Heart Rhythm
Volume 5, Issue 6 , Pages 846-854, June 2008

Rotor meandering contributes to irregularity in electrograms during atrial fibrillation

Center for Arrhythmia Research, University of Michigan, Ann Arbor, Michigan.

Received 26 September 2007; accepted 6 March 2008. published online 17 March 2008.

Background

Radiofrequency ablation therapy of atrial fibrillation (AF) recently incorporated the analysis of dominant frequency (DF) and/or electrogram fractionation for guidance. However, the relationships between DF, fractionation, and spatiotemporal characteristics of the AF source remain unclear.

Objective

We hypothesize that a meandering reentrant AF source contributes to the wave fractionation and is reflected in the power spectrum of local electrograms elsewhere in the rotor's surroundings.

Methods

Meandering rotors as AF sources were simulated in 2-dimensional models of human atrial tissue and recorded in isolated sheep hearts. Nondominant elements of the signals were differentiated from the dominant elements using singular value decomposition, whereby the purely periodic constituent (PC) relating to the rotor's DF was eliminated rendering a residual constituent (RC) that consisted of all other activity.

Results

Spectral analysis of the decomposed constituents revealed peaks corresponding to the meandering frequency of the rotor tip, the magnitudes of which were proportional to the size of and the distance to the rotor core. Similar analyses on epicardial optical signals and electrograms from isolated sheep hearts, as well as human complex fractionated atrial electrograms, showed applicability of the approach.

Conclusion

Increased meandering of the rotor driving AF reduces activation periodicity and increases fractionation. The spectral manifestation of the rotor activity beyond the meandering region makes it possible to characterize AF source stability, as well as DF in humans using electrode mapping.

Keywords: Electrocardiography, Mapping, Arrhythmia, Fourier analysis

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 Supported in part by National Heart, Lung, and Blood Institute grants PO1-HL039707, P01-HL087226, RO1-HL070074-05A1, and RO1-087055-01, American Heart Association SDG 0230311N, and American College of Cardiology Foundation/General Electric Healthcare Career Development Award.

PII: S1547-5271(08)00272-5

doi:10.1016/j.hrthm.2008.03.010

Heart Rhythm
Volume 5, Issue 6 , Pages 846-854, June 2008