Reproductive outcomes after a single dose of gonadotropin-releasing hormone agonist compared with human chorionic gonadotropin for the induction of final oocyte maturation in hyper-responder women aged 35–40 years
A single dose of gonadotropin-releasing hormone agonist results in decreased oocytes and embryo competence compared with human chorionic gonadotropin trigger in hyper-responder women aged 35–40 years.
Volume 107, Issue 6, Pages 1323–1328.e2
Samer Tannus, M.D., Rola Turki, M.D., Yoni Cohen, M.D., Ph.D., Weon-Young Son, Ph.D., Tal Shavit, M.D., M.H.A., Michael Haim Dahan, M.D.
To investigate the reproductive outcomes after the use of GnRH agonist (GnRHa) compared with hCG for the induction of final oocyte maturation in GnRH antagonist cycles performed in hyper-responder women aged 35–40 years.
Academic fertility center.
Two hundred seventy-two hyper-responder women aged 35–40 years who underwent controlled ovarian stimulation under GnRH antagonist suppression were included. Final oocyte maturation was performed with GnRHa (n = 168) or hCG (n = 104). Embryos were cryopreserved at the blastocyst stage and transferred in subsequent warming cycles (n = 542). Subjects were included in the analysis until live birth was achieved, after which they were excluded from further analysis.
Main Outcome Measure(s)
Cumulative live birth rate.
Subjects in the GnRHa group achieved a higher number of oocytes (22 vs. 21) and a higher number of mature oocytes (16 vs. 14). The number of cryopreserved blastocysts (median of five blastocysts in both groups) was similar. Women in the hCG group needed a lower number of warming cycles to achieve live birth (1.32 vs. 2.12), had higher embryo implantation rates (48% vs. 39%), and the proportion of embryos transferred until live birth was lower (33% vs. 57%). The cumulative live birth rate was similar between the groups (48.15% vs. 48%).
Although the cumulative live birth rate is similar, a single dose of GnRHa possibly results in suboptimal oocyte and embryo competence, as manifested by decreased embryo implantation rates and increased time needed to achieve live birth.