论文部分内容阅读
目的:探究PCI前负荷剂量替格瑞洛对急性心肌梗死(AMI)患者冠状动脉(冠脉)血流、炎症反应及心肌酶谱的影响.方法:选择60例急性ST段抬高型心肌梗死(STEMI)患者,随机分为替格瑞洛组(30例)和氯吡格雷组(30例),分别于术前应用负荷剂量的替格瑞洛180 mg和氯吡格雷600 mg,后行经皮冠脉介入治疗(PCI),随访12个月,比较两组患者PCI手术情况、血清肌钙蛋白I(cTnI)、磷酸肌酸激酶同工酶(CK-MB)、降钙素(PCT)、高敏C反应蛋白(hs-CRP)水平及主要不良心血管事件(MACE)发生情况.结果:两组患者植入血管数量和植入支架数量均无统计学差异(P>0.05),术后TIMI血流分级存在显著差异(P<0.05),替格瑞洛组冠脉慢血流发生率(0%)显著低于氯吡格雷组(20.00%)(P<0.05).PCI术前两组患者的cTnI和CK-MB无统计学差异(P>0.05),术后12 h均上升,但术后24 h均明显下降,且替格瑞洛组在两个时期的指标均显著低于氯吡格雷组(P<0.05).PCI术前两组患者的PCT和hs-CRP水平无统计学差异(P>0.05),术后24 h均上升,但术后48 h均明显下降,且替格瑞洛组在两个时期的指标均显著低于氯吡格雷组(P<0.05).替格瑞洛组患者的MACE发生风险(26.67%)显著低于氯吡格雷组(46.67%)(HR=0.482,P=0.045).结论:负荷剂量替格瑞洛能明显恢复AMI患者PCI治疗后的冠脉血流及减少冠脉慢血流的发生率,有效恢复cTnI和CK-MB水平,降低炎症反应,改善预后.“,”Objective:To investigate the effects of pre-PCI load dosage ticagrelor on the coronary blood flow, inflammatory response and myocardial enzymes in acute myocardial infarction patients after PCI.Method:The 60 patients with STEMI in our hospital between June 2016 and March 2017 were randomized into ticagrelor group (30 cases) and clopidogrel group (30 cases) and were treated by load dosage ticagrelor (180 mg) or clopidogrel (600 mg) before PCI, then with followed-up for 12 months.The PCI operations, cTnI, CK-MB, PCT, hs-CRP and MACE were comparatively analyzed.Result:There were no significant difference in the number of stent implantation and blood vessels implanted (P>0.05) while there was difference in TIMI blood flow grading between two groups (P<0.05), and the incidence of SCF was significantly lower in the ticagrelor group (P<0.05).The cTnI and CK-MB of ticagrelor group was significantly lower than the clopidogrel group at 24 hours after PCI (P<0.05).PCT and hs-CRP of ticagrelor group was significantly lower than theclopidogrel group at 48 hours after PCI (P<0.05).The risk of MACE in the ticagrelor group (26.67%) was significantly lower than the clopidogrel group (46.67%) (HR=0.482, P=0.045).Conclusion:Load dosage ticagrelor can obviously recover coronary blood flow and reduce SCF, recover myocardial enzymes effectively, and decrease inflammatory response.