Adjunctive Intravenous Argatroban or Eptifibatide for Ischemic Stroke

阿加曲班 依替巴肽 医学 冲程(发动机) 心脏病学 缺血性中风 内科学 麻醉 缺血 血小板 经皮冠状动脉介入治疗 机械工程 工程类 心肌梗塞 凝血酶
作者
Opeolu Adeoye,Joseph Broderick,Colin P. Derdeyn,James C. Grotta,William G. Barsan,Oladi Bentho,Scott Berry,Mauricio Concha,Iris Davis,Stacie L Demel,Jordan Elm,Nina Gentile,Todd Graves,Melissa Hoffman,Josephine F. Huang,James Ingles,Scott Janis,Adam Jasne,Pooja Khatri,Steven R. Levine
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:391 (9): 810-820 被引量:55
标识
DOI:10.1056/nejmoa2314779
摘要

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. (Funded by the National Institute of Neurological Disorders and Stroke; MOST ClinicalTrials.gov number, NCT03735979.).
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