Impact of pre-treatment in GnRH-antagonist cycles triggered with GnRH agonist on reproductive outcomes

被引:0
|
作者
Zivi, Einat [1 ,2 ]
Eldar-Geva, Talia [1 ]
Rubinstein, Esther [1 ]
Dekel, Nava [1 ]
Schonberger, Oshrat [1 ]
Ben-Ami, Ido [1 ]
机构
[1] Hebrew Univ Jerusalem, Dept Obstet & Gynecol, IVF & infertil Unit,Sch Med, Hadassah Sch Med,Shaare Zedek Med Ctr, Jerusalem, Israel
[2] Shaare Zedek Med Ctr, IVF & Infertil Unit, Jerusalem, Israel
来源
关键词
pre-treatment; GnRH-agonist; hormonal contraception; maturation response; pituitary suppression; IN-VITRO FERTILIZATION; FINAL OOCYTE MATURATION; EMPTY FOLLICLE SYNDROME; POOR RESPONDERS; OVARIAN HYPERSTIMULATION; PROTOCOL; STIMULATION; CESSATION; DURATION; FRESH;
D O I
10.5935/1518-0557.20230022
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Pre-treatment (PT) therapies in IVF are known to be used as pre -stimulation modality to improve cycle outcomes. This study aims to assess whether PT in GnRH antagonist cycles triggered with GnRH-agonist impact oocyte maturation response. Methods: Data were retrospectively collected for patients who underwent GnRH antagonist cycle with agonist triggering with and without PT. The patients were allocated to groups according to their PT status. The primary outcome evaluated was suboptimal maturation response. Suboptimal maturation to trigger was defined as no oocyte upon retrieval when adequate response was expected. Results: The study population included 196 patients who underwent GnRH antagonist cycle with agonist triggering. The study group included 69 patients who received PT. The control group included 127 patients with no PT. In univariate analysis, the PT group significantly displayed suboptimal response compared to the controls ( p = 0.008). All the patients in the study group with suboptimal response (with or without hCG re -triggering) were treated with GnRH-agonist as PT. Basal and pretrigger LH values were significantly lower in the study group compared to controls ( p < 0.001). Multivariate regression analysis revealed that PT with GnRH agonist was a significant predictor for suboptimal response. Conclusions: Pre-treatment, and particularly the use of GnRH-agonist as PT in antagonist cycles triggered with agonist, increases the risk of suboptimal response to GnRH-agonist trigger. This might be explained by prolonged pituitary suppression, which lasts beyond the PT cessation.
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页码:2 / 8
页数:7
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