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Anticoagulation with edoxaban in patients with long atrial high-rate episodes ≥24 h.
Becher, Nina; Toennis, Tobias; Bertaglia, Emanuele; Blomström-Lundqvist, Carina; Brandes, Axel; Cabanelas, Nuno; Calvert, Melanie; Camm, A John; Chlouverakis, Gregory; Dan, Gheorghe-Andrei; Dichtl, Wolfgang; Diener, Hans Christoph; Fierenz, Alexander; Goette, Andreas; de Groot, Joris R; Hermans, Astrid N L; Lip, Gregory Y H; Lubinski, Andrzej; Marijon, Eloi; Merkely, Béla; Mont, Lluís; Ozga, Ann-Kathrin; Rajappan, Kim; Sarkozy, Andrea; Scherr, Daniel; Schnabel, Renate B; Schotten, Ulrich; Sehner, Susanne; Simantirakis, Emmanuel; Vardas, Panos; Velchev, Vasil; Wichterle, Dan; Zapf, Antonia; Kirchhof, Paulus.
Affiliation
  • Becher N; Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, Hamburg 20246, Germany.
  • Toennis T; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Postdamer Str. 58, 10785 Berlin, Germany.
  • Bertaglia E; Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, Hamburg 20246, Germany.
  • Blomström-Lundqvist C; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Luebeck, Postdamer Str. 58, 10785 Berlin, Germany.
  • Brandes A; Department of Cardiac, Vascular, Thoracic and Public Health Sciences, Azienda Ospedaliera, Padua, Italy.
  • Cabanelas N; Department of Medical Science, Uppsala University, Uppsala, Sweden.
  • Calvert M; Department of Cardiology, School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
  • Camm AJ; Department of Cardiology, Esbjerg Hospital-University Hospital of Southern Denmark, Esbjerg, Denmark.
  • Chlouverakis G; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.
  • Dan GA; Cardiology Department, Fernando Fonseca Hospital, Amadora, Portugal.
  • Dichtl W; Centre for Patient Reported Outcomes Research, Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, UK.
  • Diener HC; NIHR Birmingham Biomedical Research Centre and NIHR Applied Research Collaboration West Midlands, University of Birmingham, Edgbaston, Birmingham, UK.
  • Fierenz A; Cardiovascular and Cell Sciences Research Institute, St George's, University of London, and Imperial College, London, UK.
  • Goette A; Biostatistics Lab, School of Medicine, University of Crete, Crete, Greece.
  • de Groot JR; Medicine University 'Carol Davila', Colentina University Hospital, Bucharest, Romania.
  • Hermans ANL; Department of Internal Medicine III, Cardiology and Angiology, Innsbruck Medical University, Innsbruck, Austria.
  • Lip GYH; Department of Neuroepidemiology, Institute for Medical Informatics, Biometry and Epidemiology (IMIBE), University Duisburg-Essen, Essen, Germany.
  • Lubinski A; Institute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Marijon E; Department of Cardiology and Intensive Care Medicine, St Vincenz-Hospital Paderborn, Paderborn, Germany.
  • Merkely B; Atrial Fibrillation NETwork (AFNET), Mendelstrasse 11, 48149 Muenster, Germany.
  • Mont L; Heart Center, Department of Clinical and Experimental Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
  • Ozga AK; Departments of Cardiology and Physiology, Maastricht University, Maastricht, The Netherlands.
  • Rajappan K; Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK.
  • Sarkozy A; Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
  • Scherr D; Department of Cardiology and Internal Diseases, Medical University of Gdansk, Gdansk, Poland.
  • Schnabel RB; Cardiology Division, European Georges Pompidou Hospital, Paris, France.
  • Schotten U; Heart and Vascular Centre, Semmelweis University, Budapest, Hungary.
  • Sehner S; Hospital Clinic, Universtitat de Barcelona, Catalonia, Barcelona, Spain.
  • Simantirakis E; Institut d'Investigacions Biomèdiques August Pi Sunyer (IDIBAPS), Catalonia, Barcelona, Spain.
  • Vardas P; Centro de Investigacion Biomedica en Red Cardiovascular (CIBERCV), Madrid, Spain.
  • Velchev V; Institute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Wichterle D; Cardiac Department, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Zapf A; HRMC, University Hospital Brussels, VUB, Brussels, Belgium.
  • Kirchhof P; Department of Cardiology, University Hospital Graz, Graz, Austria.
Eur Heart J ; 45(10): 837-849, 2024 Mar 07.
Article in En | MEDLINE | ID: mdl-37956458
ABSTRACT
BACKGROUND AND

AIMS:

Patients with long atrial high-rate episodes (AHREs) ≥24 h and stroke risk factors are often treated with anticoagulation for stroke prevention. Anticoagulation has never been compared with no anticoagulation in these patients.

METHODS:

This secondary pre-specified analysis of the Non-vitamin K antagonist Oral anticoagulants in patients with Atrial High-rate episodes (NOAH-AFNET 6) trial examined interactions between AHRE duration at baseline and anticoagulation with edoxaban compared with placebo in patients with AHRE and stroke risk factors. The primary efficacy outcome was a composite of stroke, systemic embolism, or cardiovascular death. The safety outcome was a composite of major bleeding and death. Key secondary outcomes were components of these outcomes and electrocardiogram (ECG)-diagnosed atrial fibrillation.

RESULTS:

Median follow-up of 2389 patients with core lab-verified AHRE was 1.8 years. AHRE ≥24 h were present at baseline in 259/2389 patients (11%, 78 ± 7 years old, 28% women, CHA2DS2-VASc 4). Clinical characteristics were not different from patients with shorter AHRE. The primary outcome occurred in 9/132 patients with AHRE ≥24 h (4.3%/patient-year, 2 strokes) treated with anticoagulation and in 14/127 patients treated with placebo (6.9%/patient-year, 2 strokes). Atrial high-rate episode duration did not interact with the efficacy (P-interaction = .65) or safety (P-interaction = .98) of anticoagulation. Analyses including AHRE as a continuous parameter confirmed this. Patients with AHRE ≥24 h developed more ECG-diagnosed atrial fibrillation (17.0%/patient-year) than patients with shorter AHRE (8.2%/patient-year; P < .001).

CONCLUSIONS:

This hypothesis-generating analysis does not find an interaction between AHRE duration and anticoagulation therapy in patients with device-detected AHRE and stroke risk factors. Further research is needed to identify patients with long AHRE at high stroke risk.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Atrial Fibrillation / Thiazoles / Stroke Limits: Aged / Aged80 / Female / Humans / Male Language: En Journal: Eur Heart J Year: 2024 Document type: Article Affiliation country: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pyridines / Atrial Fibrillation / Thiazoles / Stroke Limits: Aged / Aged80 / Female / Humans / Male Language: En Journal: Eur Heart J Year: 2024 Document type: Article Affiliation country: Alemania