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首页> 外文期刊>Archives of gynecology and obstetrics. >Comparison of multiple dose GnRH antagonist and minidose long agonist protocols in poor responders undergoing in vitro fertilization: a randomized controlled trial.
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Comparison of multiple dose GnRH antagonist and minidose long agonist protocols in poor responders undergoing in vitro fertilization: a randomized controlled trial.

机译:在接受体外受精的不良反应者中,多剂量GnRH拮抗剂和小剂量长效激动剂方案的比较:一项随机对照试验。

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摘要

OBJECTIVE: To investigate the efficacy of gonadotropin releasing hormone antagonist (GnRH) in poor responders undergoing in vitro fertilization. STUDY DESIGN: Ninety-six patients with poor ovarian response in previous treatment cycles were prospectively randomized into two groups. Forty-four patients were stimulated with GnRH antagonist multidose protocol and 45 patients received a standard long agonist protocol. Ovarian response was evaluated by transvaginal ultrasound and hormonal parameters. Cycle characteristics and treatment outcomes were statistically compared between groups. RESULTS: There was significantly reduced duration of stimulation and consumption of gonadotrophins in the antagonist group when compared to the agonist group. The estradiol concentrations on the day of human chorionic gonadotropin (hCG) injection, the number of oocytes retrieved, and the number of embryos transferred were similar for both groups. In the antagonist group, eight (18.1%) ongoing pregnancies were achieved and inthe agonist group, ten (22.2%) clinical pregnancies were achieved but the difference was not statistically significant. CONCLUSION: The present study was not powered to detect clinically relevant differences between two protocols in outcomes such as pregnancy rate, with confidence.
机译:目的:探讨促性腺激素释放激素拮抗剂(GnRH)在体外受精中的不良反应。研究设计:将先前治疗周期中的96位卵巢反应不良的患者前瞻性随机分为两组。 GnRH拮抗剂多剂量方案刺激了44名患者,而45名患者接受了标准的长效激动剂方案。通过经阴道超声和激素参数评估卵巢反应。两组之间的周期特征和治疗结果进行了统计学比较。结果:与激动剂组相比,拮抗剂组的促性腺激素的刺激和消耗的持续时间显着减少。两组人在注射绒毛膜促性腺激素(hCG)当天的雌二醇浓度,回收的卵母细胞数量和转移的胚胎数量相似。在拮抗剂组中,进行了八次(18.1%)的妊娠,而在激动剂组中,进行了十次(22.2%)的临床妊娠,但差异无统计学意义。结论:本研究没有能力可靠地检测出两种方案在诸如妊娠率等结局方面的临床相关差异。

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