Factors Associated With Major Bleeding Events

被引:189
作者
Goodman, Shaun G. [1 ,2 ]
Wojdyla, Daniel M. [3 ]
Piccini, Jonathan P. [3 ]
White, Harvey D. [4 ]
Paolini, John F. [5 ]
Nessel, Christopher C. [6 ]
Berkowitz, Scott D. [5 ]
Mahaffey, Kenneth W. [3 ]
Patel, Manesh R. [3 ]
Sherwood, Matthew W. [3 ]
Becker, Richard C. [3 ]
Halperin, Jonathan L. [7 ]
Hacke, Werner [8 ]
Singer, Daniel E. [9 ,10 ]
Hankey, Graeme J. [11 ]
Breithardt, Gunter [12 ]
Fox, Keith A. A. [13 ,14 ]
Califf, Robert M. [3 ,15 ]
机构
[1] Univ Toronto, St Michaels Hosp, Canadian Heart Res Ctr, Toronto, ON M5B 1W8, Canada
[2] Univ Toronto, St Michaels Hosp, Terrence Donnelly Heart Ctr, Div Cardiol, Toronto, ON M5B 1W8, Canada
[3] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC USA
[4] Auckland City Hosp, Green Lane Cardiovasc Serv, Auckland, New Zealand
[5] Bayer HealthCare Pharmaceut, Montville, NJ USA
[6] Janssen Res & Dev, Raritan, NJ USA
[7] Mt Sinai Med Ctr, Cardiovasc Inst, New York, NY 10029 USA
[8] Heidelberg Univ, Heidelberg, Germany
[9] Massachusetts Gen Hosp, Boston, MA 02114 USA
[10] Harvard Univ, Sch Med, Boston, MA USA
[11] Royal Perth Hosp, Perth, WA 6001, Australia
[12] Hosp Univ Munster, Munster, Germany
[13] Univ Edinburgh, Edinburgh, Midlothian, Scotland
[14] Royal Infirm Edinburgh NHS Trust, Edinburgh, Midlothian, Scotland
[15] Duke Univ, Med Ctr, Duke Translat Med Inst, Durham, NC USA
关键词
anticoagulants; atrial fibrillation; hemorrhage; ATRIAL-FIBRILLATION; RISK-FACTORS; WARFARIN; ANTICOAGULATION; COMPLICATIONS; PREVENTION; PREDICTION; DABIGATRAN; HEMORRHAGE; STROKE;
D O I
10.1016/j.jacc.2013.11.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to report additional safety results from the ROCKET AF (Rivaroxaban Once-daily oral Direct Factor Xa Inhibition Compared with Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation). Background The ROCKET AF trial demonstrated similar risks of stroke/systemic embolism and major/nonmajor clinically relevant bleeding (principal safety endpoint) with rivaroxaban and warfarin. Methods The risk of the principal safety and component bleeding endpoints with rivaroxaban versus warfarin were compared, and factors associated with major bleeding were examined in a multivariable model. Results The principal safety endpoint was similar in the rivaroxaban and warfarin groups (14.9 vs. 14.5 events/100 patient-years; hazard ratio: 1.03; 95% confidence interval: 0.96 to 1.11). Major bleeding risk increased with age, but there were no differences between treatments in each age category (<65, 65 to 74, >= 75 years; p(interaction) = 0.59). Compared with those without (n = 13,455), patients with a major bleed (n = 781) were more likely to be older, current/prior smokers, have prior gastrointestinal (GI) bleeding, mild anemia, and a lower calculated creatinine clearance and less likely to be female or have a prior stroke/transient ischemic attack. Increasing age, baseline diastolic blood pressure (DBP) >= 90 mm Hg, history of chronic obstructive pulmonary disease or GI bleeding, prior acetylsalicylic acid use, and anemia were independently associated with major bleeding risk; female sex and DBP <90 mm Hg were associated with a decreased risk. Conclusions Rivaroxaban and warfarin had similar risk for major/nonmajor clinically relevant bleeding. Age, sex, DBP, prior GI bleeding, prior acetylsalicylic acid use, and anemia were associated with the risk of major bleeding. (An Efficacy and Safety Study of Rivaroxaban With Warfarin for the Prevention of Stroke and Non-Central Nervous System Systemic Embolism in Patients With Non-Valvular Atrial Fibrillation: NCT00403767) (C) 2014 by the American College of Cardiology Foundation
引用
收藏
页码:891 / 900
页数:10
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