Evidence map›Paper›PMID 40711852›Full record

Trial reportEuropean journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery2025

Durable effectiveness and safety of hybrid ablation versus catheter ablation: 2-year results from the randomized CEASE-AF trial†.

Nicolas Doll, Timo Weimar, Dariusz A Kosior, Alan Bulava, Ales Mokracek, Gerold Mönnig, Jonathan Sahu, Steven Hunter, Maurits Wijffels, Bart van Putte and 5 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02695277 (Combined Endoscopic Epicardial and Percutaneous Endocardial Ablation Versus Repeated Catheter Ablation in Persistent and Longstanding Persistent Atrial Fibrillation), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02695277 nacompletednot on this map

Combined Endoscopic Epicardial and Percutaneous Endocardial Ablation Versus Repeated Catheter Ablation in Persistent and Longstanding Persistent Atrial Fibrillation

TypeinterventionalSponsorAtriCure, Inc.Ran2015 to 2024Enrolled146ConditionsAtrial Fibrillation, Persistent and Longstanding Persistent Atrial FibrillationArmsAtriCure Bipolar System, Standard Endocardial Ablation with Catheter, AtriClip® PRO LAA Exclusion System, Endocardial Ablation with Catheter, Repeated Endocardial ablation(s)
3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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  4. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Nicolas DollDepartement of Cardiac Surgery, Schüchtermann-Klinik, Bad Rothenfelde, Germany.
Timo WeimarEberhard Karls University, School of Medicine, Tuebingen, Germany.
Dariusz A KosiorNational Medical Institute of the Ministry of Interior and Administration, Centre of Postgraduate Medical Education, Warsaw, Poland.
Alan BulavaDepartment of Cardiology, Ceske Budejovice Hospital, Czech Republic.ORCID 0000-0002-1742-207X
Ales MokracekFaculty of Health and Social Sciences, University of South Bohemia in Ceske Budejovice, Czech Republic.
Gerold MönnigDepartment of Cardiology, Schüchtermann-Klinik, Bad Rothenfelde, Germany.
Jonathan SahuDepartement of Electrophysiology, Northern General Hospital, Sheffield, UK.ORCID 0009-0002-1180-5253
Steven HunterDepartement of Cardiac Surgery, Northern General Hospital, Sheffield, UK.
Maurits WijffelsDepartement of Electrophysiology, St Antonius Hospital, Nieuwegein, The Netherlands.
Bart van PutteDepartement of Cardiac Surgery, St Antonius Hospital, Nieuwegein, The Netherlands.
Norman RübDepartement of Electrophysiology, RKH Klinikum Ludwigsburg, Ludwigsburg, Germany.
Petr NemecDepartement of Cardiac Surgery, Center of Cardiovascular Surgery and Transplantation, Brno, Czech Republic.
Tomas OstrizekDepartement of Electrophysiology, Center of Cardiovascular Surgery and Transplantation, Brno, Czech Republic.
Erik FransenAtriCure Europe B.V., Amsterdam, The Netherlands.
Piotr SuwalskiNational Medical Institute of the Ministry of Interior and Administration, Centre of Postgraduate Medical Education, Warsaw, Poland.

Funding

AtriCure, Inc
6 · The paper itself

Abstract

objectivesThe CEASE-AF trial demonstrated that epicardial-endocardial hybrid ablation (HA) had superior effectiveness compared to endocardial catheter ablation (CA) for non-paroxysmal atrial fibrillation (AF), without significantly increasing major complications during a 12-month period. Most contemporary AF ablation trials have not evaluated durability beyond 12 months. Therefore, 24-month effectiveness and safety of HA and CA are compared.

methodsCEASE-AF is a prospective, multicentre, randomized trial. Patients 18-75 years of age with symptomatic, drug refractory persistent AF and left atrial diameter >4.0 cm or long-standing persistent AF were randomized 2:1 to HA (posterior wall and pulmonary vein isolation with left atrial appendage exclusion) or CA (pulmonary vein isolation). Secondary effectiveness was freedom from AF/atrial flutter/atrial tachycardia off class I/III anti-arrhythmic drugs except for those who previously failed at doses not exceeding those previously failed through a 24-month follow-up period. Major complications and reinterventions were evaluated.

resultsThe intention-to-treat population was 102 patients with HA and 52 patients with CA. Seventy-five percent were male, 80.5% had persistent AF and 19.5% had long-standing persistent AF, with a mean age of 60.7 ± 7.9 years. Effectiveness for 24 months was 66.3% (63/95) with HA and 33.3% (17/51) with CA [absolute difference 33.0% (95% confidence interval 14.3%, 48.3%; P < 0.001)]. Major complication rates were 10.8% (11/102) with HA and 9.6% (5/52) with CA (P = 1.0), and fewer patients had reinterventions after HA than CA [18.9% (18/95) vs 52.9% (27/51), P < 0.001].

conclusionsCEASE-AF demonstrated that the 32.4% absolute benefit of HA over CA for 12 months was durable for 24 months at 33% with continued similar safety rates and fewer reinterventions after HA (funded by AtriCure, Inc.; NCT02695277). CLINICALTRIALS.GOV REGISTRATION: NCT02695277.

Indexed as

Atrial FibrillationCatheter AblationAdolescentAdultAgedEndocardiumFemaleHumansMaleMiddle AgedProspective StudiesPulmonary VeinsTreatment OutcomeYoung AdultAtrial fibrillationCatheter ablationHybrid ablationLeft atrial appendageSurgical ablation

Identifiers

PMID40711852
PMCPMC12304665

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.