| Literature DB >> 6140231 |
Abstract
The phasic approach to oral contraception is described with a historical review of the evolution of new administration regimens aimed at lowering total steroid content from monophasic to biphasic to the new triphasic approach. The phasic regimen designs which support the intended mechanism of action of each of the phasic approaches are discussed. Emphasis is placed on the discussion of the rationale for the new triphasic oral contraceptive and the clinical demonstration of the triphasic's inhibition of ovulation and maintenance of functional integrity of the pituitary-ovarian axis. A new theoretical formula and practical concept are presented that incorporate a progestogen potency factor, and consequently provide a common denominator enabling a comparison of the magnitude of the effects of various oral contraceptive products on pituitary responsiveness. Widespread clinical studies are described which reinforce the suggestion that the triphasic is the state of the art and represents an important contribution to contraceptive technology.Entities:
Keywords: Acne; Age Factors; Amenorrhea; Biology; Blood Pressure; Body Weight; Cervical Mucus; Contraception; Contraception Termination; Contraceptive Agents; Contraceptive Agents, Estrogen--administraction and dosage; Contraceptive Agents, Female; Contraceptive Agents, Progestin--administraction and dosage; Contraceptive Agents--administraction and dosage; Contraceptive Methods--administraction and dosage; Contraceptive Methods--pharmacodynamics; Contraceptive Methods--side effects; Contraceptive Mode Of Action; Cytologic Effects; Demographic Factors; Depression; Dysmenorrhea; Economic Factors; Endocrine System; Endometrial Effects; Endometrium; Estradiol; Ethinyl Estradiol; Family Planning; Fertility; Follicle Stimulating Hormone; Headache; Incidence; Levonorgestrel; Luteinizing Hormone; Measurement; Menstrual Cycle; Menstruation; Metrorrhagia; Nausea; Oral Contraceptives--administraction and dosage; Oral Contraceptives--pharmacodynamics; Oral Contraceptives--side effects; Ovulation Suppression; Physiology; Pituitary Gland--side effects; Population; Population Dynamics; Progesterone; Prolactin; Reproduction; Reproductive Control Agents; Research And Development; Research Methodology; Technology; Testosterone
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Year: 1983 PMID: 6140231
Source DB: PubMed Journal: Int J Fertil ISSN: 0020-725X