Evolution of the organization of epicardial activation patterns during ventricular fibrillation

J Cardiovasc Electrophysiol. 1998 Dec;9(12):1291-1304. doi: 10.1111/j.1540-8167.1998.tb00105.x.

Abstract

Introduction: This study quantified how the organization of epicardial activation changes during the first 40 seconds of ventricular fibrillation (VF).

Methods and results: Unipolar potentials were mapped from a 504 (24 x 21) electrode array (2-mm interelectrode spacing) on the anterior right ventricle (RV) and left ventricle (LV) epicardium. The array covered approximately 20% of the epicardial surface. In each of seven pigs, six episodes of VF were induced by premature stimulation. One-half second epochs of VF were analyzed, starting 0, 10, 20, 30, and 40 seconds post induction and using novel pattern analysis algorithms. Eight parameters were quantified: (1) the number of wavefronts; (2) the epicardial area activated by wavefronts; (3) the fraction of wavefronts arising from epicardial breakthrough or from a focus; (4) the fraction of wavefronts terminated by conduction block; (5) the multiplicity index (number of distinct activation pathways in the rhythm); (6) the repeatability index (number of times activation pathways are traversed); (7) the activation rate; and (8) the wavefront propagation velocity. The results showed that VF patterns were less organized at 10 than at 0 seconds, with more, smaller wavefronts traversing a larger variety of pathways for fewer repetitions. VF activation patterns then gradually reorganized up to 40 seconds, but by a different mechanism: the spatial size of subpatterns grew, but the dynamics otherwise appeared unchanged. During both transitions, both activation rate and propagation velocity slowed monotonically.

Conclusion: Thus, changes in organization during VF can occur by multiple mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Action Potentials
  • Animals
  • Body Surface Potential Mapping*
  • Disease Models, Animal
  • Electric Countershock
  • Heart Ventricles / physiopathology
  • Pericardium / physiopathology*
  • Swine
  • Ventricular Fibrillation / classification
  • Ventricular Fibrillation / physiopathology*