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GnRH Agonist-only Trigger, Compared to Dual Trigger, Reduces Oocyte Retrieval Rate in High Responders Without Affecting Cumulative Live Birth Rate

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Specialty Endocrinology
Date 2024 Sep 4
PMID 39229374
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Abstract

Introduction: This study compared, in high responders undergoing IVF treatment, GnRH agonist-only trigger and dual trigger on oocyte retrieval rate and cumulative live birth rate (LBR). The aim was to determine if the GnRH agonist-only triggers had provided outcomes comparable to dual trigger, while minimizing the risk of ovarian hyperstimulation syndrome (OHSS).

Materials And Methods: A retrospective, matched case-control study was conducted at Taichung Veterans General Hospital, Taiwan, including women who underwent IVF/ICSI between January 1, 2014, and December 31, 2022. Inclusion criteria were: GnRH antagonist protocol and estrogen level >3,000 pg/ml on trigger day. Exclusion criteria were: immune/metabolic diseases, donated oocytes, and mixed stimulation cycles. Propensity score matching was applied to balance age, AMH level, and oocyte number between the GnRH agonist-only and dual trigger groups. Outcomes were analyzed for patients who had complete treatment cycles, focusing on oocyte retrieval rate and cumulative LBR.

Results: We analyzed 116 cycles in the agonist-only group, and 232 cycles in the dual trigger group. No inter-group difference was found in their age, BMI, and AMH levels. The dual trigger group had a higher oocyte retrieval rate (93% vs. 80%; p <0.05), while fertilization rates, blastocyst formation rates, and cumulative LBR were comparable. Notably, no OHSS cases had been reported in the GnRH agonist-only group, compared with 7 cases in the dual trigger group.

Conclusion: GnRH agonist-only triggers resulted in a lower oocyte retrieval rate compared to dual triggers but did not significantly affect cumulative LBR in high responders. This approach effectively reduces OHSS risk without compromising pregnancy outcomes, making it a preferable option in freeze-all strategies, despite a longer oocyte pick-up duration and a medium cost. GnRH agonist-only trigger, however, may not be suitable for fresh embryo transfers or patients with low serum LH levels on trigger day.

References
1.
Humaidan P, Alsbjerg B . GnRHa trigger for final oocyte maturation: is HCG trigger history?. Reprod Biomed Online. 2014; 29(3):274-80. DOI: 10.1016/j.rbmo.2014.05.008. View

2.
Zelinski-Wooten M, Hutchison J, Hess D, Wolf D, Stouffer R . Follicle stimulating hormone alone supports follicle growth and oocyte development in gonadotrophin-releasing hormone antagonist-treated monkeys. Hum Reprod. 1995; 10(7):1658-66. DOI: 10.1093/oxfordjournals.humrep.a136151. View

3.
Jones B, Al-Chami A, Gonzalez X, Arshad F, Green J, Bracewell-Milnes T . Is oocyte maturity influenced by ovulation trigger type in oocyte donation cycles?. Hum Fertil (Camb). 2019; 24(5):360-366. DOI: 10.1080/14647273.2019.1671614. View

4.
Alvarez C, Marti-Bonmati L, Novella-Maestre E, Sanz R, Gomez R, Fernandez-Sanchez M . Dopamine agonist cabergoline reduces hemoconcentration and ascites in hyperstimulated women undergoing assisted reproduction. J Clin Endocrinol Metab. 2007; 92(8):2931-7. DOI: 10.1210/jc.2007-0409. View

5.
Castillo J, Humaidan P, Bernabeu R . Pharmaceutical options for triggering of final oocyte maturation in ART. Biomed Res Int. 2014; 2014:580171. PMC: 4123594. DOI: 10.1155/2014/580171. View