Regional and Temporal Variation of Ventricular and Conduction Tissue Activity During Ventricular Fibrillation in Canines

Background: Rigorous study of ventricular fibrillation (VF) is not feasible in humans. The spatiotemporal characteristics of prolonged VF remain undefined, limiting our understanding of this lethal rhythm. Methods: VF was mapped in 4 canines. The endocardial and epicardial left ventricle (LV) and right ventricle (RV) were sequentially mapped at 0 to 15, 15 to 30, 30 to 45, and 45 to 60 minutes post-induction. Ten consecutive beats were used to determine the average cycle length and regularity index of ventricular and His-Purkinje system signals in discrete regions during each time interval. Results: Average VF time was 58 +/- 12 minutes. The shortest ventricular cycle length was present in the RV apical region (70 +/- 10 msec) at 0 to 15 minutes and at 15 to 30 minutes (89 +/- 31 msec) and LV apical region at 45 to 60 minutes (242 +/- 163 msec). The His-Purkinje system cycle length was the shortest at the RV outflow tract (75 +/- 3 msec) at 0 to 15 minutes, RV inflow and free wall (89 +/- 12 msec) at 15 to 30 minutes, LV apical region (83 +/- 14 msec) at 30 to 45 minutes, and inferior and inferolateral LV (145 +/- 23 msec) at 45 to 60 minutes. Regularity index was the highest in the RV inflow and free wall (78%) at 0 to 15 minutes, RV apical region (86%) at 15 to 30 minutes, LV septum and epicardial anterior RV (80%) at 30 to 45 minutes, and anterior and anterolateral LV (75%) at 45 to 60 minutes. Conclusions: These data suggest significant regional changes in electrical activity throughout VF in canines. A transition of fastest electrical activity from RV to LV apical regions across VF was observed. These novel insights of the temporal and spatial changes of VF merit further evaluation in diseased hearts to assess for reproducibility of findings.

Automated summary

By mapping ventricular fibrillation in canines, it was found that there are significant regional changes in electrical activity throughout VF, with the fastest electrical activity transitioning from the RV to the LV apical regions. These findings provide novel insights for further evaluation of temporal and spatial changes of VF in diseased hearts.