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The value of pronuclear scoring for the success of IVF and ICSI-cycles.

作者信息

Ludwig A K, Werner S, Diedrich K, Nitz B, Ludwig M

机构信息

Department of Gynecology and Obstetrics, University Clinic Schleswig-Holstein , Campus Lübeck, Ratzeburger Allee 160, 23538 Lubeck, Germany.

出版信息

Arch Gynecol Obstet. 2006 Mar;273(6):346-54. doi: 10.1007/s00404-005-0102-2. Epub 2005 Dec 7.

DOI:10.1007/s00404-005-0102-2
PMID:16333679
Abstract

BACKGROUND

Pronuclear scoring helps to identify good quality embryos already at the pronuclear stage. There are no data available, however, to demonstrate whether patients benefit from a higher pregnancy rate after pronuclear scoring.

METHODS

In a retrospective, matched cohort study 338 cycles in which patients chose to score their oocytes at the pronuclear stage (scoring group) were compared with 338 cycles without scoring (control group). The cycles were matched for maternal age, number of previous IVF and ICSI cycles, cryopreservation (yes/no) and diagnosis of primary infertility.

RESULTS

The pregnancy rate was not significantly different between the scoring group and the control group (24.0 vs. 21.0%, NS) in spite of more cycles with grade A embryos and a higher number of embryos transferred. The presence of a Z1 pronuclear oocyte was found to be associated with the retrieval of more oocytes, a higher fertilization rate and more grade A embryos, as well as a non-significant increase in pregnancy rates (25.1 vs. 18.8%).

CONCLUSIONS

Benefit from pronuclear scoring seems to be small. Apparently, experienced biologists are able to select "good-quality" pronuclear oocytes in the same way they would do after scoring. However, the results might be biased by differences between the groups.

摘要

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PLoS One. 2017 Feb 2;12(2):e0171465. doi: 10.1371/journal.pone.0171465. eCollection 2017.
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Embryo quality but not pronuclear score is associated with clinical pregnancy following IVF.胚胎质量而非原核评分与体外受精后的临床妊娠相关。
J Assist Reprod Genet. 2014 Mar;31(3):279-83. doi: 10.1007/s10815-013-0162-3. Epub 2014 Jan 5.