An all-37 °C thawing method improves the clinical outcomes of vitrified frozen-thawed embryo transfer: a retrospective study using a case-control matching analysis

被引:3
作者
Yan, Gaofeng [1 ]
Yao, Youlin [1 ]
Yang, Wenjuan [1 ]
Lu, Ling [1 ]
Wang, Longda [1 ]
Zhao, Di [1 ]
Zhao, Shuhua [1 ]
机构
[1] Kunming Med Univ, Dept Reprod & Genet, Affiliated Hosp 1, Kunming 650032, Yunnan, Peoples R China
关键词
Vitrification; Thaw/warm; 37 degrees C/room temperature; Embryo transfer; Clinical outcomes; INTRACELLULAR ICE FORMATION; MOUSE OOCYTES; CRITICAL-APPRAISAL; WARMING RATE; COOLING RATE; VITRIFICATION; CRYOPRESERVATION; SURVIVAL; CRYOPROTECTANTS; RECRYSTALLIZATION;
D O I
10.1007/s00404-023-07029-1
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose The purpose of this study is to assess the impact of different temperatures and incubation times on the clinical outcomes of FET cycles during the thawing procedure and to select a better thawing method to improve clinical outcomes. Methods This retrospective study included 1734 FET cycles from January 1, 2020, to January 30, 2022. Embryos vitrified using a KITAZATO Vitrification Kit were thawed at 37 degrees C in all steps (the case group, denoted the "all-37 degrees C" group) or at 37 degrees C and then at room temperature (RT; the control group, denoted the "37 degrees C-RT" group), according to the kit instructions. The groups were matched 1:1 to avoid confounding. Results After case-control matching, 366 all-37 degrees C cycles and 366 37 degrees C-RT cycles were included. The baseline characteristics were similar (all P > 0.05) between the two groups after matching. FET of the all-37 degrees C group yielded a higher clinical pregnancy rate (CPR; P = 0.009) and implantation rate (IR; P = 0.019) than FET of the 37 degrees C-RT group. For blastocyst transfers, the CPR (P = 0.019) and IR (P = 0.025) were significantly higher in the all-37 degrees C group than in the 37 degrees C-RT group. For D3-embryo transfers, the CPR and IR were non-significantly higher in the all-37 degrees C group than in the 37 degrees C-RT group (P > 0.05). Conclusions Thawing vitrified embryos at 37 degrees C in all steps with shortening wash time can enhance CPR and IR in FET cycles. Well-designed prospective studies are warranted to further evaluate the efficacy and safety of the all-37 degrees C thawing method.
引用
收藏
页码:1991 / 1999
页数:9
相关论文
共 48 条
[1]  
Alpha Scientists in Reproductive Medicine and ESHRE Special Interest Group of Embryology, 2011, Hum Reprod, V26, P1270, DOI 10.1093/humrep/der037
[2]   A randomized controlled study of human Day 3 embryo cryopreservation by slow freezing or vitrification: vitrification is associated with higher survival, metabolism and blastocyst formation [J].
Balaban, B. ;
Urman, B. ;
Ata, B. ;
Isiklar, A. ;
Larman, M. G. ;
Harnilton, R. ;
Gardner, D. K. .
HUMAN REPRODUCTION, 2008, 23 (09) :1976-1982
[3]   Introduction: Are we ready to eliminate the transfer of fresh embryos in in vitro fertilization? [J].
Barnhart, Kurt T. .
FERTILITY AND STERILITY, 2014, 102 (01) :1-2
[4]   Cryoprotectant Toxicity: Facts, Issues, and Questions [J].
Best, Benjamin P. .
REJUVENATION RESEARCH, 2015, 18 (05) :422-436
[5]   Are commercial warming kits interchangeable for vitrified human blastocysts? Further evidence for the adoption of a Universal Warming protocol [J].
Canosa, Stefano ;
Parmegiani, Lodovico ;
Charrier, Lorena ;
Gennarelli, Gianluca ;
Garello, Cristina ;
Granella, Francesca ;
Evangelista, Francesca ;
Monelli, Giuseppe ;
Guidetti, Daniela ;
Revelli, Alberto ;
Filicori, Marco ;
Bongioanni, Francesca .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2022, 39 (01) :67-73
[6]   The role of aquaporin 3 in the movement of water and cryoprotectants in mouse morulae [J].
Edashige, Keisuke ;
Ohta, Satoshi ;
Tanaka, Mitsunobu ;
Kuwano, Tatsunaga ;
Valdez, Delgado M., Jr. ;
Hara, Takao ;
Jin, Bo ;
Takahashi, Sei-ichi ;
Seki, Shinsuke ;
Koshimoto, Chihiro ;
Kasai, Magosaburo .
BIOLOGY OF REPRODUCTION, 2007, 77 (02) :365-375
[7]  
Edashige K, 2017, REPROD MED BIOL, V16, P36, DOI 10.1002/rmb2.12007
[8]   A critical appraisal of cryopreservation (slow cooling versus vitrification) of human oocytes and embryos [J].
Edgar, David H. ;
Gook, Debra A. .
HUMAN REPRODUCTION UPDATE, 2012, 18 (05) :536-554
[9]   A randomized controlled trial comparing two vitrification methods versus slow-freezing for cryopreservation of human cleavage stage embryos [J].
Fasano, Giovanna ;
Fontenelle, Nicolas ;
Vannin, Anne-Sophie ;
Biramane, Jamila ;
Devreker, Fabienne ;
Englert, Yvon ;
Delbaere, Anne .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2014, 31 (02) :241-247
[10]   Comparing 36.5°C with 37°C for human embryo culture: a prospective randomized controlled trial [J].
Fawzy, Mohamed ;
Emad, Mai ;
Gad, Mostafa A. ;
Sabry, Mohamed ;
Kasem, Hesham ;
Mahmoud, Manar ;
Bedaiwy, Mohamed A. .
REPRODUCTIVE BIOMEDICINE ONLINE, 2018, 36 (06) :620-626