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      Day 7 blastocyst euploidy supports routine implementation for cycles using preimplantation genetic testing

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          Abstract

          Objective:

          To determine if Day 7 blastocysts merit biopsy, vitrification and transfer consideration by contrasting their aneuploidy and implantation rates to Day 5 and 6 blastocysts.

          Methods:

          A total of 1,925 blastocysts were biopsied from 402 PGT-A cycles over a 12 to 16 month interval. All embryos were cultured under tri-gas, humidified conditions (37ºC) for up to 7 days (168 hours post-insemination). Biopsied blastocysts were vitrified and trophectoderm samples analyzed using NextGen sequencing. Single euploid embryo transfers were performed (n=254) using either a Day 5 (n=145), Day 6 (n=92) or a Day 7 blastocyst (n=16) post-warming. Euploidy rates and pregnancy outcomes were subsequently assessed and differences determined by day of development and blastocyst quality grade.

          Results:

          No differences were observed in implantation, pregnancy loss or ongoing pregnancy rates between Day 5 and Day 6 blastocysts. Development to Day 7 accounted for 6.6% of all blastocysts. Euploidy rates were higher in Day 5 blastocysts (53.5%; p<0.05) compared to Day 6 (40.4%) and Day 7 (35.9%). High implantation potential (56.3% to 79.3%) of vitrified-warmed euploid blastocyst occurred independent to the day of development. However, miscarriage/loss rates increased (22.2% vs. 2%; p<0.05) with Day 7 blastocysts, resulting in lower ( p<0.05) live birth rates (43.8% vs. 67.4-77.2%).

          Conclusion:

          Culturing blastocysts to Day 7 has proven beneficial by achieving viable euploid embryos that would have otherwise been discarded. An extra Day of embryo growth allows select patients additional opportunities for in vitro development and possible healthy term live births.

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          Most cited references25

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          Self-organisation of the human embryo in the absence of maternal tissues

          Remodelling of the human embryo at implantation is indispensable for successful pregnancy. Yet it has remained mysterious because of the experimental hurdles that beset the study of this developmental phase. Here, we establish an in vitro system to culture human embryos through implantation stages in the absence of maternal tissues and reveal the key events of early human morphogenesis. These include segregation of the pluripotent embryonic and extra-embryonic lineages and morphogenetic re-arrangements leading to: generation of a bi-laminar disc, formation of a pro-amniotic cavity within the embryonic lineage, appearance of the prospective yolk sac, and trophoblast differentiation. Using human embryos and human pluripotent stem cells, we show that the reorganisation of the embryonic lineage is mediated by cellular polarisation leading to cavity formation. Together, our results indicate that the critical remodelling events at this stage of human development are embryo-autonomous highlighting the remarkable and unanticipated self-organising properties of human embryos.
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            Cryopreservation of human embryos by vitrification or slow freezing: a systematic review and meta-analysis.

            To examine the literature systematically in order to identify prospective comparative trials answering the following question: Is vitrification of human embryos associated with a higher postthawing survival rate as compared with slow freezing? Systematic review and meta-analysis. University-based hospital. Not applicable. Vitrification versus slow freezing for cryopreservation of human embryos. Postthawing survival rate. Four eligible studies were identified, three of which were randomized controlled trials. Overall, the current review summarizes information from 8,824 cryopreserved human cleavage stage embryos/blastocysts (vitrification: n = 7,482; slow freezing: n = 1,342). Survival rate of cleavage stage embryos was significantly higher after vitrification as compared with slow freezing (odds ratio 15.57, 95% confidence interval 3.68-65.82; random effects model). Postthawing survival rate of vitrified blastocysts was significantly higher compared with that observed with slow freezing (odds ratio 2.20, 95% confidence interval 1.53-3.16; fixed effects model). Vitrification appears to be associated with a significantly higher postthawing survival rate than slow freezing. Further prospective trials are necessary to confirm the above results and, in addition, allow the evaluation of the two cryopreservation methods in terms of pregnancy achievement.
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              The effects of chemical and physical factors on mammalian embryo culture and their importance for the practice of assisted human reproduction.

              Although laboratory procedures, along with culture media formulations, have improved over the past two decades, the issue remains that human IVF is performed in vitro (literally 'in glass').
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                Author and article information

                Journal
                JBRA Assist Reprod
                JBRA Assist Reprod
                jbra
                JBRA Assisted Reproduction
                Brazilian Society of Assisted Reproduction
                1517-5693
                1518-0557
                Jan-Mar 2019
                Jan-Mar 2019
                : 23
                : 1
                : 45-50
                Affiliations
                [1 ] Ovation Fertility, ART Lab, Newport Beach, CA 92663 USA
                [2 ] Southern California Center for Reproductive Medicine, Newport Beach, CA 92663 USA
                Author notes
                Corresponding Authors: John B. Whitney, Ovation Fertility, ART Lab, Newport Beach, CA 92663, USA jwhitney@ 123456ovationfertility.com
                Corresponding Authors: Mitchel C. Schiewe, Ovation Fertility, ART Lab, Newport Beach, CA 92663, USA mschiewe@ 123456ovationfertility.com
                Article
                10.5935/1518-0557.20180089
                6364279
                30614486
                d0ea6d42-53a1-475a-ae9c-aa93439e4487

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 June 2018
                : 21 December 2018
                Categories
                Original Article

                embryo culture,day 7,blastocyst,biopsy,pgt
                embryo culture, day 7, blastocyst, biopsy, pgt

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