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Intensive Statin Therapy in NSTE-ACS Patients Undergoing PCI: Clinical and Biochemical Effects

机译:接受PCI的NSTE-ACS患者的强化他汀类药物治疗:临床和生化作用

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摘要

Early initiation of statin therapy in acute coronary syndrome patients has a favorable prognostic impact because of its anti-inflammatory and antithrombotic properties. In this study, we explored the effect of atorvastatin-loading, followed by intensive atorvastatin therapy, on clinical and biochemical outcomes in non-ST-segment-elevation acute coronary syndrome patients who were scheduled for percutaneous coronary intervention.We prospectively enrolled 140 patients (mean age, 56 ± 9 years, 68% men). Once eligible, patients were randomly assigned to receive either a moderate 20-mg daily dose of atorvastatin (Group A) or a 160-mg loading dose followed by an intensified 80-mg daily dose (Group B). High-sensitivity C-reactive protein (hs-CRP) levels were recorded before and after intervention. Evaluation after 6 months included hs-CRP levels, left ventricular systolic function, and major adverse cardiac events.We found no significant difference between the 2 groups in regard to the interventional data. However, blood sampling after coronary intervention, and again 6 months later, revealed a significant decline in mean hs-CRP level among Group B patients (P <0.001). Moreover, patients in Group B manifested a higher left ventricular ejection fraction than did patients in Group A (P <0.05). After 6 months, we found no significant difference between groups in the incidence of major adverse cardiac events.We conclude that intensive atorvastatin therapy in non-ST-segment-elevation acute coronary syndrome patients is associated with lower hs-CRP levels and with higher left ventricular ejection fraction after 6 months, with no significant impact on adverse cardiac events.
机译:由于他汀类药物具有抗炎和抗血栓形成的特性,因此在急性冠脉综合征患者中尽早开始他汀类药物的治疗对预后具有良好的影响。在这项研究中,我们探讨了阿托伐他汀负荷量加阿托伐他汀强化治疗对计划行经皮冠状动脉介入治疗的非ST段抬高急性冠脉综合征患者的临床和生化结果的影响。我们前瞻性纳入了140例患者(平均年龄为56±9岁,男性为68%)。一旦符合条件,患者被随机分配接受中度阿托伐他汀每日20 mg剂量(A组)或160 mg负荷剂量,随后接受每日80 mg强化剂量(B组)。记录干预前后的高敏C反应蛋白(hs-CRP)水平。 6个月后的评估包括hs-CRP水平,左心室收缩功能和主要不良心脏事件。我们发现两组的介入治疗数据之间无显着差异。然而,在冠状动脉介入治疗后以及六个月后再次进行的血液采样显示,B组患者的平均hs-CRP水平显着下降(P <0.001)。此外,B组患者的左心室射血分数高于A组患者(P <0.05)。 6个月后,我们发现两组主要不良心脏事件的发生率之间无显着差异。我们得出结论,在非ST段抬高的急性冠状动脉综合征患者中,强化阿托伐他汀治疗与较低的hs-CRP水平和较高的左心率相关6个月后心室射血分数,对不良心脏事件无明显影响。

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