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

atrial fibrillation device-detected atrial fibrillation oral anticoagulation stroke trial

Journal

European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263

Informations de publication

Date de publication:
02 Sep 2024
Historique:
received: 26 07 2024
revised: 06 08 2024
accepted: 28 08 2024
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 2 9 2024
Statut: aheadofprint

Résumé

The optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation. These pre-specified analyses of the NOAH-AFNET 6 (n=2534 patients) and ARTESiA (n=4012 patients) trials compared anticoagulation to no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischemic 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. In patients with vascular disease (NOAH-AFNET 6 56%, ARTESiA 46.0%), 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 randomised groups). Meta-analysis found consistent results across both trials (I2heterogeneity=6%) with a trend for interaction with randomised therapy (pinteraction=0.08). Stroke/SE behaved similarly. Anticoagulation increased major bleeding in vascular disease patients (edoxaban 2.1%/patient-year, no anticoagulation 1.3%/patient-year; apixaban 1.7%/patient-year; 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]). Patients 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.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
The optimal antithrombotic therapy in patients with device-detected atrial fibrillation (DDAF) is unknown. Concomitant vascular disease can modify the benefits and risks of anticoagulation.
METHODS METHODS
These pre-specified analyses of the NOAH-AFNET 6 (n=2534 patients) and ARTESiA (n=4012 patients) trials compared anticoagulation to no anticoagulation in patients with DDAF with or without vascular disease, defined as prior stroke/transient ischemic 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.
RESULTS RESULTS
In patients with vascular disease (NOAH-AFNET 6 56%, ARTESiA 46.0%), 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 randomised groups). Meta-analysis found consistent results across both trials (I2heterogeneity=6%) with a trend for interaction with randomised therapy (pinteraction=0.08). Stroke/SE behaved similarly. Anticoagulation increased major bleeding in vascular disease patients (edoxaban 2.1%/patient-year, no anticoagulation 1.3%/patient-year; apixaban 1.7%/patient-year; 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]).
CONCLUSIONS CONCLUSIONS
Patients 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.

Identifiants

pubmed: 39222018
pii: 7745053
doi: 10.1093/eurheartj/ehae596
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Renate B Schnabel (RB)

Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Hamburg, Germany; Atrial Fibrillation NETwork (AFNET), Muenster, Germany.

Juan Benezet-Mazuecos (J)

Arrhytmia Unit director, Cardiology Department, Hospital Universitario La Luz, Madrid, Spain.

Nina Becher (N)

Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Hamburg, Germany.

William F McIntyre (WF)

Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Alexander Fierenz (A)

Institute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Germany.

Shun Fu Lee (SF)

Department of Health Research Methods, Evaluation, and Impact, McMaster University, and Population Health Research Institute, Hamilton, Ontario, Canada.

Andreas Goette (A)

Department of Cardiology and Intensive Care Medicine, St Vincenz-Hospital Paderborn, Paderborn, Germany; Otto-von-Guericke Universität Magdeburg, Magdeburg, Germany.

Dan Atar (D)

Division of Cardiology, Oslo University Hospital Ulleval, and Institute of Clinical Medicine, University of Oslo, Norway.

Emanuele Bertaglia (E)

Cardiology Unit, Camposampiero Hospital - AULSS Euganea, Padua, Italy.

Alexander P Benz (AP)

Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada; Department of Cardiology, University Medical Center Mainz, Johannes Gutenberg-University, Mainz, Germany.

Gregory Chlouverakis (G)

Biostatistics Lab, School of Medicine, University of Crete, Crete, Greece.

David H Birnie (DH)

University of Ottawa Heart Institute, Ottawa, ON, Canada.

Wolfgang Dichtl (W)

Department of Internal Medicine III, Cardiology and Angiology, Innsbruck Medical University, Innsbruck, Austria.

Carina Blomstrom-Lundqvist (C)

Department of Medical Science, Uppsala University, Uppsala, Sweden; School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

A John Camm (AJ)

Cardiovascular and Cell Sciences Research Institute, St George´s, University of London, London, United Kingdom.

Julia W Erath (JW)

Division of Clinical Electrophysiology, Department of Cardiology, University Hospital Frankfurt, J. W. Goethe University, Frankfurt, Germany.

Emmanuel Simantirakis (E)

Department of Cardiology, Heraklion University Hospital, Heraklion, Crete, Greece.

Valentina Kutyifa (V)

University of Rochester, School of Medicine and Dentistry, Rochester, NY, US.

Gregory Y H Lip (GYH)

Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK; Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Philippe Mabo (P)

Cardiology and Vascular Disease Division, Rennes University Health Centre, Rennes, France.

Eloi Marijon (E)

Cardiology Division, European Georges Pompidou Hospital, Paris, France.

Lena Rivard (L)

Department of Cardiology, Montreal Heart Institute, Université de Montréal, Canada.

Ulrich Schotten (U)

Departments of Cardiology and Physiology, Maastricht University, Maastricht, The Netherlands; Atrial Fibrillation NETwork (AFNET), Muenster, Germany.

Marco Alings (M)

Amphia Ziekenhuis, Breda, Netherlands.

Susanne Sehner (S)

Institute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Germany.

Tobias Toennis (T)

Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Hamburg, Germany.

Cecilia Linde (C)

Karolinska Institutet, Stockholm, Sweden.

Panos Vardas (P)

Department of Cardiology, Heraklion University Hospital, Heraklion, Crete, Greece; Biomedical Research Foundation Academy of Athens (BRFAA), Greece and Hygeia Hospitals Group, Athens, Greece.

Christopher B Granger (CB)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, US.

Antonia Zapf (A)

Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University, Durham, NC, US.

Jeff S Healey (JS)

Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Paulus Kirchhof (P)

Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Hamburg, Germany; Atrial Fibrillation NETwork (AFNET), Muenster, Germany; Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.

Classifications MeSH