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Efficacy of Clopidogrel and Clinical Outcome When Clopidogrel Is Coadministered With Atorvastatin and Lansoprazole

机译:氯吡格雷与阿托伐他汀和兰索拉唑合用时氯吡格雷的疗效和临床结果

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摘要

This prospective, randomized, nonblind, controlled trial evaluated the effects of clopidogrel on platelet function upon coadministration with atorvastatin and lansoprazole.One hundred four adult patients with non-ST-segment elevated acute coronary syndrome (NSTE-ACS) who underwent percutaneous coronary intervention (PCI) with drug-eluting stent implantation were included. All patients were treated with standard dual antiplatelet therapy (DAPT) plus rosuvastatin 10 mg daily after the operation. On the sixth day after PCI, patients were randomly divided into 4 groups, Group A: DAPT + atorvastatin 20 mg daily (a change from rosuvastatin to atorvastatin) + lansoprazole 30 mg daily, Group B: DAPT + atorvastatin 20 mg daily (a change from rosuvastatin to atorvastatin), Group C: DAPT + lansoprazole 30 mg daily (continuing to take rosuvastatin), Group D is the control group. Additional drugs were used according to the situation of patients. Platelet function and concentrations of platelet activation markers (granular membrane protein 140 (P-selectin), thromboxane B2 (TXB2), and human soluble cluster of differentiation 40 ligand (sCD40L)) were assessed before randomization and at 15- and 30-day follow-up visits. All patients were maintained on treatment for 6 months and observed for bleeding and ischemic events.A total of 104 patients were enrolled, 27 patients in group A, 26 patients in Group B/C, 25 patients in Group D separately, and all the patients were analyzed. There were no differences in platelet function and the levels of platelet activation markers (P-selectin, TXB2, and sCD40L) among or within the 4 groups at the 3 time points of interest (P > 0.05). In the subsequent 6 months, no significant bleeding events occurred, and 12 patients experienced ischemic events, these results were also not significantly different among the groups (P > 0.05).In patients diagnosed with NSTE-ACS who have had drug-eluting stent implantation, simultaneously administering clopidogrel, atorvastatin, and lansoprazole did not decrease the antiplatelet efficacy of clopidogrel or increase adverse event frequency over 6 months.
机译:这项前瞻性,随机,无盲,对照试验评估了氯吡格雷与阿托伐他汀和兰索拉唑合用对血小板功能的影响.104例接受非ST段抬高的急性冠状动脉综合征(NSTE-ACS)的成人患者接受了经皮冠状动脉介入治疗(包括PCI)和药物洗脱支架植入。所有患者术后均接受标准双重抗血小板治疗(DAPT)加瑞舒伐他汀10 mg。 PCI后第6天,将患者随机分为4组,A组:DAPT +阿托伐他汀每天20 mg(从罗舒伐他汀改为阿托伐他汀)+兰索拉唑30 mg每天,B组:DAPT +阿托伐他汀每日20 mg(改变(从瑞舒伐他汀到阿托伐他汀),C组:DAPT +兰索拉唑每天30mg(继续服用瑞舒伐他汀),D组为对照组。根据患者情况使用其他药物。在随机分组之前以及随机分组后的第15天和第30天评估血小板功能和血小板激活标记物(颗粒膜蛋白140(P-选择蛋白),血栓素B2(TXB2)和人可溶性分化型40配体(sCD40L))的浓度。上门拜访。所有患者均维持治疗6个月,观察出血和局部缺血事件,共入组104例,A组27例,B / C组26例,D组25例,所有患者被分析。在三个感兴趣的时间点之间,四组之间或之内,血小板功能和血小板激活标记物(P-选择素,TXB2和sCD40L)的水平没有差异(P> 0.05)。在随后的6个月中,没有发生明显的出血事件,并且12例患者发生了缺血事件,各组之间的结果也没有显着差异(P> 0.05)。在诊断为NSTE-ACS且已进行药物洗脱支架植入的患者中,同时服用氯吡格雷,阿托伐他汀和兰索拉唑在6个月内并未降低氯吡格雷的抗血小板功效或增加不良事件发生频率。

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