Dynamic electrophysiological mechanism in patients with long-standing persistent atrial fibrillation.

atrial fibrillation electrophysiology localization of AF drivers non-invasive electrocardiographic imaging sequential mapping

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 26 05 2022
accepted: 02 09 2022
entrez: 17 10 2022
pubmed: 18 10 2022
medline: 18 10 2022
Statut: epublish

Résumé

Improved understanding of the mechanisms that sustain persistent and long-standing persistent atrial fibrillation (LSpAF) is essential for providing better ablation solutions. The findings of traditional catheter-based electrophysiological studies can be impacted by the sedation required for these procedures. This is not required in non-invasive body-surface mapping (ECGI). ECGI allows for multiple mappings in the same patient at different times. This would expose potential electrophysiological changes over time, such as the location and stability of extra-pulmonary vein drivers and activation patterns in sustained AF. In this electrophysiological study, 10 open-heart surgery candidates with LSpAF, without previous ablation procedures (6 male, median age 73 years), were mapped on two occasions with a median interval of 11 days (IQR: 8-19) between mappings. Bi-atrial epicardial activation sequences were acquired using ECGI (CardioInsight™, Minneapolis, MN, United States). Bi-atrial electrophysiological abnormalities were documented in all 20 mappings. Interestingly, the anatomic location of focal and rotor activities changed between the mappings in all patients [100% showed changes, 95%CI (69.2-100%), This clinical study documented that driver location and activation patterns in patients with LSpAF changes constantly. Furthermore, bi-atrial pathophysiology was demonstrated, which underscores the importance of treating both atria in LSpAF and the significant role that arrhythmogenic drivers outside the pulmonary veins seem to have in maintaining this complex arrhythmia.

Sections du résumé

Background UNASSIGNED
Improved understanding of the mechanisms that sustain persistent and long-standing persistent atrial fibrillation (LSpAF) is essential for providing better ablation solutions. The findings of traditional catheter-based electrophysiological studies can be impacted by the sedation required for these procedures. This is not required in non-invasive body-surface mapping (ECGI). ECGI allows for multiple mappings in the same patient at different times. This would expose potential electrophysiological changes over time, such as the location and stability of extra-pulmonary vein drivers and activation patterns in sustained AF.
Materials and methods UNASSIGNED
In this electrophysiological study, 10 open-heart surgery candidates with LSpAF, without previous ablation procedures (6 male, median age 73 years), were mapped on two occasions with a median interval of 11 days (IQR: 8-19) between mappings. Bi-atrial epicardial activation sequences were acquired using ECGI (CardioInsight™, Minneapolis, MN, United States).
Results UNASSIGNED
Bi-atrial electrophysiological abnormalities were documented in all 20 mappings. Interestingly, the anatomic location of focal and rotor activities changed between the mappings in all patients [100% showed changes, 95%CI (69.2-100%),
Conclusion UNASSIGNED
This clinical study documented that driver location and activation patterns in patients with LSpAF changes constantly. Furthermore, bi-atrial pathophysiology was demonstrated, which underscores the importance of treating both atria in LSpAF and the significant role that arrhythmogenic drivers outside the pulmonary veins seem to have in maintaining this complex arrhythmia.

Identifiants

pubmed: 36247427
doi: 10.3389/fcvm.2022.953622
pmc: PMC9556291
doi:

Types de publication

Journal Article

Langues

eng

Pagination

953622

Informations de copyright

Copyright © 2022 Osorio-Jaramillo, Cox, Klenk, Kaider, Angleitner, Werner, Strassl, Mach, Laufer, Ehrlich and Ad.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

J Cardiovasc Electrophysiol. 2020 May;31(5):1031-1037
pubmed: 32115794
Europace. 2017 Aug 01;19(8):1302-1309
pubmed: 28204452
J Clin Med. 2021 Dec 31;11(1):
pubmed: 35011953
Front Physiol. 2021 Apr 30;12:653013
pubmed: 33995122
JACC Case Rep. 2020 May 20;2(5):745-749
pubmed: 34317340
Heart Rhythm. 2022 Jun;19(6):875-884
pubmed: 35134548
Circulation. 2010 Oct 5;122(14):1364-72
pubmed: 20855661
Heart Rhythm. 2017 May;14(5):661-667
pubmed: 28434446
Circ Arrhythm Electrophysiol. 2016 May;9(5):
pubmed: 27103089
Circ Res. 2013 Mar 1;112(5):863-74
pubmed: 23449548
J Thorac Cardiovasc Surg. 2019 Jan;157(1):234-243.e9
pubmed: 30557941
Circ Arrhythm Electrophysiol. 2017 Nov;10(11):
pubmed: 29138143
Circ Arrhythm Electrophysiol. 2018 May;11(5):e006119
pubmed: 29743170
Circulation. 2000 Jan 18;101(2):194-9
pubmed: 10637208
J Am Coll Cardiol. 2017 Mar 14;69(10):1257-1269
pubmed: 28279292
Innovations (Phila). 2020 Nov/Dec;15(6):525-531
pubmed: 33052065
J Am Coll Cardiol. 2009 Mar 3;53(9):782-9
pubmed: 19245970
Heart Rhythm. 2008 Jun;5(6):846-54
pubmed: 18534369
Innovations (Phila). 2020 Sep/Oct;15(5):410-415
pubmed: 32790514
Circulation. 1997 Aug 5;96(3):1012-24
pubmed: 9264513
J Am Heart Assoc. 2020 Oct 20;9(19):e017789
pubmed: 33006292
J Thorac Cardiovasc Surg. 2006 May;131(5):1029-35
pubmed: 16678586
J Thorac Cardiovasc Surg. 2019 Jan;157(1):248-256
pubmed: 30482525
Eur Heart J. 2021 Feb 1;42(5):373-498
pubmed: 32860505
J Electrocardiol. 2006 Oct;39(4 Suppl):S7-12
pubmed: 16920139
Circulation. 2014 Aug 12;130(7):530-8
pubmed: 25028391
Circulation. 2009 Apr 7;119(13):1758-67
pubmed: 19307477
Am Heart J. 1964 Feb;67:200-20
pubmed: 14118488
Nat Med. 2004 Apr;10(4):422-8
pubmed: 15034569
Circulation. 2014 Dec 2;130(23):e199-267
pubmed: 24682347
Circulation. 2019 Jul 9;140(2):e125-e151
pubmed: 30686041
PLoS Comput Biol. 2020 Sep 23;16(9):e1008086
pubmed: 32966275

Auteurs

Emilio Osorio-Jaramillo (E)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

James L Cox (JL)

Division of Cardiac Surgery, Bluhm Cardiovascular Institute, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States.

Sarah Klenk (S)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.
Division of Cardiology, Clinic Favoriten, Vienna, Austria.

Alexandra Kaider (A)

Department of Cardiac Surgery, Informatics and Intelligent Systems, Medical University of Vienna, Vienna, Austria.

Philipp Angleitner (P)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Paul Werner (P)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Andreas Strassl (A)

Division of Cardiovascular and Interventional Radiology, Medical University of Vienna, Vienna, Austria.

Markus Mach (M)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Guenther Laufer (G)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Marek P Ehrlich (MP)

Department of Cardiac Surgery, Medical University of Vienna, Vienna, Austria.

Niv Ad (N)

Cardiothoracic Surgery, Adventist HealthCare White Oak Medical Center, Silver Spring, MD, United States.
Division of Cardiac Surgery, Johns Hopkins University, Baltimore, MD, United States.

Classifications MeSH