4.3 Article

Once versus twice daily direct oral anticoagulants in patients with recent stroke and atrial fibrillation

期刊

EUROPEAN STROKE JOURNAL
卷 7, 期 3, 页码 221-229

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/23969873221099477

关键词

Direct oral anticoagulants; once-daily; twice-daily; regimen; stroke; atrial fibrillation

资金

  1. Bayer AG (Switzerland)
  2. Science Fund Rehabilitation of the University Department of Geriatric Medicine Felix Platter Basel
  3. Stroke Fund and Scientific Fund of the University Hospital Basel
  4. Swiss Heart Foundation
  5. Daiichi-Sankyo AG (Switzerland)

向作者/读者索取更多资源

Both once-daily and twice-daily direct oral anticoagulants show lower risk for recurrent ischemic stroke, major bleeding, and all-cause death compared to vitamin K antagonists in atrial fibrillation patients with recent stroke. There is no clear evidence that one dosing regimen of direct oral anticoagulants is more advantageous than the other.
Background: Data on the safety and effectiveness of once-daily (QD) versus twice-daily (BID) direct oral anticoagulants (DOAC) in comparison to vitamin K antagonists (VKA) and to one another in patients with atrial fibrillation (AF) and recent stroke are scarce. Patients and methods: Based on prospectively obtained data from the observational registry Novel-Oral-Anticoagulants-in-Ischemic-Stroke-Patients(NOACISP)-LONGTERM (NCT03826927) from Basel, Switzerland, we compared the occurrence of the primary outcome - the composite of recurrent ischemic stroke, major bleeding, and all-cause death - among consecutive AF patients treated with either VKA, QD DOAC, or BID DOAC following a recent stroke using Cox proportional hazards regression including adjustment for potential confounders. Results: We analyzed 956 patients (median age 80 years, 46% female), of whom 128 received VKA (13.4%), 264 QD DOAC (27.6%), and 564 BID DOAC (59%). Over a total follow-up of 1596 patient-years, both QD DOAC and BID DOAC showed a lower hazard for the composite outcome compared to VKA (adjusted HR [95% CI] 0.69 [0.48, 1.01] and 0.66 [0.47, 0.91], respectively). Upon direct comparison, the hazard for the composite outcome did not differ between patients treated with QD versus BID DOAC (adjusted HR [95% CI] 0.94 [0.70, 1.26]). Secondary analyses focusing on the individual components of the composite outcome revealed no clear differences in the risk-benefit profile of QD versus BID DOAC. Discussion and conclusion: The overall benefit of DOAC over VKA seems to apply to both QD and BID DOAC in AF patients with a recent stroke, without clear evidence that one DOAC dosing regimen is more advantageous than the other.

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