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Pilot study of the optimal protocol of low dose step-up follicle stimulating hormone therapy for infertile women

机译:低剂量升压卵泡刺激激素治疗促进妇女的试验研究

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Purpose: To evaluate the optimized protocol of low dose follicle-stimulating hormone (FSH) therapy that has a starting dose of 50 IU/62.5 IU with a small increment dose (12.5 IU) for women with World Health Organization (WHO) II ovulatory disorder and unexplained infertility. Methods: Anovulatory women with WHO group II ovulatory disorder (ovulation induction [O1] patients, n = 29), and with an unexplained infertility (ovarian stimulation [OS] patients, n = 21) were enrolled. The protocol of low dose step-up FSH therapy was optimized for the starting dose as 50 IU (body mass index [BMI] < 20 group) and 62.5 IU (BMI ≥ 20 group) with the increment dose of 12.5 IU. Study outcomes were ovulation, monofollicular development and other variables. Results: In the Olpatients, the ovulation rate was 100% (BMI < 20 group) and 90.9% (BMI ≥ 20 group). Monofollicular development was 80.0% (BMI < 20) and 77.3% (BMI ≥ 20). The pregnancy rate was 60% (3/5 BMI < 20) and 18.2% (4/22 BMI ≥ 20). There was no multiple pregnancy. In the OSpatients, the ovulation rate was 100%. Monofollicular development was 85.7% (BMI < 20) and 76.6% (BMI ≥ 20). No pregnancy was achieved in the OSpatients. Conclusion: Optimized protocol of low dose FSH therapy setting a starting dose 50 IU/62.5 IU by BMI with an increment dose of 12.5 IU was safe and highly effective in WHO group II anovulatory patients. However, this protocol seemed uneffective for patients with unexplained infertility.
机译:目的:评估低剂量卵泡刺激激素(FSH)治疗的优化方案,其具有50 IU / 62.5 IU的起始剂量,用于世界卫生组织(WHO)II排卵障碍的妇女和无法解释的不孕症。方法:患有世卫组织II族排卵障碍(排卵诱导患者,N = 29)和未解释的不孕症(卵巢刺激[OS]患者,N = 21)的逆转录妇女。优化低剂量升压FSH治疗的方案针对50IU(体重指数[BMI] <20组)和62.5IU(BMI≥20组)的起始剂量进行了优化,增量剂量为12.5 IU。研究结果是排卵,单褶皱的发育和其他变量。结果:在奥尔氏菌,排卵率为100%(BMI <20组)和90.9%(BMI≥20组)。单褶皱的发育是80.0%(BMI <20)和77.3%(BMI≥20)。妊娠率为60%(3/5 bmi <20)和18.2%(4/22bmi≥20)。没有多次怀孕。在osatives中,排卵率为100%。单褶皱的发育为85.7%(BMI <20)和76.6%(BMI≥20)。 oSpatorient中没有妊娠。结论:低剂量FSH治疗的优化方案设定BMI的起始剂量50 IU / 62.5 IU,增量剂量为12.5 IU,在II组无助性患者中是安全且高效的。然而,该协议对于具有无法苛刻的不孕症的患者似乎是不利的。

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