2013
DOI: 10.1016/j.fertnstert.2013.06.021
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Should embryos developing to blastocysts on day 7 be cryopreserved and transferred: an analysis of pregnancy and implantation rates

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Cited by 57 publications
(54 citation statements)
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“…The final inclusion was 13 studies that met the selection criteria for our meta‐analysis. Hence, 23 studies were included in the following meta‐analyses . The main characteristics and assessment for risk of bias of the included studies are presented in Table .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The final inclusion was 13 studies that met the selection criteria for our meta‐analysis. Hence, 23 studies were included in the following meta‐analyses . The main characteristics and assessment for risk of bias of the included studies are presented in Table .…”
Section: Resultsmentioning
confidence: 99%
“…The widespread application of blastocysts transfer has helped us to confirm that day 6 blastocyst formation is, in reality, a relatively frequent event. It is estimated that this phenomenon occurs in 30% of blastocyst cultivation . Given the high frequency of day 6 blastocyst formation, understanding the pregnancy outcomes of day 6 BET becomes clinically important.…”
Section: Introductionmentioning
confidence: 99%
“…Many studies have shown that the chromosomal status of embryo may affect the embryo cleavage rate and morphology [18,23,24]. Most of the researchers used fluorescence in situ hybridization (FISH) techniques and found a higher incidence of chromosomal abnormality of cleavage-stage embryos with poor morphology.…”
Section: Discussionmentioning
confidence: 99%
“…ongoing pregnancy rates of the D5 blastocyst were significantly higher than those of blastocysts in the D6 and D7 groups [6]. Similarly, the results of the study by Liebermann et al also suggested that the pregnancy outcome of D5 was better than that of the D6 blastocyst [8].…”
Section: Discussionmentioning
confidence: 83%
“…Our center used vitrification freezing to freeze the embryos, which was based on the previously described [6]. The blastocysts were subjected to artificial shrinkage before being frozen, and then allowed to equilibrate for 2 min in a pre-equilibrated solution containing 7.5% (v/v) dimethylsulfoxide (DMSO) and 7.5% (v/v) ethylene glycol (EG), followed by transfer to a vitrification freezing solution-15% (v/v) DMSO + 15% (v/v) EG + 0.65 mol/l sucrose + 10 mg/ml Ficoll-where the blastocysts were allowed to equilibrate for 30 s. Subsequently, the blastocysts were transferred to a Cryoloop, which was then preserved in liquid nitrogen.…”
Section: Methodsmentioning
confidence: 99%