EIKELBOOM, J.W., S.J. CONNOLLY, J. BOSCH, G.R. DAGENAIS, R.G. HART, O. SHESTAKOVSKA, R. DIAZ, M. ALINGS, E.M. LONN, S.S. ANAND, P. WIDIMSKY, M. HORI, A. AVEZUM, L.S. PIEGAS, K.R.H. BRANCH, J. PROBSTFIELD, D.L. BHATT, J. ZHU, Y. LIANG, A.P. MAGGIONI, P. LOPEZ-JARAMILLO, M. O´DONNELL, A.K. KAKKAR, K.A.A. FOX, A.N. PARKHOMENKO, G. ERTL, S. STORK, M. KELTAI, L. RYDEN, N. POGOSOVA, A.L. DANS, F. LANAS, P.J. COMMERFORD, C. TORP-PEDERSEN, T.J. GUZIK, P.B. VERHAMME, D. VINEREANU, J.H. KIM, A.M. TONKIN, B.S. LEWIS, C. FELIX, K. YUSOFF, P.G. STEG, K.P. METSARINNE, N.C. BRUNS, F. MISSELWITZ, E. CHEN, D. LEONG and S. YUSUF. Rivaroxaban with or without Aspirin in Stable Cardiovascular Disease. New England Journal of Medicine. Waltham: Massachussetts Medical Society, 2017, vol. 377, No 14, p. 1319-1330. ISSN 0028-4793. Available from: https://dx.doi.org/10.1056/NEJMoa1709118.
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Basic information
Original name Rivaroxaban with or without Aspirin in Stable Cardiovascular Disease
Authors EIKELBOOM, J.W., S.J. CONNOLLY, J. BOSCH, G.R. DAGENAIS, R.G. HART, O. SHESTAKOVSKA, R. DIAZ, M. ALINGS, E.M. LONN, S.S. ANAND, P. WIDIMSKY, M. HORI, A. AVEZUM, L.S. PIEGAS, K.R.H. BRANCH, J. PROBSTFIELD, D.L. BHATT, J. ZHU, Y. LIANG, A.P. MAGGIONI, P. LOPEZ-JARAMILLO, M. O´DONNELL, A.K. KAKKAR, K.A.A. FOX, A.N. PARKHOMENKO, G. ERTL, S. STORK, M. KELTAI, L. RYDEN, N. POGOSOVA, A.L. DANS, F. LANAS, P.J. COMMERFORD, C. TORP-PEDERSEN, T.J. GUZIK, P.B. VERHAMME, D. VINEREANU, J.H. KIM, A.M. TONKIN, B.S. LEWIS, C. FELIX, K. YUSOFF, P.G. STEG, K.P. METSARINNE, N.C. BRUNS, F. MISSELWITZ, E. CHEN, D. LEONG and S. YUSUF.
Edition New England Journal of Medicine, Waltham, Massachussetts Medical Society, 2017, 0028-4793.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30201 Cardiac and Cardiovascular systems
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 79.260
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1056/NEJMoa1709118
UT WoS 000412375000012
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 9/5/2022 10:31.
Abstract
BACKGROUND We evaluated whether rivaroxaban alone or in combination with aspirin would be more effective than aspirin alone for secondary cardiovascular prevention. METHODS In this double-blind trial, we randomly assigned 27,395 participants with stable atherosclerotic vascular disease to receive rivaroxaban (2.5 mg twice daily) plus aspirin (100 mg once daily), rivaroxaban (5 mg twice daily), or aspirin (100 mg once daily). The primary outcome was a composite of cardiovascular death, stroke, or myocardial infarction. The study was stopped for superiority of the rivaroxaban-plus-aspirin group after a mean follow-up of 23 months. RESULTS The primary outcome occurred in fewer patients in the rivaroxaban-plus-aspirin group than in the aspirin-alone group (379 patients [4.1%] vs. 496 patients [5.4%]; hazard ratio, 0.76; 95% confidence interval [CI], 0.66 to 0.86; P< 0.001; z = -4.126), but major bleeding events occurred in more patients in the rivaroxaban-plus-aspirin group (288 patients [3.1%] vs. 170 patients [1.9%]; hazard ratio, 1.70; 95% CI, 1.40 to 2.05; P< 0.001). There was no significant difference in intracranial or fatal bleeding between these two groups. There were 313 deaths (3.4%) in the rivaroxaban-plus-aspirin group as compared with 378 (4.1%) in the aspirin-alone group (hazard ratio, 0.82; 95% CI, 0.71 to 0.96; P = 0.01; threshold P value for significance, 0.0025). The primary outcome did not occur in significantly fewer patients in the rivaroxaban-alone group than in the aspirin-alone group, but major bleeding events occurred in more patients in the rivaroxaban- alone group. CONCLUSIONS Among patients with stable atherosclerotic vascular disease, those assigned to rivaroxaban (2.5 mg twice daily) plus aspirin had better cardiovascular outcomes and more major bleeding events than those assigned to aspirin alone. Rivaroxaban (5 mg twice daily) alone did not result in better cardiovascular outcomes than aspirin alone and resulted in more major bleeding events.
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