在GnRH拮抗剂周期中,GnRH激动剂联合hCG与单独hCG对最终卵母细胞成熟触发的影响。

IF 1.9
Condesmar M de Oliveira, Carlos A M de Oliveira, Larissa L Fonseca, Kelly R R de Souza, Moacir R M Radaelli
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引用次数: 1

摘要

目的:分析促性腺激素释放激素(GnRH)激动剂联合人绒毛膜促性腺激素(hCG)(双重触发)与单独hCG(常规触发)对GnRH拮抗剂周期中最终卵母细胞成熟触发的影响。方法:本前瞻性病例对照研究纳入了2018年2月至2019年8月期间接受自体体外受精治疗的114例患者,无论年龄、不孕因素或周期数。根据触发卵母细胞成熟的方法将患者随机分为两组:A组(n = 48) -仅hCG;B组(66例)- hCG + GnRH激动剂。测量的主要结果是总卵母细胞和中期(MII)卵母细胞的数量。结果:各组在年龄上具有同质性。无中度或重度卵巢过度刺激综合征事件。两组间总卵母细胞数及MII数比较,差异均无统计学意义(p > 0.05)。A组MII/总卵母细胞率为70.9%,B组为74.5% (p = 0.679)。A组2/48例(4.16%)、b组1/66例(1.5%)未检出卵母细胞。A组4/48例(8.3%)、b组2/66例(3%)未检出MII卵母细胞。年龄与总卵母细胞数和检出MII卵母细胞数直接相关(p < 0.05)。结论:在一般人群中,双触发与常规hCH触发在总卵母细胞数量和MII卵母细胞数量方面相当。在选定的妇女群体中,需要进一步的研究来确定双重触发指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

GnRH agonist in association with hCG versus hCG alone for final oocyte maturation triggering in GnRH antagonist cycles.

GnRH agonist in association with hCG versus hCG alone for final oocyte maturation triggering in GnRH antagonist cycles.

GnRH agonist in association with hCG versus hCG alone for final oocyte maturation triggering in GnRH antagonist cycles.

Objective: To analyze gonadotropin-releasing hormone (GnRH) agonist in association with human chorionic gonadotropin (hCG) (dual triggering) versus hCG alone (conventional triggering) for final oocyte maturation triggering in GnRH antagonist cycles in an unselected population of Brazilian women.

Methods: This prospective case-control study involved 114 patients referred to autologous in vitro fertilization treatment between February 2018 and August 2019, recruited regardless of age, infertility factor or number of cycles. The patients were randomly allocated into two groups according to oocyte maturation triggering approach: group A (n = 48) - hCG only; and group B (n = 66) - hCG plus GnRH agonist. The main outcomes measured were the number of total and metaphase II (MII) oocytes retrieved.

Results: The groups were homogenous in terms of age. There were no moderate or severe ovarian hyperstimulation syndrome events. There were no statistical differences concerning total or MII oocytes retrieved between the groups (p > 0.05). The MII/total oocyte rate was 70.9% in group A, and 74.5% in group B (p = 0.679). There was no oocyte retrieved in 2/48 patients (4.16%) in group A, 1/66 (1.5%) in group B. There were no MII oocytes in 4/48 patients (8.3%) in group A, and 2/66 (3%) in group B. Age was directly correlated to the number of total and MII oocytes retrieved (p < 0.05).

Conclusions: Dual triggering was equivalent to conventional hCH triggering in terms of the number of total and MII oocytes retrieved in the general population. Further studies are necessary to ascertain dual triggering indication in selected groups of women.

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