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Volume 92, Issue 3, Pages 907-912 (September 2009)


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Comparison of low-dose human menopausal gonadotropin and micronized 17β-estradiol supplementation in in vitro maturation cycles with thin endometrial lining

Shai E. Elizur, M.D.Corresponding Author Informationemail address, Weon-Young Son, Ph.D., Raymond Yap, Yariv Gidoni, M.D., Dan Levin, M.D., Ezgi Demirtas, M.D., Seang-Lin Tan, M.D., M.B.A.

Received 5 May 2008; received in revised form 8 July 2008; accepted 15 July 2008. published online 30 October 2008.

Objective

A challenge of in vitro maturation (IVM) treatment in some women is insufficient development of the endometrium prior to embryo transfer.

Design

Retrospective study.

Setting

McGill Reproductive Center, Montreal, Canada.

Patient(s)

Women with endometrial thickness <6 mm on days 6–10 ultrasound (US) scan of IVM treatment.

Intervention(s)

In the human menopausal gonadotropin (hMG) group, 150 IU/day of hMG was started and in the estradiol group, 6 to 12 mg/day of micronized 17β-estradiol was initiated. Additional US scans were performed 2 to 3 days apart, until endometrial thickness reached ≥8 mm or a dominant follicle (>10 mm) was identified.

Main Outcome Measure(s)

Endometrial lining before oocyte retrival.

Result(s)

In both groups endometrial lining significantly thickened following treatment. However, hMG treatment resulted in a higher number of follicles ≥7 mm compared to estradiol (7.4 ± 4.8 vs. 3.4 ± 2.5, respectively) and a significantly higher percentage of mature oocytes that were identified on the day of oocyte retrieval (in vivo matured oocytes) (15.1% vs. 10.5%).

Conclusion(s)

In IVM designated cycles with a thin endometrium both low-dose hMG and micronized 17β-estradiol supplementation significantly improve endometrial thickness. However, low-dose hMG results in larger follicles and a greater number of in vivo matured oocytes.

Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, McGill Reproductive Center, McGill University Health Center, Montreal, Quebec, Canada

Corresponding Author InformationReprint requests: Shai E. Elizur, M.D., Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, McGill University, Montreal, Quebec, Canada. H3A 1A1 (FAX: 514-843-1496).

 S.E.E. has nothing to disclose. W.-Y.S. has nothing to disclose. R.Y. has nothing to disclose. Y.G. has nothing to disclose. D.L. has nothings to disclose. E.D. has nothing to disclose. S.-L-T. has nothing to disclose.

PII: S0015-0282(08)03270-6

doi:10.1016/j.fertnstert.2008.07.1750


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