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急诊冠状动脉支架术联合国产替罗非班治疗急性ST段抬高性心肌梗死的临床疗效和安全性 被引量:23

Clinical outcomes and safety of primary percutaneous coronary intervention combined with tirofiban therapy in patients with acute ST-segment elevation myocardial infarction
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摘要 目的前瞻性评价急性 ST 段抬高性心肌梗死(STEMI)患者急诊经皮冠状动脉介入治疗(PCI)联合应用国产替罗非班治疗的临床疗效及安全性。方法入选连续160例接受急诊 PCI 治疗的急性 STEMI 患者,随机分为替罗非班组(80例)和对照组(80例)。比较两组基础临床情况、介入治疗结果、术后即刻疗效、术后30天和180天主要心脏不良事件(MACE,包括死亡、再梗死、再次靶血管重建)发生率及左室射血分数(LVEF)。结果两组基础临床情况、介入治疗结果差异均无统计学意义。与对照组相比,替罗非班组术后即刻心肌梗死溶栓试验(TIMI)3级复流血流差异无统计学意义(95.0%比87.5%,P>0.05),但即刻心肌组织灌注(TMP)3级(75.0%比56.3%,P<0.05)、校正 TIMI 帧数[(23.56±5.19)帧比(31.05±6.92)帧,P<0.01)]、ST 段抬高总和回落[(6.51±3.56)mm 比(4.53±2.47)mm,P<0.01]、肌酸激酶同工酶(CK-MB)峰值[(225.02±105.81)μg/L比(269.20±110.88)μg/L,P<0.05)、肌钙蛋白 I(TnI)峰值[(45.25±33.00)μg/L 比(56.46±29.48)μg/L,P<0.05]及平均住院天数[(11.38±4.63)天比(14.68±6.90)天,P<0.01]均显著优于对照组。替罗非班组术后 MACE 发生率30天(5.0%比16.3%,P<0.05)和180天(7.5%比18.8%,P<0.05)明显降低,LVEF(术后30天:53%±7%比49%±9%,P<0.01;术后180天:59%±8%比53%±9%,P<0.01)显著提高。多因素 logistic 回归分析表明,年龄>65岁[比值比(OR)=3.42,P<0.01]、替罗非班治疗(OR=0.56,P<0.05)、住院期 LVEF<0.5(OR=2.56,P<0.01)是术后180天 MACE 发生率的主要决定因素。替罗非班组术后出血并发症发生率高于对照组(16.3%和7.5%),但差异无统计学意义(P>0.05)。结论急诊冠状动脉支架术联合应用国产替罗非班治疗STEMI 能显著提高相关梗死区域再灌注水平,明显改善术后即刻、术后30天及180天临床预后和左心室收缩功能。 Objective This prospective study was conducted to investigate the clinical outcomes and safety of primary percutaneous coronary intervention ( PCI ) combined with tirofiban therapy in patients with acute ST-segment elevation myocardial infarction (STEMI). Methods One hundred and sixty consecutive patients with acute STEMI were randomly allocated to either primary PCI combined with tirofiban therapy (Tirofiban group, n = 80 ) or primary PCI treatment alone (Control group, n = 80 ). Baseline characteristics, PCI features and clinical outcomes during hospitalization were compared between the two groups. Left ventricular ejection fraction (LVEF) and major adverse cardiac events (MACE, including death, re-infarction and target vessel revascularization) at 30 and 180 days after discharge were also compared. Results The baseline clinical characteristics were comparable between the two groups. Despite similar TIMI grade 3 flow ( 95% vs. 87.5% , P 〉 0. 05 ) between the tirofiban and control groups immediately after the procedure, TMP grade 3 (75% vs. 56. 3%, P 〈 0. 05) , corrected TIMI frame count (cTFC, 23.56±5. 19 vs. 31.05±6. 92,P 〈0. 01 ), resolution of sum of ST-segment elevation (6. 51 ± 3.56 mm vs. 4. 53 ± 2.47 mm, P 〈 0. 01 ), peak value of CK-MB (225.02 ± 105.81 μg/L vs. 269. 20 ± 110. 88 μg/L,P 〈 0. 05 ) and TnI ( 45.25 ± 33.00 μg/L vs. 56.46 ± 29.48 μg/L, P 〈 0.05 ) in tirofiban group were significantly superior to the control group related to a shorter hospital stay ( 11.38 ± 4. 63 days vs. 14. 68±6. 90 days,P 〈 0. 01 ). Compared to control group, the MACE rates at 30 days (5. 0% vs. 16. 3% ,P 〈0. 05)and 180 days(7.5% vs. 18.8% ,P 〈 0. 05) were also significantly reduced and LVEF was significantly improved(30 days :53% ±7% vs. 49% ±9%,P〈0.01; 180 days:59% ±8% vs. 53% ±9% ,P 〈0. 01 ) in tirofiban group. Multivariate logistic analysis revealed that age 〉 65 years( OR = 3.42 ,P 〈0.01 ), tirofiban therapy ( OR = 0. 56, P 〈 0. 05 ) and LVEF 〈 0. 5 during hospitalization ( OR = 2. 56, P 〈 0. 01 ) were independent predictors of MACE rates at 180 days follow up. There was no significant difference in hemorrhagic complications between the two groups ( 16. 3 % vs. 7. 5 % , P 〉 0. 05 ). Conclusion Adjunctive therapy with tirofiban for patients with acute STEMI who undergo primary PCI is safe and can significantly improve re-perfusion in the infarct area and clinical outcomes at 30 as well as 180 days after procedure.
出处 《中华心血管病杂志》 CAS CSCD 北大核心 2007年第11期1005-1009,共5页 Chinese Journal of Cardiology
基金 上海市科学技术委员会资助项目(05DZ19503)
关键词 冠状动脉疾病 心肌梗塞 血管成形术 经腔 经皮冠状动脉 支架 替罗非班 预后 Coronary disease Myocardial infarction Angioplasty, transluminal, percutaneous coronary Stents Tirofiban Prognosis
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