Early antiplatelet for minor stroke following thrombolysis (EAST): Rationale and design

医学 溶栓 冲程(发动机) 氯吡格雷 阿司匹林 改良兰金量表 轻微中风 安慰剂 抗血栓 内科学 纤溶剂 随机对照试验 外科 心肌梗塞 缺血性中风 缺血 替代医学 病理 工程类 狭窄 机械工程
作者
Xiaoqiu Li,Yu Cui,Xinhong Wang,Dawei Chen
出处
期刊:International Journal of Stroke [SAGE]
卷期号:18 (5): 615-619 被引量:3
标识
DOI:10.1177/17474930221118900
摘要

Background: Early neurological deterioration (END) occurs in about 10% of patients after intravenous thrombolysis (IVT) and is related to poor outcome. In theory, early antiplatelet following IVT could reduce END by preventing re-occlusion and stroke progression, but current guidelines recommend starting antiplatelet treatment at 24 h after IVT due to concerns about hemorrhagic transformation. Given higher risk of hemorrhagic transformation in severe stroke, we hypothesized that minor stroke patients following IVT can safely benefit from early antiplatelet treatment. Aims: To explore the efficacy and safety of early antiplatelet in minor stroke patients after IVT. Sample size estimates: A maximum of 1022 patients are required to test the superiority hypothesis with 80% power according to a two-side 0.05 level of significance, stratified by age, gender, history of stroke or transient ischemic attack, history of hypertension, history of diabetes mellitus, systolic blood pressure at admission, time from IVT to treatment, thrombolysis drug, stroke territory, and stroke etiology. Design: Early antiplatelet for minor stroke following thrombolysis is a prospective, double-blinded, multicenter, randomized and placebo-controlled trial. Minor stroke patients within 6 h following IVT are randomly assigned into experimental group and control group with the ratio of 1:1. The experimental group is orally administered with 300 mg clopidogrel and 100 mg aspirin, and control group with placebo. Subsequently, both groups received guideline-based antithrombotic treatment from 24 h after IVT to 90 days. Outcome: The primary efficacy endpoint is excellent functional outcome, defined as the modified Rankin Scale 0–1 at 90 days after randomization, while primary safety endpoint is symptomatic intracerebral hemorrhage, defined as National Institutes of Health Stroke Scale score increase ⩾ 4 caused by intracranial hemorrhage within 36 h after randomization. Conclusions: The results of EAST will provide us powerful early antiplatelet evidence for minor stroke population following intravenous thrombolysis in clinical practice.
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