Thromb Haemost 2016; 115(02): 424-432
DOI: 10.1160/th15-06-0474
Stroke, Systemic or Venous Thromboembolism
Schattauer GmbH

Risk of major bleeding in patients with venous thromboembolism treated with rivaroxaban or with heparin and vitamin K antagonists

Marcello Di Nisio
1   Department of Medical, Oral and Biotechnological Sciences, University “G. D’Annunzio” of Chieti-Pescara, Chieti, Italy
2   Department of Vascular Medicine, Academic Medical Center, Amsterdam, Netherlands
,
Walter Ageno
3   Department of Clinical and Experimental Medicine, University of Insubria, Varese
,
Anne W. S. Rutjes
4   Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland
5   Centre for Systematic Reviews, Foundation, University “G. D’Annunzio” of Chieti-Pescara, Chieti, Italy
,
Akos F. Pap
6   Bayer Pharma AG, Wuppertal, Germany
,
Harry R. Büller
2   Department of Vascular Medicine, Academic Medical Center, Amsterdam, Netherlands
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Weitere Informationen

Publikationsverlauf

Received: 11. Juni 2015

Accepted after major revision: 18. September 2015

Publikationsdatum:
22. November 2017 (online)

Summary

The study aim was to identify predictive factors for major bleeding in patients receiving the novel oral factor Xa inhibitor rivaroxaban or enoxaparin-vitamin K antagonists (VKAs) for the treatment of acute symptomatic venous thromboembolism. We analysed data from patients included in the phase III EINSTEIN DVT and EINSTEIN PE studies. Factors associated with major bleeding events were assessed with best subset variable selection using Cox proportional hazards regression model. Three time windows were considered, i. e. the initial three weeks, after the third week onwards, and the entire duration of the anticoagulant treatment. Model discrimination was estimated using the C-statistic and validated internally by bootstrap techniques. Major bleeding occurred in 40 (1.0 %) of 4130 patients receiving rivaroxaban and in 72 (1.7 %) of 4116 receiving enoxaparin/VKAs, with 44 % of the major bleeding events occurring in the first three weeks of treatment. Significant risk factors for major bleeding were older age, black race, low haemoglobin concentrations, active cancer, and antiplatelet or non-steroidal anti-inflammatory drug therapy. The discrimination of the model for major bleeding was high for the first three weeks (C-statistic 0.73), from the fourth week onwards (C-statistic 0.68), and the entire period of anticoagulant treatment (C-statistic 0.74). This analysis identified risk factors for major bleeding in patients receiving the novel oral anticoagulant rivaroxaban or enoxaparin/VKAs for the treatment of acute venous thromboembolism. The prognostic model based on the combination of identified risk factors may be informative to estimate the risk of major bleeding both during the initial and later phases of anticoagulation.

Supplementary Material to this article is available online at www.thrombosis-online.com.

 
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