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Am J Physiol Heart Circ Physiol 285: H1705-H1719, 2003. First published June 5, 2003; doi:10.1152/ajpheart.01108.2001
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Characterization of fibrillatory rhythms by ensemble vector directional analysis

Alan Kadish, David Johnson, Willie Choe, Jeffrey Goldberger, and George Horvath

Feinberg Cardiovascular Research Institute and Division of Cardiology, Department of Medicine, Northwestern University, Chicago, Illinois 60611

Submitted 2 January 2002 ; accepted in final form 27 May 2003

Recent studies have demonstrated that fibrillatory rhythms are not random phenomena but have definable patterns. However, standard mapping techniques may have limitations in their ability to identify the organization of fibrillation. The purpose of this study was to develop and apply a method, "ensemble vector mapping," for characterizing the spatiotemporal organization of fibrillation. Ventricular fibrillation was induced by burst pacing in normal mongrel dogs. In a separate protocol, atrial fibrillation was induced by epicardial aconitine application. Epicardial electrograms were recorded from a 112-electrode plaque array using a computerized mapping system. Vectors were created by summing orthogonal bipolar electrograms. The magnitude of the vectors was transformed using a logarithmic function, integrated over time, and normalized for local electrogram amplitude to produce an "ensemble vector" index whose magnitude is high when beat-to-beat activation direction is consistent and low when activation direction is variable. The mean index was 137 ± 36 mV/s during ventricular pacing at a cycle length of 300 ms but only 39 ± 23 mV/s during ventricular fibrillation (P < 0.001). The ensemble vector index was also lower during atrial fibrillation (60 ± 54 mV/s) than during atrial pacing (115 ± 27 mV/s, P < 0.01 vs. atrial fibrillation) but not as low as during ventricular fibrillation (P < 0.05, atrial vs. ventricular fibrillation). The index was also capable of distinguishing atrial tachycardia from atrial fibrillation. Ensemble vector mapping produces an objective assessment of the consistency of myocardial activation during fibrillation. The consistency of activation direction differs in different models of fibrillation and is higher during atrial than ventricular fibrillation. This technique has the potential to rapidly characterize repetitive activation patterns in fibrillatory rhythms and may help distinguish among different characteristics of fibrillatory rhythms.

cardiac mapping; activation direction; linking



Address for reprint requests and other correspondence: A. Kadish, Northwestern Memorial Hospital, Feinberg Pavilion, Suite 8-536, 251 E. Huron St., Chicago, IL 60611 (E-mail: a-kadish{at}northwestern.edu).




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