Epiphenomenal Re-Entry and Spurious Focal Activation Detection by Atrial Fibrillation Mapping Algorithms
- PMID: 33812838
- PMCID: PMC9146411
- DOI: 10.1016/j.jacep.2020.12.005
Epiphenomenal Re-Entry and Spurious Focal Activation Detection by Atrial Fibrillation Mapping Algorithms
Abstract
Objectives: The purpose of this study was to validate the ability of mapping algorithms to detect rotational activations (RoA) and focal activations (FoA) during fibrillatory conduction (FC) and atrial fibrillation (AF) and understand their mechanistic relevance.
Background: Mapping algorithms have been proposed to detect RoA and FoA to guide AF ablation.
Methods: Rapid left atrial pacing created FC-fibrillatory electrograms-with and without AF induction in dogs (n = 17). Activation maps were constructed using Topera (Abbott, St. Paul, Minnesota) or CARTOFINDER (Biosense Webster, Irvine, California) algorithms. Mapping strategies included: panoramic noncontact mapping with a basket catheter (CARTOFINDER n = 6, Topera n = 5); and sequential contact mapping using 8-spline OctaRay catheter (Biosense Webster) (n = 6). Offline frequency and spectral analysis were also performed. Algorithm-detected RoA was manually verified.
Results: The right atrium (RA) consistently exhibited fibrillatory signals during FC. FC with and without AF had similar left-to-right frequency gradients. Basket maps were either uninterpretable (847 of 990 Topera, 132 of 148 Cartofinder) or had unverifiable RoA. OctaRay contact mapping showed 4% RoA (n = 30 of 679) and 63% FoA (n = 429 of 679). Verified RoA clustered at consistent sites, was more common in the RA than left atrium (odds ratio: 3.5), and colocalized with sites of frequency breakdown in the crista terminalis and RA appendage. During pacing, spurious FoA sites were identified around the atria, but not at the actual pacing sites. RoA and FoA site distribution was similar during pacing with and without induction, and during induced AF.
Conclusions: Mapping algorithms were unable to detect pacing sites as true drivers of FC, and detected epiphenomenal RoA and FoA sites unrelated to AF induction or maintenance. Algorithm-detected RoA and FoA did not identify true AF drivers.
Keywords: 3D; CARTOFINDER; atrial fibrillation; focal activation; frequency; mapping; repetitive patterns; rotational activation; rotors; spectral analysis.
Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures This study was supported by the Lois and Carl Davis Centennial Chair, the Charles Burnett III endowment, the Antonio Pacifico fellowship fund, and National Heart, Lung, and Blood Institute grant R01HL115003. Biosense-Webster donated catheters and lent processing workstations for this study. Dr. Valderrábano has received consulting and speaking honoraria from Biosense Webster and Boston Scientific. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Figures






Comment in
-
Patient-Specific Mapping of Atrial Fibrillation Mechanisms: The Quest Continues.JACC Clin Electrophysiol. 2021 Jul;7(7):933-935. doi: 10.1016/j.jacep.2021.02.006. JACC Clin Electrophysiol. 2021. PMID: 34294391 No abstract available.
References
-
- Mandapati R, Skanes A, Chen J, Berenfeld O, Jalife J. Stable microreentrant sources as a mechanism of atrial fibrillation in the isolated sheep heart. Circulation 2000;101:194–9. - PubMed
-
- Skanes AC, Mandapati R, Berenfeld O, Davidenko JM, Jalife J. Spatiotemporal periodicity during atrial fibrillation in the isolated sheep heart. Circulation 1998;98:1236–48. - PubMed
-
- Chen J, Mandapati R, Berenfeld O, Skanes AC, Gray RA, Jalife J. Dynamics of wavelets and their role in atrial fibrillation in the isolated sheep heart. Cardiovasc Res 2000;48:220–32. - PubMed
-
- Prinzmetal M, Corday E, Brill IC, et al. Mechanism of the auricular arrhythmias. Circulation 1950;1:241–5. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources