Relationship Between Nonuniform Isochrone-Area in Late Activation Mapping and Arrhythmogenic Substrates Related to

Tomonori Watanabe1, Masashi Kamioka1, Hisaki Makimoto1

  • 1Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.

Insights

Non-uniform isochrone-areas in late activation mapping may indicate non-pulmonary vein triggers in atrial fibrillation (AF) patients. This finding aids in identifying potential arrhythmogenic sources during ablation procedures.

Area of Science:

  • Electrophysiology
  • Cardiac Mapping
  • Atrial Fibrillation Pathophysiology

Background:

  • Arrhythmogenic substrates in the atrial myocardium can initiate atrial fibrillation (AF).
  • The link between nonuniform isochrone-areas in late activation mapping and these arrhythmogenic substrates is not well understood.

Purpose of the Study:

  • To investigate the relationship between nonuniform isochrone-areas identified through high-density mapping and the presence of arrhythmogenic substrates in patients undergoing AF ablation.
  • To determine if these mapped areas are predictive of non-pulmonary vein (PV) triggers.

Main Methods:

  • Sixty-two patients undergoing AF catheter ablation had high-density left atrial (LA) activation mapping post-pulmonary vein isolation.
  • Late activation mapping was reconstructed, defining nonuniform isochrone-areas as regions with ≥3 color-isochrones within a 1-cm radius.
  • The association between these areas and AF triggers was evaluated.

Main Results:

  • Non-PV triggers were found in 11 patients, often located on the LA wall.
  • Patients with non-PV triggers exhibited significantly more nonuniform isochrone-areas compared to those without (median 5.0 vs. 2.0).
  • Nonuniform isochrone-areas on the LA low-posterior wall independently predicted the presence of non-PV triggers (OR: 6.9).

Conclusions:

  • Identification of nonuniform isochrone-areas on the LA low-posterior wall during late activation mapping can suggest potential sources of non-PV triggers.
  • This mapping technique may help localize arrhythmogenic substrates contributing to AF initiation.
Abstract

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