Microdose Flare-up Gonadotropin-releasing Hormone (GnRH) Agonist Protocol and GnRH Antagonist Protocol: Effects on In-vitro Fertilization in Patients with Poor-responder Diagnosis According to Bologna Criteria

Gökşen Görgülü, Merve Çakır Köle, O. Aldemir, E. Köle, S. Dilbaz
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Abstract

Objective: The aim of the study was to evaluate microdose flare-up Gonadotropin-Releasing Hormone (GnRH) agonist protocol and GnRH antagonist protocol with respect to their effects on in-vitro fertilization (IVF) results in patients with poor ovarian response according to the Bologna Criteria. Material Methods: This was a retrospective cohort study conducted in the Assisted Reproduction clinic of University of Health Sciences, Etlik Zübeyde Hanım Gynaecology Training and Research Hospital. A total of 645 patients who had been diagnosed as poor responders in our clinic, between 2007 and 2018, and received treatment with either microdose flare-up GnRH agonist protocol (n=250, 38.8%) or GnRH antagonist protocol (n=395, 61.2%), were included in the study. Results: The mean age of the study group was 34.5±5.5 years. Comparisons showed that IVF cycle cancellation frequency (p<0.01), third day estradiol level (p=0.04) and third day follicle stimulating hormone level (p<0.01) were significantly greater in patients who underwent the microdose flare-up protocol. In the GnRH antagonist group, the number of surviving children (p=0.01), antral follicle count (p<0.01), follicle count on day of human chorionic gonadotropin (hCG) administration (p<0.01), endometrial thickness on hCG day (p<0.01), number of oocytes collected (p<0.01), mature oocyte count (p<0.01), embryo transfer number (p<0.01) were higher compared to the microdose flare-up protocol group. The two groups were similar in terms of clinical pregnancy rate. Conclusions: In terms of clinical pregnancy rate, the IVF results of microdose flare-up and GnRH antagonist protocols are similar. Further studies are needed to reach more comprehensive results on the subject.
微剂量促性腺激素释放激素(GnRH)激动剂方案和GnRH拮抗剂方案:根据博洛尼亚标准诊断为不良反应的患者对体外受精的影响
目的:本研究的目的是根据博洛尼亚标准评估微剂量促性腺激素释放激素(GnRH)激动剂方案和GnRH拮抗剂方案对卵巢反应差的患者体外受精(IVF)结果的影响。材料方法:本研究是一项回顾性队列研究,在健康科学大学辅助生殖诊所进行,Etlik z beyde Hanım妇科培训与研究医院。在2007年至2018年期间,共有645名患者在我们的诊所被诊断为不良反应,并接受了微剂量突发GnRH激动剂方案(n=250, 38.8%)或GnRH拮抗剂方案(n=395, 61.2%)的治疗。结果:研究组患者平均年龄34.5±5.5岁。比较发现,接受微剂量发作方案的患者体外受精周期取消频率(p<0.01)、第3天雌二醇水平(p=0.04)和第3天促卵泡激素水平(p<0.01)显著高于接受微剂量发作方案的患者。GnRH拮抗剂组患儿存活数(p=0.01)、窦卵泡计数(p<0.01)、人绒毛膜促性腺激素(hCG)给药第1天卵泡计数(p<0.01)、hCG第1天子宫内膜厚度(p<0.01)、收集卵母细胞数(p<0.01)、成熟卵母细胞计数(p<0.01)、胚胎移植数(p<0.01)均高于微剂量启动方案组。两组临床妊娠率相近。结论:在临床妊娠率方面,微剂量急性发作与GnRH拮抗剂方案的IVF结果相似。需要进一步的研究才能在这个问题上取得更全面的结果。
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