2014•Journal of Qiqihar University of MedicineRequires access

Feasibility of selecting viable embryos from poor quality embryos by blastocyst culture

Xian Ying-ji

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Abstract

Objective To investigate the feasibility of screening viable embryos from poor quality embryos by extending blastocyst culture. Methods 538 D3 poor quality embryos from 142 cases IVF /ICSI treatment were collected after embryo transfer or freezing,and observe the blastocyst formation by blastocyst cultured for up to the sixth days( D6). The embryos were divided into four groups( 4 cells grade Ⅰ /Ⅱ /Ⅲembryos,5 cells grade Ⅰ /Ⅱ /Ⅲ embryos,6 ~ 9 cells grade Ⅲ embryos and exceed 9 cells grade Ⅰ /Ⅱ /Ⅲembryos) according to different blastomere and grade,and then compared the blastula development. Results The blastula formation rate and the high-quality blastula rate from D3 poor quality embryos were 65. 6% and 51.3%,the blastula formation rate of the four groups were 55. 6%,56. 6%,70. 4% and 66. 7%,there were significant difference among the four groups( P 0. 05). And the high-quality blastula rate were 8. 9%,32. 6%,61. 0% and 63. 3%,there were significant difference among the four groups( P 0. 05). Conclusions Extending blastocysts cultured can select the developmental potential embryos from those poor quality embryos remnant effectively,and make better use of the embryos.

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Objective To investigate the feasibility of screening viable embryos from poor quality embryos by extending blastocyst culture. Methods 538 D3 poor quality embryos from 142 cases IVF /ICSI treatment were collected after embryo transfer or freezing,and observe the blastocyst formation by blastocyst cultured for up to the sixth days( D6). The embryos were divided into four groups( 4 cells grade Ⅰ /Ⅱ /Ⅲembryos,5 cells grade Ⅰ /Ⅱ /Ⅲ embryos,6 ~ 9 cells grade Ⅲ embryos and exceed 9 cells grade Ⅰ /Ⅱ /Ⅲembryos) according to different blastomere and grade,and then compared the blastula development. Results The blastula formation rate and the high-quality blastula rate from D3 poor quality embryos were 65. 6% and 51.3%,the blastula formation rate of the four groups were 55. 6%,56. 6%,70. 4% and 66. 7%,there were significant difference among the four groups( P 0. 05). And the high-quality blastula rate were 8. 9%,32. 6%,61. 0% and 63. 3%,there were significant difference among the four groups( P 0. 05). Conclusions Extending blastocysts cultured can select the developmental potential embryos from those poor quality embryos remnant effectively,and make better use of the embryos.

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Available abstract

Objective To investigate the feasibility of screening viable embryos from poor quality embryos by extending blastocyst culture. Methods 538 D3 poor quality embryos from 142 cases IVF /ICSI treatment were collected after embryo transfer or freezing,and observe the blastocyst formation by blastocyst cultured for up to the sixth days( D6). The embryos were divided into four groups( 4 cells grade Ⅰ /Ⅱ /Ⅲembryos,5 cells grade Ⅰ /Ⅱ /Ⅲ embryos,6 ~ 9 cells grade Ⅲ embryos and exceed 9 cells grade Ⅰ /Ⅱ /Ⅲembryos) according to different blastomere and grade,and then compared the blastula development. Results The blastula formation rate and the high-quality blastula rate from D3 poor quality embryos were 65. 6% and 51.3%,the blastula formation rate of the four groups were 55. 6%,56. 6%,70. 4% and 66. 7%,there were significant difference among the four groups( P 0. 05). And the high-quality blastula rate were 8. 9%,32. 6%,61. 0% and 63. 3%,there were significant difference among the four groups( P 0. 05). Conclusions Extending blastocysts cultured can select the developmental potential embryos from those poor quality embryos remnant effectively,and make better use of the embryos.

Key concepts: Blastula, Embryo, Blastocyst, Blastomere, Andrology, Significant difference, Embryo quality, Medicine

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