Direct Oral Anticoagulants for Stroke Prevention in Patients with Device-Detected Atrial Fibrillation: A Study-Level Meta-Analysis of the NOAH-AFNET 6 and ARTESiA Trials

Author:

McIntyre William F.1ORCID,Benz Alexander P.1ORCID,Becher Nina2ORCID,Healey Jeffrey S.1ORCID,Granger Christopher B.3ORCID,Rivard Lena4ORCID,Camm A. John5ORCID,Goette Andreas6ORCID,Zapf Antonia7ORCID,Alings Marco8ORCID,Connolly Stuart J.1ORCID,Kirchhof Paulus2ORCID,Lopes Renato D.3ORCID

Affiliation:

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

2. Department of Cardiology, University Heart and Vascular Center Hamburg, Germany

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

4. Montreal Heart Institute, Montreal, Quebec, Canada

5. St. George's University of London and Imperial College London, London, United Kingdom

6. Department of Cardiology and Intensive Care Medicine, St. Vincenz Hospital Paderborn, Germany

7. Institute of Medical Biometry and Epidemiology, University Medical Center Hamburg–Eppendorf

8. Amphia Ziekenhuis, Breda, Netherlands

Abstract

Background: Device-detected atrial fibrillation (AF) (also known as subclinical AF or atrial high-rate episodes) is a common finding in patients with an implanted cardiac rhythm device and is associated with an increased risk of ischemic stroke. Whether oral anticoagulation is effective and safe in this patient population is unclear. Methods: We performed a systematic review of MEDLINE and Embase for randomized trials comparing oral anticoagulation to antiplatelet or no antithrombotic therapy in adults with device-detected AF recorded by a pacemaker, implantable cardioverter-defibrillator, cardiac resynchronization therapy device or implanted cardiac monitor. We used random-effects models for meta-analysis and rated the quality of evidence using the GRADE framework. The review was pre-registered (PROSPERO CRD42023463212). Results: From 785 unique citations, we identified two randomized trials with relevant clinical outcome data; NOAH-AFNET 6 (2,536 participants) evaluated edoxaban and ARTESiA (4,012 participants) evaluated apixaban. Meta-analysis demonstrated that oral anticoagulation with these agents reduced ischemic stroke (relative risk [RR] 0.68, 95% confidence interval [CI] 0.50-0.92; high-quality evidence). The results from the two trials were consistent (I 2 statistic for heterogeneity=0%). Oral anticoagulation also reduced a composite of cardiovascular death, all-cause stroke, peripheral arterial embolism, myocardial infarction or pulmonary embolism (RR 0.85, 95% CI 0.73-1.00, I 2 =0%; moderate-quality evidence). There was no reduction in cardiovascular death (RR 0.95, 95% CI 0.76-1.17, I 2 =0%; moderate-quality evidence) or all-cause mortality (RR 1.08, 95% CI 0.96-1.21 I 2 =0%; moderate-quality evidence). Oral anticoagulation increased major bleeding (RR 1.62, 95% CI 1.05-2.5 I ² =61%; high-quality evidence). Conclusions: The results of the NOAH-AFNET 6 and ARTESiA trials are consistent with each other. Meta-analysis of these two large randomized trials provides high-quality evidence that oral anticoagulation with edoxaban or apixaban reduces the risk of stroke in patients with device-detected AF and increases the risk of major bleeding.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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