Ethinylestradiol and dl-Norgestrel as a Postcoital Contraceptive *

Oral contraceptive steroids are of 2 types: oestrogens, of which ethinyloestradiol is the most important, and progestagens, of which levonorgestrel and norethisterone are the most commonly used. All these steroids can be measured by a number of analytical techniques but there is little doubt that radioimmunoassay is the most convenient. All the steroids are well absorbed in humans but while levonorgestrel is completely bioavailable, norethisterone has an average bioavailability of 70%. Ethinyloestradiol, too, is subject to presystemic metabolism with a mean bioavailability of 40 to 45%. The main site of presystemic metabolism is the gut wall, with the production of ethinyloestradiol sulphate. The progestagens norethynodrel, ethynodiol diacetate and lynoestrenol are quantitatively metabolised to norethisterone. The pharmacokinetics of the contraceptive steroids are best described by a 2-compartment open model. The terminal plasma half-life of levonorgestrel varies from 11 to 45 hours and of norethisterone from 5 to 14 hours. The β-phase half-life of ethinyloestradiol varies from 6 to 20 hours. The apparent volume of distribution of these contraceptive steroids (after intravenous administration) is between 1.5 and 4.3 L/kg. During long term treatment with oral contraceptive steroids, steady-state plasma concentrations of ethinyloestradiol (24 hours after administration) are between 10 and 200 pg/ml. Plasma concentrations of norethisterone and levonorgestrel at steady-state are higher than predicted from the single-dose kinetics because of enhanced binding of the progestagens following the induction of sex hormone binding globulin (SHBG) by ethinyloestradiol. Concentrations are in the range of 1.6 to 15.2 ng/ml for norethisterone and 0.8 to 4.5 ng/ml for levonorgestrel. All the contraceptive steroids are bound to proteins in plasma. Ethinyloestradiol is 97 to 98% bound to plasma albumin. The progestagens are bound both to albumin (levonorgestrel 93 to 95%; norethisterone 79 to 80%) and more specifically to SHBG. The binding capacity of SHBG can be enhanced by treatment with ethinyloestradiol or with more conventional enzyme-inducing drugs such as phenobarbitone, carbamazepine or rifampicin. Norethisterone and levonorgestrel are chiefly metabolised by reduction in the A ring and this is followed by conjugation with glucuronide or sulphate. The metabolism of levonorgestrel is stereoselective. Ethinyloestradiol is primarily hydroxylated at the 2 position but a wide variety of hydroxylated and methylated metabolites are formed and these are present both free and as glucuronide and sulphate conjugates. Ethinyloestradiol is conjugated directly at the 3 position (unlike the progestagens) and thus is liable to enterohepatic recirculation. Ethinyloestradiol sulphate concentrations in plasma are many times higher than that of the unchanged drug. The oral contraceptive steroids are involved in drug interactions of clinical significance. While the effect of contraceptive steroids on other drugs is small and unlikely to be of clinical significance, failure of contraception often occurs if enzyme-inducing agents such as rifampkin, phenobarbitone or carbamazepine are coadministered. Oral antibiotics do not seem to cause a significant loss of contraception in the large majority of women. Vitamin C will enhance the effect of contraceptive steroids by competing for sulphate conjugation in the gut wall, thus leading to increased bioavailability of ethinyloestradiol.

Clinical pharmacokinetics of oral contraceptive steroids.

A system for the clinical evaluation of menstrual patterns is presen ted. The standardized approach to the collection analysis and evaluation of menstrual data is designed to facilitate objective compari sons between the effects of contraceptive methods on the menstrual cycle and menstruation. The conceptual framework of the method includes: 1) the use of the woman as the unit of analysis 2) bleeding episodes as the basis of assessment rather than the menstrual cycle and 3) a series of variables that are descriptive of salient features of bleeding patterns. A temporal reference frame is developed and bleeding patterns are analyzed in relation to the reference period. A series of computer programs are presented for the proposed system and multivariate statistical procedures for the analysis of menstrual patterns are described.

An approach to the analysis of menstrual patterns in the critical evaluation of contraceptives.

The hormonal and peripheral effects of d -norgestrel in postcoital contraception

Contraceptive And Sterilization Practices And Extrauterine Pregnancy: A Realistic Perspective *

A Pill-a-Month Contraceptive

Clinical study of a once-a-month oral contraceptive: quinestrol-quingestanol.

A new postcoital oral contraceptive

Further experience with quingestanol acetate as a postcoital oral contraceptive.

Contraception with a daily low-dose progestogen: quingestanol acetate.

Edel Berman

Papers

A Pill-a-Month Contraceptive

Clinical study of a once-a-month oral contraceptive: quinestrol-quingestanol.

A new postcoital oral contraceptive

Further experience with quingestanol acetate as a postcoital oral contraceptive.

Contraception with a daily low-dose progestogen: quingestanol acetate.