Meyer Dawn M, Albright Karen C, Allison Teresa A, Grotta James C
Neurology Department, University of Texas Health Science Center at Houston, Texas, USA.
J Stroke Cerebrovasc Dis. 2008 Jan-Feb;17(1):26-9. doi: 10.1016/j.jstrokecerebrovasdis.2007.09.006.
Most patients with ischemic stroke present to the emergency department beyond the approved 3-hour time window for thrombolytic or other revascularization therapies. Clopidogrel and aspirin loading is commonly used to prevent deterioration in other acute vascular occlusive events. This pilot study examined the safety of antiplatelet loading in acute ischemic stroke and transient ischemic attack.
Forty patients with stroke or transient ischemic attack symptoms, not eligible for revascularization, received a single dose of 375 mg of clopidogrel and 325 mg of aspirin within 36 hours of stroke onset. All patients were admitted to a comprehensive stroke department and monitored for neurologic deterioration (2-point increase on National Institutes of Health stroke scale [NIHSS] score) and bleeding complications until hospital day 7 or discharge. NIHSS was performed at 24 hours postadmission and on hospital day 7 or discharge, whichever came first.
A total of 40 patients were loaded with 375 mg of clopidogrel and 325 mg of aspirin (mean 12 hours 32 minutes). Mean admission NIHSS score was 6. There were no cases of systemic hemorrhage or mortality. A single symptomatic intracranial hemorrhage (2.5%) was detected 43 hours posttreatment. When compared with matched control subjects, loaded patients were no more likely to experience hemorrhage and significantly less likely to experience neurologic deterioration (odds ratio 17.2; P < .002).
Loading with 375 mg of clopidogrel and 325 mg of aspirin appears to be safe when administered up to 36 hours after stroke and transient ischemic attack onset in this pilot study. Neurologic deterioration may be decreased and warrants further study.
大多数缺血性卒中患者在急诊科就诊时已超出批准的3小时溶栓或其他血管再通治疗时间窗。氯吡格雷和阿司匹林负荷剂量常用于预防其他急性血管闭塞事件的病情恶化。这项前瞻性研究探讨了急性缺血性卒中和短暂性脑缺血发作时抗血小板负荷剂量治疗的安全性。
40例有卒中或短暂性脑缺血发作症状、不符合血管再通条件的患者在卒中发作36小时内接受了一剂375毫克氯吡格雷和325毫克阿司匹林治疗。所有患者均入住综合性卒中病房,监测神经功能恶化情况(美国国立卫生研究院卒中量表[NIHSS]评分增加2分)和出血并发症,直至住院第7天或出院。入院后24小时以及住院第7天或出院时(以先到者为准)进行NIHSS评分。
共有40例患者接受了375毫克氯吡格雷和325毫克阿司匹林负荷剂量治疗(平均12小时32分钟)。入院时NIHSS评分平均为6分。未发生系统性出血或死亡病例。治疗后43小时发现1例有症状性颅内出血(2.5%)。与匹配的对照受试者相比,接受负荷剂量治疗的患者发生出血的可能性并不更高,而发生神经功能恶化的可能性显著更低(优势比17.2;P<0.002)。
在这项前瞻性研究中,卒中及短暂性脑缺血发作后36小时内给予375毫克氯吡格雷和325毫克阿司匹林负荷剂量治疗似乎是安全的。神经功能恶化情况可能会减少,值得进一步研究。