A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Pregnancy potential and perinatal outcomes of embryos cryopreserved twice: a case–control study




Julkaisun tekijät: Hallamaa Marianne, Seikkula Jaana, Willman Sami, Ollila Helena, Jokimaa Varpu

Kustantaja: Elsevier Ltd

Julkaisuvuosi: 2021

Journal: Reproductive BioMedicine Online

Tietokannassa oleva lehden nimi: Reproductive BioMedicine Online

eISSN: 1472-6491

DOI: http://dx.doi.org/10.1016/j.rbmo.2021.06.028

Verkko-osoite: https://www.sciencedirect.com/science/article/pii/S1472648321003126?via%3Dihub


Tiivistelmä

Research question

What are the pregnancy and perinatal outcomes of twice-cryopreserved embryos compared with embryos cryopreserved once?

Design

Retrospective register-based case–control study. The case group consisted of transfers of twice-cryopreserved embryos (n = 89), and the control group of transfers of embryos cryopreserved once (n = 304). Matching criteria were embryonic age at transfer and female age category of less than 35 years or 35 and greater.

Results

The survival rate of twice-cryopreserved embryos was 92.2%, and 93.7% of the planned frozen embryo transfers (FET) could be completed. FET was performed with cleavage-stage embryos in 17 cases and 68 controls and with blastocysts in 72 cases and 238 controls. The rates of live birth (27.0% versus 31.9%, adjusted odds ratio [OR] 0.70, 95% CI 0.40–1.22, P = 0.21), clinical pregnancy (31.5% versus 36.8%, adjusted OR 0.71, 95% CI 0.42–1.21, P = 0.21) and miscarriage (4.5% versus 3.9%, adjusted OR 1.10, 95% CI 0.33–3.60, P = 0.88) in the case and the control groups were comparable. No difference was seen in the preterm delivery rate (cases 4.2% versus controls 10.3%, P = 0.69). Twenty-five children were born in the case group and 100 in the control group. No difference in birthweight was detected between the groups and there were no large for gestational age fetuses or congenital malformations in the case group.

Conclusions

Uncompromised live birth rates and neonatal outcomes may be expected after the transfer of twice-cryopreserved embryos. To avoid embryo wastage and transfer of multiple embryos, good quality surplus embryos from FET cycles may be cryopreserved again by vitrification.


Ladattava julkaisu

This is an electronic reprint of the original article.
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Last updated on 2021-14-09 at 11:24