Recommendations for the management of GnRH-ant for ovarian stimulation in the assistant reproductive process: Benefits and harms for different ovarian response population

Rong Li, Rui Yang, Junhao Yan, Yang Song, Yunxia Cao, Zijiang Chen, Chenchen Xu, Zhan Zhao, Yichun Guan, Fei Gong, Guimin Hao, Hefeng Huang, Li Jin, Fenghua Liu, Jiayin Liu, Xiaoyan Liang, Xiaolin La, Yun Sun, Xiaohong Wang, Yanwen Xu, Cuilian Zhang, Jie Qiao
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Abstract

Introduction: Gonadotropin-releasing hormone antagonists (GnRH-ant) are commonly used during controlled ovarian stimulation (COS) in the in vitro fertilization (IVF) process to prevent premature luteinization and to ensure follicles mature synchronously. The 2020 guideline from European Society of Human Reproduction and Embryology (ESHRE) recommends the use of GnRH-ant for patients with varying levels of ovarian response. However, the question of how to manage the protocol pathway for these patients requires further investigation.

Methods: The current clinical practice guideline (CPG) adheres to the World Health Organization's (WHO) recommended development process, and covers eight clinical questions, all focusing on the application of GnRH antagonists in COS. We conducted Cochrane-standard systematic reviews, utilized GRADE for evidence certainty assessment, and employed GRADE Evidence-to-Decision Framework to derive recommendations. We pre-defined clinically important outcomes, and the common critical outcomes shared by all clinical questions as follows: live birth rate, implantation rate, clinical pregnancy rate, and moderate to severe ovarian hyperstimulation syndrome (OHSS). We strictly followed the RIGHT guideline and AGREE-II criteria throughout the CPG development.

Recommendations: The guideline development group (GDG) agreed on 14 recommendations on the application of GnRH-ant during COS. In summary, low certainty of evidence supported the benefits of using GnRH-ant protocol in IVF patients with high ovarian response (HOR), following with very low certainty of evidence to use Oral Contraceptive Pill (OCP) or estrogen as pretreatment in normal ovarian response (NOR) patients, low certainty of evidence to use fixed GnRH-ant protocol and very low certainty of evidence to use GnRH agonist (GnRH-a) add on trigger. For patients using GnRH-ant protocol, very low certainty of evidence in HOR patients and low certainty of evidence in NOR patients supported the “freeze-all” strategy considering the potential risk associated with fresh embryo transfer. However, multiple fresh embryo transfer may still provide benefits in some cases.

在辅助生殖过程中使用GnRH-ant刺激卵巢的建议:对不同卵巢反应人群的利与弊
简介:促性腺激素释放激素拮抗剂(Gonadotropin-releasing hormone antagonists, GnRH-ant)是体外受精(IVF)过程中控制性卵巢刺激(COS)中常用的药物,用于防止黄体素过早生成和确保卵泡同步成熟。欧洲人类生殖与胚胎学会(ESHRE)的2020年指南建议对卵巢反应水平不同的患者使用GnRH-ant。然而,如何管理这些患者的方案途径的问题需要进一步研究。方法:现行临床实践指南(CPG)遵循世界卫生组织(WHO)推荐的制定流程,涵盖8个临床问题,重点关注GnRH拮抗剂在COS中的应用。我们进行了cochrane标准的系统评价,使用GRADE进行证据确定性评估,并使用GRADE证据到决策框架得出建议。我们预先定义了临床重要结局和所有临床问题共有的常见关键结局:活产率、着床率、临床妊娠率和中度至重度卵巢过度刺激综合征(OHSS)。在整个CPG开发过程中,我们严格遵循了RIGHT指南和AGREE-II标准。建议:指南制定小组(GDG)就COS期间GnRH-ant的应用达成了14项建议。总之,低确定性的证据支持在卵巢高反应(HOR)的IVF患者中使用GnRH-ant方案的益处,在正常卵巢反应(NOR)患者中使用口服避孕药(OCP)或雌激素作为预处理的证据非常低确定性,使用固定GnRH-ant方案的证据很低确定性,以及使用GnRH激动剂(GnRH-a)添加触发的证据非常低确定性。对于使用GnRH-ant方案的患者,考虑到与新鲜胚胎移植相关的潜在风险,HOR患者的证据确定性非常低,NOR患者的证据确定性也很低,支持“冷冻全部”策略。然而,在某些情况下,多个新鲜胚胎移植仍然可能提供益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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