Evidence map›Paper›PMID 39222018›Full record

SynthesisEuropean heart journal2024

Anticoagulation in device-detected atrial fibrillation with or without vascular disease: a combined analysis of the NOAH-AFNET 6 and ARTESiA trials.

Renate B Schnabel, Juan Benezet-Mazuecos, Nina Becher, William F McIntyre, Alexander Fierenz, Shun Fu Lee, Andreas Goette, Dan Atar, Emanuele Bertaglia, Alexander P Benz and 23 more

Registry-linked trialAbstract readMeta-Analysis
In one paragraph

Synthesis in European heart journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07713615 (Device-Detected Atrial Fibrillation - Haemostatic Profile and Echocardiographic Variables), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

NCT07713615 recruitingnot on this mapstarted 2026, after this paper: background citation

Device-Detected Atrial Fibrillation - Haemostatic Profile and Echocardiographic Variables

Typeobservational_patient_registrySponsorAndreas Sjøholm-ChristensenRan2026 to 2037Enrolled222ConditionsDevice-detected Atrial Fibrillation, Subclinical Atrial Fibrillation, Atrial High Rate Episodes
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Trial
  2. Cost-effectiveness of apixaban vs. aspirin for the reduction of thrombo-embolism in high-risk patients with device-detected atrial fibrillation: insights from the ARTESiA trial.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    Trial
  3. Review
  4. Review
  5. Review
  6. Irregular atrial arrhythmias shorter than 30 s and the risk of atrial fibrillation on continuous monitoring.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2026
    Article
  7. Device-detected Atrial Fibrillation: How Much is Too Much?Arrhythmia & electrophysiology review · 2026
    Review
  8. Article
  9. Review
  10. Review
  11. Apixaban in subclinical atrial fibrillation: stroke-driven value amid economic uncertainty.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    Article
  12. Article
  13. Article
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

33 authors.

Renate B SchnabelDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0001-7170-9509
Juan Benezet-MazuecosCardiology Department, Hospital Universitario La Luz, Madrid, Spain.ORCID 0000-0003-3912-8901
Nina BecherDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0002-4476-1341
William F McIntyrePopulation Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
Alexander FierenzInstitute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-5233-215X
Shun Fu LeeDepartment of Health Research Methods, Evaluation, and Impact, McMaster University, and Population Health Research Institute, Hamilton, Ontario, Canada.ORCID 0000-0001-9795-1045
Andreas GoetteDepartment of Cardiology and Intensive Care Medicine, St Vincenz-Hospital Paderborn, Paderborn, Germany.
Dan AtarDivision of Cardiology, Oslo University Hospital Ulleval, and Institute of Clinical Medicine, University of Oslo, Norway.ORCID 0000-0003-1513-8793
Emanuele BertagliaCardiology Unit, Camposampiero Hospital-AULSS, Padua, Italy.
Alexander P BenzPopulation Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
Gregory ChlouverakisBiostatistics Lab, School of Medicine, University of Crete, Crete, Greece.ORCID 0000-0002-2855-772X
David H BirnieUniversity of Ottawa Heart Institute, Ottawa, ON, Canada.
Wolfgang DichtlDepartment of Internal Medicine III, Cardiology and Angiology, Innsbruck Medical University, Innsbruck, Austria.
Carina Blomstrom-LundqvistDepartment of Medical Science, Uppsala University, Uppsala, Sweden.
A John CammCardiovascular and Cell Sciences Research Institute, St George´s, University of London, London, UK.ORCID 0000-0002-2536-2871
Julia W ErathDivision of Clinical Electrophysiology, Department of Cardiology, University Hospital Frankfurt, J. W. Goethe University, Frankfurt, Germany.
Emmanuel SimantirakisDepartment of Cardiology, Heraklion University Hospital, Heraklion, Crete, Greece.ORCID 0000-0001-9615-6293
Valentina KutyifaSchool of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.ORCID 0000-0002-0016-289X
Gregory Y H LipLiverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK.
Philippe MaboCardiology and Vascular Disease Division, Rennes University Health Centre, Rennes, France.
Eloi MarijonCardiology Division, European Georges Pompidou Hospital, Paris, France.ORCID 0000-0001-7227-3428
Lena RivardDepartment of Cardiology, Montreal Heart Institute, Université de Montréal, Montréal, Canada.ORCID 0000-0002-1340-0850
Ulrich SchottenAtrial Fibrillation NETwork (AFNET), Mendelstraße 11, 48149 Muenster, Germany.ORCID 0000-0003-1532-3315
Marco AlingsAmphia Ziekenhuis, Breda, Netherlands.
Susanne SehnerInstitute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-2415-9302
Tobias ToennisDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0002-7351-0621
Cecilia LindeDepartment of Cardiology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-9039-6023
Panos VardasDepartment of Cardiology, Heraklion University Hospital, Heraklion, Crete, Greece.
Christopher B GrangerDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Antonia ZapfInstitute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8467-0508
Renato D LopesDuke Clinical Research Institute, Duke University, Durham, NC, USA.
Jeff S HealeyPopulation Health Research Institute, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0003-1216-7580
Paulus KirchhofDepartment of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.ORCID 0000-0002-1881-0197

Funding

Accelerating Clinical Trials NetworkAFFECT EU 847770BMBFBristol Myers Squibb-Pfizer AllianceBritish Heart Foundation AA/18/2/34218Canadian Institutes of HealthResearch 201610PTJ-378238Canadian Stroke Prevention Intervention NetworkDaiichi Sankyo EuropeDutch Heart Foundation 01-002-2022-0118ERACoSysMed3 031L0239European Union CATCH ME 633196European Union's Horizon 2020 research and innovation programme 847770European Union's Horizon Europe research and innovation programme 101095480German Centre for Cardiovascular ResearchGerman Centre for Cardiovascular Research, Berlin, Germany FKZ 81X2800182German Ministry of Education and Research, Berlin, GermanyGerman Ministry of Research and Education BMBF 01ZX1408AGerman Research Foundation Ki 509167694Hamilton Health SciencesHeart and Stroke Foundation of CanadaLeducq FoundationMAESTRIA 965286MedtronicPopulation Health Research InstituteUnion's Horizon 2020 research and innovation programme 648131Wolfgang Seefried project funding German Heart Foundation
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation.

methodsThese pre-specified analyses of the NOAH-AFNET 6 (n = 2534 patients) and ARTESiA (n = 4012 patients) trials compared anticoagulation with no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischaemic attack, coronary or peripheral artery disease. Efficacy outcomes were the primary outcomes of both trials, a composite of stroke, systemic arterial embolism (SE), myocardial infarction, pulmonary embolism or cardiovascular death, and stroke or SE. Safety outcomes were major bleeding or major bleeding and death.

resultsIn patients with vascular disease (NOAH-AFNET 6, 56%; ARTESiA, 46%), stroke, myocardial infarction, systemic or pulmonary embolism, or cardiovascular death occurred at 3.9%/patient-year with and 5.0%/patient-year without anticoagulation (NOAH-AFNET 6), and 3.2%/patient-year with and 4.4%/patient-year without anticoagulation (ARTESiA). Without vascular disease, outcomes were equal with and without anticoagulation (NOAH-AFNET 6, 2.7%/patient-year; ARTESiA, 2.3%/patient-year in both randomized groups). Meta-analysis found consistent results across both trials (I2heterogeneity = 6%) with a trend for interaction with randomized therapy (pinteraction = .08). Stroke/SE behaved similarly. Anticoagulation equally increased major bleeding in vascular disease patients [edoxaban, 2.1%/patient-year; no anticoagulation, 1.3%/patient-year; apixaban, 1.7%/patient-years; no anticoagulation, 1.1%/patient-year; incidence rate ratio 1.55 (1.10-2.20)] and without vascular disease [edoxaban, 2.2%/patient-year; no anticoagulation, 0.6%/patient-year; apixaban, 1.4%/patient-year; no anticoagulation, 1.1%/patient-year; incidence rate ratio 1.93 (0.72-5.20)].

conclusionsPatients with DDAF and vascular disease are at higher risk of stroke and cardiovascular events and may derive a greater benefit from anticoagulation than patients with DDAF without vascular disease.

Indexed as

AnticoagulantsAtrial FibrillationStrokeAgedFemaleHemorrhageHumansIschemic Attack, TransientMaleMiddle AgedMyocardial InfarctionTreatment OutcomeAnticoagulantsAtrial fibrillationDevice-detected atrial fibrillationOral anticoagulationStrokeTrial

Identifiers

PMID39222018
PMCPMC11631065

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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 Socratic graph.