Gonadotropin-releasing hormone antagonists - Implications for oocyte quality and uterine receptivity

被引:17
作者
Gordon, K [1 ]
机构
[1] Organon Inc, Reprod Med, W Orange, NJ 07052 USA
来源
HUMAN FERTILITY AND REPRODUCTION: THE OOCYTE, THE EMBRYO, AND THE UTERUS | 2001年 / 943卷
关键词
GnRH antagonist; controlled ovarian (hyper)stimulation; in vitro fertilization/embryo transfer; uterine receptivity;
D O I
10.1111/j.1749-6632.2001.tb03789.x
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Until recently, gonadotropin-releasing hormone (GnRH) agonists were the only choice available to physicians for prevention of premature luteinizing hormone (LH) surges in women undergoing controlled ovarian stimulation. The recent FDA approval of GnRH antagonists for this indication gives clinicians some new options. Results of clinical trials to date suggest that, with GnRH antagonists, much shorter treatment regimens with fewer injections and possibly less gonadotropin can achieve good clinical results. In most of the trials performed to date, however, the GnRH antagonist regimens have been associated with a slightly lower pregnancy and implantation rate than the established GnRH agonist protocols. This remains the biggest hurdle to their more general acceptance. Herein, the possible contributing factors are discussed, and the proposal made that differences in serum estradiol patterns preceding oocyte retrieval are the most likely contributing factor.
引用
收藏
页码:49 / 54
页数:6
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