Skip to main navigation Skip to search Skip to main content

Adjunctive Intravenous Argatroban or Eptifibatide for Ischemic Stroke

  • O. Adeoye
  • , J. Broderick
  • , C. P. Derdeyn
  • , J. C. Grotta
  • , W. Barsan
  • , O. Bentho
  • , S. Berry
  • , M. Concha
  • , I. Davis
  • , S. Demel
  • , J. Elm
  • , N. Gentile
  • , T. Graves
  • , M. Hoffman
  • , J. Huang
  • , J. Ingles
  • , S. Janis
  • , A. S. Jasne
  • , P. Khatri
  • , S. R. Levine
  • A. Majjhoo, P. Panagos, A. Pancioli, S. Pizzella, T. Ranasinghe, N. Sabagha, S. Sivakumar, C. Streib, A. Vagal, A. Wilson, M. Wintermark, A. J. Yoo, A. D. Barreto
  • Washington University St. Louis
  • Departments of Neurology and Rehabilitation Medicine
  • University of Virginia
  • Memorial Hermann Healthcare System
  • University of Michigan, Ann Arbor
  • University of Minnesota Twin Cities
  • Berry Consultants LLC
  • Sarasota Memorial Hospital
  • Medical University of South Carolina
  • Temple University
  • Mayo Clinic Rochester, MN
  • National Institutes of Health
  • Yale University
  • McLaren Flint
  • Emergency Medicine
  • Wake Forest University
  • University of Cincinnati
  • University of South Carolina
  • Radiology Associates
  • University of Glasgow
  • University of Texas MD Anderson Cancer Center
  • Medical City Healthcare
  • University of Texas Health Science Center

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

BACKGROUND Intravenous thrombolysis is a standard treatment of acute ischemic stroke. The efficacy and safety of combining intravenous thrombolysis with argatroban (an anticoagulant agent) or eptifibatide (an antiplatelet agent) are unclear. METHODS We conducted a phase 3, three-group, adaptive, single-blind, randomized, controlled clinical trial at 57 sites in the United States. Patients with acute ischemic stroke who had received intravenous thrombolysis within 3 hours after symptom onset were assigned to receive intravenous argatroban, eptifibatide, or placebo within 75 minutes after the initiation of thrombolysis. The primary efficacy outcome, the utility-weighted 90-day modified Rankin scale score (range, 0 to 10, with higher scores reflecting better outcomes), was assessed by means of centralized adjudication. The primary safety outcome was symptomatic intracranial hemorrhage within 36 hours after randomization. RESULTS A total of 514 patients were assigned to receive argatroban (59 patients), eptifibatide (227 patients), or placebo (228 patients). All the patients received intravenous thrombolysis (70% received alteplase, and 30% received tenecteplase), and 225 patients (44%) underwent endovascular thrombectomy. At 90 days, the mean (±SD) utility-weighted modified Rankin scale scores were 5.2±3.7 with argatroban, 6.3±3.2 with eptifibatide, and 6.8±3.0 with placebo. The posterior probability that argatroban was better than placebo was 0.002 (posterior mean difference in utility-weighted modified Rankin scale score, −1.51±0.51) and that eptifibatide was better than placebo was 0.041 (posterior mean difference, −0.50±0.29). The incidence of symptomatic intracranial hemorrhage was similar in the three groups (4% with argatroban, 3% with eptifibatide, and 2% with placebo). Mortality at 90 days was higher in the argatroban group (24%) and the eptifibatide group (12%) than in the placebo group (8%). CONCLUSIONS In patients with acute ischemic stroke treated with intravenous thrombolysis within 3 hours after symptom onset, adjunctive treatment with intravenous argatroban or eptifibatide did not reduce poststroke disability and was associated with increased mortality.

Original languageEnglish
Pages (from-to)810-820
Number of pages11
JournalNew England Journal of Medicine
Volume391
Issue number9
DOIs
StatePublished - Sep 5 2024

Fingerprint

Dive into the research topics of 'Adjunctive Intravenous Argatroban or Eptifibatide for Ischemic Stroke'. Together they form a unique fingerprint.

Cite this