TY - JOUR
T1 - Dabigatran versus warfarin in patients with atrial fibrillation
AU - RE-LY Steering Committee and Investigators
AU - Connolly, Stuart J.
AU - Ezekowitz, Michael D.
AU - Yusuf, Salim
AU - Eikelboom, John
AU - Oldgren, Jonas
AU - Parekh, Amit
AU - Pogue, Janice
AU - Reilly, Paul A.
AU - Themeles, Ellison
AU - Varrone, Jeanne
AU - Wang, Susan
AU - Alings, Marco
AU - Xavier, Denis
AU - Zhu, Jun
AU - Diaz, Rafael
AU - Lewis, Basil S.
AU - Darius, Harald
AU - Diener, Hans Christoph
AU - Joyner, Campbell D.
AU - Wallentin, Lars
AU - Palmcrantz-Graf, E.
AU - Haehl, M.
AU - Alings, A. M.W.
AU - Amerena, J. V.
AU - Avezum, A.
AU - Baumgartner, I.
AU - Brugada, J.
AU - Budaj, A.
AU - Caicedo, V.
AU - Ceremuzynski, L.
AU - Chen, J. H.
AU - Commerford, P. J.
AU - Dans, A. L.
AU - Di Pasquale, G.
AU - Erol, C.
AU - Ferreira, J.
AU - Flaker, G. C.
AU - Flather, M. D.
AU - Franzosi, M. G.
AU - Gamboa, R.
AU - Golitsyn, S. P.
AU - Gonzalez Hermosillo, J. A.
AU - Halon, D.
AU - Heidbuchel, H.
AU - Hohnloser, S. H.
AU - Hori, M.
AU - Huber, K.
AU - Jansky, P.
AU - Kamensky, G.
AU - Ilia, R.
PY - 2009/9/17
Y1 - 2009/9/17
N2 - BACKGROUND: Warfarin reduces the risk of stroke in patients with atrial fibrillation but increases the risk of hemorrhage and is difficult to use. Dabigatran is a new oral direct thrombin inhibitor. METHODS: In this noninferiority trial, we randomly assigned 18,113 patients who had atrial fibrillation and a risk of stroke to receive, in a blinded fashion, fixed doses of dabigatran - 110 mg or 150 mg twice daily - or, in an unblinded fashion, adjusted-dose warfarin. The median duration of the follow-up period was 2.0 years. The primary outcome was stroke or systemic embolism. RESULTS: Rates of the primary outcome were 1.69% per year in the warfarin group, as compared with 1.53% per year in the group that received 110 mg of dabigatran (relative risk with dabigatran, 0.91; 95% confidence interval [CI], 0.74 to 1.11; P<0.001 for noninferiority) and 1.11% per year in the group that received 150 mg of dabigatran (relative risk, 0.66; 95% CI, 0.53 to 0.82; P<0.001 for superiority). The rate of major bleeding was 3.36% per year in the warfarin group, as compared with 2.71% per year in the group receiving 110 mg of dabigatran (P=0.003) and 3.11% per year in the group receiving 150 mg of dabigatran (P=0.31). The rate of hemorrhagic stroke was 0.38% per year in the warfarin group, as compared with 0.12% per year with 110 mg of dabigatran (P<0.001) and 0.10% per year with 150 mg of dabigatran (P<0.001). The mortality rate was 4.13% per year in the warfarin group, as compared with 3.75% per year with 110 mg of dabigatran (P=0.13) and 3.64% per year with 150 mg of dabigatran (P=0.051). CONCLUSIONS: In patients with atrial fibrillation, dabigatran given at a dose of 110 mg was associated with rates of stroke and systemic embolism that were similar to those associated with warfarin, as well as lower rates of major hemorrhage. Dabigatran administered at a dose of 150 mg, as compared with warfarin, was associated with lower rates of stroke and systemic embolism but similar rates of major hemorrhage. (ClinicalTrials.gov number, NCT00262600.)
AB - BACKGROUND: Warfarin reduces the risk of stroke in patients with atrial fibrillation but increases the risk of hemorrhage and is difficult to use. Dabigatran is a new oral direct thrombin inhibitor. METHODS: In this noninferiority trial, we randomly assigned 18,113 patients who had atrial fibrillation and a risk of stroke to receive, in a blinded fashion, fixed doses of dabigatran - 110 mg or 150 mg twice daily - or, in an unblinded fashion, adjusted-dose warfarin. The median duration of the follow-up period was 2.0 years. The primary outcome was stroke or systemic embolism. RESULTS: Rates of the primary outcome were 1.69% per year in the warfarin group, as compared with 1.53% per year in the group that received 110 mg of dabigatran (relative risk with dabigatran, 0.91; 95% confidence interval [CI], 0.74 to 1.11; P<0.001 for noninferiority) and 1.11% per year in the group that received 150 mg of dabigatran (relative risk, 0.66; 95% CI, 0.53 to 0.82; P<0.001 for superiority). The rate of major bleeding was 3.36% per year in the warfarin group, as compared with 2.71% per year in the group receiving 110 mg of dabigatran (P=0.003) and 3.11% per year in the group receiving 150 mg of dabigatran (P=0.31). The rate of hemorrhagic stroke was 0.38% per year in the warfarin group, as compared with 0.12% per year with 110 mg of dabigatran (P<0.001) and 0.10% per year with 150 mg of dabigatran (P<0.001). The mortality rate was 4.13% per year in the warfarin group, as compared with 3.75% per year with 110 mg of dabigatran (P=0.13) and 3.64% per year with 150 mg of dabigatran (P=0.051). CONCLUSIONS: In patients with atrial fibrillation, dabigatran given at a dose of 110 mg was associated with rates of stroke and systemic embolism that were similar to those associated with warfarin, as well as lower rates of major hemorrhage. Dabigatran administered at a dose of 150 mg, as compared with warfarin, was associated with lower rates of stroke and systemic embolism but similar rates of major hemorrhage. (ClinicalTrials.gov number, NCT00262600.)
UR - http://www.scopus.com/inward/record.url?scp=70349306707&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa0905561
DO - 10.1056/NEJMoa0905561
M3 - Article
C2 - 19717844
AN - SCOPUS:70349306707
SN - 0028-4793
VL - 361
SP - 1139
EP - 1151
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 12
ER -