About this item:

67 Views | 25 Downloads

Author Notes:

Sanjiv M. Narayan, MD, PhD, Stanford University School of Medicine, 780 Welch Road, MC 5773, Stanford CA 94305, Tel: +1 650-7362563, Fax: +1 650-7246131. Email: sanjiv1@stanford.edu

Drs. Bhatia and Kapoor report no disclosures. Drs Shah reports consulting reimbursement from Abbott Laboratories. Dr. Narayan reports consulting from Life Signals.ai, TDK Inc., Up to Date, Abbott Laboratories, and American College of Cardiology Foundation; Intellectual Property Rights from University of California Regents and Stanford University.

Subject:

Research Funding:

This work was funded in part by grants to SMN by the National Institutes of Health (R01 HL 83359, R01 HL149134).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cardiac & Cardiovascular Systems
  • Cardiovascular System & Cardiology
  • atrial fibrillation
  • catheters
  • humans
  • pulmonary veins
  • surgery
  • POSTERIOR WALL ISOLATION
  • CATHETER ABLATION
  • SINGLE-CENTER

Mapping Atrial Fibrillation After Surgical Therapy to Guide Endocardial Ablation

Show all authors Show less authors

Tools:

Journal Title:

CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY

Volume:

Volume 15, Number 6

Publisher:

, Pages E010502-E010502

Type of Work:

Article | Post-print: After Peer Review

Abstract:

BACKGROUND: Surgical ablation for atrial fibrillation (AF) can be effective, yet has mixed results. It is unclear which endocardial lesions delivered as part of hybrid therapy‚ will best augment surgical lesion sets in individual patients. We addressed this question by systematically mapping AF endocardially after surgical ablation and relating findings to early recurrence, then performing tailored endocardial ablation as part of hybrid therapy. METHODS: We studied 81 consecutive patients undergoing epicardial surgical ablation (stage 1 hybrid), of whom 64 proceeded to endocardial catheter mapping and ablation (stage 2). Stage 2 comprised high-density mapping of pulmonary vein (PV) or posterior wall (PW) reconnections, low-voltage zones (LVZs), and potential localized AF drivers. We related findings to postsurgical recurrence of AF. RESULTS: Mapping at stage 2 revealed PW isolation reconnection in 59.4%, PV isolation reconnection in 28.1%, and LVZ in 42.2% of patients. Postsurgical recurrence of AF occurred in 36 patients (56.3%), particularly those with long-standing persistent AF (P=0.017), but had no relationship to reconnection of PVs (P=0.53) or PW isolation (P=0.75) when compared with those without postsurgical recurrence of AF. LVZs were more common in patients with postsurgical recurrence of AF (P=0.002), long-standing persistent AF (P=0.002), advanced age (P=0.03), and elevated CHA2DS2-VASc (P=0.046). AF mapping revealed 4.4±2.7 localized focal/rotational sites near and also remote from PV or PW reconnection. After ablation at patient-specific targets, arrhythmia freedom at 1 year was 81.0% including and 73.0% excluding previously ineffective antiarrhythmic medications. CONCLUSIONS: After surgical ablation, AF may recur by several modes particularly related to localized mechanisms near low voltage zones, recovery of posterior wall or pulmonary vein isolation, or other sustaining mechanisms. LVZs are more common in patients at high clinical risk for recurrence. Patient-specific targeting of these mechanisms yields excellent long-term outcomes from hybrid ablation.
Export to EndNote