Pharmacokinetics of terbutaline during pregnancy

European Journal of Clinical Pharmacology - Tập 29 - Trang 619-623 - 1986
S. Lyrenäs1, A. Grahnén2, B. Lindberg1, B. Lindström2, G. Lönnerholm2
1Department of Obstetrics and Gynecology, University Hospital, Uppsala, Sweden
2Department of Drugs, National Board of Health and Welfare, Uppsala, Sweden

Tóm tắt

Terbutaline in plasma was determined in three groups of women by gas chromatography-mass spectrometry. Eight women received a single i.v. dose of 0.25 mg terbutaline sulphate during pregnancy and 3–6 months after delivery. Mean plasma clearance was 29% higher during pregnancy than after delivery. There was a subsequent decrease in mean terminal half-life from 5.3 to 3.7 h and in mean residence time from 5.3 to 3.4 h. There was no change in volume of distribution. A second group of pregnant women in premature labour (n=8) received oral terbutaline 5 mg t.d.s. The dosing was repeated after delivery. The mean steady state plasma concentration of terbutaline was about 30% lower during pregnancy than after delivery. A third group of women in preterm labour (n=8) was treated with an i.v. infusion of terbutaline. The concentrations of terbutaline found on cessation of uterine contractions ranged between 12.8 and 31.5 ng/ml. At present there is no basis for formulation of a “therapeutic plasma level” of terbutaline for the treatment of preterm labour.

Tài liệu tham khảo

Hemminki E, Starfield B (1978) Prevention and treatment of premature labour by drugs: Review of controlled clinical trials. Br J Obstet Gynaecol 85: 411–417

Gomeni C, Gomeni R (1978) Interactive package for pharmacokinetic analysis. Comp Biomed Res 11: 345–361

Parker WA (1984) Effects of pregnancy on pharmacokinetics. In: Benet LZ, et al. (eds) Pharmacokinetic basis of drug treatment. Raven Press, New York, pp 249–268