Residual Stroke Risk Among Patients With Atrial Fibrillation Prescribed Oral Anticoagulants: A Patient‐Level Meta‐Analysis From COMBINE AF

Author:

Johnson Linda S.12ORCID,Benz Alexander P.13ORCID,Shoamanesh Ashkan14ORCID,Eikelboom John W.1ORCID,Ezekowitz Michael56ORCID,Giugliano Robert P.78ORCID,Wallentin Lars910ORCID,Ruff Christian T.78ORCID,Lopes Renato D.1011ORCID,Jolly Sanjit112ORCID,Whitlock Richard112ORCID,Granger Christopher B.1311ORCID,Connolly Stuart1ORCID,Healey Jeffrey S.112ORCID

Affiliation:

1. Population Health Research Institute, McMaster University Hamilton Canada

2. Department of Clinical Sciences Lund University Malmö Sweden

3. Department of Cardiology University Medical Center Mainz, Johannes Gutenberg‐University Mainz Germany

4. Division of Neurology McMaster University Hamilton ON Canada

5. Sydney Kimmel Medical School Thomas Jefferson University Philadelphia PA USA

6. Cardiology Department, Lankenau Medical Center Bryn Mawr Hospital/Mainline Health Wynnewood PA USA

7. Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School Boston MA USA

8. Thrombolysis in Myocardial Infarction Study Group Boston MA USA

9. Uppsala Clinical Research Centre Uppsala University Uppsala Sweden

10. Department of Medical Sciences, Cardiology Uppsala University Uppsala Sweden

11. Duke Clinical Research Institute, Duke University Durham NC USA

12. Department of Medicine McMaster University Hamilton ON Canada

13. Division of Cardiology Duke University Durham NC USA

Abstract

Background Despite oral anticoagulation, patients with atrial fibrillation (AF) remain at risk of ischemic stroke and systemic embolism (SE) events. For patients whose residual risk is sufficiently high, additional therapies might be useful to mitigate stroke risk. Methods and Results Individual patient data from 5 landmark trials testing oral anticoagulation in AF were pooled in A Collaboration Between Multiple Institutions to Better Investigate Non‐Vitamin K Antagonist Oral Anticoagulant Use in AF (COMBINE AF). We calculated the rate of ischemic stroke/SE among oral anticoagulation–treated patients with a CHA 2 DS 2 ‐VASc score≥2, across strata of CHA 2 DS 2 ‐VASc score, stroke history, and AF type, as either paroxysmal or nonparoxysmal. We included 71 794 patients with AF (median age 72 years, interquartile range, 13 years, 61.3% male) randomized to a direct oral anticoagulant or vitamin K antagonist, and followed for a mean of 2.1 (±0.8) years. The median CHA 2 DS 2 ‐VASc score was 4 (interquartile range, 3–5), 18.8% had a prior stroke, and 76.4% had nonparoxysmal AF. The overall rate of stroke/SE was 1.33%/y (95% CI, 1.27–1.39); 1.38%/y (95% CI, 1.31–1.45) for nonparoxysmal AF, and 1.15%/y (95% CI, 1.05–1.27) for paroxysmal AF. The rate of ischemic stroke/SE increased by a rate ratio of 1.36 (95% CI, 1.32–1.41) per 1‐point increase in CHA 2 DS 2 ‐VASc, reaching 1.67%/y (95% CI, 1.59–1.75) ≥4 CHA 2 DS 2 ‐VASc points. Patients with both nonparoxysmal AF and CHA 2 DS 2 ‐VASc ≥4 had a stroke/SE rate of 1.75%/y (95% CI, 1.66–1.85). In patients with a prior stroke, the risk was 2.51%/y (95% CI, 2.33–2.71). Conclusions AF type, CHA 2 DS 2 ‐VASc score, and stroke history can identify patients with AF, who despite oral anticoagulation have a residual stroke/SE risk of 1.5% to 2.5% per year. Evaluation of additional stroke/SE prevention strategies in high‐risk patients is warranted.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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