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February 6, 2006Circulation415 citationsOpen Access

Mechanisms of Wave Fractionation at Boundaries of High-Frequency Excitation in the Posterior Left Atrium of the Isolated Sheep Heart During Atrial Fibrillation

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JKJérôme KalifaKTKazuhiko TanakaАЗА. В. Зайцев

Key Result

In isolated sheep hearts with induced AF, wave fractionation was highest at the boundaries of the maximal dominant frequency domain compared to within the domain (regularity index 0.16 vs 0.19; P=0.047).

Key Points

  • The aim is to explore how high-frequency electrical waves in the posterior left atrium during atrial fibrillation relate to fractionated electrograms.
  • Induction of sustained atrial fibrillation in 8 isolated sheep hearts using acetylcholine.
  • Endocardial videoimaging and electrical mapping of the posterior left atrium to determine dominant frequencies and regularity index.
  • Assessment of spatiotemporal periodic episodes and conduction dynamics in both experimental and simulation setups.
  • Fractionation was lower in the DFmax domain (0.19±0.02) compared to boundary areas (0.16±0.02; P=0.047).
  • Average number of periodic episodes was 25.9±2.3 with 1.9±0.7 rotors per experiment.
  • Outward propagation towards the atria occurred in 76.8±8.1% of breakthrough wave instances; P<0.01.

Structured PICO

P
Population
8 isolated sheep hearts with sustained atrial fibrillation induced by 0.5 micromol/L acetylcholine
I
Intervention
Endocardial videoimaging (DI-4-ANEPPS) and electric mapping of the posterior left atrium (PLA)
O
Outcome
Spatial characterization of dominant frequencies (DFs) and a regularity index (ratio of DF to total power) to assess wave fractionationsurrogate

In an isolated sheep heart model of atrial fibrillation, the most fractionated electrograms occur at the boundaries of high-frequency excitation domains, providing mechanistic insight for localizing AF sources during ablation.

Abstract

BACKGROUND: High-frequency fractionated electrograms recorded during atrial fibrillation (AF) in the posterior left atrium (PLA) and elsewhere are being used as target sites for catheter ablation. We tested the hypothesis that highly periodic electric waves emerging from AF sources at or near the PLA give rise to the most fractionated activity in adjacent locations. METHODS AND RESULTS: Sustained AF was induced in 8 isolated sheep hearts (0.5 micromol/L acetylcholine). Endocardial videoimaging (DI-4-ANEPPS) and electric mapping of the PLA enabled spatial characterization of dominant frequencies (DFs) and a regularity index (ratio of DF to total power). Regularity index showed that fractionation was lowest within the area with the maximal DF (DFmax domain; 0.19+/-0.02) and highest within a band of P=0.047) at boundaries with lower-frequency domains. The numbers of spatiotemporal periodic episodes (25.9+/-2.3) and rotors per experiment (1.9+/-0.7) were also highest within the DFmax domain. Most commonly, breakthrough waves at the PLA traveled toward the rest of the atria (76.8+/-8.1% outward versus 23.2+/-8.1% inward; P<0.01). In both experiments and simulations with an atrial ionic model, fractionation at DFmax boundaries was associated with increased beat-to-beat variability of conduction velocity and directionality with wavebreak formation. CONCLUSIONS: During stable AF, the PLA harbors regular, fast, and highly organized activity; the outer limit of the DFmax domain is the area where the most propagation pattern variability and fractionated activity occur. These new concepts introduce a new perspective in the clinical use of high-frequency fractionated electrograms to localize sources of AF precisely at the PLA and elsewhere.

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Cite This Study

Kalifa et al. (2006) studied Atrial fibrillation (n=8). Acetylcholine was evaluated on Spatial characterization of dominant frequencies and regularity index. In isolated sheep hearts with induced AF, wave fractionation was highest at the boundaries of the maximal dominant frequency domain compared to within the domain (regularity index 0.16 vs 0.19; P=0.047).

synapsesocial.com/papers/6a0f808d9e54838161fccc8ahttps://doi.org/10.1161/circulationaha.105.575340
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