Division of Obstetrics and Gynaecology, Department of Human Reproduction, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Department of Gynaecology and Obstetrics, Ptuj General Hospital, Ptuj, Slovenia.
Front Endocrinol (Lausanne). 2022 Apr 6;13:826411. doi: 10.3389/fendo.2022.826411. eCollection 2022.
While triggering oocyte maturation with GnRH agonist (GnRHa) seems to be safe and effective in terms of the risk of developing OHSS and the number of metaphase II oocytes, it nevertheless results in luteal phase deficiency. To date, strategies have been developed in order to rescue defective luteal phase of GnRHa triggered cycles. Our study aimed to assess the reproductive outcome of GnRHa triggered cycles combined with modified luteal support (1500 IU hCG at the day of oocyte retrieval) in women with high ovarian response and to compare the outcome with hCG triggered cycles in GnRH antagonist IVF-ICSI procedures. A retrospective cohort database review of the results of GnRH antagonist IVF-ICSI cycles was conducted at a tertiary-care IVF center in Ljubljana, Slovenia. A total of 6126 cycles, performed from January 1, 2014, to December 31, 2020, were included in the final analysis. Final oocyte maturation was performed with either 5000, 6500, or 10,000 IU hCG (women with normal ovarian response) or 0.6 mg GnRHa (buserelin), supplemented with 1500 IU hCG on the day of oocyte retrieval (in women with high ovarian response). In cases of excessive ovarian response and/or high risk of OHSS luteal support was not introduced and all good quality blastocysts were frozen. According to significant differences in patients' age and the number of oocytes in the two groups, matching by age and number of oocytes was performed. No significant differences were observed regarding pregnancy rate per embryo transfer, rate of early pregnancy loss, and livebirth rate per pregnancy between the GnRHa and hCG trigger groups, respectively. A significant difference in the number of developed embryos and blastocysts, as well as the number of frozen blastocysts, was seen in favor of the GnRHa trigger. However, the birth weight in the GnRHa trigger group was significantly lower.
The results of our study support the use of GnRHa for final oocyte maturation in GnRH antagonist IVF cycles in women with high ovarian response. Luteal phase rescue was performed by co-administration of 1500 IU hCG on the day of oocyte retrieval and estradiol and progesterone supplementation. In our experience, such an approach results in a comparable reproductive outcome with hCG trigger group.
评估 GnRH 拮抗剂 IVF-ICSI 中高卵巢反应患者使用 GnRH 激动剂(GnRHa)触发卵子成熟并联合改良黄体支持(取卵日给予 1500 IU hCG)的治疗结局,并与 hCG 触发周期进行比较。
这是斯洛文尼亚卢布尔雅那的一家三级试管婴儿中心回顾性队列数据库研究。纳入 2014 年 1 月 1 日至 2020 年 12 月 31 日进行的 GnRH 拮抗剂 IVF-ICSI 周期,最终分析纳入 6126 个周期。正常卵巢反应者(n=4877)最终卵母细胞成熟采用 5000、6500 或 10000 IU hCG,高卵巢反应者(n=1249)采用 0.6 mg GnRHa(布舍瑞林)加取卵日 1500 IU hCG。如果发生卵巢过度刺激和/或发生 OHSS 的风险高,则不给予黄体支持,所有优质囊胚均被冷冻。根据两组患者年龄和获卵数的显著差异,进行了年龄和获卵数的匹配。
GnRHa 触发组和 hCG 触发组之间,胚胎移植妊娠率、早期妊娠丢失率和活产率无显著差异。GnRHa 触发组胚胎和囊胚的发育数量以及冷冻囊胚数量均显著增加,但 GnRHa 触发组的出生体重显著降低。
本研究结果支持在高卵巢反应患者的 GnRH 拮抗剂 IVF 周期中使用 GnRHa 进行最终卵母细胞成熟。取卵日给予 1500 IU hCG 并联合雌二醇和孕酮补充进行黄体期补救。根据我们的经验,这种方法与 hCG 触发组的生殖结局相当。