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来曲唑与枸橼酸氯米芬联合促性腺激素在宫腔内人工授精周期中的应用:一项初步研究。

Use of letrozole versus clomiphene citrate combined with gonadotropins in intrauterine insemination cycles: a pilot study.

作者信息

Jee Byung Chul, Ku Seung Yup, Suh Chang Suk, Kim Ki Chul, Lee Won Don, Kim Seok Hyun

机构信息

Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.

出版信息

Fertil Steril. 2006 Jun;85(6):1774-7. doi: 10.1016/j.fertnstert.2006.02.070. Epub 2006 May 4.

Abstract

OBJECTIVE

To compare the clinical outcomes between letrozole and clomiphene citrate (CC) in gonadotropin-combined intrauterine insemination (IUI) cycles.

DESIGN

Prospective pilot study.

SETTING

One university hospital and two private infertility clinics.

PATIENT(S): Ninety-three infertile couples eligible for superovulation and IUI.

INTERVENTION(S): A letrozole dose of 2.5 mg/day (n = 66) or a CC dose of 100 mg/day (n = 27) was given on day 3-7 of the menstrual cycle, combined with human menopausal gonadotropin (hMG) at a dose 150 IU every other day starting on day 5.

MAIN OUTCOME MEASURE(S): The number of mature follicles, serum estradiol (E2) and progesterone (P) levels, endometrial thicknesses on the day of human chorionic gonadotropin (hCG), and clinical pregnancy rates.

RESULT(S): The patients' clinical characteristics were comparable between the two groups. The number of mature follicles (3.2 +/- 1.7 vs. 5.6 +/- 2.4) and serum E2 levels on the day of hCG (231.0 +/- 179.8 vs. 1,371.7 +/- 750.5 pg/mL) were significantly lower in the letrozole group. No significant differences were found in endometrial thickness measured on the day of hCG or clinical pregnancy rates (18.2% vs. 25.9%). The rate of patients with serum P levels > 1.0 ng/mL on the day of hCG was significantly lower in the letrozole group (4.5% vs. 25.9%).

CONCLUSION(S): Letrozole produced a comparable pregnancy rate vs. CC in gonadotropin-combined IUI cycles. Our results should be confirmed in larger populations with proper randomization.

摘要

目的

比较来曲唑与枸橼酸氯米芬(CC)在促性腺激素联合宫腔内人工授精(IUI)周期中的临床结局。

设计

前瞻性试验研究。

地点

一家大学医院和两家私立不孕不育诊所。

患者

93对符合超排卵和IUI条件的不孕夫妇。

干预措施

在月经周期第3 - 7天给予来曲唑剂量为2.5 mg/天(n = 66)或CC剂量为100 mg/天(n = 27),从第5天开始每隔一天联合给予人绝经期促性腺激素(hMG),剂量为150 IU。

主要观察指标

成熟卵泡数量、血清雌二醇(E2)和孕酮(P)水平、人绒毛膜促性腺激素(hCG)日的子宫内膜厚度以及临床妊娠率。

结果

两组患者的临床特征具有可比性。来曲唑组的成熟卵泡数量(3.2±1.7 vs. 5.6±2.4)和hCG日的血清E2水平(231.0±179.8 vs. 1371.7±750.5 pg/mL)显著较低。hCG日测量的子宫内膜厚度或临床妊娠率(18.2% vs. 25.9%)未发现显著差异。来曲唑组hCG日血清P水平>1.0 ng/mL的患者比例显著较低(4.5% vs. 25.9%)。

结论

在促性腺激素联合IUI周期中,来曲唑产生的妊娠率与CC相当。我们的结果应在更大规模且适当随机分组的人群中得到证实。

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