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首页> 外文期刊>Journal of the Chinese Medical Association: JCMA >Comparing the clinical outcomes of intrauterine insemination by two different density gradient preparation methods.
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Comparing the clinical outcomes of intrauterine insemination by two different density gradient preparation methods.

机译:通过两种不同的密度梯度制备方法比较宫腔内人工授精的临床结果。

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摘要

BACKGROUND: Sperm preparation has play an integral part in the success of in-vitro fertilization. The aim of this study was to compare 2 different density gradient preparations for sperm separation in respect to sperm recovery, motility, motion parameters and clinical outcome after intrauterine insemination. METHODS: One-hundred and 21 women who received intrauterine insemination due to ovulation dysfunction were randomly allocated into 2 groups, using either the Percoll (Amersham, Pharmacia Biotech AB, Sweden) or the PureSperm (Nidacon, Goteborg, Sweden) density gradient method for sperm preparation. The characteristics of sperm before and after separation and the clinical outcome of intrauterine insemination were compared between the 2 groups. RESULTS: PureSperm and Percoll demonstrated comparable ability to recover the sperms with progressive motility. There was no difference in motion parameters and the number of sperm recovered with progressive motility between the Percoll and the PureSperm density gradient preparations. The clinical pregnancy rate was also comparable between the 2 groups, 12.5% (7/56) in the PureSperm group compared to 13.8% (9/65) in the Percoll group, (p > 0.05). CONCLUSIONS: Despite using different density composition and volume, PureSperm demonstrated clinical effect comparable to that of Percoll in preparing sperm for intrauterine insemination.
机译:背景:精子制备在体外受精的成功中起着不可或缺的作用。这项研究的目的是比较两种不同密度梯度的精子分离制剂,它们涉及精子恢复,活力,运动参数和宫腔内人工授精后的临床结局。方法:将一百二十一例因排卵障碍而接受宫内授精的妇女随机分为两组,分别采用Percoll(Amersham,Pharmacia Biotech AB,瑞典)或PureSperm(Nidacon,哥德堡,瑞典)密度梯度法进行。精子准备。比较两组分离前后的精子特征和宫内授精的临床结局。结果:PureSperm和Percoll表现出相当的恢复精子的能力,并具有进行性运动能力。 Percoll和PureSperm密度梯度制剂之间的运动参数和随着进行性运动而恢复的精子数量没有差异。两组之间的临床妊娠率也相当,PureSperm组为12.5%(7/56),而Percoll组为13.8%(9/65),(p> 0.05)。结论:尽管使用不同的密度成分和体积,PureSperm在制备用于子宫内授精的精子方面具有与Percoll相当的临床效果。

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