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β-地中海贫血心肌病的心律失常表现:复杂的管理。

Arrhythmic manifestation in β-thalassemia cardiomyopathy: a complex management.

机构信息

Department of Cardiology, ASST Ospedale Maggiore, Crema.

Department of Cardiology, Ospedale San Paolo, Savona.

出版信息

J Cardiovasc Med (Hagerstown). 2021 Dec 1;22(12):e41-e42. doi: 10.2459/JCM.0000000000001265.

Abstract

A young male with β-thalassemia major was implanted with a single-chamber Implantable cardioverter-defibrillator (ICD) for a cardiac arrest due to ventricular fibrillation. He received multiple inappropriate shocks due to atrioventricular nodal re-entrant tachycardia (AVNRT) treated with radiofrequency catheter ablation and then to high-rate atrial tachycardia refractory to amiodarone and not inducible during electrophysiological study. He refused empirical pulmonary vein isolation. Upgrading to biventricular ICD and performing atrioventricular node ablation avoided further inappropriate shocks.

摘要

一名患有重型β-地中海贫血的年轻男性因心室颤动导致心脏骤停而植入了单腔植入式心脏转复除颤器(ICD)。他因房室结折返性心动过速(AVNRT)接受射频导管消融治疗后,多次出现不适当的电击,随后出现对胺碘酮无效且电生理检查时不能诱发的快速性心房心动过速。他拒绝经验性肺静脉隔离。升级为双心室 ICD 并进行房室结消融术可避免进一步出现不适当的电击。

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