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This analysis investigates the cumulative hazard rates associated with Warfarin and two doses of Dabigatran (110 mg and 150 mg) in the context of stroke or systemic embolism prevention. The primary endpoint focuses on the efficacy of these anticoagulants over a period of 30 months, referencing the landmark RE-LY trial as conducted by Connolly et al. The findings aim to provide insights into the safety and effectiveness of both treatment options in patients at risk for thromboembolic events.
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0.05 0.04 Cumulative hazard rate 0.03 0.02 0.01 0.00 Warfarin 0 6 12 18 24 30 Dabigatran 110 mg Months Dabigatran 150 mg RE-LY: Primary endpoint: Stroke or systemic embolism Connolly et al. N Eng J Med 2009;361:1139–1151.