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Nuchal Translucency Measurement Did Not Significantly Predict Trisomy Cases in Tertiary Referral Center

机译:颈部半透明测量未显着预测三级转诊中心的三体病例

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OBJECTIVE: We sought to determine the value of well defined screening method in predicting trisomy?cases in our institution. STUDY DESIGN: Totally 300 amniocentesis cases were screened from prospectively collected database.?Subjects were referred to amniocentesis according to the sequential results of first and second?trimester screening tests. Each case had nuchal translucency measurement between 11th to 14th weeks?of gestation. All values of NT measurement were analyzed to predict trisomy cases. RESUlTS:There were 7 trisomy cases , non of the screening methods significantly predicted trisomy?cases (p0.05) rather than the simply age (Area under curve 0.724, p=0.043). Mean NT did not differ?between groups with normal and abnormal chromosomes(p0.05). CONClUSION: This data led us to conclude that in our country there is still need for more accurate and?standardized method to predict abnormal cases with higher sensitivity and specificiy to decrease invasive?procedures.
机译:目的:我们试图确定定义明确的筛查方法在预测本院三体性病例中的价值。研究设计:从前瞻性收集的数据库中筛选出300例羊膜穿刺术。根据早孕和孕中期筛查试验的顺序结果,将受试者称为羊膜穿刺术。每个病例在妊娠的第11至14周之间进行颈部透明性测量。分析NT测量的所有值以预测三体性病例。结果:有7例三体性病例,没有一种筛查方法能显着预测三体性病例(p> 0.05),而不是单纯年龄(曲线下面积0.724,p = 0.043)。正常染色体和异常染色体组的平均NT无差异(p> 0.05)。结论:这些数据使我们得出结论,在我国,仍需要更准确,更标准化的方法来预测异常病例,并且具有更高的敏感性和特异性,以减少侵入性手术。

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