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使用不同触发方法对促性腺激素释放激素激动剂方案卵巢反应正常的女性妊娠结局的比较:一项基于倾向评分匹配的单中心回顾性队列研究

Comparison of pregnancy outcomes in women with normal ovarian response to the gonadotropin-releasing hormone agonist protocol using different trigger methods: a single-center retrospective cohort study based on propensity score matching.

作者信息

Guo Danyang, Pang Conghui, Wang Kehua

机构信息

The First Clinical College, Shandong University of Traditional Chinese Medicine, Jinan, China.

Reproductive and Genetic Center of Integrative Medicine, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.

出版信息

Arch Gynecol Obstet. 2024 May;309(5):2153-2165. doi: 10.1007/s00404-024-07404-6. Epub 2024 Mar 18.

DOI:10.1007/s00404-024-07404-6
PMID:38494512
Abstract

PURPOSE

To investigate whether gonadotropin-releasing hormone agonist (GnRH-a) combined with human chorionic gonadotropin (HCG) can improve pregnancy outcomes in patients with normal ovarian response (NOR).

METHODS

In this retrospective cohort study, data of 404 NOR patients undergoing fresh embryo transfer (ET) from 2018 to 2022 were studied. Patients were divided into HCG group and HCG plus GnRH-a group according to trigger methods. After confounding factors were controlled by propensity score matching, 67 cases were included in HCG group and HCG plus GnRH-a group, respectively, and pregnancy outcomes were assessed. Basal data, ovarian stimulation, embryological data and pregnancy outcomes were compared. The effect of trigger methods on pregnancy outcomes was analyzed by binary logistic regression.

RESULTS

There was no statistically significant differences in embryological data, embryo implantation rate, clinical pregnancy rate, live birth rate of ET, number of fresh embryos transferred and total number of embryos transferred after one cycle of oocyte retrieval. While, cumulative live birth rate (CLBR) was better in the dual-trigger group than in the HCG group. The binary logistic regression analysis indicated that the trigger methods had an independent influence on embryo implantation and cumulative live birth.

CONCLUSIONS

During IVF/ICSI, dual-trigger could potentially play a role in improving oocyte quality, ensuring embryo implantation rate, clinical pregnancy rate, live birth rate of ET and cumulative live birth rate at the end of one ovum pick-up (OPU) cycle, and reducing the physical, temporal and financial negative consequences due to repeated OPU cycle.

摘要

目的

探讨促性腺激素释放激素激动剂(GnRH-a)联合人绒毛膜促性腺激素(HCG)能否改善卵巢反应正常(NOR)患者的妊娠结局。

方法

在这项回顾性队列研究中,研究了2018年至2022年期间404例接受新鲜胚胎移植(ET)的NOR患者的数据。根据扳机方法将患者分为HCG组和HCG加GnRH-a组。通过倾向评分匹配控制混杂因素后,HCG组和HCG加GnRH-a组分别纳入67例患者,并评估妊娠结局。比较基础数据、卵巢刺激、胚胎学数据和妊娠结局。采用二元逻辑回归分析扳机方法对妊娠结局的影响。

结果

在一次取卵周期后的胚胎学数据、胚胎着床率、临床妊娠率、ET活产率、移植新鲜胚胎数和移植胚胎总数方面,两组之间无统计学显著差异。然而,双扳机组的累积活产率(CLBR)优于HCG组。二元逻辑回归分析表明,扳机方法对胚胎着床和累积活产有独立影响。

结论

在体外受精/卵胞浆内单精子注射(IVF/ICSI)过程中,双扳机可能在改善卵母细胞质量、确保胚胎着床率、临床妊娠率、ET活产率和一次取卵(OPU)周期结束时的累积活产率方面发挥作用,并减少因重复OPU周期带来的身体、时间和经济方面的负面影响。

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Reprod Biol Endocrinol. 2022 Sep 24;20(1):144. doi: 10.1186/s12958-022-01017-x.
2
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Hum Reprod. 2022 Jul 30;37(8):1795-1805. doi: 10.1093/humrep/deac114.
3
Dual Trigger with hCG Plus GnRHa for Final Oocyte Maturation in PGT-A Cycles Results in Similar Euploidy Rates when Compared to hCG-Only Trigger.
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Reprod Sci. 2022 Aug;29(8):2265-2271. doi: 10.1007/s43032-022-00954-7. Epub 2022 Apr 27.
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Prediction, assessment, and management of suboptimal GnRH agonist trigger: a systematic review.预测、评估和管理 GnRH 激动剂扳机时机不当:系统评价。
J Assist Reprod Genet. 2022 Feb;39(2):291-303. doi: 10.1007/s10815-021-02359-y. Epub 2022 Mar 19.
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9
Comparative study between single versus dual trigger for poor responders in GnRH-antagonist ICSI cycles: A randomized controlled study.在 GnRH 拮抗剂 ICSI 周期中对反应不良者进行单扳机与双扳机的比较研究:一项随机对照研究。
Int J Gynaecol Obstet. 2021 Mar;152(3):395-400. doi: 10.1002/ijgo.13405. Epub 2020 Oct 22.
10
Dual-trigger improves the outcomes of in vitro fertilization cycles in older patients with diminished ovarian reserve: A retrospective cohort study.双扳机方案提高了卵巢储备功能减退的高龄患者体外受精周期的结局:一项回顾性队列研究。
PLoS One. 2020 Jul 6;15(7):e0235707. doi: 10.1371/journal.pone.0235707. eCollection 2020.