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Anticoagulation with edoxaban in patients with long atrial high-rate episodes ≥24 h

Authors :
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, Bela
Mont, Lluis
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
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, Bela
Mont, Lluis
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
Publication Year :
2024

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.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1457644331
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1093.eurheartj.ehad771