Comparative study on clinical efficacy of indobufen and aspirin in acute mild ischemic stroke
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摘要: 目的 对比吲哚布芬与阿司匹林治疗急性轻型缺血性脑卒中的临床疗效。方法 选取2021年1月—2021年9月期间住院治疗的急性轻型缺血性脑卒中患者60例，采用随机数字表法分为2组：观察组(n=30)与对照组(n=30)。2组均接受基础治疗，观察组口服吲哚布芬，对照组口服阿司匹林，前3周2组均联合氯吡格雷口服，3周后观察血小板聚集功能，90 d后观察2组患者的美国国立卫生院神经功能缺损(NIHSS)评分变化、Barthel指数(BI)变化及不良反应发生情况。结果 2组患者的基线特征具有可比性(P>0.05)。2组患者治疗前花生四烯酸(AA)诱导的血小板最大聚集率(MAR-AA)和二磷酸腺苷(ADP)诱导的血小板最大聚集率(MAR-ADP)具有可比性(P>0.05)；治疗3周后均降低，差异有统计学意义(P< 0.05)，2组治疗后比较差异无统计学意义(P>0.05)。治疗前2组NIHSS评分具有可比性(P>0.05)；治疗3个月后均降低，差异有统计学意义(P< 0.05)，治疗后2组NIHSS评分比较差异无统计学意义(P>0.05)。治疗前2组BI指数比较差异无统计学意义(P>0.05)；治疗后，2组BI指数较用药前均升高，差异有统计学意义(P< 0.05)，且2组间BI指数评分差异无统计学意义(P>0.05)。观察组发生不良反应情况较对照组低(3.33% vs. 23.33%,P< 0.05)。结论 2组药物方案抗血小板聚集效果相当，且均能改善急性轻型缺血性脑卒中患者的神经功能缺损、日常生活能力，但吲哚布芬不良反应发生率更低，安全性更高。吲哚布芬对急性轻型缺血性脑卒中的治疗作用与阿司匹林相当，且不良反应更小。
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关键词:
- 吲哚布芬 /
- 阿司匹林 /
- 急性轻型缺血性脑卒中 /
- 疗效
Abstract: Objective To compare the clinical efficacy of indobufen and aspirin in the treatment of acute mild ischemic stroke.Methods Sixty patients with acute mild ischemic stroke hospitalized in the Department of Neurology of our hospital from January 2021 to September 2021 were selected and divided into 2 groups by random number table method: observation group(n=30) and control group(n=30), both groups received basic treatment, the observation group orally indocybufen, the control group orally aspirin, the first 3 weeks of both groups combined with clopidogrel, 3 weeks after observation of platelet aggregation function, 90 days after observation of NIH stroke scale(NIHSS), Barthe index(BI) changes, and the occurrence of adverse reactions in 2 groups.Results The baseline characteristics of the two groups were comparable(P>0.05). Before treatment, MAR-AA and MAR-ADP were comparable between 2 groups(P>0.05). There was significant difference before and after treatment(P< 0.05), but there was no significant difference between the two groups after treatment(P>0.05). NIHSS scores were comparable between 2 groups before treatment(P>0.05). There was significant difference before and after treatment(P< 0.05), while NIHSS score after treatment between the two groups had no statistical significance(P>0.05). BI index was comparable between 2 groups before treatment(P>0.05). After 3 months of treatment, BI index scores of patients in both groups increased(P< 0.05). There was no significant difference in BI index between the two groups after treatment(P>0.05). After treatment, there were fewer adverse reactions in the observation group than the control group(3.33% vs. 23.33%,P< 0.05).Conclusion The anti-platelet aggregation effect of the two groups of drug regimen is similar, and both can improve the neurological deficit and daily living ability of patients with acute mild ischemic stroke, but the incidence of adverse reactions of indocybufen is lower, and the safety is higher. In conclusion, indocybufen has the same therapeutic effect as aspirin in the treatment of acute mild ischemic stroke with fewer side effects.-
Key words:
- indobufen /
- aspirin /
- acute mild ischemic stroke /
- efficacy
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表 1 2组患者基本资料的比较
例，X±S 基本资料 实验组(n=30) 对照组(n=30) P 性别 男 19 22 0.405 女 11 8 年龄/岁 60.57±7.68 62.70±6.98 0.682 高血压病史 有 12 19 0.070 无 18 11 高脂血症病史 有 4 3 0.688 无 26 27 糖尿病史 有 9 8 0.774 无 21 22 吸烟史 有 16 15 0.796 无 14 15 饮酒史 有 8 13 0.176 无 22 17 
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表 2 2组患者治疗前后MAR-AA的比较
%，X±S 组别 MAR-AA P 治疗前 治疗后 观察组 50.786 7±19.165 5 34.683 3±11.876 9 0.015 对照组 44.946 7±19.658 9 31.630 0±10.355 4 < 0.001 P 0.249 0.293
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表 3 2组患者治疗前后MAR-ADP的比较
%，X±S 组别 MAR-ADP P 治疗前 治疗后 观察组 45.683 3±14.950 5 32.456 7±11.292 8 0.024 对照组 43.573 3±14.673 4 29.496 7±8.226 1 0.001 P 0.583 0.251
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表 4 2组患者治疗前后NIHSS评分的比较
分，M(Q1，Q3) 组别 NIHSS评分 P 治疗前 治疗后 观察组 2.00(1.00，2.25) 1.00(1.00，1.00) < 0.001 对照组 2.00(1.00，2.00) 1.00(0.75，1.00) 0.001 P 0.873 0.692
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表 5 2组患者治疗前后BI指数的比较
分，X±S 组别 BI指数 P 治疗前 治疗后 实验组 85.500 0±8.024 7 91.500 0±7.673 3 0.004 对照组 87.000 0±8.051 6 91.500 0±6.966 7 0.001 P 0.860 0.607
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