陆胜, 余再新, 黄友良, 谭碧峰. 不同剂量替罗非班联合替格瑞洛对NSTEMI患者短期心血管事件及血小板聚集率的影响[J]. 心脏杂志, 2017, 29(4): 427-430. DOI: 10.13191/j.chj.2017.0108
    引用本文: 陆胜, 余再新, 黄友良, 谭碧峰. 不同剂量替罗非班联合替格瑞洛对NSTEMI患者短期心血管事件及血小板聚集率的影响[J]. 心脏杂志, 2017, 29(4): 427-430. DOI: 10.13191/j.chj.2017.0108
    LU Sheng, YU Zai-xin, HUANG You-liang, TAN Bi-feng. Effect of different doses of terofiban combined with ticagrelor on short-term cardiovascular events and platelet aggregation rate in patients with non-ST-elevation myocardial infarction[J]. Chinese Heart Journal, 2017, 29(4): 427-430. DOI: 10.13191/j.chj.2017.0108
    Citation: LU Sheng, YU Zai-xin, HUANG You-liang, TAN Bi-feng. Effect of different doses of terofiban combined with ticagrelor on short-term cardiovascular events and platelet aggregation rate in patients with non-ST-elevation myocardial infarction[J]. Chinese Heart Journal, 2017, 29(4): 427-430. DOI: 10.13191/j.chj.2017.0108

    不同剂量替罗非班联合替格瑞洛对NSTEMI患者短期心血管事件及血小板聚集率的影响

    Effect of different doses of terofiban combined with ticagrelor on short-term cardiovascular events and platelet aggregation rate in patients with non-ST-elevation myocardial infarction

    • 摘要: 目的 探讨不同剂量替罗非班联合替格瑞洛对急性非ST段抬高型心肌梗死(NSTEMI)患者短期心血管事件及血小板聚集率的影响。 方法 收集128例NSTEMI患者,根据不同用药方式分为替格瑞洛组(A组,n=39)、常规剂量替罗非班联合替格瑞洛组(B组,n=46)和小剂量替罗非班联合替格瑞洛组(C组,n=41)。治疗4周后,比较3组患者的血小板聚集率、血纤维蛋白原(Fib)水平以及心血管事件、不良反应发生率。 结果 治疗4周后,A组复合项终点事件发生率明显高于B组和C组,差异有统计学意义(P<0.05);治疗1、4周后,B组和C组血小板聚集率、血Fib水平均显著低于A组,差异有统计学意义(P<0.05),B组和C组血小板聚集率、血Fib水平比较差异均无统计学意义 ;B组不良反应发生率明显高于A组和C组,差异有统计学意义(P<0.05)。 结论 常规剂量和小剂量替罗非班联合替格瑞洛均可减少NSTEMI患者短期心血管事件的发生,增强血小板聚集的抑制作用,且小剂量的替罗非班减少了不良反应的发生。

       

      Abstract: AIM To investigate the effect of different doses of terofiban combined with ticagrelor on short-term cardiovascular events and platelet aggregation rate in patients with (NSTEMI). METHODS One hundred and twenty-eight NSTEMI patients in our hospital were included in the study. According to different treatment methods, the patients were divided into ticagrelor group (group A, n=39), the conventional dose of tirofiban combined with ticagrelor group (group B, n=46) and small dose of tirofiban combined with Grillo group (group C, n=41). After 4 weeks of treatment, the platelet aggregation rate, fibrinogen (Fib) level and cardiovascular events, and incidence of adverse events were compared between the three groups. RESULTS After 4 weeks of treatment, the occurrence rate of composite endpoint in group A was significantly higher than those in group B and group C (P<0.05). The platelet aggregation rate and blood Fib levels in group B and group C were significantly lower than those in group A (P<0.05). The incidence of adverse reactions in group B was significantly higher than those in group A and group C (P<0.05). CONCLUSION Conventional dose and small dose of tirofiban combined with ticagrelor can reduce short-term cardiovascular events in NSTEMI patients and enhance the inhibition of platelet aggregation. Small dose of tirofiban reduces the incidence of adverse reactions.

       

    /

    返回文章
    返回