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Prenatal Diagnosis of Complete Atrioventricular Septal Defect: Perinatal and Neonatal Outcomes

机译:完全房室间隔缺损的产前诊断:围产期和新生儿结局

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摘要

Objective. The purpose of this study was to establish the outlook for fetuses diagnosed with complete atrioventricular septal defect (cAVSD) prenatally and its relation to additional cardiac, extracardiac, and chromosomal abnormalities. Methods. We retrospectively reviewed fetal echocardiograms diagnosed with cAVSD from January 2002 to December 2007, comparing fetuses with and without aneuploidy. Results. Complete antrioventricular septal defect was confirmed in 62 fetuses. Mean maternal age was 28.79 ± 4.78 years (range 20–38). Mean gestational age was 23.69 ± 5.48 weeks (range 12–38). Fetal karyotype was known in all fetuses. An abnormal karyotype was found in 21 fetuses. Complete AVSD occurred without any other intracardiac abnormality in 28 fetuses. Extracardiac anomalies were present in 38 fetuses. As for pregnancy outcomes, there were 36 (58%) terminations of pregnancy and 4 (6.4%) intrauterine fetal deaths. In these four fetuses, complex cAVSD was associated with atrioventricular block (one case), heterotaxy (one case), and fetal hydrops (two cases). Of the 22 live births, 5 were neonatal deaths without surgery while 17 babies underwent surgery and 13 have survived to date. The mean survival age was 53 ± 4 months (range 22–64 m). Conclusion. AVSD is associated with chromosomal, other cardiac, and extracardiac abnormalities. The detection of these abnormalities is important in order to give the best indication of the likely outcome when counselling parents.
机译:目的。这项研究的目的是确定产前诊断为完全房室间隔缺损(cAVSD)的胎儿的前景及其与其他心脏,心外膜和染色体异常的关系。方法。我们回顾性地回顾了2002年1月至2007年12月诊断为cAVSD的胎儿超声心动图,比较了有和没有非整倍性的胎儿。结果。确诊62例胎儿完全房室间隔缺损。平均产妇年龄为28.79±4.78岁(范围20-38)。平均胎龄为23.69±5.48周(范围12-38)。胎儿核型在所有胎儿中都是已知的。在21个胎儿中发现了异常的核型。在28例胎儿中发生了完整的AVSD,而没有任何其他心内异常。 38例胎儿存在心外异常。至于妊娠结局,终止妊娠36例(58%),宫内胎儿死亡4例(6.4%)。在这四个胎儿中,复杂的cAVSD与房室传导阻滞(1例),异型性(1例)和胎儿积液(2例)相关。在22例活产婴儿中,有5例是未经手术的新生儿死亡,而17例接受了手术,迄今为止有13例存活。平均生存年龄为53±4个月(范围22–64μm)。结论。 AVSD与染色体异常,其他心脏异常和心脏外异常有关。这些异常的检测很重要,以便在咨询父母时最好地表明可能的结果。

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