Successful Catheter Ablation Under ECMO for Fatal Ventricular Tachycardia from RV Papillary Muscle in an Infant.

IF 1.3
Shigehito Baba, Aya Miyazaki, Sou Otsuki, Shuichi Shiraishi, Kei Nishiyama, Akihiko Saitoh
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引用次数: 0

Abstract

Right ventricular papillary muscle (RVPM)-originating ventricular tachycardia (VT) is a potentially life-threatening arrhythmia that can rapidly lead to hemodynamic collapse. To the best of our knowledge, no cases have been reported in infants. We present the case of a 2-month-old male who developed RVPM-VT and subsequently underwent successful catheter ablation while on extracorporeal membrane oxygenation (ECMO). Due to the risk of air entry through the sheath from ECMO suction, catheter exchange was performed in a water-filled tray. Pace mapping was utilized to accurately localize the VT origin, followed by ablation using an irrigated catheter, which effectively delivered the necessary power to ablate the RVPM. The VT was successfully terminated post-ablation, with no recurrence observed.

ECMO下导管消融治疗婴儿右室乳头肌致死性室性心动过速成功一例。
右心室乳头状肌(RVPM)源性室性心动过速(VT)是一种潜在的危及生命的心律失常,可迅速导致血流动力学衰竭。据我们所知,没有婴儿病例报告。我们提出了一个2个月大的男性病例,他发展为RVPM-VT,随后在体外膜氧合(ECMO)下进行了成功的导管消融。由于ECMO吸入有空气通过鞘进入的风险,导管交换在一个充满水的托盘中进行。利用起搏图准确定位室性室起源,然后使用冲洗导管消融,有效地提供消融RVPM所需的能量。消融后室速成功终止,未见复发。
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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