developmental stage on day-5 and fragmentation rate on day-3 can influence the implantation potential of top-quality blastocysts in ivf cycles with single embryo transfer

developmental stage on day-5 and fragmentation rate on day-3 can influence the implantation potential of top-quality blastocysts in ivf cycles with single embryo transfer

;Devroey Paul;Van Landuyt Lisbet;Papanikolaou Evangelos G;Verheyen Greta;della Ragione Tiziana;Van Steirteghem Andre
international entrepreneurship and management journal 2007 Vol. 5 pp. 2-
236
paul2007reproductivedevelopmental

Abstract

Abstract

Background

In IVF-ICSI cycles with single embryo transfer (SET), embryo selection for transfer is of crucial importance. The present study aimed to define which embryo parameters might be related to the implantation potential of advanced blastocysts.

Methods

Overall, in 203 cycles with SET, developmental characteristics of 93 implanted (group A) and 110 non-implanted (group B) advanced blastocysts of good quality were compared. The following developmental parameters were assessed in the two groups: normal fertilization, developmental stage on day 5, number of blastomeres on day 2 and on day 3, fragmentation rate on day 3, compaction on day 4 and cleavage pattern on day 2 and day 3.

Results

Expanded blastocysts compared to full blastocysts have higher implantation potential (56.5% vs. 29.3%, p < 0.05). In group B, a higher proportion of advanced blastocysts showed between 10% and 50% anucleated fragments on day 3 than in group A (23.6 vs 11.8, P = 0.03). Advanced blastocysts with >10–50% fragments on day 3 showed a significant lower implantation (29.7%) than those with ≤ 10%fragments (49.4%, P = 0.03). All the other parameters analysed were comparable for the two groups.

Conclusion

Developmental stage on day 5 and fragmentation rate on day 3 were related to the implantation potential of advanced blastocysts and should also be taken into account in the selection of the best advanced blastocyst for transfer.

Citation

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10.1186/1477-7827-5-2
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