Key result
High dominant frequency (86%) and continuous complex fractionated electrogram regions (77%) were predominantly located within 15 mm of pulmonary vein ostia, mostly relating to arrhythmogenic PVs.
Why the study?
What are the atrial substrate properties around arrhythmogenic pulmonary veins in patients with paroxysmal atrial fibrillation?
Observational (n=23)
What are the atrial substrate properties around arrhythmogenic pulmonary veins in patients with paroxysmal atrial fibrillation?
High-frequency and fractionated electrogram regions are predominantly located within 15 mm of arrhythmogenic pulmonary veins, suggesting this area is a key target for ablation in paroxysmal AF.
Substrate mapping near PVs may help identify triggers in paroxysmal AF ablation; leaves open whether it improves long-term outcomes.
INTRODUCTION: The relationship between pulmonary veins (PVs) with atrial fibrillation (AF) initiating triggers and their surrounding atrial substrate has not been elucidated. We aimed to clarify the atrial substrate properties around the PVs. METHODS AND RESULTS: Twenty-three paroxysmal AF patients were studied with the identification of PV initiating triggers. High-density mapping of the dominant frequency (DF, 1200 Hz) and the mean degree of the complex fractionated electrograms (CFE mean interval over 6 seconds) was evaluated in 2 zones (zone 1: < 5 mm, zone 2: 5-15 mm from the PVs) and the left atrial (LA) using a NavX system prior to the PV isolation. High-DFs (>8 Hz) and continuous CFEs (<50 ms) were identified in 1.5 ± 0.9 and 2.3 ± 1.1 regions per patient, respectively. Most of the high-DF regions (86%) and continuous CFE regions (77%) were located within 15 mm of the PV ostia. Of those, 75% of the high-DF regions and 54% of the continuous CFE regions were related to arrhythmogenic PVs. There was a significant DF gradient from arrhythmogenic PV zone 1 to zone 2, while the mean CFE exhibited a significant gradient between arrhythmogenic PV zone 2 and the rest of the LA. Additionally, 69% of the procedural AF termination sites were at arrhythmogenic PV zone 2. CONCLUSION: Evaluation of the atrial substrate properties may be useful for locating arrhythmogenic PVs during AF and defining the extent of the circumferential PV isolation.
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Suenari et al. (2010) conducted an observational in Paroxysmal Atrial Fibrillation (n=23). Arrhythmogenic pulmonary veins vs. Non-arrhythmogenic pulmonary veins or rest of the left atrium was evaluated on Dominant frequency (DF) and complex fractionated electrograms (CFE) distribution. High dominant frequency (86%) and continuous complex fractionated electrogram regions (77%) were predominantly located within 15 mm of pulmonary vein ostia, mostly relating to arrhythmogenic PVs.
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