首页> 外文期刊>Journal of the American College of Cardiology >Effect of intensive statin therapy on clinical outcomes among patients undergoing percutaneous coronary intervention for acute coronary syndrome. PCI-PROVE IT: A PROVE IT-TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis In Myocardial Infarction 22) Substudy.
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Effect of intensive statin therapy on clinical outcomes among patients undergoing percutaneous coronary intervention for acute coronary syndrome. PCI-PROVE IT: A PROVE IT-TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis In Myocardial Infarction 22) Substudy.

机译:他汀类药物强化治疗对急性冠脉综合征经皮冠状动脉介入治疗患者的临床效果的影响。 PCI-PROVE IT:PROVE IT-TIMI 22(普伐他汀或阿托伐他汀评估和心肌梗塞的感染治疗-血栓溶解22)亚研究。

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OBJECTIVES: The goal of this analysis was to determine whether intensive statin therapy, compared with moderate-dose statin therapy, leads to a reduction in major adverse cardiovascular events (MACE) among patients undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS). BACKGROUND: When compared with moderate-dose statins, intensive statin therapy reduces MACE among patients with ACS. The role of intensive statin therapy specifically among patients who undergo PCI for ACS is unknown. METHODS: Outcomes were compared in 2,868 patients who underwent PCI for ACS just prior to enrollment in the PROVE IT-TIMI 22 (Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis In Myocardial Infarction 22) trial, which randomized patients to either atorvastatin 80 mg or pravastatin 40 mg daily. The incidence of the primary composite end point of all-cause mortality, myocardial infarction, unstable angina leading to hospitalization, and revascularization after 30 days and stroke was evaluated, as was the incidence of target vessel revascularization (TVR) and non-TVR during follow-up. RESULTS: Treatment with 80 mg atorvastatin reduced the incidence of the composite end point (21.5% vs. 26.5%, hazard ratio: 0.78, 95% confidence interval: 0.67 to 0.91, p=0.002) and lowered the incidence of both TVR (11.4% vs. 15.4%, p=0.001) and non-TVR (8.0% vs. 10.5%, p=0.017) compared with 40 mg pravastatin. After adjusting for on-treatment serum low-density lipoprotein cholesterol and C-reactive protein concentrations, the odds of TVR with high-dose statin therapy remained significant (odds ratio: 0.74, p=0.015) while the odds of non-TVR did not (odds ratio: 0.92, p=0.55). CONCLUSIONS: Among patients with ACS who undergo PCI, intensive statin therapy reduces MACE compared with moderate-dose statin therapy. The reduction in the incidence of TVR was independent of low-density lipoprotein cholesterol and C-reactive protein lowering and may therefore be due, at least in part, to a pleiotropic effect of high-dose statin therapy. (PROVE IT-TIMI 22; NCT00382460).
机译:目的:本分析的目的是确定与中剂量他汀类药物治疗相比,强化他汀类药物治疗是否导致急性冠脉综合征(ACS)的经皮冠状动脉介入治疗(PCI)患者的主要不良心血管事件(MACE)减少)。背景:与中等剂量他汀类药物相比,强化他汀类药物治疗可降低ACS患者的MACE。他汀类药物强化治疗的作用,尤其是在接受PCI治疗ACS的患者中,尚不清楚。方法:比较了2868例在入选PROVE IT-TIMI 22(普伐他汀或阿托伐他汀评估和心肌梗死的感染治疗-血栓溶解)试验之前接受PCI ACS治疗的患者的研究,该研究将患者随机分为80 mg阿托伐他汀或80 mg阿托伐他汀普伐他汀40毫克每天。评估了全因死亡率,心肌梗塞,导致住院的不稳定型心绞痛以及30天和中风后的血运重建的主要复合终点的发生率,以及随访期间目标血管血运重建(TVR)和非TVR的发生率-向上。结果:阿托伐他汀80 mg治疗降低了复合终点的发生率(21.5%vs. 26.5%,危险比:0.78,95%置信区间:0.67至0.91,p = 0.002),并降低了两种TVR的发生率(11.4)与40 mg普伐他汀相比,%vs. 15.4%,p = 0.001)和非TVR(8.0%vs. 10.5%,p = 0.017)。调整治疗中的血清低密度脂蛋白胆固醇和C反应蛋白浓度后,大剂量他汀类药物治疗的TVR几率仍然很高(优势比:0.74,p = 0.015),而非TVR的几率没有(比值:0.92,p = 0.55)。结论:在接受PCI的ACS患者中,相比中剂量他汀类药物,强化他汀类药物治疗可降低MACE。 TVR发生率的降低与低密度脂蛋白胆固醇和C反应蛋白的降低无关,因此可能至少部分是由于大剂量他汀类药物治疗的多效性所致。 (证明IT-TIMI 22; NCT00382460)。

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