B. Faguer et al., AMENORRHEA DURING HORMONE REPLACEMENT THE RAPY BY THE ASSOCIATION OF PERCUTANEOUS 17-BETA-ESTRADIOL AND ORAL MICRONIZED PROGESTERONE, Contraception fertilite sexualite, 21(11), 1993, pp. 849-852
The effects of oral micronized progesterone - administered at a low do
se - on the endometrium and on bleeding pattern have been evaluated du
ring a multicenter study in which 101 patients were involved. For a mi
nimum of 6 months, patients who did not wish to have withdrawal bleedi
ng (98) received the association of 17 beta-percutaneous estradiol (1,
5 mg / d) and oral micronized progesterone (100 mg / d, at bedtime) du
ring 25 days per month (or 21 d / 28). The few women (3) who wished re
gular bleeding were given progesterone (300 mg / d) with estradiol (3
mg / d), from the 16th to the 25th of the month. No hyperplasia was ob
served among the endometrial biopsies performed after 6 months minimum
of treatment. 8 % of the endometria were partially secretory, 4 %were
sub-atrophic, 23 % were mildly active with rare mitoses and 61 % were
quiescent without mitoses. The remaining 4 % were considered inadequa
te. Mitotic activity of the glands was minimal in all samplings (mean
< 0,53 / 1 000 cells). The average thickness of the mucosa was measure
d by ultrasonography at 3,9 mm, in the cases of insufficient samplings
. No bleeding (or spotting, or cyclic bleeding) occurred in 73,3 % and
80,9 % of the cycles, in the 3rd and 6th month of therapy. Therefore
a low dose of oral Pg (100 mg / d) combined with E(2) during 25 days /
month efficiently controls endometrial proliferation, while allowing
a very weak cyclic activity. This situation makes it possible to minim
ize spottings and to maintain an amenorrhea in the majority of patient
s, thus letting us hoping for an improvement in the observance of this
simplified therapy