W. Hanggi et al., COMPARISON OF TRANSVAGINAL ULTRASONOGRAPHY AND ENDOMETRIAL BIOPSY IN ENDOMETRIAL SURVEILLANCE IN POSTMENOPAUSAL HRT USERS, Maturitas, 27(2), 1997, pp. 133-143
Objectives: To compare transvaginal ultrasonography with histological
findings in endometrial evaluation of postmenopausal women using hormo
ne replacement therapy and to evaluate endometrial safety of three hor
mone replacement therapy regimens. Methods: in a randomized, comparati
ve study in postmenopausal women, endometrial safety was evaluated usi
ng (1) no hormone replacement therapy, (2) oral micronized 17 beta-est
radiol/oral sequential dydrogesterone, (3) transdermal 17 beta-estradi
ol/oral sequential dydrogesterone, or (4) oral tibolone, 85 Non-hyster
ectomised subjects underwent transvaginal ultrasonography immediately
before Pipelle biopsy at baseline and subsequently after 12 and 24 mon
ths. Endometrial thickness and uterine dimensions were determined by t
ransvaginal ultrasonography and endometrial thickness (double-layer) w
as compared with biopsy results. Results: Endometrial evaluation was c
onveniently performed by transvaginal ultrasonography, and endometrial
thickness correlated well with biopsy findings, If endometrial thickn
ess was < 5 mm, the endometrial biopsy sample was either inactive/atro
phic or insufficient for histopathological diagnosis. Hyperplastic or
malignant changes were not reported. After 24 months, endometrial thic
kness was increased both in the oral (P < 0.001) and transdermal (P <
0.001) 17 beta-estradiol/dydrogesterone groups, whereas with tibolone
the change in endometrial thickness was not different from controls. C
onclusion: transvaginal ultrasonography of the endometrium reliably pr
edicts the histological picture in hormone replacement therapy users.
Using 5 mm endometrial thickness as cut-off point, more than 75% of bi
opsies could be avoided. All three hormone replacement therapies were
safe with respect to the endometrium. With sequential 17 beta-estradio
l/dydrogesterone the expected progestogen-induced secretory pattern wa
s observed, whereas endometrial histology under tibolone closely mimic
ked the natural atrophic postmenopausal state. (C) 1997 Elsevier Scien
ce Ireland Ltd.