effects of α/β- and β-blockers on pregnant women and fetuses are limited. We examined the risks of neonatal hypoglycemia and small for gestational age (SGA) associated with maternal exposure to α/β- and β-blockers.
Methods And Results:
All consecutive pregnant women with heart disease admitted to our hospital between January 2014 and October 2020 were included. Of 306 pregnancies (267 women), 32 were in the α/β-blocker group, 11 were in the β-blocker group, and 263 were in the control group. All 32 pregnancies in the α/β-blocker group were treated with carvedilol. In the β-blocker group, 4 women were treated with bisoprolol, 3 were treated with propranolol, 2 were treated with atenolol, 1 was treated with metoprolol, and 1 was treated nadolol. The incidence of neonatal hypoglycemia was higher in pregnant women taking carvedilol than in the control group (P=0.025). SGA was observed significantly more frequently in pregnant women taking β-blockers than in the carvedilol and control groups (P<0.001).
Conclusions:
Carvedilol administration during pregnancy was associated with neonatal hypoglycemia; however, it did not occur in a time- or dose-dependent manner. Routine monitoring of blood glucose levels in newborns exposed to α/β- and β-blockers is essential.
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