Epicardial and hybrid surgical ablation of atrial fibrillation: 1-year follow-up outcomes of the EORP EHAFA registry
Language English Country Great Britain, England Media print
Document type Journal Article, Observational Study, Multicenter Study
Grant support
European Heart Rhythm Association
260, 1101 EE
AtriCure Europe BV
Abbott Vascular Int.
Amgen Cardiovascular
AstraZeneca
Bayer AG
Boehringer Ingelheim
Boston Scientific
Bristol Myers Squibb
Pfizer Alliance
Daiichi Sankyo Europe GmbH
Alliance Daiichi Sankyo Europe GmbH and Eli Lilly and Company
Edwards
Gedeon Richter Plc.
Menarini Int. Op.
MSD-Merck & Co.
Novartis Pharma AG
ResMed
Sanofi
Servier
Vifor
PubMed
40971527
PubMed Central
PMC12449207
DOI
10.1093/europace/euaf196
PII: 8258717
Knihovny.cz E-resources
- Keywords
- Atrial fibrillation, Epicardial ablation, Hybrid ablation, Registry, Surgical ablation,
- MeSH
- Time Factors MeSH
- Atrial Fibrillation * surgery physiopathology diagnosis MeSH
- Catheter Ablation * methods adverse effects MeSH
- Middle Aged MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Pericardium * surgery MeSH
- Prospective Studies MeSH
- Recurrence MeSH
- Registries MeSH
- Aged MeSH
- Pulmonary Veins * surgery physiopathology MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Observational Study MeSH
- Geographicals
- Europe MeSH
AIMS: Stand-alone minimal invasive epicardial and hybrid atrial fibrillation ablation (EHAFA) has evolved to a recognized treatment option in challenging patients. The EHAFA registry was initiated to describe the applied diagnostic and therapeutic approaches used in routine practice for these procedures, as well as the outcomes in terms of rhythm, symptoms, and complications. METHODS AND RESULTS: Between January 2016 and March 2018, patients who underwent an EHAFA procedure for all types of atrial fibrillation (AF) were consecutively enrolled in the international, prospective, observational EHAFA registry. Follow-up occurred after 1 year. A total of 468 patients were enrolled from 17 centres in 10 countries. Stand-alone ablation (n = 464) was performed epicardially in 47% (n = 220) or as epi-/endocardial hybrid in 53% (n = 244). The predominate type of AF was non-paroxysmal in 74% (n = 342), and 36% (n = 166) of patients had failed previous catheter ablation. The main lesion sets applied consisted of pulmonary vein isolation (99%, n = 460) and isolation of the left atrial (LA) posterior wall (82%, n = 383). In 82% (n = 382), the LA appendage was managed. The overall in-hospital major complication rate was 8.2% (n = 38/464). Freedom from atrial arrhythmias > 30 s with and without antiarrhythmic drug usage was 79% and 64% (n = 279/353, n = 223/351, respectively). The EHRA score at follow-up was clearly reduced compared to preoperatively (EHRA I: 72%, n = 233/325, vs. 3%, n = 14/464). CONCLUSION: This international registry revealed good rhythm control efficacy for epicardial and hybrid AF ablation in patients with advanced AF, leading to improvement in AF-related symptoms. However, a certain associated complication rate needs to be considered.
Cardiac Surgery Department Ceske Budejovice Hospital Ceske Budejovice Czech Republic
Cardiac Surgery Department CHVZ UZ Brussel Brussels Belgium
Cardiac Surgery Department Heart Center Schuechtermann Klinik Bad Rothenfelde Germany
Department of Cardiology Arrhythmia Section Hospital Clínic Universitat de Barcelona Barcelona Spain
Department of Cardiology Ziekenhuis Oost Limburg Genk Belgium
Department of Medical Science Uppsala University Uppsala Sweden
Faculty of Medicine and Life Sciences Hasselt University Hasselt Belgium
National Heart and Lung Institute Cardiac Function Imperial College London London UK
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