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The Circle of Reentry: Characteristics of Trigger-substrate Interaction Leading to Sudden Cardiac Arrest

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Abstract

Sudden cardiac death is often caused by ventricular arrhythmias driven by reentry. Comprehensive characterization of the potential triggers and substrate in survivors of sudden cardiac arrest has provided insights into the trigger-substrate interaction leading to reentry. Previously, a "Triangle of Arrhythmogenesis", reflecting interactions between substrate, trigger and modulating factors, has been proposed to reason about arrhythmia initiation. Here, we expand upon this concept by separating the trigger and substrate characteristics in their spatial and temporal components. This yields four key elements that are required for the initiation of reentry: local dispersion of excitability (e.g., the presence of steep repolarization time gradients), a critical relative size of the region of excitability and the region of inexcitability (e.g., a sufficiently large region with early repolarization), a trigger that originates at a time when some tissue is excitable and other tissue is inexcitable (e.g., an early premature complex), and which occurs from an excitable region (e.g., from a region with early repolarization). We discuss how these findings yield a new mechanistic framework for reasoning about reentry initiation, the "Circle of Reentry." In a patient case of unexplained ventricular fibrillation, we then illustrate how a comprehensive clinical investigation of these trigger-substrate characteristics may help to understand the associated arrhythmia mechanism. We will also discuss how this reentry initiation concept may help to identify patients at risk, and how similar reasoning may apply to other reentrant arrhythmias.

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References
1.
Rivaud M, Bayer J, Cluitmans M, van der Waal J, Bear L, Boukens B . Critical repolarization gradients determine the induction of reentry-based torsades de pointes arrhythmia in models of long QT syndrome. Heart Rhythm. 2020; 18(2):278-287. DOI: 10.1016/j.hrthm.2020.09.020. View

2.
Wu W, Wang H, Zhao P, Talcott M, Lai S, McKinstry R . Noninvasive high-resolution electromyometrial imaging of uterine contractions in a translational sheep model. Sci Transl Med. 2019; 11(483). DOI: 10.1126/scitranslmed.aau1428. View

3.
Durrer D, VAN DAM R, Freud G, Janse M, Meijler F, ARZBAECHER R . Total excitation of the isolated human heart. Circulation. 1970; 41(6):899-912. DOI: 10.1161/01.cir.41.6.899. View

4.
Haws C, Lux R . Correlation between in vivo transmembrane action potential durations and activation-recovery intervals from electrograms. Effects of interventions that alter repolarization time. Circulation. 1990; 81(1):281-8. DOI: 10.1161/01.cir.81.1.281. View

5.
de Bakker J, van Capelle F, Janse M, Wilde A, Coronel R, Becker A . Reentry as a cause of ventricular tachycardia in patients with chronic ischemic heart disease: electrophysiologic and anatomic correlation. Circulation. 1988; 77(3):589-606. DOI: 10.1161/01.cir.77.3.589. View