Combined gonadotropin releasing hormone agonist/human menopausal gonadotropin therapy (GnRH-a/hMG) in normal, high, and poor responders to hMG

Zion Ben-Rafael*, David Bider, Uzi Dan, Mati Zolti, David Levran, Shlomo Mashiach

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Patients who failed to conceive after gonadotropin stimulation in in vitro fertilization treatment were classified into normal, high, or poor responders. They were routinely offered another cycle with a combination of a gonadotropin releasing hormone agonist and gonadotropin therapy (in order to evaluate whether this combined therapy could improve their response). The gonadotropin-induced cycle was compared with the combined therapy cycle. With the combination treatment, in the normal responders the phase of ovarian stimulation was significantly (P<0.001) prolonged, and the number of follicles and oocytes collected (5.7±0.7 vs 3.1±0.4) was increased, without any change in serum estradiol level compared to the control cycle. In high responders the number of oocytes was not modified by the combined treatment compared with the control cycle. However, serum estradiol level was significantly (P<0.005) decreased. The combined therapy did not modify any parameter of response in poor responders. We conclude that the response to combined agonist/gonadotropin therapy is dependent on the patient's own basal response. No improvement in response was expected in poor responders.

Original languageEnglish
Pages (from-to)33-36
Number of pages4
JournalJournal of in Vitro Fertilization and Embryo Transfer
Volume8
Issue number1
DOIs
StatePublished - Feb 1991

Keywords

  • gonadotropin releasing hormone (GnRH) analogue
  • human menopausal gonadotropin (hMG)
  • patient response

Fingerprint

Dive into the research topics of 'Combined gonadotropin releasing hormone agonist/human menopausal gonadotropin therapy (GnRH-a/hMG) in normal, high, and poor responders to hMG'. Together they form a unique fingerprint.

Cite this