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中国医药导刊 ›› 2019, Vol. 21 ›› Issue (12): 744-748.

• 药物临床研究及应用 • 上一篇    下一篇

急性脑梗死患者不同抗血小板聚集治疗方案的疗效差异探讨

章袁,朱立勤,徐彦贵,马春潮,刘志伟,汪志云   

  1. 天津市第一中心医院
  • 收稿日期:2020-02-10 修回日期:2019-12-17 出版日期:2019-12-31 发布日期:2019-12-31

Investigation on the Difference in Efficacy of Antiplatelet Aggregation Regiments in Patients with Acute Cerebral Infarction

  • Received:2020-02-10 Revised:2019-12-17 Online:2019-12-31 Published:2019-12-31

摘要: 目的:探讨本院急性脑梗死患者口服阿司匹林、氯吡格雷及其联合治疗的疗效差异并分析原因,为临床提供理论参考。方法:共纳入本院急性脑梗死患者208例,根据治疗方案,分为A组(阿司匹林组)53例、B组(氯吡格雷组)59例和C组(阿司匹林+氯吡格雷组)96例,收集所有患者的一般资料,并检测血小板抑制率,进行统计分析。结果:B组和C组较A组有较高的质子泵抑制剂(PPI)类药物使用率(P<0.05)。比较显示,AA途径与ADP途径诱导的血小板抑制率比较差异有统计学意义(P<0.05),前者高于后者;单药组与联合组比较,AA途径或ADP途径诱导的血小板抑制率比较差异均无统计学意义(P>0.05)。C组与A组和B组血小板抑制疗效比较差异有统计学意义(P<0.05),C组高于A组与B组。结论:临床氯吡格雷抵抗现象明显高于阿司匹林,须关注氯吡格雷代谢基因型,提高对氯吡格雷代谢动力学及药物相互作用的认识;联合抗血小板聚集治疗通过AA和ADP两个条途径一并提高抗血小板聚集疗效,但无协同作用。

Abstract: Objective: To investigate the difference in efficacy of oral aspirin, clopidogrel and combined anti-platelet aggregation therapy in acute cerebral infarction patients, and analyze the cause, so as to provide the theoretical reference for clinical practice. Methods: The 208 hospitalized patients with acute cerebral infarction were divided into group A (aspirin group) 53 cases, group B (clopidogrel group) 59 cases and group C (combination group) 96 cases. The platelet inhibition rate was measured in all patients, and the patients’ general information were collected and analyzed. Results: The usage of PPI drugs in group B and group C was higher than group A (P<0.05). The comparison of platelet inhibition rate among three groups showed that the platelet inhibition rate induced by AA pathway were higher than that induced by ADP pathway (P<0.05), but there was no statistical difference in platelet inhibition rate induced by AA or ADP pathway between sigle drug group and combination group(P>0.05). The effective rate of platelet inhibition in group C was higher than that in group A and B(P<0.05). Conclusion: The clinical resistance rate of clopidogrel is more common than that of aspirin. Attention should be paid to the metabolic genotype of clopidogrel. The understanding of the pharmacokinetics of clopidogrel and the drug interaction should be improved. Combined antiplatelet therapy can improve antiplatelet aggregation through AA and ADP pathway, but there is no synergistic effect.

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