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Dabigatran etexilate for thromboembolic prophylaxis in non-valvular atrial fibrillation: the RE-LY study and substudies with commentary.

Abstract
In 2010, dabigatran etexilate, a direct thrombin inhibitor, was the first new oral anticoagulant to be approved for thromboembolic prophylaxis in atrial fibrillation in over 50 years. Dabigatran, unlike warfarin, has a short half-life with a rapid onset of anticoagulant effect, does not require dose adjustment or monitoring, and does not interact with food. The RE-LY trial compared two doses of dabigatran (110 and 150 mg twice daily) with adjusted dose warfarin in patients with non-valvular atrial fibrillation and at least 1 stroke risk factor. Compared with warfarin, dabigatran 150 mg twice daily was superior in reducing the risk of stroke or systemic embolism and was associated with a similar rate of major bleeding, while dabigatran 110 mg twice daily was equally effective in reducing stroke or systemic embolism and was associated with less major bleeding. Despite these favorable results, there remains disagreement regarding the optimal dose and overall safety of dabigatran in certain patient populations including the elderly and those with renal dysfunction.
AuthorsJonathan W Waks, Peter J Zimetbaum
JournalExpert review of cardiovascular therapy (Expert Rev Cardiovasc Ther) Vol. 11 Issue 11 Pg. 1461-71 (Nov 2013) ISSN: 1744-8344 [Electronic] England
PMID24147516 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Anticoagulants
  • Antithrombins
  • Benzimidazoles
  • Pyridines
  • Warfarin
  • Dabigatran
Topics
  • Administration, Oral
  • Aged
  • Anticoagulants (adverse effects, therapeutic use)
  • Antithrombins (administration & dosage, adverse effects, therapeutic use)
  • Atrial Fibrillation (complications, drug therapy)
  • Benzimidazoles (administration & dosage, adverse effects, therapeutic use)
  • Clinical Trials, Phase III as Topic
  • Dabigatran
  • Dose-Response Relationship, Drug
  • Female
  • Half-Life
  • Hemorrhage (chemically induced, epidemiology)
  • Humans
  • Kidney Diseases (physiopathology)
  • Male
  • Pyridines (administration & dosage, adverse effects, therapeutic use)
  • Randomized Controlled Trials as Topic
  • Risk Factors
  • Stroke (etiology, prevention & control)
  • Thromboembolism (etiology, prevention & control)
  • Warfarin (adverse effects, therapeutic use)

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