{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T22:53:45Z","timestamp":1793400825373,"version":"4.5.0"},"reference-count":42,"publisher":"American Medical Association (AMA)","issue":"23","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA"],"published-print":{"date-parts":[[2021,12,21]]},"abstract":"<jats:sec id=\"ab-joi210130-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>The comparative effectiveness of rivaroxaban and apixaban, the most frequently prescribed oral anticoagulants for ischemic stroke prevention in patients with atrial fibrillation, is uncertain.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To compare major ischemic and hemorrhagic outcomes in patients with atrial fibrillation treated with rivaroxaban or apixaban.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>Retrospective cohort study using computerized enrollment and claims files for US Medicare beneficiaries 65 years or older. Between January 1, 2013, and November 30, 2018, a total of 581\u202f451 patients with atrial fibrillation began rivaroxaban or apixaban treatment and were followed up for 4 years, through November 30, 2018.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Rivaroxaban (n\u2009=\u2009227\u202f572) and apixaban (n\u2009=\u2009353\u202f879), either standard or reduced dose.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>The primary outcome was a composite of major ischemic (stroke\/systemic embolism) and hemorrhagic (intracerebral hemorrhage\/other intracranial bleeding\/fatal extracranial bleeding) events. Secondary outcomes were nonfatal extracranial bleeding and total mortality (fatal ischemic\/hemorrhagic event or other death during follow-up). Rates, hazard ratios (HRs), and rate differences (RDs) were adjusted for baseline differences in comorbidity with inverse probability of treatment weighting.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Study patients (mean age, 77.0 years; 291\u202f966 [50.2%] women; 134\u202f393 [23.1%] receiving reduced dose) had 474\u202f605 person-years of follow-up (median [IQR]\u2009of 174 [62-397] days). The adjusted primary outcome rate for rivaroxaban was 16.1 per 1000 person-years vs 13.4 per 1000 person-years for apixaban (RD,\u20092.7 [95% CI, 1.9-3.5]; HR, 1.18 [95% CI, 1.12-1.24]). The rivaroxaban group had increased risk for both major ischemic events (8.6 vs 7.6 per 1000 person-years; RD, 1.1 [95% CI, 0.5-1.7]; HR, 1.12 [95% CI, 1.04-1.20]) and hemorrhagic events (7.5 vs 5.9 per 1000 person-years; RD, 1.6 [95% CI, 1.1-2.1]; HR, 1.26 [95% CI, 1.16-1.36]), including fatal extracranial bleeding (1.4 vs 1.0 per 1000 person-years; RD, 0.4 [95% CI, 0.2-0.7]; HR, 1.41 [95% CI, 1.18-1.70]). Patients receiving rivaroxaban had increased risk of nonfatal extracranial bleeding (39.7 vs 18.5 per 1000 person-years; RD, 21.1 [95% CI, 20.0-22.3]; HR, 2.07 [95% CI, 1.99-2.15]), fatal ischemic\/hemorrhagic events (4.5 vs 3.3 per 1000 person-years; RD, 1.2 [95% CI, 0.8-1.6]; HR, 1.34 [95% CI, 1.21-1.48]), and total mortality (44.2 vs 41.0 per 1000 person-years; RD, 3.1 [95% CI, 1.8-4.5]; HR, 1.06 [95% CI, 1.02-1.09]). The risk of the primary outcome was increased for rivaroxaban in both those receiving the reduced dose (27.4 vs 21.0 per 1000 person-years; RD, 6.4 [95% CI, 4.1-8.7]; HR, 1.28 [95% CI, 1.16-1.40]) and the standard dose (13.2 vs 11.4 per 1000 person-years; RD, 1.8 [95% CI, 1.0-2.6]; HR, 1.13 [95% CI, 1.06-1.21]) groups.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-joi210130-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>Among Medicare beneficiaries 65 years or older with atrial fibrillation, treatment with rivaroxaban compared with apixaban was associated with a significantly increased risk of major ischemic or hemorrhagic events.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jama.2021.21222","type":"journal-article","created":{"date-parts":[[2021,12,21]],"date-time":"2021-12-21T11:03:50Z","timestamp":1640084630000},"page":"2395","source":"Crossref","is-referenced-by-count":146,"title":["Association of Rivaroxaban vs Apixaban With Major Ischemic or Hemorrhagic Events in Patients With Atrial Fibrillation"],"prefix":"10.1001","volume":"326","author":[{"given":"Wayne A.","family":"Ray","sequence":"first","affiliation":[{"name":"Department of Health Policy, Vanderbilt University School of Medicine, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cecilia P.","family":"Chung","sequence":"additional","affiliation":[{"name":"Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C. 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