Abstract

ObjectiveTo compare the clinical outcomes of dydrogesterone (DYG) and medroxyprogesterone (MPA) in the progestin-primed ovarian stimulation (PPOS) protocol for patients with poor ovarian response (POR).Patients and MethodsThis was a retrospective cohort study. Women with POR who underwent IVF/ICSI at the Reproductive Center of Third Affiliated Hospital of Zhengzhou University between January 2020 and January 2021 were included. The primary outcome measure of our study was the number of oocytes retrieved. The secondary outcome measures in the present study were the number of 2PN, number of available embryos, oocyte retrieval rate, fertilization rate, viable embryo rate per oocyte retrieved, cancellation rate and pregnancy outcomes of the first embryo transfer cycle, including the biochemical pregnancy, clinical pregnancy and miscarriage rates.ResultsIn total, 118 women underwent hMG +DYG protocols, and 692 women who underwent hMG +MPA met the Bologna criteria for POR. After baseline characteristics were balanced using the PSM model, 118 hMG +DYG protocols were matched to 118 hMG +MPA protocols, and the baseline characteristics were comparable between the two groups. The numbers of oocytes retrieved, 2PN, and available embryos and the oocyte retrieval rate, fertilization rate, viable embryo rate per oocyte retrieved and cancellation rate of the hMG+DYG and hMG+MPA protocols were comparable. Altogether, 66 women in the hMG+DYG group and 87 women in the hMG+MPA group underwent first embryo transfers. In the hMG+DYG group, 81.8% (54/66) of the patients underwent cleavage embryo transfers; similarly, 79.3% (69/87) of patients in the hMG+MPA group had cleavage embryo transfers (P=0.70).The biochemical pregnancy rate of the hMG+DYG group was 42.4%, and this was comparable to the rate in the hMG+DYG group, at 34.5% (P=0.32). The clinical pregnancy rates were similar between the two groups (36.4% vs. 31.0%, P=0.49), and there was no significant difference in the rate of miscarriage between the two groups (12.5% vs. 29.6%, P=0.14).ConclusionFor women with POR, the clinical outcome of the hMG + DYG group was similar to that of the hMG + MPA group, indicating that both combinations can be useful options for PPOS protocols.

Highlights

  • Infertility affects approximately 10% of reproductive-aged couples worldwide [1]

  • A randomized controlled trial (RCT) including 516 first In vitro fertilization (IVF)/ICSI cycles of women with normal ovarian reserve compared DYG and MPA in the progestin-primed ovarian stimulation (PPOS) protocol, and the results showed that DYG can be used as an appropriate alternative progestin in a PPOS protocol [12]

  • After balancing the baseline characteristics using the prospective score matching (PSM) model, 118 human menopausal gonadotropin (hMG) +DYG protocols were matched with 118 hMG +MPA protocols

Read more

Summary

Introduction

Infertility affects approximately 10% of reproductive-aged couples worldwide [1]. In vitro fertilization (IVF) has become the most effective treatment for infertility caused by tubal or other factors as well as for unexplained infertility [2]. Controlled ovarian hyperstimulation (COH), which suppresses the luteinizing hormone (LH) surge, increases the efficacy of treatment by promoting the maturation of multiple oocytes and availability of embryos for transfer, making COH a crucial step in IVF [3]. In routine clinical practice with COH, up to 9% ~24% of patients have poor ovarian response (POR) [4]. POR is characterized mainly by a number of follicles that develop during COH below the intended target, a high level of gonadotropin (Gn), a high cycle cancellation rate, low numbers of harvested oocytes and available embryos, and a low pregnancy rate and live birth rate (LBR). The Bologna criteria, discussed and formulated by the European Society of Human Embryology and Reproduction and the American Society of Reproductive Medicine in 2011, are the most widely used standards in clinical practice

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.