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[体外受精中促性腺激素释放激素激动剂触发及对有卵巢过度刺激综合征风险女性的黄体期支持]

[GnRH agonist triggering in IVF and luteal phase support in women at risk of ovarian hyperstimulation syndrome].

作者信息

Guivarc'h-Levêque A, Jaffré F, Homer L, Moy L, Priou G, Colleu D, Denis I, Arvis P

机构信息

Centre AMP, clinique mutualiste La Sagesse, 3, place Saint-Guénolé, 35000 Rennes, France.

出版信息

Gynecol Obstet Fertil. 2013 Sep;41(9):511-4. doi: 10.1016/j.gyobfe.2013.06.014. Epub 2013 Aug 22.

DOI:10.1016/j.gyobfe.2013.06.014
PMID:23972925
Abstract

OBJECTIVE

To evaluate the efficacy and safety of ovulation triggering by agonists in antagonists IVF cycles with fresh embryo transfer in modulating low HCG dose for luteal phase support in patients at risk of ovarian hyperstimulation syndrome (OHSS).

PATIENTS AND METHODS

In an observational study from September 2011 to March 2013, we triggered with agonist 107 cycles with OHSS risk, we initially triggered 39 cycles with 2 doses of Triptorelin 0.1 mg. Injection of 1500 IU HCG was performed one hour after the pick up and a second injection of 1500 IU was made 5 days later (group 1) combined with 400 mg of natural progesterone vaginally. In the following 68 cycles we removed the second HCG injection and increased to 600 mg vaginal progesterone associated with E2 4 mg orally (group 2).

RESULTS

Group 1: the ongoing pregnancy rate and birth rate in fresh cycle is respectively 37.1% and 34.3% and the cumulative ongoing pregnancy rate and birth rate per patient is 43.6% and 41%. We recorded three late onset OHSS in pregnant women. Group 2: ongoing pregnancy rate in fresh cycle is 39.6%, the current cumulative ongoing pregnancy rate per patient was 45.6%. We observed a case of early onset OHSS.

DISCUSSION AND CONCLUSION

Triggering with agonist and administering an injection of 1500 IU of HCG the day of the pick up appears to be effective in women at risk of OHSS. The exclusion of all OHSS is still not reached. The search for the best protocol and its indications should continue.

摘要

目的

评估在有卵巢过度刺激综合征(OHSS)风险的患者中,拮抗剂方案体外受精-胚胎移植(IVF-ET)周期中使用激动剂触发排卵,同时调整低剂量人绒毛膜促性腺激素(HCG)进行黄体支持的有效性和安全性。

患者与方法

在一项2011年9月至2013年3月的观察性研究中,我们对107个有OHSS风险的周期使用激动剂触发排卵。最初,对39个周期使用0.1mg曲普瑞林分两次注射触发排卵。取卵后1小时注射1500IU HCG,5天后再注射1500IU(第1组),同时阴道给予400mg天然孕酮。在接下来的68个周期中,取消第二次HCG注射,将阴道孕酮剂量增加至600mg,并联合口服4mg雌二醇(E2)(第2组)。

结果

第1组:新鲜周期的持续妊娠率和出生率分别为37.1%和34.3%,每位患者的累积持续妊娠率和出生率分别为43.6%和41%。我们记录到3例孕妇发生迟发性OHSS。第2组:新鲜周期的持续妊娠率为39.6%,目前每位患者的累积持续妊娠率为45.6%。我们观察到1例早发性OHSS。

讨论与结论

对于有OHSS风险的女性,在取卵日使用激动剂触发排卵并注射1500IU HCG似乎是有效的。但仍未达到完全排除所有OHSS的目标。寻找最佳方案及其适应证的研究应继续进行。

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