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Atrioventricular and ventriculoarterial discordance (congenitally corrected transposition of the great arteries): echocardiographic features, associations, and outcome in 34 fetuses

机译:房室和心室动脉不协调(先天校正大动脉移位):34位胎儿的超声心动图特征,关联和结局

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Objective: To identify fetal echocardiographic features, associations, and outcome of atrioventricular and ventriculoarterial discordance. Design: Retrospective analysis of videotape recordings of fetal echocardiograms and examination of departmental database and patient records to establish outcome. Setting: Tertiary centre for fetal cardiology. Patients: 34 consecutive fetuses with a prenatal diagnosis of double discordance seen between January 1993 and December 2003. Main outcome measures: Echocardiographic features including reversed differential insertion, identification of the right ventricle through the moderator band, and the origin and orientation of the great arteries. All associated cardiac abnormalities and outcome. Results: Reversed differential insertion was identified in 26 fetuses. The right ventricle could be identified by the moderator band in 30 fetuses and was left sided in all but one. A parallel or abnormal orientation of the great arteries was seen in all fetuses. Only five of 34 cases were isolated from a cardiac viewpoint. There was a ventricular septal defect in 21, Ebstein's anomaly in 8, pulmonary stenosis in 12, coarctation of the aorta in 6, tricuspid atresia in 2, congenital heart block in 2 fetuses prenatally, and dextrocardia in 6. Nineteen babies survived; one baby died in the neonatal period and three in infancy. Eleven pregnancies were interrupted. Conclusions: A left sided or posterior right ventricle, identified by reversed differential insertion or the moderator band, in association with abnormal orientation of the great arteries should alert a sonographer to the diagnosis of double discordance. Isolated cases are rare prenatally (14%) but the short term survival in our fetal series is good. Where pregnancy was continued, 19 of 23 babies (82%) remained alive.
机译:目的:确定胎儿的超声心动图特征,关联和房室与心室动脉不协调的结果。设计:回顾性分析胎儿超声心动图的录像带,并检查部门数据库和患者记录以确定结果。地点:胎儿心脏病学三级中心。患者:1993年1月至2003年12月间,有34例连续胎儿被产前诊断为双不和谐。主要预后指标:超声心动图特征包括反向插入差异,通过调节带识别右心室以及大动脉的起源和方向。 。所有相关的心脏异常和预后。结果:在26名胎儿中发现了反向差异插入。右心室可被30个胎儿的减速带识别,除一个外,其余全部位于左侧。在所有胎儿中都观察到大动脉平行或异常的方向。从心脏角度出发,仅34例病例中有5例是孤立的。室间隔缺损21例,埃伯斯坦异常8例,肺狭窄12例,主动脉缩窄6例,三尖瓣闭锁2例,先天性心脏阻滞2例胎儿,右旋心底6例,存活19例;一名婴儿在新生儿期死亡,三名在婴儿期死亡。十一次怀孕被中断。结论:左心室或右心室后侧,经反向差分插入或减速带识别,并伴有大动脉的异常定向,应提醒超声医师双重不和谐的诊断。孤立的病例在产前很少见(占14%),但在我们的胎儿系列中短期生存是好的。在继续怀孕的情况下,23个婴儿中有19个(82%)仍然活着。

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