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High versus low dose statin therapy in Indian patients with acute ST-segment elevation myocardial infarction undergoing thrombolysis

机译:在印度患者急性ST段抬高心肌梗死中的印度患者高与低剂量他汀类药物治疗接受溶栓栓塞

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Objectives: This study sought to compare high dose versus low dose statin therapy in Indian patients with ST-segment elevation myocardial infarction (STEMI) undergoing thrombolysis. Background: Randomized trials have demonstrated that statin treatment reduced major adverse cardiac events (MACEs) in patients with stable angina pectoris and acute coronary syndrome. However, randomized studies of statin therapy in Indian patients with STEMI are scarce. Methods: Of 1859 patients with acute STEMI, 1027 eligible patients were randomized to 80-mg (n = 512) or 10-mg (n = 515) atorvastatin. Primary end point was 30-day incidence of MACE (death from any cause, myocardial infarction, NSTE-ACS requiring readmission, ischemia driven revascularization, and stroke). Secondary end points included individual components of primary end point and ST-segment resolution at 90 min after thrombolysis. Results: Two groups did not differ in primary endpoints of MACEs (8.79% in high dose vs 9.32% in low dose atorvastatin group, OR = 0.938, 95% CI = 0.612-1.436, P = 0.764). With 80 mg atorvastatin, there was insignificant reduction in rate of reinfarction, revascularization and death. Stroke and readmission for NSTE-ACS increased in 80 mg atrovastatin group, but was not statistically significant. ST-segment resolution was significantly higher in 80-mg atorvastatin arm (45.90% vs. 37.67%; p = 0.008). Myalgia was more in 80 mg statin group (18.06% vs 7.57%, p = 0.0001). Conclusions: High-dose atorvastatin did not show significant difference of MACEs in STEMI patients undergoing thrombolysis but showed significant improvement in immediate coronary flow depicted by ST-segment resolution. This benefit of high dose statin is to be weighed against greater myalgia, drug discontinuation and cost in Indian patients.
机译:目的:该研究寻求比较高剂量与低剂量他汀类药物治疗在印度患者中,患有溶栓的ST段抬高心肌梗死(Stemi)。背景:随机试验表明,他汀类药物治疗减少了稳定的心绞痛和急性冠状动脉综合征患者的主要不良心脏事件(拟合)。然而,在印度患者中对他汀类药物治疗的随机研究是稀缺的。方法:1859例急性STEMI,1027名符合条件的患者患者随机分配至80mg(n = 512)或10mg(n = 515)阿托伐他汀。主要终点是MACE的30天发生率(来自任何原因的死亡,心肌梗塞,不需要阅约,缺血驱动的血运重建和中风)。次要终点包括溶栓后90分钟的主要终点和ST段分辨率的单个组分。结果:两组在摩羯座的主要终点(高剂量与低剂量阿托替司汀组中的8.79%8.79%,或= 0.938,95%CI = 0.612-1.436,P = 0.764)。含有80毫克阿托伐他汀,减少速度降低,血运重建和死亡率微不足道。 NSTE-ACs的中风和入院增加了80毫克阿马托汀组,但没有统计学意义。 80mg阿托伐他汀臂(45.90%vs.37.67%; P = 0.008),ST段分辨率显着高。 Myalgia在80毫克他汀类动物组中更多(18.06%Vs 7.57%,P = 0.0001)。结论:高剂量阿托伐他汀在接受溶栓术后的术中未显示出巨大差异,但表达了ST段分辨率所描绘的即时冠状动脉的显着改善。高剂量他汀类药物的这种益处将受到印度患者的更大的肌痛,药物停药和成本。

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