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西洛他唑联合阿司匹林可预防急性缺血性脑卒中患者早期神经功能恶化:一项初步研究。

Cilostazol combined with aspirin prevents early neurological deterioration in patients with acute ischemic stroke: a pilot study.

机构信息

Department of Neurology, Tokyo Women's Medical University, Tokyo, Japan.

出版信息

J Neurol Sci. 2012 Feb 15;313(1-2):22-6. doi: 10.1016/j.jns.2011.09.038. Epub 2011 Oct 19.

DOI:10.1016/j.jns.2011.09.038
PMID:22014645
Abstract

Recent randomized trials have shown that cilostazol is superior to aspirin for secondary stroke prevention. We hypothesized that combining cilostazol with aspirin is more effective than aspirin alone in patients with acute ischemic stroke. This randomized study compared the effects of oral aspirin alone to aspirin plus cilostazol in patients with non-cardioembolic ischemic stroke within 48 h of stroke onset. NIH Stroke Scale (NIHSS) and modified Rankin Scale (mRS) scores were checked before and after 14 days and 6 months of drug administration. The primary and secondary endpoints were neurological deterioration or stroke recurrence (NIHSS score ≥ 1) within 14 days and 6 months, respectively. For statistical analysis, on-treatment analysis was conducted. Seventy-six patients were enrolled in the study. The primary endpoint was significantly higher in the aspirin group than in the aspirin plus cilostazol group (28% vs. 6%, relative risk (RR): 0.21, 95% confidence intervals (CI): 0.05-0.87, p=0.013). Among the patients who did not reach these endpoints, the mean improvement in the NIHSS score at day 14 tended to be better (-1.8 ± 1.2 vs. -1.2 ± 1.0, p=0.078) and the frequency of the favorable functional status of mRS 0-1 at month 6 was significantly higher (RR: 1.48, 95% CI: 1.07-2.06, p=0.0048) in the aspirin plus cilostazol group than in the aspirin group. Patients treated with aspirin plus cilostazol during the acute phase of stroke had less neurological deterioration and more favorable functional status than those treated with aspirin alone.

摘要

最近的随机试验表明,西洛他唑在预防二级卒中方面优于阿司匹林。我们假设,在急性缺血性卒中患者中,西洛他唑联合阿司匹林比单独使用阿司匹林更有效。这项随机研究比较了在卒中发病后 48 小时内,口服阿司匹林单独治疗与阿司匹林联合西洛他唑治疗非心源性缺血性卒中患者的效果。在药物治疗前、后 14 天和 6 个月,分别采用 NIH 卒中量表(NIHSS)和改良 Rankin 量表(mRS)评分。主要和次要终点分别为 14 天和 6 个月内神经功能恶化或卒中复发(NIHSS 评分≥1)。为了进行统计分析,进行了治疗期间分析。这项研究共纳入了 76 例患者。阿司匹林组的主要终点显著高于阿司匹林联合西洛他唑组(28% vs. 6%,相对风险(RR):0.21,95%置信区间(CI):0.05-0.87,p=0.013)。在未达到这些终点的患者中,第 14 天 NIHSS 评分的平均改善程度倾向于更好(-1.8 ± 1.2 vs. -1.2 ± 1.0,p=0.078),6 个月时 mRS 0-1 的良好功能状态的频率在阿司匹林联合西洛他唑组也显著更高(RR:1.48,95% CI:1.07-2.06,p=0.0048)。在卒中急性期接受阿司匹林联合西洛他唑治疗的患者,神经功能恶化程度较轻,功能状态较好。

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