Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Both scar and left-to-right ventricular (LV/RV) differences in repolarization properties have been implicated as risk factors for lethal arrhythmias. As a possible mechanism for the initiation of re-entry, a recent study has indicated that LV/RV heterogeneities in the adaptation of action potential duration (APD) to changes in heart rate can cause a transient increase in APD dispersion following rate acceleration, promoting unidirectional block of conduction at the LV/RV junction. In the presence of an ischemic region and ectopic stimulation, a pathological dispersion in repolarization has been suggested to increase the risk of electrical re-entry. However, the exact location and timing of the ectopic activation play a crucial role in initiation of re-entry, and certain combinations may lead to re-entry even under normal LV/RV dispersion in repolarization. This suggests that the phenomenon needs to be investigated in a probabilistic way. In this study we employ a computationally efficient, phenomenological model to quantify the pro-arrhythmic effects associated with a range of combinations of position and timing of an ectopic activation. This allows us to probabilistically study how increasing interventricular dispersion of repolarization increases arrhythmic risk. Results indicate that a larger LV/RV dispersion more than doubles the length of the time window during which the ventricles are vulnerable to re-entry, and leads to a four-fold increase in the probability of re-entry within the vulnerable window. © 2013 CCAL.

Type

Conference paper

Publication Date

01/12/2013

Volume

40

Pages

711 - 714