Efficacy and Safety of Apixaban Compared With Warfarin at Different Levels of Predicted International Normalized Ratio Control for Stroke Prevention in Atrial Fibrillation

Author:

Wallentin Lars1,Lopes Renato D.1,Hanna Michael1,Thomas Laine1,Hellkamp Anne1,Nepal Sunil1,Hylek Elaine M.1,Al-Khatib Sana M.1,Alexander John H.1,Alings Marco1,Amerena John1,Ansell Jack1,Aylward Philip1,Bartunek Jozef1,Commerford Patrick1,De Caterina Raffaele1,Erol Cetin1,Harjola Veli-Pekka1,Held Claes1,Horowitz John D.1,Huber Kurt1,Husted Steen1,Keltai Matyas1,Lanas Fernando1,Lisheng Liu1,McMurray John J.V.1,Oh Byung-Hee1,Rosenqvist Mårten1,Ruzyllo Witold1,Steg Philippe Gabriel1,Vinereanu Dragos1,Xavier Denis1,Granger Christopher B.1

Affiliation:

1. From the Department of Medical Sciences, Cardiology, and Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden (L.W., C.H.); Duke Clinical Research Institute, Duke University Medical Center, Durham, NC (R.D.L., L.T., A.H., S.M.A.-K., J.H.A., C.B.G.); Bristol-Myers Squibb, Princeton, NJ (M.H.); Novartis Pharmaceuticals, Florham Park, NJ (S.N.); Boston University Medical Center, Boston, MA (E.M.H.); Working Group on Cardiovascular Research the Netherlands, Utrecht, Netherlands (M.A.);...

Abstract

Background— In the Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation (ARISTOTLE) trial, apixaban compared with warfarin reduced stroke and systemic embolism, major bleeding, and mortality. We evaluated treatment effects in relation to 2 predictions of time in therapeutic range (TTR). Methods and Results— The trial randomized 18 201 patients with atrial fibrillation to apixaban 5 mg twice daily or warfarin for at least 12 months. For each patient, a center average TTR was estimated with the use of a linear mixed model on the basis of the real TTRs in its warfarin-treated patients, with a fixed effect for country and random effect for center. For each patient, an individual TTR was also predicted with the use of a linear mixed effects model including patient characteristics as well. Median center average TTR was 66% (interquartile limits, 61% and 71%). Rates of stroke or systemic embolism, major bleeding, and mortality were consistently lower with apixaban than with warfarin across center average TTR and individual TTR quartiles. In the lowest and highest center average TTR quartiles, hazard ratios for stroke or systemic embolism were 0.73 (95% confidence interval [CI], 0.53–1.00) and 0.88 (95% CI, 0.57–1.35) ( P interaction =0.078), for mortality were 0.91 (95% CI, 0.74–1.13) and 0.91 (95% CI, 0.71–1.16) ( P interaction =0.34), and for major bleeding were 0.50 (95% CI, 0.36–0.70) and 0.75 (95% CI, 0.58–0.97) ( P interaction =0.095), respectively. Similar results were seen for quartiles of individual TTR. Conclusions— The benefits of apixaban compared with warfarin for stroke or systemic embolism, bleeding, and mortality appear similar across the range of centers’ and patients’ predicted quality of international normalized ratio control. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT00412984.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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