Catheter ablation in adult congenital heart disease on uninterrupted oral anticoagulation: Is it safe? Data from a large single-center study.


Journal

Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317

Informations de publication

Date de publication:
04 2022
Historique:
received: 16 08 2021
revised: 16 12 2021
accepted: 17 12 2021
pubmed: 28 12 2021
medline: 6 4 2022
entrez: 27 12 2021
Statut: ppublish

Résumé

Catheter ablation in adult congenital heart disease (ACHD) patients is a critical treatment strategy for complex arrhythmias including atrial fibrillation (AF) and atrial tachycardia (AT). In addition to vitamin K antagonists (VKAs), direct oral anticoagulants (DOACs) are increasingly used in this patient population. The purpose of this study was to assess the safety of catheter ablation in ACHD patients on uninterrupted oral anticoagulation with VKA or DOAC, examining thromboembolic, bleeding, and vascular access complications. Retrospective analysis of 234 ACHD patients with simple (n = 83), moderate (n = 66), or complex (n = 85) CHD (mean age 46 years) undergoing 368 ablation procedures on uninterrupted oral anticoagulation with VKA (45.4%) or DOAC (54.6%) was undertaken. Arrhythmias were AF in 97, right AT in 181, left AT in 65, or a combination of AF and AT in 25. No thromboembolic complications occurred. Major complications occurred in 4 patients (1.1%; 1 VKA, 3 DOAC), including retroperitoneal hematoma in 2 and arteriovenous (AV) fistula requiring surgical treatment in 2. Minor bleeding or vascular access complications occurred in 46 cases (12.5%), including hematomas >5 cm in 26, AV fistulas (not requiring surgical intervention) in 13, and pseudoaneurysms in 7 (thrombin injection in 3/7). Overall, no significant difference was found between DOAC (14.9%) and VKA groups (12.0%; P = .411). Catheter ablation in ACHD patients on uninterrupted oral anticoagulation with VKA or DOAC is feasible and safe. No thromboembolic events occurred, and major bleeding or vascular access complications were rare. No significant differences regarding minor bleeding or vascular access complications between patients on DOAC or VKA were found.

Sections du résumé

BACKGROUND
Catheter ablation in adult congenital heart disease (ACHD) patients is a critical treatment strategy for complex arrhythmias including atrial fibrillation (AF) and atrial tachycardia (AT). In addition to vitamin K antagonists (VKAs), direct oral anticoagulants (DOACs) are increasingly used in this patient population.
OBJECTIVE
The purpose of this study was to assess the safety of catheter ablation in ACHD patients on uninterrupted oral anticoagulation with VKA or DOAC, examining thromboembolic, bleeding, and vascular access complications.
METHODS
Retrospective analysis of 234 ACHD patients with simple (n = 83), moderate (n = 66), or complex (n = 85) CHD (mean age 46 years) undergoing 368 ablation procedures on uninterrupted oral anticoagulation with VKA (45.4%) or DOAC (54.6%) was undertaken. Arrhythmias were AF in 97, right AT in 181, left AT in 65, or a combination of AF and AT in 25.
RESULTS
No thromboembolic complications occurred. Major complications occurred in 4 patients (1.1%; 1 VKA, 3 DOAC), including retroperitoneal hematoma in 2 and arteriovenous (AV) fistula requiring surgical treatment in 2. Minor bleeding or vascular access complications occurred in 46 cases (12.5%), including hematomas >5 cm in 26, AV fistulas (not requiring surgical intervention) in 13, and pseudoaneurysms in 7 (thrombin injection in 3/7). Overall, no significant difference was found between DOAC (14.9%) and VKA groups (12.0%; P = .411).
CONCLUSION
Catheter ablation in ACHD patients on uninterrupted oral anticoagulation with VKA or DOAC is feasible and safe. No thromboembolic events occurred, and major bleeding or vascular access complications were rare. No significant differences regarding minor bleeding or vascular access complications between patients on DOAC or VKA were found.

Identifiants

pubmed: 34958942
pii: S1547-5271(21)02510-8
doi: 10.1016/j.hrthm.2021.12.018
pii:
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

648-655

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Leonie Foerschner (L)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany. Electronic address: foerschner@dhm.mhn.de.

Julia Kriesmair (J)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Marta Telishevska (M)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Marc Kottmaier (M)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Felix Bourier (F)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Tilko Reents (T)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Sarah Lengauer (S)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Carsten Lennerz (C)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Hannah Krafft (H)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Susanne Maurer (S)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Miruna Popa (M)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Christof Kolb (C)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Isabel Deisenhofer (I)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

Gabriele Hessling (G)

Department of Electrophysiology, German Heart Center Munich, Technical University Munich, Munich, Germany.

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