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. Author manuscript; available in PMC: 2020 Jan 8.
Published in final edited form as: J Am Coll Cardiol. 2019 Jan 8;73(1):70–88. doi: 10.1016/j.jacc.2018.09.083

Table 3.

Potential Mechanistic Axes for Sudden Cardiac Arrest

Mechanism Comment Reference
Electrophysiological
Reentry Most common mechanism. Multiple subtypes. Myocardial reentry related to scar; bundle branch reentry; rotors (118,124)
Repolarization prolongation Pathophysiology likely related to temporo-spatial dispersion. Long QT; Acute ischemia; potassium channel blockade; enhanced late sodium current. (118,125)
Repolarization dispersion Measured as T peak to T end; phase 2 reentry in ischemia or Brugada syndrome; T-wave area dispersion; microvolt T-wave alternans (TWA). (76,126,127)
Triggered -Early After Depolarizations (EADs) Long QT syndromes; Heart failure-related Enhanced late inward Na current (INa-L) (128)
Triggered -Delayed After Depolarizations (DADs) CPVT; Idiopathic OT and annular VPDs and VT (129)
Wavebreak Transition from organized circuits, foci to fibrillation (89,130)
Myocardial Ischemia
Myocardium Myocardial infarction; Myocardial ischemia (6)
Coronary Atherosclerosis and collaterals; Coronary dissection; Coronary artery spasm; Myocardial- arterial bridge (131)
Inflammation Coronary events; QT modulation. (132)
Mechanical
Stretch LV dysfunction; mitral valve prolapse; sleep apnea; left bundle branch block (91,93)
Fibrosis/scar Post infarct; NICM; HCM. Facilitates reentry, other rhythms (87)
Dyssynchrony Bundle branch may cause cardiomyopathy; predispose to SCA (133)
Mechanical Disruption Commotio cordis, Aortic dissection (134)
Neurologic
Sympathetic stimulation Stellate ganglion activity may precede ventricular arrhythmias; takotsubo syndrome. (135,136)
Neural sprouting Infarction can cause sympathetic nerve sprouting and excessive regional sympathetic innervation. (135)
Regional Myocardial inhomogeneity (MIBG) Regionally inhomogeneously denervated myocardium is Arrhythmogenic. (137)
Cerebral Events Known causes of Sudden death (10,49)
Genetic Monogenic disorders (LQTS, CPVT, Brugada, HCM, ARVC, etc); familial pattern of death in acute MI (47)