Ablation versus Anti-Arrhythmic Therapy for Reducing All Hospital Episodes from Recurrent Atrial Fibrillation (AVATAR-AF): Design and rationale.


Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
08 2019
Historique:
received: 30 05 2018
accepted: 25 04 2019
pubmed: 4 6 2019
medline: 7 3 2020
entrez: 2 6 2019
Statut: ppublish

Résumé

Atrial Fibrillation (AF) ablation using the cryoballoon is effective at reducing symptomatic AF episodes. The prevalence of AF is increasing with the aging population and access to such treatment would be enhanced by reducing the resource requirements. Relinquishing electrical mapping of the pulmonary veins (PV) removes the need for PV catheters, electrical recording equipment and staff trained in using this equipment. Moreover, the majority of complications are peri-procedural so overnight hospitalization maybe unnecessary. We tested this streamlined approach to AF ablation against medical therapy using the endpoint of time to all hospital episodes. METHODS: The AVATAR-AF study is a prospective, multicenter, randomized controlled trial testing the primary hypothesis that AF ablation done without PV mapping or overnight hospitalization is more effective than anti-arrhythmic drugs at reducing all hospital episodes related to recurrent atrial arrhythmias. We included a third arm to test a secondary hypothesis that confirming PV entrance block as per consensus guidelines can improve outcomes. Three hundred twenty-one patients with documented paroxysmal AF will be randomized in a 1:1:1 manner to one of three investigation arms: (1) AVATAR protocol cryoballoon ablation without assessment of acute PV isolation or overnight hospitalization; (2) medical therapy with anti-arrhythmic drugs; or (3) conventional cryoballoon ablation with assessment of acute PV isolation. The primary endpoint is defined as the time to all hospital episodes (including outpatient consultation) related to treatment for atrial arrhythmia. CONCLUSION: The AVATAR-AF study will determine whether the resource utilization for AF ablation can be reduced whilst maintaining superiority over medical therapy.

Identifiants

pubmed: 31152874
pii: S0002-8703(19)30104-8
doi: 10.1016/j.ahj.2019.04.015
pii:
doi:

Substances chimiques

Anti-Arrhythmia Agents 0

Banques de données

ClinicalTrials.gov
['NCT02459574']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

36-45

Subventions

Organisme : British Heart Foundation
ID : PG/15/36/31425
Pays : United Kingdom

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Ian Mann (I)

Imperial College London, London, UK.

Thiagarajah Sasikaran (T)

Imperial Clinical Trials Unit, Imperial College London, London, UK.

Belinda Sandler (B)

Imperial College London, London, UK.

Daphne Babalis (D)

Imperial Clinical Trials Unit, Imperial College London, London, UK.

Nicholas Johnson (N)

Imperial Clinical Trials Unit, Imperial College London, London, UK.

Emanuela Falaschetti (E)

Imperial Clinical Trials Unit, Imperial College London, London, UK.

Andrew Copley (A)

Imperial Clinical Trials Unit, Imperial College London, London, UK.

Muzahir Tayebjee (M)

Leeds Teaching Hospitals NHS Trust, Leeds, UK.

Derick Todd (D)

Liverpool Heart and Chest Hospital, Liverpool, UK.

Ewen Shepherd (E)

Newcastle-upon-Tyne NHS Foundation Trust, Newcastle, UK.

James McCready (J)

Brighton & Sussex University Hospital, Brighton, UK.

Neil Poulter (N)

Imperial College London, London, UK; Imperial College Healthcare NHS Trust, London, UK.

Prapa Kanagaratnam (P)

Imperial College London, London, UK; Imperial College Healthcare NHS Trust, London, UK. Electronic address: p.kanagaratnam@ic.ac.uk.

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