多囊卵巢综合征 (PCOS) 妇女的孕激素促排卵 (PPOS) 与灵活 GnRH 拮抗剂方案 (FGnRHan):对大量群体的临床结果和卵巢反应的回顾性分析

Fatma Darwish, Ashraf Elmantwe, Hossam Elbanhawy, Ahmed Abbas, Mohamed El noury, Ahmed Ahmed
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引用次数: 0

摘要

:背景:多囊卵巢综合征(PCOS)女性的卵巢刺激反应(OSR)是一个有争议的问题。目的:评估固定孕激素卵巢刺激(FPPOS)和灵活GnRH拮抗剂方案(FGnRHan)对接受卵胞浆内单精子注射-冷冻胚胎移植(ICSI-FET)的多囊卵巢综合征女性卵巢刺激反应和妊娠结局的影响。患者和方法:对过去5年中在吉萨省阿古扎的利雅得生殖中心(RFC)和贝哈大学医院(BUH)接受ICSI-FET周期治疗的多囊卵巢综合征女性进行回顾性评估。研究结果包括临床妊娠、持续妊娠、活产、受精、早期 LH 激增和其他 OSR 结果。结果:在纳入的 950 名女性中,420 人(研究组)采用了 FPPOS,390 人(对照组)采用了 GnRHan 方案。两组的基线指标相似。成熟和受精的卵母细胞在两组之间没有明显差异(P > 0.5)。两组中都很少出现过早黄体化的情况,差异无统计学意义(P > 0.5)。此外,FGnRHan 组和 FPPOS 组每个冷冻胚胎移植周期(FETC)的临床妊娠率也没有明显差异(P > 0.5)。此外,各组的持续妊娠率、流产率、生化妊娠率和植入率在统计学上也有相似之处(P > 0.05)。虽然 FPPOS 组和 FGnRHan 组以当地货币计算的费用有显著下降(5.8±3.1 vs. 8.8±4.1,P =0.001)。结论:在接受ICSI-FET的多囊卵巢综合症女性患者中,FPPOS方案被证明是一种功能强大、实用、操作简便、经济实惠且在临床上等同于标准FGnRHan方案的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progestin-Primed Ovarian Stimulation (PPOS) Versus Flexible GnRH Antagonist Protocol (FGnRHan) In Women with Polycystic Ovary Syndrome (PCOS): A Retrospective Analysis of Clinical Outcomes and Ovarian Response of a Substantial Cohort
: Background : Ovarian Stimulation Response (OSR) in polycystic ovarian syndrome (PCOS) ladies is controversial issues . Aim: to evaluate outcomes of Fixed Progestin-Primed Ovarian Stimulation (FPPOS) and Flexible GnRH Antagonist Protocol (FGnRHan) on OSR and pregnancy outcomes in PCOS ladies undergone intracytoplasmic sperm injection-frozen embryo transfer (ICSI-FET). Patients and Methods: A retrospective assessment of PCOS ladies undergoing ICSI-FET cycles at Riyadh fertility center, Agouza, Giza Governorate (RFC) and Benha University Hospital (BUH), over the last 5 years. The frequencies of clinical pregnancy, continued pregnancy, live births, fertilization, early LH surge, and other OSR results were the outcomes. Results: of 950 ladies included, 420 had FPPOS (study group) and 390 (control group) had the GnRHan protocol. Both groups' baseline metrics showed similarities. Oocytes that were mature and fertilized showed no discernible difference between the two groups (P > 0.5). Premature luteinization was rare in both groups, and there was no statistically significant difference (P > 0.5). Additionally, there was no discernible difference in the clinical pregnancy rate per frozen embryo transfer cycle (FETC) between the FGnRHan and FPPOS groups (P > 0.5). Also, continuing pregnancy rates, miscarriage rates, biochemical pregnancy rates, and implantation rates, showed statistically similarities across the groups (P > 0.05). Although there was a considerable decrease in cost calculated in local currency (5.8±3.1 vs. 8.8±4.1, p =0.001) between the FPPOS and FGnRHan groups. Conclusion: in PCOS ladies who had ICSI-FET, the FPPOS protocol proves to be a powerful, practical, user-friendly, economical, and clinically equivalent alternative to the standard FGnRHan protocol.
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