Early initiation of rivaroxaban after reperfusion therapy for stroke patients with nonvalvular atrial fibrillation

PLoS One. 2022 Apr 6;17(4):e0264760. doi: 10.1371/journal.pone.0264760. eCollection 2022.

Abstract

Background: The optimal timing of initiating oral anticoagulants after reperfusion therapy for ischemic stroke is unknown. Factors related to early initiation of rivaroxaban and differences in clinical outcomes of stroke patients with nonvalvular atrial fibrillation (NVAF) who underwent reperfusion therapy was investigated.

Methods: From data of 1,333 NVAF patients with ischemic stroke or transient ischemic attack (TIA) in a prospective multicenter study, patients who started rivaroxaban after intravenous thrombolysis and/or mechanical thrombectomy were included. The clinical outcomes included the composite of ischemic events (recurrent ischemic stroke, TIA, or systemic embolism) and major bleeding at 3 months.

Results: Among the 424 patients, the median time from index stroke to starting rivaroxaban was 3.2 days. On multivariable logistic regression analysis, infarct size (odds ratio [OR], 0.99; 95%CI, 0.99-1.00) was inversely and successful reperfusion (OR, 2.13; 95%CI, 1.24-3.72) was positively associated with initiation of rivaroxaban within 72 hours. 205 patients were assigned to the early group (< 72 hours) and 219 patients (≥ 72 hours) to the late group. Multivariable Cox regression models showed comparable hazard ratios between the two groups at 3 months for ischemic events (hazard ratio [HR], 0.18; 95%CI, 0.03-1.32) and major bleeding (HR, 1.80; 95%CI, 0.24-13.54).

Conclusions: Infarct size and results of reperfusion therapy were associated with the timing of starting rivaroxaban. There were no significant differences in the rates of ischemic events and major bleeding between patients after reperfusion therapy who started rivaroxaban < 72 hours and ≥ 72 hours after the index stroke.

Clinical trial registration: Unique identifier: NCT02129920; URL: https://www.clinicaltrials.gov.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticoagulants / therapeutic use
  • Atrial Fibrillation* / chemically induced
  • Atrial Fibrillation* / complications
  • Atrial Fibrillation* / drug therapy
  • Hemorrhage / chemically induced
  • Humans
  • Infarction
  • Ischemic Attack, Transient* / complications
  • Ischemic Stroke*
  • Prospective Studies
  • Reperfusion
  • Retrospective Studies
  • Rivaroxaban / adverse effects
  • Stroke* / chemically induced
  • Stroke* / complications
  • Stroke* / drug therapy
  • Treatment Outcome

Substances

  • Anticoagulants
  • Rivaroxaban

Associated data

  • ClinicalTrials.gov/NCT02129920

Grants and funding

This study was planned by Japan Cardiovascular Research Foundation and funded by Bayer Yakuhin Ltd. (contract No.:017926). The study was partly supported by the Japan Agency for Medical Research and Development (AMED) (20lk0201094h0002 and 20lk0201109h0001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.