UBC Faculty Research and Publications

Dabigatran for atrial fibrillation : Why we can not rely on RE-LY Therapeutics Initiative (University of British Columbia)

Description

Therapeutics Letter 80 provides a detailed analysis of the RE-LY trial, which compared dabigatran to warfarin in patients with atrial fibrillation. Conclusions: Licensing of dabigatran 150 mg BID for atrial fibrillation is premature, pharmacologically irrational and unsafe for many patients. The optimal dose of dabigatran for non-valvular atrial fibrillation is not yet clear. An independent audit of RE-LY is needed to check for irregularities in conduct, sources of bias and the cause of the unusually high incidence of intracranial hemorrhage in the warfarin arm. An independently conducted double-blind RCT comparing dabigatran with warfarin in patients with non-valvular atrial fibrillation is required. Taking antiplatelet drugs in combination with oral anticoagulants doubles the incidence of major bleeding events.

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Attribution-NonCommercial-NoDerivatives 4.0 International