This editorial refers to 'Acute effects of complex fractionated atrial electrogram ablation on dominant frequency and regulatory index for the fibrillatory process' by G. Bencsik et al., on page 1011
Mechanisms underlying fractionation of extracellular potentialsFractionated electrograms are defined as extracellular potentials consisting of multiple negative deflections which are the result of local asynchronous activation of atrial tissue beneath the recording electrode.1 Experimental studies have suggested that fractionation of electrograms can be either functional (spatial dispersion of action potential duration) or structural (e.g. tissue anisotropy, collageneous septa) in nature. 2 -4 Spach has demonstrated that the fractionation of extracellular potentials is caused by the deposition of fibrous tissue between muscle fibres. 2,3 The number of side-to-side electrical coupling in the transverse direction is diminished, whereas the electrical coupling in the longitudinal direction remains unaffected. A decrease in side-to-side electrical coupling in the transverse direction leads to an increase in effective axial resistance and hence a local conduction delays in this direction (nonuniform anisotropy). The resulting asynchronous activation of muscle bundles gives rise to fractionation of electrograms. In the goat model of persistent of atrial fibrillation, prolongation of atrial fibrillation cycle length by infusion of a Class I drug was associated with a significant reduction in the incidence of fractionation. 4 Class I drugs prolong atrial fibrillation cycle length more than atrial refractoriness, thereby widening the excitable gap. These findings indicate that the decrease of fractionation was due to widening of the excitable gap as in the presence of a wider excitable gap the wavefront will propagate through muscle which is in a higher state of excitability, suggesting that the fractionation is functionally determined. The importance of fractionated fibrillation potentials as possible indicators of the arrhythmogenic substrate was first suggested by Allessie et al.
5The relation between the morphology of fibrillation electrograms and spatial patterns of activation during atrial fibrillation was studied. For this purpose, fibrillation electrograms recorded from the right atrial free wall in humans were classified as fragmented potentials. Short double potentials were the result of collision of fibrillation waves; long double potentials were recorded along long lines of functional conduction block, whereas fragmented potentials occurred either during pivoting of fibrillatory waves at the end of a line of block or at areas of slow conduction. As abnormalities in conduction resulted in long double and fractionated potentials, it was hypothesized that fibrillation potentials could be used to guide a selective ablation approach.On the basis of this hypothesis, ablative therapy targeting fractionated atrial electrograms have become a topic of interest. Ever since, a series of clinical studies have indeed provided...