Low-dose human chorionic gonadotropin versus estradiol/progesterone luteal phase support in gonadotropin-releasing hormone agonist-triggered assisted reproductive technique cycles: understanding a new approach
- PMID: 20673892
- DOI: 10.1016/j.fertnstert.2010.06.035
Low-dose human chorionic gonadotropin versus estradiol/progesterone luteal phase support in gonadotropin-releasing hormone agonist-triggered assisted reproductive technique cycles: understanding a new approach
Abstract
It remains unclear how GnRH agonist (GnRHa) triggering affects the luteal phase, so we investigated the luteal phase after GnRHa triggering, supported with conventional E(2)/P with or without low-dose hCG. E(2)/P support, compared with low-dose hCG, induced a shorter luteal phase (11.2 ± 1.1 vs. 15.0 ± 1.6 days) and fewer subjective complaints (0 vs. 42%), whereas hCG caused more free fluid accumulation and enlarged ovaries than E(2)/P alone. Steroids and low-dose hCG differentially affected corpus luteum function, ovarian size, free fluid accumulation, and patient comfort.
Copyright © 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
Similar articles
-
Safety and efficacy of low dose hCG for luteal support after triggering ovulation with a GnRH agonist in cases of polyfollicular development.Eur J Obstet Gynecol Reprod Biol. 2006 May 1;126(1):87-92. doi: 10.1016/j.ejogrb.2005.11.013. Epub 2005 Dec 22. Eur J Obstet Gynecol Reprod Biol. 2006. PMID: 16377065 Clinical Trial.
-
Early luteal phase endocrine profile is affected by the mode of triggering final oocyte maturation and the luteal phase support used in recombinant follicle-stimulating hormone-gonadotropin-releasing hormone antagonist in vitro fertilization cycles.Fertil Steril. 2013 Sep;100(3):742-7. doi: 10.1016/j.fertnstert.2013.05.028. Epub 2013 Jun 24. Fertil Steril. 2013. PMID: 23806846 Clinical Trial.
-
1,500 IU human chorionic gonadotropin administered at oocyte retrieval rescues the luteal phase when gonadotropin-releasing hormone agonist is used for ovulation induction: a prospective, randomized, controlled study.Fertil Steril. 2010 Feb;93(3):847-54. doi: 10.1016/j.fertnstert.2008.12.042. Epub 2009 Feb 6. Fertil Steril. 2010. PMID: 19200959 Clinical Trial.
-
Ovarian hyperstimulation syndrome prevention strategies: Luteal support strategies to optimize pregnancy success in cycles with gonadotropin-releasing hormone agonist ovulatory trigger.Semin Reprod Med. 2010 Nov;28(6):506-12. doi: 10.1055/s-0030-1265678. Epub 2010 Nov 16. Semin Reprod Med. 2010. PMID: 21082510 Review.
-
GnRHa to trigger final oocyte maturation: a time to reconsider.Hum Reprod. 2009 Oct;24(10):2389-94. doi: 10.1093/humrep/dep246. Epub 2009 Jul 16. Hum Reprod. 2009. PMID: 19608565 Review.
Cited by
-
Dual trigger improves response to ovarian stimulation and ICSI outcomes in patients with a previous r-hCG triggered ICSI cycle.JBRA Assist Reprod. 2022 Apr 17;26(2):255-260. doi: 10.5935/1518-0557.20210065. JBRA Assist Reprod. 2022. PMID: 34609808 Free PMC article.
-
The Effects of Three Methods of Luteal Phase Support on Pregnancy Outcomes in Poor Ovarian Responders: A Randomized Clinical Trial.Int J Fertil Steril. 2025 Jan 5;19(1):10-16. doi: 10.22074/ijfs.2024.2007292.1500. Int J Fertil Steril. 2025. PMID: 39827385 Free PMC article.
-
Efficacy of daily GnRH agonist for luteal phase support following GnRH agonist triggered ICSI cycles versus conventional strategy: A Randomized controlled trial.JBRA Assist Reprod. 2021 Jul 21;25(3):368-372. doi: 10.5935/1518-0557.20200077. JBRA Assist Reprod. 2021. PMID: 33507722 Free PMC article. Clinical Trial.
-
Luteal phase support for assisted reproduction cycles.Cochrane Database Syst Rev. 2015 Jul 7;2015(7):CD009154. doi: 10.1002/14651858.CD009154.pub3. Cochrane Database Syst Rev. 2015. PMID: 26148507 Free PMC article.
-
An update on the prevention of ovarian hyperstimulation syndrome.Womens Health (Lond). 2016 Sep;12(5):496-503. doi: 10.1177/1745505716664743. Epub 2016 Aug 19. Womens Health (Lond). 2016. PMID: 27543490 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical