Comparison of the clinical outcomes between fresh embryo transfer and frozen-thawed embryo transfer in the gonadotropin-releasing hormone antagonist protocol

Sun Li, Li Xinxin, Li Yue, Ge Mingxiao, Ou Jianping, Ge Shuqi

Chinese Journal of Clinical Anatomy ›› 2024, Vol. 42 ›› Issue (2) : 181-185.

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Chinese Journal of Clinical Anatomy ›› 2024, Vol. 42 ›› Issue (2) : 181-185. DOI: 10.13418/j.issn.1001-165x.2024.2.11

Comparison of the clinical outcomes between fresh embryo transfer and frozen-thawed embryo transfer in the gonadotropin-releasing hormone antagonist protocol

  • Sun Li1, Li Xinxin1, Li Yue2, Ge Mingxiao1, Ou Jianping1, Ge Shuqi1*
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Abstract

Objective   To compare the clinical outcomes of fresh embryo transfer and frozen-thawed embryo transfer (FET) in the gonadotropin-releasing hormone antagonist (GnRH-A) protocol.   Method   The clinical data of 2575 women undergoing GnRH antagonist protocol cycle, including 1328 cases of fresh embryo transfer and 1247 cases of FET were retrospectively analyzed.    Results    The AMH level and AFC in the FET group were significantly higher than those in the fresh embryo transfer group (P<0.05), and there was no significant difference in other baseline characteristics between the two group (P>0.05). The FSH level on hCG day in the FET group was significantly lower than that in the fresh embryo transfer group, and E2, P level on hCG day in the FET group were significantly higher than those in the fresh embryo transfer group (P<0.05). The total number of oocytes retrieved, matured oocyte, high-quality embryos in the FET group were significantly higher than those in the fresh embryo transfer group (P<0.05). The mean number of embryos transfer in the FET group was significantly lower than that in the fresh embryo transfer group, the clinical pregnancy rate, implantation rate and live birth rate in the FET group were significantly higher than those in the fresh embryo transfer group, the ectopic pregnancy rate and the multiple pregnancy rate in the FET group were significantly lower than those in the fresh embryo transfer group (P<0.05). There was no significant difference in the incidence of moderate-severe OHSS, miscarriage rate, incidence of GDM and gestational hypertension between the two groups (P>0.05). The singleton birth weight in the FET group was significantly higher than that in the fresh embryo transfer group, with statistical difference (P<0.05).    Conclusions   In the GnRH antagonist protocol cycle, FET can obtain good clinical outcome and can be used as an effective supplemental regimen.

Key words

GnRH antagonist protocol /   /   / Fresh embryo transfer /   /   / Frozen-thawed embryo transfer / Whole embryo freezing

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Sun Li, Li Xinxin, Li Yue, Ge Mingxiao, Ou Jianping, Ge Shuqi. Comparison of the clinical outcomes between fresh embryo transfer and frozen-thawed embryo transfer in the gonadotropin-releasing hormone antagonist protocol[J]. Chinese Journal of Clinical Anatomy. 2024, 42(2): 181-185 https://doi.org/10.13418/j.issn.1001-165x.2024.2.11

References

[1] Grow D, Kawwass JF, Kulkarni AD, et al. GnRH agonist and GnRH antagonist protocols: comparison of outcomes among good-prognosis patients using national surveillance data[J]. Reprod Biomed Online, 2014,29(3):299-304. DOI: 10.1016/j.rbmo.2014.05.007.
[2] Roque M, Valle M, Guimaraes F, et al. Freeze-all policy: fresh vs. frozen-thawed embryo transfer[J]. Fertil Steril, 2015,103(5):1190-1193. DOI: 10.1016/j.fertnstert.2015.01.045.
[3] Ozgur K, Bulut H, Berkkanoglu M, et al. Frozen embryo transfer can be performed in the cycle immediately following the freeze-all cycle[J]. J Assist Reprod Genet, 2018,35(1):135-142. DOI: 10.1007/s10815-017-1048-6.
[4] Isikoglu M. Is it too early for a major change? A critical objection to the freeze all policy[J]. Arch Gynecol Obstet, 2016,293(6):1359-1360. DOI: 10.1007/s00404-016-4039-4.
[5] Vuong LN, Dang VQ, Ho TM, et al. IVF Transfer of Fresh or Frozen Embryos in Women without Polycystic Ovaries[J]. N Engl J Med, 2018,378(2):137-147. DOI: 10.1056/NEJMoa1703768.
[6] Jing M, Lin C, Zhu W, et al. Cost-effectiveness analysis of GnRH-agonist long-protocol and GnRH-antagonist  protocol for in vitro fertilization[J]. Sci Rep, 2020,10(1):8732. DOI: 10.1038/s41598-020-65558-0.
[7] Al-Inany HG, Youssef MA, Ayeleke RO, et al. Gonadotrophin-releasing hormone antagonists for assisted reproductive technology[J]. Cochrane Database Syst Rev, 2016,4(4):CD1750. DOI: 10.1002/14651858.CD001750.
[8] Simon C, Moreau J, Gatimel N, et al. Impact of estradiol and progesterone levels during the late follicular stage on the outcome of GnRH antagonist protocols[J]. Gynecol Endocrinol, 2019,35(6):481-484. DOI: 10.1080/09513590.2018.1538346.
[9] Racca A, Santos-Ribeiro S, De Munck N, et al. Impact of late-follicular phase elevated serum progesterone on cumulative live  birth rates: is there a deleterious effect on embryo quality?[J]. Hum Reprod, 2018,33(5):860-868. DOI: 10.1093/humrep/dey031.
[10] Simon C, Branet L, Moreau J, et al. Association between progesterone to number of mature oocytes index and live birth in GnRH antagonist protocols[J]. Reprod Biomed Online, 2019, 38(6):901-907. DOI: 10.1016/j.rbmo.2019.01.009.
[11] Tomas C, Toftager M, Lossl K, et al. Perinatal outcomes in 521 gestations after fresh and frozen cycles: a secondary outcome of a randomized controlled trial comparing GnRH antagonist versus GnRH agonist protocols[J]. Reprod Biomed Online, 2019,39(4):659-664. DOI: 10.1016/j.rbmo.2019.05.010.
[12] Huang MC, Tzeng SL, Lee CI, et al. GnRH agonist long protocol versus GnRH antagonist protocol for various aged  patients with diminished ovarian reserve: A retrospective study[J]. PLoS One, 2018, 13(11):e207081. DOI: 10.1371/journal.pone.0207081.
[13] Zhai XH, Zhang P, Wu FX, et al. GnRH antagonist for patients with polycystic ovary syndrome undergoing controlled  ovarian hyperstimulation for in vitro fertilization and embryo transfer in fresh  cycles[J]. Exp Ther Med, 2017,13(6):3097-3102. DOI: 10.3892/etm.2017.4309.
[14] Trounson A, Mohr L. Human pregnancy following cryopreservation, thawing and transfer of an eight-cell embryo[J]. Nature, 1983, 305(5936):707-709. DOI: 10.1038/305707a0.
[15] Zeilmaker GH, Alberda AT, van Gent I, et al. Two pregnancies following transfer of intact frozen-thawed embryos[J]. Fertil Steril, 1984,42(2):293-296. DOI: 10.1016/s0015-0282(16)48029-5.
[16] Liebermann J. Vitrification: A Simple and Successful Method for Cryostorage of Human Blastocysts[J]. Methods Mol Biol, 2021,2180:501-515. DOI: 10.1007/978-1-0716-0783-1_24.
[17] Nagy ZP, Shapiro D, Chang CC. Vitrification of the human embryo: a more efficient and safer in vitro fertilization treatment[J]. Fertil Steril, 2020,113(2):241-247. DOI: 10.1016/j.fertnstert.2019.12.009.
[18] Chen T, Li B, Shi H, et al. Reproductive Outcomes of Single Embryo Transfer in Women with Previous Cesarean  Section[J]. Reprod Sci, 2021,28(4):1049-1059. DOI: 10.1007/s43032-020-00345-w.
[19] Blockeel C, Drakopoulos P, Santos-Ribeiro S, et al. A fresh look at the freeze-all protocol: a SWOT analysis[J]. Hum Reprod, 2016,31(3):491-497. DOI: 10.1093/humrep/dev339.
[20] Chen ZJ, Shi Y, Sun Y, et al. Fresh versus Frozen Embryos for Infertility in the Polycystic Ovary Syndrome[J]. N Engl J Med, 2016, 375(6):523-533. DOI: 10.1056/NEJMoa1513873.
[21] Shi Y, Sun Y, Hao C, et al. Transfer of Fresh versus Frozen Embryos in Ovulatory Women[J]. N Engl J Med, 2018, 378(2):126-136. DOI: 10.1056/NEJMoa1705334.
[22] Roque M, Valle M, Sampaio M, et al. Does freeze-all policy affect IVF outcome in poor ovarian responders?[J]. Ultrasound Obstet Gynecol, 2018,52(4):530-534. DOI: 10.1002/uog.19000.
[23] Roque M, Valle M, Sampaio M, et al. Obstetric outcomes after fresh versus frozen-thawed embryo transfers: A systematic review and meta-analysis[J]. JBRA Assist Reprod, 2018, 22(3):253-260. DOI: 10.5935/1518-0557.20180049.
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