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) |