首页|阿托伐他汀联合氯吡格雷治疗脑血栓的安全性及对凝血功能的改善研究

阿托伐他汀联合氯吡格雷治疗脑血栓的安全性及对凝血功能的改善研究

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目的 分析脑血栓采取阿托伐他汀联合氯吡格雷治疗的安全性以及对凝血功能的改善情况.方法 100 例脑血栓患者,取随机数字法分成参照组、试验组,每组 50 例.两组均接受对症治疗,参照组给予阿托伐他汀治疗,试验组给予阿托伐他汀联合氯吡格雷治疗.比较两组安全性,凝血功能[D-二聚体(D-D)、纤维蛋白原(Fib)、凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)],血液流变学(低切全血粘度、高切全血粘度、血浆粘度),治疗效果,预后不良事件发生情况.结果 试验组不良反应发生率为 4.00%,参照组不良反应发生率为 18.00%,组间不良反应发生率存在统计学差异(χ2=5.0051,P=0.0253<0.05).两组间的D-D、Fib、PT、APTT在治疗前并不存在差异(P>0.05);但治疗后试验组的D-D(151.26±23.17)ng/ml、Fib(3.02±0.27)g/L低于参照组的(179.02±26.14)ng/ml、(3.95±0.38)g/L,PT(12.29±1.79)s、APTT(35.33±2.16)s长于参照组的(11.68±1.15)、(32.37±2.09)s,存在统计学差异(P<0.05).两组治疗前的低切全血粘度、高切全血粘度、血浆粘度并不存在差异(P>0.05);但治疗后试验组的低切全血粘度、高切全血粘度、血浆粘度分别为(4.51±0.63)、(3.27±0.36)、(1.58±0.38)mPa·s,均低于参照组的(5.83±0.73)、(4.15±0.68)、(2.16±0.52)mPa·s,存在统计学差异(P<0.05).试验组总有效率 96.00%显著高于参照组的 84.00%,存在统计学差异(P<0.05).经跟踪随访发现,试验组预后不良事件发生率 6.00%低于参照组的 22.00%,存在统计学差异(P<0.05).结论 在治疗脑血栓时,阿托伐他汀联合氯吡格雷是一种具有价值的方案,可在保证用药安全的前提下有效改善凝血功能,值得推广.
Study on the safety of atorvastatin combined with clopidogrel in the treatment of cerebral thrombosis and the improvement of coagulation function
Objective To analyze the safety of atorvastatin combined with clopidogrel in the treatment of cerebral thrombosis and the improvement of coagulation function.Methods 100 patients with cerebral thrombosis were divided into a reference group and an experimental group according to the random numerical table,each with 50 cases.Both groups received conventional treatment.On this basis,the reference group was given atorvastatin treatment,and the experimental group was given atorvastatin combined with clopidogrel for treatment.Both groups were compared in terms of safety,coagulation function[D-dimer(D-D),fibrinogen(Fib),prothrombin time(PT),activated partial thromboplastin time(APTT)],hemorheology(whole blood low shear viscosity,whole blood high shear viscosity,plasma viscosity),treatment effect,and occurrence of adverse events.Results The incidence of adverse reactions was 4.00%in the experimental group and 18.00%in reference group,and there was statistical difference(χ2=5.0051,P=0.0253<0.05).Before treatment,there were no statistical differences in D-D,Fib,PT and APTT between the two groups(P>0.05).After treatment,the experimental group had D-D of(151.26±23.17)ng/ml and Fib levels of(3.02±0.27)g/L,which were lower than(179.02±26.14)ng/ml and(3.95±0.38)g/L of the reference group;the experimental group had PT of(12.29±1.79)s and APTT of(35.33±2.16)s,which were longer than(11.68±1.15)and(32.37±2.09)s in the reference group;there was a statistical difference(P<0.05).Before treatment,there was no difference in whole blood low shear viscosity,whole blood high shear viscosity and plasma viscosity between the two groups(P>0.05).After treatment,the whole blood low shear viscosity,whole blood high shear viscosity and plasma viscosity in the experimental group were(4.51±0.63),(3.27±0.36)and(1.58±0.38)mPa·s,which were lower than(5.83±0.73),(4.15±0.68)and(2.16±0.52)mPa·s in the the reference group.There was a statistical difference(P<0.05).The total effective rate of 96.00%in the experimental group was significantly higher than 84.00%in the reference group,and there was a statistical difference(P<0.05).After follow-up,it was found that the incidence of adverse events in the experimental group was 6.00%,which was lower than 22.00%in the reference group,and the difference was statistically significant(P<0.05).Conclusion In the treatment of cerebral thrombosis,atorvastatin combined with clopidogrel is a valuable scheme,which can effectively improve the coagulation function under the premise of ensuring the safety of medication,and is worthy of promotion.

AtorvastatinClopidogrelCerebral thrombosisSafetyCoagulation function

张涛

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115200 盖州博海医院

阿托伐他汀 氯吡格雷 脑血栓 安全性 凝血功能

2024

中国实用医药
中国康复医学会

中国实用医药

影响因子:0.797
ISSN:1673-7555
年,卷(期):2024.19(8)
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