氟伐他汀治疗急性冠脉综合征:一项多中心、随机、双盲、安慰剂对照试验(FACS试验)的基本原理和设计[ISRCTN81331696]。

Petr Ostadal, David Alan, Petr Hajek, Jiri Vejvoda, Martin Mates, Peter Blasko, Josef Veselka, Milan Kvapil, Jiri Kettner, Martin Wiendl, Ondrej Aschermann, Josef Slaby, Eduard Nemecek, Frantisek Holm, Marek Rac, Milan Macek, Jana Cepova
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引用次数: 6

摘要

背景:炎症通路的激活在冠状动脉斑块不稳定和随后的破裂中起重要作用,这可能导致急性冠状动脉综合征(ACS)的发展。血清炎症标志物如c反应蛋白(CRP)水平升高是进一步心血管事件的独立危险因素。最近的证据表明,除了降低胆固醇水平外,他汀类药物还能降低炎症标志物的水平。先前的对照临床试验报告了他汀类药物对ACS患者的积极作用,这些试验是为早期二级预防设计的。据我们所知,没有对照试验评估他汀类药物治疗在入院时立即开始的潜在益处。我们小组先前进行的一项试点研究侧重于早期开始cerivastatin治疗。我们发现炎症标志物(CRP和白细胞介素-6)水平显著降低。基于这些初步发现,我们正在进行一项临床试验,以评估另一种他汀类药物氟伐他汀作为ACS患者早期干预的疗效。方法:facs试验(氟伐他汀治疗急性冠脉综合征)是一项多中心、随机、双盲、安慰剂对照研究,评估入院时开始的氟伐他汀治疗的效果。该研究将招募1000名因ACS住院的参与者(包括ST段抬高和ST段抬高)。该研究的主要终点是氟伐他汀治疗对炎症标志物(CRP和白细胞介素-6)水平和妊娠相关血浆蛋白A (pap -A)水平的影响。联合次要终点是30天和1年的死亡发生、非致死性心肌梗死、复发性症状性缺血、紧急血运重建和心脏骤停。结论:FACS试验的主要目的是证明他汀类药物治疗,在ACS住院后立即开始治疗,可减少炎症和改善预后。本研究可能为ACS患者的治疗策略提供新的知识,并可能为他汀类药物的使用提供额外的临床适应症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Fluvastatin in the therapy of acute coronary syndrome: Rationale and design of a multicenter, randomized, double-blind, placebo-controlled trial (The FACS Trial)[ISRCTN81331696].

BACKGROUND: Activation of inflammatory pathways plays an important contributory role in coronary plaque instability and subsequent rupture, which can lead to the development of acute coronary syndrome (ACS). Elevated levels of serum inflammatory markers such as C-reactive protein (CRP) represent independent risk factors for further cardiovascular events. Recent evidence indicates that in addition to lowering cholesterol levels, statins also decrease levels of inflammatory markers. Previous controlled clinical trials reporting the positive effects of statins in participants with ACS were designed for very early secondary prevention. To our knowledge, no controlled trials have evaluated the potential benefits of statin therapy, beginning immediately at the time of hospital admission. A previous pilot study performed by our group focused on early initiation of cerivastatin therapy. We demonstrated a highly significant reduction in levels of inflammatory markers (CRP and interleukin-6). Based on these preliminary findings, we are conducting a clinical trial to evaluate the efficacy of another statin, fluvastatin, as an early intervention in patients with ACS. METHODS: The FACS-trial (Fluvastatin in the therapy of Acute Coronary Syndrome) is a multicenter, randomized, double-blind, placebo-controlled study evaluating the effects of fluvastatin therapy initiated at the time of hospital admission. The study will enroll 1,000 participants admitted to hospital for ACS (both with and without ST elevation). The primary endpoint for the study is the influence of fluvastatin therapy on levels of inflammatory markers (CRP and interleukin-6) and on pregnancy associated plasma protein A (PAPP-A). A combined secondary endpoint is 30-day and one-year occurrence of death, nonfatal myocardial infarction, recurrent symptomatic ischemia, urgent revascularization, and cardiac arrest. CONCLUSION: The primary objective of the FACS trial is to demonstrate that statin therapy, when started immediately after hospital admission for ACS, results in reduction of inflammation and improvement of prognosis. This study may contribute to new knowledge regarding therapeutic strategies for patients suffering from ACS and may offer additional clinical indications for the use of statins.

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