Research Institute-Heart Hospital (HCor), Rua Abílio Soares 250, 12th floor, 04005-000, São Paulo, SP, Brazil.
Research Institute-Heart Hospital (HCor), Rua Abílio Soares 250, 12th floor, 04005-000, São Paulo, SP, Brazil.
Am Heart J. 2018 Apr;198:129-134. doi: 10.1016/j.ahj.2017.12.018. Epub 2018 Jan 8.
Previous evidence suggests that acute treatment with statins reduce atherosclerotic complications, including periprocedural myocardial infarction, but currently, there are no large, adequately powered studies to define the effects of early, high-dose statins in patients with acute coronary syndrome (ACS) and planned invasive management.
The main goal of Statins Evaluation in Coronary procedUres and REvascularization (SECURE-PCI) Trial is to determine whether the early use of a loading dose of 80 mg of atorvastatin before an intended percutaneous coronary intervention followed by an additional dose of 80 mg 24 hours after the procedure will be able to reduce the rates of major cardiovascular events at 30 days in patients with an ACS.
The SECURE-PCI study is a pragmatic, multicenter, double-blind, placebo-controlled randomized trial planned to enroll around 4,200 patients in 58 different sites in Brazil. The primary outcome is the rate of major cardiovascular events at 30 days defined as a composite of all-cause mortality, nonfatal acute myocardial infarction, nonfatal stroke, and coronary revascularization.
The SECURE PCI is a large randomized trial testing a strategy of early, high-dose statin in patients with ACS and will provide important information about the acute treatment of this patient population.
先前的证据表明,他汀类药物的急性治疗可减少动脉粥样硬化并发症,包括围手术期心肌梗死,但目前尚无大型、充分有力的研究来定义急性冠状动脉综合征(ACS)和计划进行介入治疗的患者中早期高剂量他汀类药物的效果。
Statins Evaluation in Coronary procedUres and REvascularization(SECURE-PCI)试验的主要目标是确定在计划进行经皮冠状动脉介入治疗之前使用 80mg 阿托伐他汀负荷剂量,并在术后 24 小时再给予 80mg 剂量,是否能降低 ACS 患者 30 天内主要心血管事件的发生率。
SECURE-PCI 研究是一项实用的、多中心、双盲、安慰剂对照的随机试验,计划在巴西的 58 个不同地点招募约 4200 名患者。主要终点是 30 天内主要心血管事件的发生率,定义为全因死亡率、非致死性急性心肌梗死、非致死性卒中和冠状动脉血运重建的复合终点。
SECURE PCI 是一项大型随机试验,旨在测试 ACS 患者早期高剂量他汀类药物的治疗策略,将为该患者人群的急性治疗提供重要信息。