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Late complete heart block post-tetralogy of Fallot repair: a possible new predicting precipitating factor and review of related cases

机译:晚期完全心阻滞后图解的乳房修复:可能的新预测促进因子和相关病例的审查

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摘要

Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease beyond the age of 3 months. Complete heart block (CHB) is rare but a serious sequalae post-repair of TOF. We present a case of an 18-month-old child who developed late CHB after around 1 year of the corrective surgery of the congenital anomaly. On the regular follow-up visit, the patient assessment was unremarkable. However, there was bradycardia, 55 beats/min. The ECG showed complete atrioventricular dissociation. Echocardiogram was done and demonstrated severe tricuspid regurgitation (TR). The patient required a permanent pacemaker and he is currently well. We are presenting this case as a late unexpected CHB, with a possibility of progressive right-side dilatation as a contributing factor to CHB due to severe TR.
机译:Fallot(TOF)的Tetralogy是超过3个月的紫绀型心脏病的最常见形式。完整的心脏块(CHB)是罕见的,但是一个严重的TOF后修复后的蛋白葡萄糖。我们提出了一个18个月大的孩子,在先天性异常的矫正手术左右后开发了晚期CHB。在经常随访的访问中,患者评估不起眼。但是,有前心动物,55次/分钟。心电图显示出完全的房室分离。已经完成了超声心动图并证明了严重的三尖瓣反流(TR)。患者需要永久的起搏器,他目前很好。我们将这种情况呈现为晚期意外的CHB,由于严重TR,逐步右侧扩张的可能性是CHB的贡献因素。

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