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Perinatal Outcomes in Children Born After Fresh or Frozen Embryo Transfer: a Catalan Cohort Study Based on 14,262 Newborns

Overview
Journal Fertil Steril
Date 2017 Mar 16
PMID 28292612
Citations 24
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Abstract

Objective: To ascertain whether perinatal outcomes are affected by vitrification and/or controlled ovarian hyperstimulation (COH).

Design: Register-based cohort study.

Setting: Not applicable.

Patient(s): Women undergoing in vitro fertilization (IVF) between 2008 and 2012 using autologous or donated eggs who had a singleton pregnancy delivered from the 24th week onward.

Intervention(s): Fresh embryo transfer (ET) or frozen-thawed ET in women undergoing IVF.

Main Outcome Measure(s): Primary outcome birthweight, and secondary outcomes gestational age at delivery, small for gestational age, mode of delivery, and perinatal mortality.

Result(s): In the autologous egg population, newborns from the fresh ET group had lower birthweight than the frozen-thawed ET group (3,152.9 ± 545.5g and 3,343.2 ± 532.3g, respectively), and this difference persisted even after adjusting for confounding factors, and the newborns had a higher risk of being small for gestational age (SGA). In contrast, among egg-donor recipients undergoing ET, the mean birthweight did not differ between the groups (3,165 ± 604.15 g and 3,143.60 ± 604.21g in the fresh and frozen-thawed ET groups, respectively); however, in the adjusted regression model birthweight was statistically significantly higher in the fresh ET group than the frozen-thawed ET group. The risk of SGA remained comparable between the fresh versus frozen-thawed ET groups. We observed no statistically significant differences in perinatal mortality between groups either in the autologous egg population or in the donor recipient group.

Conclusion(s): Perinatal outcomes are negatively affected by COH and not affected by the vitrification process.

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Higher risk of pre-eclampsia and other vascular disorders with artificial cycle for frozen-thawed embryo transfer compared to ovulatory cycle or to fresh embryo transfer following fertilization.

Epelboin S, Labrosse J, de Mouzon J, Devaux A, Gervoise-Boyer M, Hesters L Front Endocrinol (Lausanne). 2023; 14:1182148.

PMID: 37284215 PMC: 10240394. DOI: 10.3389/fendo.2023.1182148.