| Literature DB >> 857675 |
J L Ambrus, N G Courey, B J Browne, I B Mink, R H Moore, C M Ambrus.
Abstract
Changes in the blood coagulation system were studied in three groups of 20 patients each. The first group received 0.5 mg. of norethindrone daily, plus 0.06 mg. of ethinyl estradiol on alternate days from cycle Day 5 through 25. The second group, all of whom had been fitted with an intrauterine contraceptive device (IUD), received no hormonal treatment and served as a control group. The third group received 0.5 mg. of norethindrone daily, combined with 0.045 mg. of ethinyl estradiol given on alternate days from cycle Day 5 through 25. Blood samples were drawn prior to the initiation of the study and after three months of treatment. Tests of the following parameters of the blood coagulation system were performed: direct platelet count; platelet adhesiveness; prothrombin time; thrombin time; fibrinogen; factor II assay; activity of factors V, VII, VIII, IX, and X; antithrombin III; and fibrin/fibrinogen degradation products. For a number of these factors, both fresh and frozen blood samples were examined. It was concluded that the two treatment regimens, with the use of alternate-day estrogen administration over a three-month period, had no clinically significant effect on the blood coagulation system.Entities:
Keywords: Biology; Blood Coagulation Effects; Clinical Research; Contraceptive Agents, Female; Ethinyl Estradiol; Hematological Effects; Hemic System; Norethindrone Acetate; Oral Contraceptives; Oral Contraceptives, Combined; Physiology; Platelet Aggregation; Research Methodology
Mesh:
Substances:
Year: 1977 PMID: 857675 DOI: 10.1016/0002-9378(77)90680-9
Source DB: PubMed Journal: Am J Obstet Gynecol ISSN: 0002-9378 Impact factor: 8.661