Zuo Feng-Tong, Liu Hui, Wu Hui-Jun, Su Na, Liu Jie-Qiong, Dong Ai-Qin
Department of Neurology, Cangzhou Central Hospital Department of Internal Medicine, Cangzhou Peace Hospital, Cangzhou, Hebei, China.
Medicine (Baltimore). 2017 Jan;96(1):e5497. doi: 10.1097/MD.0000000000005497.
There are limited data on the effect of dual antiplatelet treatment with clopidogrel plus aspirin in patients with ischemic cerebrovascular disease and intracranial and extracranial arteriostenosis. The aim of our study was to evaluate the efficacy and safety of aspirin plus clopidogrel in the treatment of ischemic cerebrovascular disease with intracranial and extracranial arteriostenosis.
Patients with clinically evident acute cerebral infarction or transient ischemic attack combined with intracranial and extracranial arteriostenosis (greater than 50%) who were unsuitable or reluctance to perform stent implantation were enrolled in this study. We randomly assigned these patients to receive clopidogrel (75 or 50 mg) plus aspirin (100 mg) or aspirin (100 mg) once daily through 90 days, and followed them for 90 days. We examined the main endpoints including the recurrence of stroke, death from cardiovascular causes, and bleeding events.
In all, 200 patients were recruited and followed for 90 days. Ischemic stroke occurred in 6 patients (9.1%) treated with 50 mg clopidogrel and aspirin, 6 patients (9.1%) receiving 75 mg clopidogrel and aspirin, whereas 19 patients (27.9%) in the aspirin group (aspirin alone vs copidogrel 50 mg plus aspirin; 95% confidence intervals 1.704-23.779, P < 0.05; aspirin alone vs copidogrel 75 mg plus aspirin; 95% confidence intervals 1.190-13.240, P < 0.05). There were more hemorrhagic events among recipients (3 patients [2.3%]) in the copidogrel plus aspirin group than aspirin recipients (0 patient [0%]), including 1 subcutaneous hemorrhage in the group of 50 mg clopidogrel and aspirin, doubling the number of nasal and gum bleeding in the group of 75 mg clopidogrel and aspirin (P > 0.05). No intracranial hemorrhage and gastro-intestinal hemorrhage occurred in these 3 groups.
Accordingly, 50 mg clopidogrel plus aspirin, and 75 mg clopidogrel plus aspirin were all superior to aspirin alone as stroke prevention in patients with cerebral infarction or transient ischemic attack combined with intracranial and extracranial arteriostenosis. The effect of secondary stroke prevention was similar between 50 mg clopidogrel plus aspirin and 75 mg clopidogrel plus aspirin. The therapy of 75 mg clopidogrel plus aspirin resulted in a worrisome tread in bleeding events.
关于氯吡格雷联合阿司匹林双重抗血小板治疗对缺血性脑血管病合并颅内和颅外动脉狭窄患者的影响,相关数据有限。我们研究的目的是评估阿司匹林联合氯吡格雷治疗缺血性脑血管病合并颅内和颅外动脉狭窄的疗效和安全性。
将临床上有明显急性脑梗死或短暂性脑缺血发作且合并颅内和颅外动脉狭窄(大于50%)、不适合或不愿进行支架植入的患者纳入本研究。我们将这些患者随机分为两组,一组接受氯吡格雷(75或50毫克)加阿司匹林(100毫克),另一组接受阿司匹林(100毫克),均每日一次,持续90天,并对他们进行90天的随访。我们检查了主要终点,包括中风复发、心血管原因导致的死亡以及出血事件。
总共招募了200名患者并随访90天。接受50毫克氯吡格雷和阿司匹林治疗的患者中有6例(9.1%)发生缺血性中风,接受75毫克氯吡格雷和阿司匹林治疗的患者中有6例(9.1%)发生缺血性中风,而阿司匹林组有19例(27.9%)发生缺血性中风(单独使用阿司匹林与50毫克氯吡格雷加阿司匹林相比;95%置信区间为1.704 - 23.779,P < 0.05;单独使用阿司匹林与75毫克氯吡格雷加阿司匹林相比;95%置信区间为1.190 - 13.240,P < 0.05)。氯吡格雷加阿司匹林组的接受者中出血事件更多(3例患者[2.3%]),高于阿司匹林组接受者(0例患者[0%]),包括50毫克氯吡格雷和阿司匹林组有1例皮下出血,75毫克氯吡格雷和阿司匹林组鼻出血和牙龈出血数量翻倍(P > 0.05)。这3组均未发生颅内出血和胃肠道出血。
因此,50毫克氯吡格雷加阿司匹林以及75毫克氯吡格雷加阿司匹林在预防脑梗死或短暂性脑缺血发作合并颅内和颅外动脉狭窄患者的中风方面均优于单独使用阿司匹林。50毫克氯吡格雷加阿司匹林与75毫克氯吡格雷加阿司匹林在二级预防中风方面的效果相似。75毫克氯吡格雷加阿司匹林的治疗导致出血事件出现令人担忧的趋势。