Infertility and IVF Unit, Department of Obstetrics and Gynecology, Chaim Sheba Medical Center, Tel Hashomer, Affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv, Israel.
Front Endocrinol (Lausanne). 2020 May 22;11:182. doi: 10.3389/fendo.2020.00182. eCollection 2020.
To examine whether the Stop GnRH-agonist combined with multiple-dose GnRH-antagonist protocol may improve conventional IVF/intracytoplasmic sperm injection (ICSI) cycle in poor ovarian response (POR) patients. Cohort historical, proof of concept study. Tertiary, University affiliated Medical Center. Thirty POR patients, defined according to the Bologna criteria, who underwent a subsequent Stop GnRH-agonist combined with multiple-dose GnRH-antagonist controlled ovarian hyperstimulation (COH) protocol, within 3 months of the previous failed conventional IVF/ICSI cycle, were included. For the purposes of this study, we eliminated a bias in this selection by including only "genuine" poor responder patients, defined as those who yielded up to 3 oocytes following COH with a minimal gonadotropin daily dose of 300 IU. Number of oocytes retrieved, number of top-quality embryos, COH variables. The Stop GnRH-agonist combined with multiple-dose GnRH-antagonist COH protocol revealed significantly higher numbers of follicles >13 mm on the day of hCG administration, higher numbers of oocytes retrieved, and top-quality embryos (TQE) with an acceptable clinical pregnancy rate (16.6%). Moreover, as expected, patients undergoing the Stop GnRH-agonist combined with multiple-dose GnRH-antagonist COH protocol required significantly higher doses and a longer duration of gonadotropins stimulation. The combined Stop GnRH-ag/GnRH-ant COH protocol is a valuable tool in the armamentarium for treating "genuine" poor ovarian responders. Further, large prospective studies are needed to elucidate its role in POR and to characterize the appropriate patients subgroup (before initiating ovarian stimulation) that may benefit from the combined Stop GnRH-ag/GnRH-ant COH protocol.
探讨促性腺激素释放激素激动剂(GnRH-a)停药联合多次应用促性腺激素释放激素拮抗剂(GnRH-ant)方案是否可以改善卵巢低反应(POR)患者的常规体外受精/卵胞浆内单精子注射(ICSI)周期。 队列历史对照研究。 三级大学附属医院。 30 例 POR 患者,根据博洛尼亚标准定义,在先前常规 IVF/ICSI 周期失败后 3 个月内接受 GnRH-a 停药联合多次 GnRH-ant 拮抗剂控制性卵巢刺激(COH)方案。为了消除这种选择偏倚,我们仅纳入“真正”的 POR 患者,即那些在 COH 中给予最小剂量 300IU 促性腺激素后仅获得 3 个卵母细胞的患者。 获卵数、优质胚胎数、COH 变量。 GnRH-a 停药联合多次 GnRH-ant 拮抗剂 COH 方案显示 hCG 给药日≥13mm 的卵泡数明显增多,获卵数和优质胚胎(TQE)明显增多,可接受的临床妊娠率(16.6%)也较高。而且,正如预期的那样,接受 GnRH-a 停药联合多次 GnRH-ant 拮抗剂 COH 方案的患者需要更高剂量和更长时间的促性腺激素刺激。 GnRH-a 联合 GnRH-ant COH 方案是治疗“真正”POR 患者的有效工具。此外,需要进行大型前瞻性研究来阐明其在 POR 中的作用,并确定可能受益于 GnRH-a 联合 GnRH-ant COH 方案的合适患者亚组(在开始卵巢刺激前)的特征。