MedicineObstetricsPharmacologyClinical PharmacologyMaternal-fetal MedicinePharmacodynamicsHypertension PharmacotherapyHypertensive DisordersNeonatal PharmacologyPregnancyPregnancy PharmacologyPregnancy-induced HypertensionArea Under The Concentration - Time CurveBlood PressurePharmacodynamic Changes In PregnancyPharmacological TherapyPharmacotherapy In PregnancyPregnancy-related HypertensionPregnancy-related Pharmacokinetic ChangesPregnancy-related Pharmacokinetics
The disposition and effect of orally administered prazosin have been studied in eight women with hypertension which was uncontrolled by beta-adrenoceptor blockade during the last trimester of pregnancy. Results were compared with healthy men of similar age. The median time to peak concentration was 165 min during pregnancy and 120 min in the men (P less than 0.04). Area under the concentration vs time curve was 3914 ng l-1 min in pregnancy and 2439 ng l-1 min in the men (P less than 0.06). Mean elimination half-life was 171 min in the pregnant women and 130 min in the men (P less than 0.01). Blood pressure was lowered by prazosin in both supine and standing positions. Blood pressure control remained satisfactory in six of the eight women and the median prolongation of pregnancy was 22 days. Neonatal outcome was satisfactory and all babies are developing normally. We conclude that prazosin is more slowly, but apparently more completely, absorbed during pregnancy and that its half-life is slightly prolonged. Prazosin appears to be both effective and safe when used during the last trimester to control blood pressure.
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PLACEBO-CONTROLLED TRIAL OF ATENOLOL IN TREATMENT OF PREGNANCY-ASSOCIATED HYPERTENSION
P. C. Rubin, DonaldM. Clark, Davidj Sumner et al. · The Lancet · 1983 · 222 citations
Randomised comparison of methyldopa and oxprenolol for treatment of hypertension in pregnancy.
Eileen D.M. Gallery, DM Saunders, Stephen N. Hunyor et al. · BMJ · 1979 · 156 citations · Full text
Prazosin disposition in young and elderly subjects.
PC Rubin, PJ Scott, JL Reid · British Journal of Clinical Pharmacology · 1981 · 60 citations · Full text