Blood Pressure Control and Risk of Stroke or Systemic Embolism in Patients With Atrial Fibrillation: Results From the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) Trial

Author:

Rao Meena P.1,Halvorsen Sigrun2,Wojdyla Daniel1,Thomas Laine1,Alexander John H.1,Hylek Elaine M.3,Hanna Michael4,Bahit M. Cecilia5,Lopes Renato D.1,De Caterina Raffaele6,Erol Cetin7,Goto Shinya8,Lanas Fernando9,Lewis Basil S.10,Husted Steen11,Gersh Bernard J.12,Wallentin Lars13,Granger Christopher B.1,

Affiliation:

1. Duke Clinical Research Institute Duke University Medical Center Durham NC

2. Oslo University Hospital Oslo Norway

3. Boston University Medical Center Boston MA

4. Bristol‐Myers Squibb Princeton NJ

5. INECO Neurociencias Oroño Rosario, Santa Fe Argentina

6. G. D'Annunzio Universita‐Chieti and Fondazione Toscana G. Monasterio Pisa Italy

7. Ankara University Ankara Turkey

8. Tokai University School of Medicine Isehara Japan

9. Universidad de La Frontera Temuco Chile

10. Lady Davis Carmel Medical Center and the Ruth and Bruce Rappaport School of Medicine Technion‐IIT Haifa Israel

11. Hospital UnitWest Herning/Holstbro Denmark

12. Mayo Clinic College of Medicine Rochester MN

13. Uppsala Clinical Research Center Uppsala University Uppsala Sweden

Abstract

Background Patients with atrial fibrillation ( AF ) and hypertension are at high risk for stroke. Previous studies have shown elevated risk of stroke in patients with AF who have a history of hypertension (regardless of blood pressure [ BP ] control) and in patients with elevated BP . We assessed the association of hypertension and BP control on clinical outcomes. Methods and Results In ARISTOTLE (n=18 201), BP was evaluated as history of hypertension requiring treatment and elevated BP (systolic ≥140 and/or diastolic ≥90 mm Hg) at study entry and any point during the trial. Hazard ratios ( HR s) were derived from Cox proportional hazards models including BP as a time‐dependent covariate. A total of 15 916 (87.5%) patients had a history of hypertension requiring treatment. In patients with elevated BP measurement at any point during the trial, the rate of stroke or systemic embolism was significantly higher ( HR , 1.53; 95% confidence interval [ CI ], 1.25–1.86), as was hemorrhagic stroke ( HR 1.85; 95% CI , 1.26–2.72) and ischemic stroke ( HR , 1.50; 95% CI , 1.18–1.90). Rates of major bleeding were lower in patients with a history of hypertension ( HR , 0.80; 95% CI , 0.66–0.98) and nonsignificantly lower in patients with elevated BP at study entry ( HR , 0.89; 95% CI , 0.77–1.03). The benefit of apixaban versus warfarin on preventing stroke or systemic embolism was consistent among patients with and without a history of hypertension ( P interaction=0.27), BP control at baseline ( P interaction=0.43), and BP control during the trial ( P interaction=0.97). Conclusions High BP measurement at any point during the trial was independently associated with a substantially higher risk of stroke or systemic embolism. These results strongly support efforts to treat elevated BP as an important strategy to optimally lower risk of stroke in patients with AF . Clinical Trial Registration URL : https://ClinicalTrials.gov/ . Unique identifier: NCT 00412984.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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