Qi Fan-Xing, Hu Ying, Wang Sen
Fan-xing Qi, Department of Neurology, Baoding First Central Hospital, Baoding 071000, Hebei, China.
Ying Hu, Department of Cardiology, Baoding First Central Hospital, Baoding 071000, Hebei, China.
Pak J Med Sci. 2021 Jul-Aug;37(4):1145-1150. doi: 10.12669/pjms.37.4.3986.
This study aims to evaluate the clinical effect of alteplase combined with butylphthalide in treating patients with acute anterior circulation cerebral infarction.
Retrospective study methods were used. Eighty patient cases with acute anterior circulation cerebral infarction treated in Baoding First Central Hospital, China from January 2018 to December 2020 were randomly and averagely divided into two groups. Patients in the two groups were given symptomatic treatment. Patients in the experimental group were treated with alteplase combined with butylphthalide for thrombolytic therapy, whereas patients in the control group were treated with urokinase thrombolytic therapy. The NIHSS score, effective rates and neurological function recovery were analysed one day, seven days and 30 days after treatment were analyzed, respectively. So as the incidence of adverse reactions within seven days after drug adminutesistration.
The NIHSS scores of the two groups were significantly lower than those before treatment on one day, seven days and 30 days after treatment (experimental group, =0.00; control group, =0.02). The experimental group was more significantly lower than the control group (=0.00). The effective rate of the experimental group was significantly higher than that of the control group (=0.03), and the recovery rate after treatment was significantly higher than that of the control group (=0.04). Within one week after treatment, the complication rate was 15% in the experimental group and 20% in the control group but was not significantly different (=0.56).
Alteplase combined with butylphthalide is effective and safe in the treatment of acute anterior circulation cerebral infarction without obvious complications.
本研究旨在评估阿替普酶联合丁苯酞治疗急性前循环脑梗死患者的临床疗效。
采用回顾性研究方法。选取2018年1月至2020年12月在中国保定市第一中心医院接受治疗的80例急性前循环脑梗死患者,随机平均分为两组。两组患者均给予对症治疗。试验组患者采用阿替普酶联合丁苯酞进行溶栓治疗,而对照组患者采用尿激酶溶栓治疗。分别分析治疗后1天、7天和30天的美国国立卫生研究院卒中量表(NIHSS)评分、有效率及神经功能恢复情况。同时分析给药后7天内的不良反应发生率。
两组患者治疗后1天、7天和30天的NIHSS评分均显著低于治疗前(试验组,=0.00;对照组,=0.02)。试验组显著低于对照组(=0.00)。试验组的有效率显著高于对照组(=0.03),治疗后的恢复率显著高于对照组(=0.04)。治疗后1周内,试验组并发症发生率为15%,对照组为20%,但差异无统计学意义(=0.56)。
阿替普酶联合丁苯酞治疗急性前循环脑梗死有效且安全,无明显并发症。