Letrozole versus Clomiphene Citrate for Induction of Ovulation in Patients with Polycystic Ovarian Syndrome Undergoing Intrauterine Insemination.

Sherif F Hendawy, Hanan E Samaha, Mohamed F Elkholy
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引用次数: 26

Abstract

Background: Polycystic ovary syndrome (PCOS) is one of the most common endocrinopathies affecting women in the reproductive age group, and is one of the most common causes of hyperandrogenic anovulatory infertility. The aromatase inhibitor, letrozole, has been used for induction of ovulation. The purpose of this study was to compare the effects of letrozole and clomiphene citrate in induction of ovulation among patients with PCOS undergoing intrauterine insemination.

Methods: In a double-blind randomized study, 60 infertile patients with PCOS received standard doses of either clomiphene citrate or letrozole as an induction protocol prior to intrauterine insemination. A hormonal profile, pelvic ultrasound, hysterosalpingogram, and/ or laparoscopy were done for all patients. The patients were monitored for ovulation by translational ultrasonographic folliculometry, with measurement of number and size of the follicles, as well as endometrial thickness. Human chorionic gonadotrophin (HCG) was injected intramuscularly when at least one mature follicle ≥18 mm diameter was detected, and intrauterine insemination was performed 32-36 hours later. Transvaginal ultrasound and β-HCG measurement were performed for confirmation of pregnancy.

Results: Letrozole and clomiphene citrate achieved follicle maturation within a mean ± standard deviation (SD) of 13.2 ± 1.53 and 14.1 ± 1.35 days, respectively, showing no significant difference (P > 0.05). The mean number of follicles reaching ≥18 mm on the day of HCG administration was significantly higher in patients who received clomiphene citrate (2.9 ± 1.77) than in those receiving letrozole (1.2 ± 0.9). Letrozole had a significantly greater effect than clomiphene citrate on endometrial thickness (9.16 ± 1.36 versus 4.46 ± 1.71). The number of pregnancies achieved in the letrozole group was significantly (P < 0.05) greater than in the clomiphene group.

Conclusion: Letrozole in patients with PCOS is as effective as clomiphene citrate in inducing ovulation, and although the number of follicles produced by induction with letrozole were less than those produced by clomiphene, letrozole had a significantly greater effect on endometrial thickness than clomiphene citrate, and the incidence of pregnancy after intrauterine insemination was significantly higher, with a lower incidence of multiple pregnancy.

Abstract Image

来曲唑与枸橼酸克罗米芬对宫内人工授精多囊卵巢综合征患者的促排卵作用。
背景:多囊卵巢综合征(PCOS)是影响育龄妇女最常见的内分泌疾病之一,也是高雄激素无排卵性不孕的最常见原因之一。芳香化酶抑制剂来曲唑已被用于诱导排卵。本研究的目的是比较来曲唑和枸橼酸克罗米芬对宫内人工授精的多囊卵巢综合征患者的促排卵效果。方法:在一项双盲随机研究中,60名患有多囊卵巢综合征的不孕患者在宫内人工授精前接受标准剂量的枸橼酸克罗米芬或来曲唑作为诱导方案。对所有患者进行激素谱、盆腔超声、子宫输卵管造影和/或腹腔镜检查。通过平移超声卵泡测量术监测患者的排卵情况,测量卵泡的数量和大小,以及子宫内膜厚度。当检测到至少一个成熟卵泡直径≥18 mm时,肌内注射人绒毛膜促性腺激素(HCG), 32-36小时后进行宫内人工授精。经阴道超声及β-HCG测定证实妊娠。结果:来曲唑和枸橼酸克罗米芬实现卵泡成熟的平均±标准偏差(SD)分别为13.2±1.53和14.1±1.35天,差异无统计学意义(P > 0.05)。给药当天卵泡≥18 mm的平均卵泡数,克罗米芬组(2.9±1.77)明显高于来曲唑组(1.2±0.9)。来曲唑对子宫内膜厚度的影响显著大于克罗米芬(9.16±1.36比4.46±1.71)。来曲唑组成功妊娠数显著高于克罗米芬组(P < 0.05)。结论:来曲唑对PCOS患者的诱导排卵效果与枸橼酸克罗米芬相当,虽然来曲唑诱导产生的卵泡数量少于克罗米芬,但来曲唑对子宫内膜厚度的影响明显大于枸橼酸克罗米芬,且宫内人工授精后妊娠发生率明显高于克罗米芬,多胎妊娠发生率较低。
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来源期刊
自引率
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审稿时长
8 weeks
期刊介绍: Clinical Medicine Insights: Reproductive Health is a peer reviewed; open access journal, which covers all aspects of Reproduction: Gynecology, Obstetrics, and Infertility, spanning both male and female issues, from the physical to the psychological and the social, including: sex, contraception, pregnancy, childbirth, and related topics such as social and emotional impacts. It welcomes original research and review articles from across the health sciences. Clinical subjects include fertility and sterility, infertility and assisted reproduction, IVF, fertility preservation despite gonadotoxic chemo- and/or radiotherapy, pregnancy problems, PPD, infections and disease, surgery, diagnosis, menopause, HRT, pelvic floor problems, reproductive cancers and environmental impacts on reproduction, although this list is by no means exhaustive Subjects covered include, but are not limited to: • fertility and sterility, • infertility and ART, • ART/IVF, • fertility preservation despite gonadotoxic chemo- and/or radiotherapy, • pregnancy problems, • Postpartum depression • Infections and disease, • Gyn/Ob surgery, • diagnosis, • Contraception • Premenstrual tension • Gynecologic Oncology • reproductive cancers • environmental impacts on reproduction, • Obstetrics/Gynaecology • Women''s Health • menopause, • HRT, • pelvic floor problems, • Paediatric and adolescent gynaecology • PID
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