Intensified ovarian stimulation in a GnRH antagonist protocol with agonist triggering: a prospective, clinical feasibility study

被引:7
作者
Griesinger, Georg [1 ,2 ]
Berndt, Henriette [1 ]
Schultz, Laura [1 ]
Schultze-Mosgau, Askan [1 ]
Diedrich, Klaus [1 ]
von Otte, Soeren [1 ]
机构
[1] Univ Clin Schleswig Holstein, Dept Obstet & Gynecol, Lubeck, Germany
[2] Univ Vienna, Dept Obstet, A-1010 Vienna, Austria
关键词
cryopreserved embryo transfer; GnRH agonist; GnRH antagonist; OHSS; ovarian stimulation; vitrification; FINAL OOCYTE MATURATION; IN-VITRO FERTILIZATION; HUMAN CHORIONIC-GONADOTROPIN; DOUBLE-BLIND; RECOMBINANT FSH; HYPERSTIMULATION SYNDROME; HORMONE AGONIST; INHIBIN-A; HIGH-RISK; WOMEN;
D O I
10.1016/j.rbmo.2010.10.017
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The threat of severe ovarian hyperstimulation syndrome (OHSS) and the increase in discomfort for the patient has limited the feasibility of maximizing the oocyte yield per treatment cycle. A gonadotrophin-releasing hormone (GnRH) antagonist protocol with agonist triggering and vitrification of all 2PN oocytes can eliminate the risk of OHSS. This prospective, single-centre, cohort study in 30 good-responder IVF patients <= 36 years reports the feasibility of arbitrarily intensifying stimulation in a GnRH antagonist protocol in terms of tolerability, safety and efficacy. Ovarian stimulation was performed with 225-375 IU FSH, induction of final oocyte maturation with 0.2 mg GnRH agonist followed by vitrification of all 2 pronuclear (2PN) oocytes and repetitive vitrified-warmed embryo transfer cycles. Main outcomes were severe OHSS incidence, tolerability, assessed by a questionnaire, and cumulative live birth rate. On average, 17 oocytes were retrieved (range 4-42) and 8.4 oocytes at the 2PN stage were cryopreserved (range 3-22). No case of severe OHSS was observed (0%, 95 CI 0-11.4%). Tolerability was good. The cumulative live birth rate per patient undergoing at least one vitrified-warmed embryo transfer was 26.9% (7/26, 95% CI 13.7-46.1%). This approach can be explored in future larger-sized controlled studies. (C) 2010, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:133 / 139
页数:7
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