Effects of estradiol supplementation during the luteal phase of in vitro fertilization cycles: a meta-analysis

Fertil Steril. 2010 Feb;93(2):428-36. doi: 10.1016/j.fertnstert.2009.02.033. Epub 2009 Apr 1.

Abstract

Objective: To clarify whether adding E(2) to standard luteal P supplementation is beneficial both in GnRH agonist and antagonist IVF cycles.

Design: Meta-analysis of nine randomized controlled trials.

Setting: University hospital center for reproductive medicine and IVF.

Intervention(s): None.

Main outcome measure(s): Clinical pregnancy rate (PR) per patient, clinical PR per embryo transfer (ET), implantation rate, ongoing PR per patient, clinical abortion rate, and ectopic PR.

Result(s): There were no statistically significant differences between E(2)+P versus P-only group regarding overall IVF outcomes. From seven studies including GnRH agonist cycles, no statistical significant differences were found between the two groups in clinical PR per patient (relative risk [RR] 1.32, 95% confidence interval [CI] 0.79-2.19), clinical PR per ET (RR 1.83, 95% CI 0.96-3.49), implantation rate (RR 1.20, 95% CI 0.34-4.21), ongoing PR per patient (RR 1.34, 95% CI 0.37-4.82), clinical abortion rate (RR 1.05, 95% CI 0.48-2.28), and ectopic PR (RR 0.53, 95% CI 0.07-4.10). Clinical PR per patient (RR 0.94, 95% CI 0.62-1.42) and ongoing PR per patient (RR 1.09, 95% CI 0.79-1.50) from three studies including GnRH antagonist cycles only were all similar between the two groups.

Conclusion(s): The combined data presented in this meta-analysis suggest that the addition of E(2) to P for luteal phase support does not improve IVF outcomes in GnRH agonist and antagonist cycles. However, the authors feel that there is an obvious need for further large-scale studies regarding GnRH antagonist cycles.

Publication types

  • Meta-Analysis

MeSH terms

  • Estradiol / therapeutic use*
  • Female
  • Fertilization in Vitro / methods*
  • Humans
  • Luteal Phase / drug effects*
  • Ovary / drug effects
  • Ovary / physiology
  • Patient Selection
  • Pregnancy / drug effects
  • Pregnancy / physiology
  • Pregnancy Outcome / epidemiology
  • Pregnancy Rate*
  • Treatment Outcome

Substances

  • Estradiol