Bleeding rate of rivaroxaban in real world clinical practice consistent with trial resultsLiterature - Tamayo S et al., Clin Cardiol 2015
Characterizing Major Bleeding in Patients With Nonvalvular Atrial Fibrillation: A Pharmacovigilance Study of 27 467 Patients Taking Rivaroxaban
Tamayo S, Peacock F, Patel M, et al.
Clin. Cardiol. 2015 (in press); Published online in wileyonlinelibrary.com; DOI:10.1002/clc.22373
BackgroundAtrial fibrillation (AF) is associated with a 5-fold risk of stroke [1,2]. For several decades, Vitamin K antagonists (eg, warfarin) have been a standard prophylactic therapy in reducing the risk of stroke in patients with AF. Rivaroxaban is a novel direct factor Xa inhibitor oral anticoagulant to reduce the risk of stroke and systemic embolism in patients who have nonvalvular AF (NVAF).
An inherent risk associated with the use of anticoagulants is bleeding [3,4]. The objective of the present study is to provide longitudinal safety data on major bleeding (MB) among rivaroxaban users with NVAF in a real-world clinical setting. This observational, retrospective study retrieved information from electronic health care records and a cohort of 27467 rivaroxaban users with NVAF was followed for 15 months.
- Of 27 467 patients receiving rivaroxaban, 496 MB events occurred in 478 patients, an incidence of 2.86 per 100 person-years (95%CI:2.61-3.13).
- Patients with MB were older (mean age of 78.4 vs 75.7 years) compared with non-MB patients, and had higher rates of hypertension (95.6% vs 75.8%), coronary artery disease (64.2% vs 36.7%), heart failure (48.5% vs 23.7%), and renal disease (38.7% vs 16.7%).
- Major bleeding was most commonly gastrointestinal (88.5%) or intracranial (7.5%).
- Fourteen of the 478 patients died during their MB hospitalisation (fatal bleeding rate of 0.08 per 100 person-years; 95%CI: 0.05-0.14).
ConclusionsThe present study showed that the MB rate was 2.86 per 100 person-years and fatal bleeds were rare. Major bleeding was usually gastrointestinal or intracranial in origin. Patients who experienced MB were older and more likely to have comorbidity at baseline. These outcomes are similar to those reported in the in the ROCKET-AF registration trial [3,4], in which the reported MB rates were 3.6 for rivaroxaban and 3.5 for warfarin (per 100 person years) in patients with NVAF.
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