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dc.creatorHart R.G., Sharma M., Mundl H., Kasner S.E., Bangdiwala S.I., Berkowitz S.D., Swaminathan B., Lavados P., Wang Y., Wang Y., Davalos A., Shamalov N., Mikulik R., Cunha L., Lindgren A., Arauz A., Lang W., Czlonkowska A., Eckstein J., Gagliardi R.J., Amarenco P., Ameriso S.F., Tatlisumak T., Veltkamp R., Hankey G.J., Toni D., Bereczki D., Uchiyama S., Ntaios G., Yoon B.-W., Brouns R., Endres M., Muir K.W., Bornstein N., Ozturk S., O'Donnell M.J., De Vries Basson M.M., Pare G., Pater C., Kirsch B., Sheridan P., Peters G., Weitz J.I., Peacock W.F., Shoamanesh A., Benavente O.R., Joyner C., Themeles E., Connolly S.J., for the NAVIGATE ESUS Investigatorsen
dc.date.accessioned2023-01-31T08:27:54Z
dc.date.available2023-01-31T08:27:54Z
dc.date.issued2018
dc.identifier10.1056/NEJMoa1802686
dc.identifier.issn00284793
dc.identifier.urihttp://hdl.handle.net/11615/73909
dc.description.abstractBACKGROUND Embolic strokes of undetermined source represent 20% of ischemic strokes and are associated with a high rate of recurrence. Anticoagulant treatment with rivaroxaban, an oral factor Xa inhibitor, may result in a lower risk of recurrent stroke than aspirin. METHODS We compared the efficacy and safety of rivaroxaban (at a daily dose of 15 mg) with aspirin (at a daily dose of 100 mg) for the prevention of recurrent stroke in patients with recent ischemic stroke that was presumed to be from cerebral embolism but without arterial stenosis, lacune, or an identified cardioembolic source.The primary efficacy outcome was the first recurrence of ischemic or hemorrhagic stroke or systemic embolism in a time-to-event analysis; the primary safety outcome was the rate of major bleeding. RESULTS A total of 7213 participants were enrolled at 459 sites; 3609 patients were randomly assigned to receive rivaroxaban and 3604 to receive aspirin. Patients had been followed for a median of 11 months when the trial was terminated early because of a lack of benefit with regard to stroke risk and because of bleeding associated with rivaroxaban.The primary efficacy outcome occurred in 172 patients in the rivaroxaban group (annualized rate, 5.1%) and in 160 in the aspirin group (annualized rate, 4.8%) (hazard ratio, 1.07; 95% confidence interval [CI], 0.87 to 1.33; P = 0.52). Recurrent ischemic stroke occurred in 158 patients in the rivaroxaban group (annualized rate, 4.7%) and in 156 in the aspirin group (annualized rate, 4.7%). Major bleeding occurred in 62 patients in the rivaroxaban group (annualized rate, 1.8%) and in 23 in the aspirin group (annualized rate, 0.7%) (hazard ratio, 2.72; 95% CI, 1.68 to 4.39; P<0.001). CONCLUSIONS Rivaroxaban was not superior to aspirin with regard to the prevention of recurrent stroke after an initial embolic stroke of undetermined source and was associated with a higher risk of bleeding. © 2018 Massachussetts Medical Society. All rights reserved.en
dc.language.isoenen
dc.sourceNew England Journal of Medicineen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85047954755&doi=10.1056%2fNEJMoa1802686&partnerID=40&md5=cb2075f5b2087cab98a55faecf3ab429
dc.subjectacetylsalicylic aciden
dc.subjectplaceboen
dc.subjectrivaroxabanen
dc.subjectacetylsalicylic aciden
dc.subjectantithrombocytic agenten
dc.subjectblood clotting factor 10a inhibitoren
dc.subjectrivaroxabanen
dc.subjectageden
dc.subjectArticleen
dc.subjectbleedingen
dc.subjectbrain ischemiaen
dc.subjectcerebrovascular accidenten
dc.subjectcomorbidityen
dc.subjectcomparative effectivenessen
dc.subjectcontrolled studyen
dc.subjectdrug safetyen
dc.subjectdrug treatment failureen
dc.subjectfemaleen
dc.subjectfollow upen
dc.subjecthumanen
dc.subjectintention to treat analysisen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectNational Institutes of Health Stroke Scaleen
dc.subjectoutcome assessmenten
dc.subjectphase 3 clinical trialen
dc.subjectpreventive medicineen
dc.subjectpriority journalen
dc.subjectrandomized controlled trialen
dc.subjectrecurrent diseaseen
dc.subjectrisk assessmenten
dc.subjectrisk factoren
dc.subjecttreatment outcomeen
dc.subjecttreatment responseen
dc.subjecttreatment withdrawalen
dc.subjectbrain embolismen
dc.subjectbrain ischemiaen
dc.subjectcerebrovascular accidenten
dc.subjectchemically induceden
dc.subjectclinical trialen
dc.subjectcomparative studyen
dc.subjectKaplan Meier methoden
dc.subjectmiddle ageden
dc.subjectmulticenter studyen
dc.subjectproceduresen
dc.subjectsecondary preventionen
dc.subjectAgeden
dc.subjectAspirinen
dc.subjectBrain Ischemiaen
dc.subjectFactor Xa Inhibitorsen
dc.subjectFemaleen
dc.subjectHemorrhageen
dc.subjectHumansen
dc.subjectIntracranial Embolismen
dc.subjectKaplan-Meier Estimateen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPlatelet Aggregation Inhibitorsen
dc.subjectRivaroxabanen
dc.subjectSecondary Preventionen
dc.subjectStrokeen
dc.subjectMassachussetts Medical Societyen
dc.titleRivaroxaban for stroke prevention after embolic stroke of undetermined sourceen
dc.typejournalArticleen


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