Approach to the Diagnosis and Management of Complex Fascicular Ventricular Tachycardias.

IF 9.1 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation. Arrhythmia and electrophysiology Pub Date : 2024-12-16 DOI:10.1161/CIRCEP.124.013450
Christopher X Wong, Henry H Hsia, Adam C Lee, Robert M Hayward, Coleen J Johnson, Edgar Antezana-Chavez, Pichmanil Khmao, Melvin M Scheinman
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Abstract

Complex ventricular tachycardias involving the fascicular system (fascicular ventricular tachycardias [FVTs]) can be challenging. In this review, we describe our approach to the diagnosis and ablation of these arrhythmias with 10 illustrative cases that involve (1) differentiation from supraventricular tachycardia; (2) assessment for atypical bundle branch reentry and other interfascicular FVTs; (3) examination of P1/P2 activation sequences in sinus rhythm, pacing, and tachycardia; and (4) entrainment techniques to establish the tachycardia mechanism and aid circuit localization. To summarize, 5 cases had prior ablation with 2 previously misdiagnosed as supraventricular tachycardia. A short His-ventricular interval supported ventricular tachycardia. Atrial stimulation could initiate and entrain 4 FVTs. P1 potentials were recorded in all cases of left posterior FVT. Entrainment at P1 and P1 to P2 connection sites at the mid-septal region, and the postablation emergence of a late P1 with decremental properties, is consistent with the left septal fascicle being the slowly conducting, retrograde limb of the left posterior FVT circuit. Ablation targeting the mid-septal left septal fascicle and P1 to P2 connection sites successfully eliminated left posterior FVT. Right ventricular apical pacing was useful in differentiating bundle branch reentry and focal FVTs from reentrant FVTs. Two cases exhibited bundle branch reentry and other interfascicular FVTs. Three cases were postinfarct FVTs involving the LPF, where pacing and entrainment at sites of conduction system potentials were able to localize sites critical for ablation, in contrast to previously unsuccessful substrate modification. In conclusion, several ventricular tachycardia mechanisms involving the fascicular system can occur in both structurally normal and abnormal hearts. A high index of suspicion is required given their rarity and potential for misdiagnosis. Once identified, we emphasize a structured approach to the diagnosis and management of FVTs to confirm the mechanism and localize suitable ablation targets involving careful recording of conduction system potentials and pacing/entrainment maneuvers.

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复杂性筋膜室性心动过速的诊断和处理方法。
涉及筋膜系统的复杂室性心动过速(筋膜室性心动过速 [FVT])可能具有挑战性。在这篇综述中,我们通过 10 个典型病例介绍了诊断和消融这些心律失常的方法,包括:(1)与室上性心动过速的鉴别;(2)评估非典型束支再入及其他束间室速;(3)检查窦性心律、起搏和心动过速时的 P1/P2 激活序列;以及(4)采用夹带技术确定心动过速机制并帮助电路定位。总之,5 个病例曾做过消融术,其中 2 个病例曾被误诊为室上性心动过速。His-ventricular 间期短支持室性心动过速。心房刺激可启动和诱导 4 个室上性心动过速。所有左后房室速病例均记录到 P1 电位。P1电位和P1至P2连接点的夹带位于室隔中部,消融后出现的晚期P1电位具有递减特性,这与左室间隔束是左后室上性心动过速回路的慢传导逆行肢是一致的。针对左室间隔中束和 P1 至 P2 连接点的消融成功地消除了左室后 FVT。右室心尖起搏有助于区分束支再入和局灶性 FVT 与再发性 FVT。有两个病例表现出束支返支和其他筋膜间快速室上性心动过速。三个病例是涉及 LPF 的梗死后 FVT,在传导系统电位部位进行起搏和夹带能够定位消融的关键部位,这与之前不成功的基底改造形成了鲜明对比。总之,在结构正常和异常的心脏中都可能发生涉及筋膜系统的几种室性心动过速机制。鉴于其罕见性和误诊的可能性,需要高度怀疑。一旦发现,我们强调采用结构化的方法来诊断和处理室速,以确认机制并定位合适的消融目标,包括仔细记录传导系统电位和起搏/诱导操作。
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来源期刊
CiteScore
13.70
自引率
4.80%
发文量
187
审稿时长
4-8 weeks
期刊介绍: Circulation: Arrhythmia and Electrophysiology is a journal dedicated to the study and application of clinical cardiac electrophysiology. It covers a wide range of topics including the diagnosis and treatment of cardiac arrhythmias, as well as research in this field. The journal accepts various types of studies, including observational research, clinical trials, epidemiological studies, and advancements in translational research.
期刊最新文献
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