Ventricular Conduction Stability Noninvasively Identifies an Arrhythmic Substrate in Survivors of Idiopathic Ventricular Fibrillation

• Published in: Journal of the American Heart Association Vol. 12; no. 8; p. e028661
• Main Authors: Chow, Ji‐Jian, Leong, Kevin M. W., Shun‐Shin, Matthew J., Ormerod, Julian O. M., Koa‐Wing, Michael, Lefroy, David C., Lim, Phang Boon, Linton, Nicholas W. F., Ng, Fu Siong, Qureshi, Norman A., Whinnett, Zachary I., Peters, Nicholas S., Francis, Darrel P., Varnava, Amanda M., Kanagaratnam, Prapa
• Format: Journal Article
• Language: English
• Published: England John Wiley and Sons Inc 18.04.2023; Wiley
• Subjects: Brugada Syndrome - complications; Brugada Syndrome - diagnosis; Electrocardiography; exercise testing; Heart Conduction System; Humans; idiopathic ventricular fibrillation; myocardial ischemia; Original Research; premature ventricular complex; Survivors; Ventricular Fibrillation - diagnosis; Ventricular Fibrillation - etiology; Ventricular Premature Complexes - complications; Ventricular Premature Complexes - etiology; idiopathic ventricular fibrillation; exercise testing; myocardial ischemia; premature ventricular complex
• ISSN: 2047-9980; 2047-9980
• DOI: 10.1161/JAHA.122.028661

Background Idiopathic ventricular fibrillation (VF) is a diagnosis of exclusion following normal cardiac investigations. We sought to determine if exercise-induced changes in electrical substrate could distinguish patient groups with various ventricular arrhythmic pathophysiological conditions and identify patients susceptible to VF. Methods and Results Computed tomography and exercise testing in patients wearing a 252-electrode vest were combined to determine ventricular conduction stability between rest and peak exercise, as previously described. Using ventricular conduction stability, conduction heterogeneity in idiopathic VF survivors (n=14) was compared with those surviving VF during acute ischemia with preserved ventricular function following full revascularization (n=10), patients with benign ventricular ectopy (n=11), and patients with normal hearts, no arrhythmic history, and negative Ajmaline challenge during Brugada family screening (Brugada syndrome relatives; n=11). Activation patterns in normal subjects (Brugada syndrome relatives) are preserved following exercise, with mean ventricular conduction stability of 99.2±0.9%. Increased heterogeneity of activation occurred in the idiopathic VF survivors (ventricular conduction stability: 96.9±2.3%) compared with the other groups combined (versus 98.8±1.6%; =0.001). All groups demonstrated periodic variation in activation heterogeneity (frequency, 0.3-1 Hz), but magnitude was greater in idiopathic VF survivors than Brugada syndrome relatives or patients with ventricular ectopy (7.6±4.1%, 2.9±2.9%, and 2.8±1.2%, respectively). The cause of this periodicity is unknown and was not replicable by introducing exercise-induced noise at comparable frequencies. Conclusions In normal subjects, ventricular activation patterns change little with exercise. In contrast, patients with susceptibility to VF experience activation heterogeneity following exercise that requires further investigation as a testable manifestation of underlying myocardial abnormalities otherwise silent during routine testing.