BLEEDING PATTERN AND CLIMACTERIC SYMPTOMS DURING DIFFERENT SEQUENTIAL COMBINED HRT REGIMENS IN CURRENT USE

Four sequential combined oestrogen and progestogen regimens were compared in terms of bleeding pattern and relief of climacteric symptoms. Treatment was with either 2 mg 17 beta-oestradiol with 1 mg norethisterone acetate [E(2) + NETA]; 2 mg oestradiol valerate with 75 mu g levonorgestrel [E(2)V + LNG]; 2 mg oestradiol valerate with 10 mg medroxyprogesterone acetate [E(2)V + MPA]; or 1.5 mg 17 beta-oestradiol with 150 mu g desogestrel [E(2) + DG]. A placebo-controlled study lasting 12-24 months was completed by 143 healthy early postmenopausal women. Bleeding lengths were not substantially different; in all regimens the majority of women were bleeding for 3-6 days. Bleeding onset showed differences when related to the 11th day of progestogen addition; in the regimen with E(2)V + LNG, 21% of the women were bleeding before the 11th day of progestogen addition 26% on, and 53% after that day. In the regimen with E(2)V + MPA, 56% of the women were bleeding before the 11th day, 28% on, and 17% after that day, whereas in the regimen with E(2) + DG, 15% of the women were bleeding before the 11th day, 5% on, and 80% after that day. All regimens reduced climacteric symptoms to the same extent. Breast tenderness occurred in all the regimens, except in the E(2) + DG. Conclusively, the differences between the responses to treatment were not conspicuous. However, our data indicate that one regimen (E(2) + DG) resulted in optimal bleeding control, optimal effect on climacteric symptoms, and no production of breast tenderness.