Impact of Modifiable Bleeding Risk Factors on Major Bleeding in Patients With Atrial Fibrillation Anticoagulated With Rivaroxaban

Author:

Kirchhof Paulus12,Haas Sylvia3,Amarenco Pierre4,Hess Susanne56,Lambelet Marc6,van Eickels Martin5,Turpie Alexander G. G.7,Camm A. John8,

Affiliation:

1. Institute of Cardiovascular Sciences UHB and Sandwell & West Birmingham Hospitals NHS Trusts University of Birmingham United Kingdom

2. University Heart and Vascular Center Hamburg Hamburg Germany

3. Formerly Technical University of Munich Munich Germany

4. Department of Neurology and Stroke Centre Paris‐Diderot‐Sorbonne University Paris France

5. Medical Affairs Bayer AG Berlin Germany

6. Chrestos Concept GmbH & Co KG Essen Germany

7. Department of Medicine McMaster University Hamilton Ontario Canada

8. Cardiovascular and Cell Sciences Research Institute and Cardiology Clinical Academic Group St George's, University of London London United Kingdom

Abstract

Background Reducing major bleeding events is a challenge when managing anticoagulation in patients with atrial fibrillation. This study evaluated the impact of modifiable and nonmodifiable bleeding risk factors in patients with atrial fibrillation receiving rivaroxaban and estimated the impact of risk factor modification on major bleeding events. Methods and Results Modifiable and nonmodifiable risk factors associated with major bleeding events were identified from the XANTUS (Xarelto for Prevention of Stroke in Patients With Atrial Fibrillation) prospective registry data set (6784 rivaroxaban‐treated patients). Parameters showing univariate association with bleeding were used to construct a multivariable model identifying independent risk factors. Modeling was used to estimate attributed weights to risk factors. Heavy alcohol use (hazard ratio [ HR ]=2.37; 95% CI 1.24–4.53); uncontrolled hypertension ( HR after parameter‐wise shrinkage=1.79; 95% CI 1.05–3.05); and concomitant treatment with antiplatelets, nonsteroidal anti‐inflammatory drugs, or paracetamol ( HR =1.80; 95% CI 1.24–2.61) were identified as modifiable, independent bleeding risk factors. Increasing age ( HR =1.25 [per 5‐year increment]; 95% CI 1.12–1.38); heart failure ( HR =1.97; 95% CI 1.36–2.86); and vascular disease ( HR =1.91; 95% CI 1.32–2.77) were identified as nonmodifiable bleeding risk factors. Overall, 128 (1.9%) patients experienced major bleeding events; of these, 11% had no identified bleeding risk factors, 50% had nonmodifiable bleeding risk factors only, and 39% had modifiable bleeding risk factors (with or without nonmodifiable risk factors). The presence of 1 modifiable bleeding risk factor doubled the risk of major bleeding. Conclusions Elimination of modifiable bleeding risk factors is a potentially effective strategy to reduce bleeding risk in atrial fibrillation patients receiving rivaroxaban. Clinical Trial Registration URL : http://www.clinicaltrials.gov . Unique identifier: NCT 01606995.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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