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非ST段抬高型急性冠脉综合征早期糖蛋白IIb/IIIa抑制(EARLY ACS)试验:一项随机安慰剂对照试验,评估早期负荷剂量依替巴肽治疗非ST段抬高型急性冠脉综合征患者的临床益处——研究设计与原理

The early glycoprotein IIb/IIIa inhibition in non-ST-segment elevation acute coronary syndrome (EARLY ACS) trial: a randomized placebo-controlled trial evaluating the clinical benefits of early front-loaded eptifibatide in the treatment of patients with non-ST-segment elevation acute coronary syndrome--study design and rationale.

作者信息

Giugliano Robert P, Newby L Kristin, Harrington Robert A, Gibson C Michael, Van de Werf Frans, Armstrong Paul, Montalescot Gilles, Gilbert James, Strony John T, Califf Robert M, Braunwald Eugene

机构信息

TIMI Study Group, Boston, MA 02115, USA.

出版信息

Am Heart J. 2005 Jun;149(6):994-1002. doi: 10.1016/j.ahj.2005.03.029.

Abstract

BACKGROUND

The recent North American and European practice guidelines in patients with non-ST-segment elevation acute coronary syndrome (nSTE ACS) recommend glycoprotein IIb/IIIa (GpIIb-IIIa) inhibition in patients undergoing an early invasive treatment strategy. However, the guidelines are not explicit regarding the timing of initiation of GpIIb-IIIa antagonists, and there is marked variation in clinical practice regarding their use.

STUDY DESIGN

The EARLY ACS trial will enroll 10,500 patients in a prospective, randomized, double blind, international, multicenter investigation of early eptifibatide compared with placebo (with provisional eptifibatide in the catheterization laboratory) in patients with high-risk nSTE ACS in whom an invasive strategy is planned no sooner than the next calendar day. The primary efficacy end point is the 96-hour composite of all-cause mortality, nonfatal myocardial infarction, recurrent ischemia requiring urgent revascularization, or need for thrombotic bailout with GpIIb-IIIa inhibitor during percutaneous coronary intervention. The key secondary end point is the composite of death or nonfatal myocardial infarction within 30 days of enrollment.

IMPLICATIONS

The EARLY ACS trial will be the largest study to date to evaluate the utility of early GpIIb-IIIa inhibition in patients with nSTE ACS in whom an invasive approach is planned. This trial will provide important evidence regarding the benefit of initiating eptifibatide early after presentation with high-risk ACS versus delayed provisional use after coronary angiography. Furthermore, it will explore the ability of biomarkers to identify high-risk patients who may benefit from such an early aggressive approach.

摘要

背景

近期北美和欧洲针对非ST段抬高型急性冠状动脉综合征(nSTE ACS)患者的实践指南建议,在接受早期侵入性治疗策略的患者中使用糖蛋白IIb/IIIa(GpIIb-IIIa)抑制剂。然而,指南并未明确GpIIb-IIIa拮抗剂的起始时间,并且在其使用的临床实践中存在显著差异。

研究设计

早期急性冠状动脉综合征(EARLY ACS)试验将纳入10500例患者,进行一项前瞻性、随机、双盲、国际性、多中心研究,比较早期使用依替巴肽与安慰剂(在导管室临时使用依替巴肽)对计划在下一个日历日之后进行侵入性策略的高危nSTE ACS患者的效果。主要疗效终点是96小时内全因死亡率、非致命性心肌梗死、需要紧急血运重建的复发性缺血或在经皮冠状动脉介入治疗期间需要使用GpIIb-IIIa抑制剂进行血栓解救的复合终点。关键次要终点是入组后30天内死亡或非致命性心肌梗死的复合终点。

意义

EARLY ACS试验将是迄今为止评估早期GpIIb-IIIa抑制对计划采用侵入性方法的nSTE ACS患者效用的最大规模研究。该试验将提供重要证据,证明在高危急性冠状动脉综合征(ACS)发病后早期启动依替巴肽与冠状动脉造影后延迟临时使用相比的益处。此外,它还将探索生物标志物识别可能从此类早期积极治疗方法中获益的高危患者的能力。

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