Atenolol in the treatment of pregnancy-induced hypertension

Br J Clin Pharmacol. 1981 Nov;12(5):725-30. doi: 10.1111/j.1365-2125.1981.tb01296.x.

Abstract

1 The pharmacological properties of atenolol suggest its possible usefulness in pregnancy-induced hypertension. The pharmacokinetics of atenolol in the pregnant woman, concentrations in cord blood, and its effects on maternal blood pressure and the foetus, are evaluated. 2 We studied 13 pregnant women with hypertension, most of them uncontrolled on methyldopa. Whole blood concentrations and urinary excretion of the drug were measured over 24 h following a 100 mg dose. Effects on maternal blood pressure, pulse rate and foetal heart rate and cardiotocograph were compared for the 4 days before treatment and the first 4 days of treatment. The birth weights and Apgar scores of the babies were recorded. 2 The pharmacokinetics of atenolol (plasma half-life of about 8 h) in pregnant women do not differ from the findings in the non-pregnant. The levels of atenolol in the cord blood were confirmed as approximately equal to those in the maternal blood. 4 In the ten women in whom blood pressure was assessed a small significant fall in blood pressure was observed. 5 A 5% mean fall in foetal heart rate resulted but in one case was a rate below 120 beats/min recorded. There was no evidence of depression of the stress response of the foetal heart. Apgar scores 5 min post partum were satisfactory. 6 Atenolol appears to be safe for use in hypertensive pregnancies. Its effectiveness as an antihypertensive agent in pregnancy requires further controlled evaluation.

MeSH terms

  • Adult
  • Atenolol / adverse effects
  • Atenolol / metabolism
  • Atenolol / therapeutic use*
  • Female
  • Fetus / drug effects
  • Humans
  • Hypertension / drug therapy*
  • Kinetics
  • Pregnancy
  • Pregnancy Complications, Cardiovascular / drug therapy*
  • Propanolamines / therapeutic use*

Substances

  • Propanolamines
  • Atenolol