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先天性心脏病且核型正常胎儿中颈项透明层增厚的患病率。

Prevalence of increased nuchal translucency in fetuses with congenital cardiac disease and a normal karyotype.

作者信息

Vogel Melanie, Sharland Gurleen K, McElhinney Doff B, Zidere Vita, Simpson John M, Miller Owen I, Allan Lindsey D

机构信息

Department of Fetal and Paediatric Cardiology, Evelina Children's Hospital, London, UK.

出版信息

Cardiol Young. 2009 Sep;19(5):441-5. doi: 10.1017/S1047951109990655. Epub 2009 Jul 29.

Abstract

OBJECTIVES

Our aims were to estimate the prevalence of increased nuchal translucency in fetuses with a normal karyotype that were subsequently diagnosed with congenital cardiac disease on fetal echocardiography, and to assess whether there is a link between increased nuchal translucency and specific congenital cardiac malformations.

METHODS

We reviewed all patients referred to King's College Hospital and the Evelina Children's Hospital in London for fetal echocardiography between January 1998 and December 2007. We investigated the proportion of chromosomally normal fetuses with congenitally malformed hearts in which nuchal thickness was increased, both overall and with specific defects.

RESULTS

We identified 2133 fetuses with congenital cardiac disease by prenatal echocardiography. Of those, 707 were excluded due to abnormal karyotype, and 690 were excluded due to unknown karyotype. The remaining 736 were eligible for inclusion. Among 481 fetuses with documented congenital cardiac disease and normal chromosomes, making up 23% of the overall cohort, 224 had increased nuchal thickness defined as equal or greater than 2.5 millimetres, this being 0.47 of the inclusive cohort, with 95% confidence intervals from 0.42 to 0.51. These proportions were significantly higher than the expected proportion of the normal population, which was 0.05 (p < 0.001). The only diagnosis for which the proportion of fetuses with nuchal translucency measurement equal or greater than 2.5 millimetres was higher than the others was atrioventricular septal defect, with 0.62 of this cohort having abnormal values, with 95% confidence intervals from 0.47 to 0.77 (p = 0.038).

CONCLUSION

We found that nearly half of prenatally diagnosed fetuses with congenitally malformed hearts, when examined ultrasonically in the first or early-second trimester, had increased nuchal thickness. We recommend, therefore, referral of all fetuses with increased nuchal translucency for fetal echocardiography.

摘要

目的

我们的目标是评估核型正常但随后经胎儿超声心动图诊断为先天性心脏病的胎儿中颈项透明层增厚的发生率,并评估颈项透明层增厚与特定先天性心脏畸形之间是否存在关联。

方法

我们回顾了1998年1月至2007年12月间转诊至伦敦国王学院医院和伊芙琳儿童医院进行胎儿超声心动图检查的所有患者。我们调查了染色体正常但心脏先天性畸形且颈项厚度增加的胎儿比例,包括总体情况以及特定缺陷情况。

结果

通过产前超声心动图,我们识别出2133例患有先天性心脏病的胎儿。其中,707例因核型异常被排除,690例因核型未知被排除。其余736例符合纳入标准。在481例记录有先天性心脏病且染色体正常的胎儿中,占整个队列的23%,224例颈项厚度增加,定义为等于或大于2.5毫米,这占纳入队列的0.47,95%置信区间为0.42至0.51。这些比例显著高于正常人群的预期比例0.05(p<0.001)。颈项透明层测量值等于或大于2.5毫米的胎儿比例高于其他诊断的唯一情况是房室间隔缺损,该队列中有0.62的胎儿值异常,95%置信区间为0.47至0.77(p = 0.038)。

结论

我们发现,在孕早期或孕中期进行超声检查时,近一半产前诊断为心脏先天性畸形的胎儿颈项厚度增加。因此,我们建议将所有颈项透明层增厚的胎儿转诊进行胎儿超声心动图检查。

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