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Spatial and transmural properties of the reentrant ventricular tachycardia circuit in arrhythmogenic right ventricular cardiomyopathy: Simultaneous epicardial and endocardial recordings
Journal article   Peer reviewed

Spatial and transmural properties of the reentrant ventricular tachycardia circuit in arrhythmogenic right ventricular cardiomyopathy: Simultaneous epicardial and endocardial recordings

Ruhong Jiang, Takuro Nishimura, Andrew D Beaser, Zaid A Aziz, Gaurav A Upadhyay, Dalise Y Shatz, Hemal M Nayak, Hongtao Liao, Xianzhang Zhan, Fa Po Chung, …
Heart rhythm, Vol.18(6), pp.916-925
06/2021
PMID: 33524624

Abstract

Adult Aged Arrhythmogenic Right Ventricular Dysplasia - etiology Arrhythmogenic Right Ventricular Dysplasia - physiopathology Arrhythmogenic Right Ventricular Dysplasia - surgery Catheter Ablation - methods Epicardial Mapping - methods Female Follow-Up Studies Humans Male Middle Aged Retrospective Studies Tachycardia, Ventricular - complications Tachycardia, Ventricular - physiopathology Young Adult
While advances in the characterization of the structural substrate in arrhythmogenic right ventricular cardiomyopathy (ARVC) have been made, the ventricular tachycardia (VT) circuit remains incompletely described. The purpose of this study was to delineate the reentrant VT circuit with simultaneous epicardial and endocardial mapping (SEEM) in ARVC. Twenty-three consecutive patients with ARVC and VT underwent SEEM at 4 centers between 2014 and 2020. Retrospective analysis was performed on combined isochronal activation maps. Of the 30 VT circuits, 24 were delineated with SEEM (956 [341-1843] endocardial points and 1763 [882-3054] epicardial points). The apex and outflow tract rarely harbored VT circuits, with 50% distributed in the inferior wall and 43% in the free wall. The entire tachycardia cycle length was recorded from the epicardium in 71% of circuits. In all circuits, a large proportion of the tachycardia cycle length was recorded from the epicardium relative to the endocardium. Localized epicardial reentry was observed in 35% of patients (14 mm × 15 mm), which was associated with smaller endocardial low voltage area (39 cm vs 104 cm ; P = .002) and preserved right ventricular ejection fraction (35% vs 25%; P = .046) compared with those with larger circuit dimensions. Seventy percent of termination sites were achieved from the epicardium. High-resolution recordings from both myocardial surfaces confirm a consistent predominance of epicardial participation during reentry in ARVC. Only the perivalvular inflow region of the "triangle of dysplasia" had a strong propensity to harbor VT circuits, with the greatest proportion located in the inferior wall. Localized epicardial reentry may be a manifestation of earlier stage disease with a relative paucity of endocardial substrate.

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