Atrial Fibrillation with Ventricular Pre-Excitation: A Diagnosis That Must Not Be Missed

A. Ioannou
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Abstract

Wolff-Parkinson-White (WPW) syndrome is caused by an accessory pathway that communicates between the atria and ventricles known as the Bundle of Kent. The development of atrial fibrillation, can result in the atrial impulses all being conducted via the accessory pathway and result in a sinister, board complex, irregular tachycardia, with varying QRS morphology (known as pre-excited atrial fibrillation) Adenosine is a potent atrioventricular node blocker, which can be used in the treatment of supraventricular tachycardias, but also has diagnostic utility, particularly in differentiating between supraventricular tachycardia with aberrant conduction (which would often terminate) and a ventricular tachycardia (which would not respond to adenosine). However, the administration of adenosine in pre-excited atrial fibrillation can precipitate 1:1 atrial to ventricular conduction, which can degenerate into life-threatening ventricular arrythmias. This case describes a patient who presented with pre-excited atrial fibrillation and received intravenous adenosine that resulted in development of broad complex tachycardia with haemodynamic compromise. In patients with pre-exited atrial fibrillation, AV nodal blocking agents should be avoided and direct current cardioversion should be utilised.
房颤伴心室预激:一个不容错过的诊断
Wolff-Parkinson-White (WPW)综合征是由心房和心室之间的辅助通路(称为肯特束)引起的。房颤的发展,可导致心房脉冲全部通过辅助通路传导,导致一种危险的,板复杂的,不规则的心动过速,具有不同的QRS形态(称为预兴奋性房颤)腺苷是一种有效的房室结阻滞剂,可用于治疗室上性心动过速,但也有诊断用途。特别是在区分传导异常的室上性心动过速(通常会终止)和室性心动过速(对腺苷没有反应)时。然而,在预兴奋性房颤中给药腺苷可使1:1的房室传导沉淀,并可退化为危及生命的室性心律失常。这个病例描述了一个病人谁提出了预兴奋性心房颤动,并接受静脉腺苷,导致发展广泛的复杂心动过速与血流动力学妥协。对于房颤患者,应避免房室结阻滞剂,并应使用直流电复律。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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