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经皮直接冠状动脉介入治疗后梗死相关冠状动脉通畅性和微循环功能的评估:FINESSE-ANGIO(增强再灌注速度以停止事件-血管造影)研究。

Evaluation of infarct-related coronary artery patency and microcirculatory function after facilitated percutaneous primary coronary angioplasty: the FINESSE-ANGIO (Facilitated Intervention With Enhanced Reperfusion Speed to Stop Events-Angiographic) study.

机构信息

San Giovanni Hospital and Centro per la Lotta Contro l'Infarto, Fondazione Onlus, Via dell’amba Aradam 9, Rome, Italy.

出版信息

JACC Cardiovasc Interv. 2010 Dec;3(12):1284-91. doi: 10.1016/j.jcin.2010.08.023.

Abstract

OBJECTIVES

The FINESSE-ANGIO (Facilitated Intervention with Enhanced Reperfusion Speed to Stop Events-Angiographic) study evaluated acute treatment effects on infarct-related artery (IRA) patency and angiographic correlates of coronary microcirculatory function.

BACKGROUND

The FINESSE trial evaluated the effects on clinical outcomes of primary percutaneous coronary intervention (PCI) facilitated with pre-catheterization laboratory administration of abciximab with half-dose reteplase (combination-facilitated group), abciximab alone (abciximab-facilitated group), or with abciximab administered immediately before the procedure (primary PCI).

METHODS

The FINESSE-ANGIO substudy compared the effects of the 3 treatment strategies on patency (TIMI [Thrombolysis In Myocardial Infarction] flow grade 2/3) of the IRA at basal coronary angiography. The secondary efficacy end points were corrected TIMI frame count, percentage of patients achieving TIMI flow grade 3, and the percentage achieving myocardial blush grade 2/3 of the IRA at post-PCI angiography. All angiographies were evaluated at a central core laboratory.

RESULTS

Of the 2,452 FINESSE patients, 637 were included in the FINESSE-ANGIO substudy. Patients in the combination-facilitated group exhibited significantly higher rates of baseline IRA patency compared with the abciximab-facilitated and the primary PCI groups (76.1% vs. 43.7% and 32.7%, respectively; p < 0.0001 for both; p = 0.025 abciximab-facilitated vs. primary PCI). There were no significant differences in the post-PCI corrected TIMI frame count (17.1 ± 15.8, 17.4 ± 17.3, and 15.8 ± 14.1) or the rates of post-PCI TIMI flow grade 3 (79.8%, 77.7%, and 76.6%), myocardial blush grade 2/3 (85.6%, 79.5%, and 86.4%), respectively.

CONCLUSIONS

Pre-catheterization laboratory administration of abciximab alone and especially in combination with half-dose reteplase resulted in higher rates of IRA patency at baseline coronary angiography compared with no pre-treatment. However, post-procedural angiographic and microcirculatory variables were unaffected by facilitation therapy.

摘要

目的

FINESSE-ANGIO(促进再灌注速度以停止事件-血管造影的优化干预)研究评估了急性治疗对梗死相关动脉(IRA)通畅性的影响,以及冠状动脉微循环功能的血管造影相关性。

背景

FINESSE 试验评估了三种治疗策略对IRA 通畅性(TIMI [心肌梗死溶栓治疗] 血流分级 2/3)的影响,三种治疗策略分别为:经皮冠状动脉介入治疗(PCI)前在导管室给予半剂量瑞替普酶的阿昔单抗联合治疗(联合辅助治疗组)、阿昔单抗单独治疗(阿昔单抗辅助治疗组)和直接在 PCI 前给予阿昔单抗治疗(直接 PCI 组)。

方法

FINESSE-ANGIO 亚研究比较了三种治疗策略对基础冠状动脉造影时 IRA 通畅性(TIMI 血流分级 2/3)的影响。次要疗效终点为校正 TIMI 帧数、达到 IRA 术后 TIMI 血流分级 3 的患者比例,以及达到 IRA 术后心肌灌注分级 2/3 的患者比例。所有血管造影均由中心核心实验室进行评估。

结果

在 2452 例 FINESSE 患者中,637 例纳入 FINESSE-ANGIO 亚研究。与阿昔单抗辅助治疗组和直接 PCI 组相比,联合辅助治疗组 IRA 的基线通畅率明显更高(分别为 76.1%、43.7%和 32.7%;p<0.0001;p=0.025 阿昔单抗辅助治疗组与直接 PCI 组)。校正 TIMI 帧数(17.1±15.8、17.4±17.3 和 15.8±14.1)或术后 TIMI 血流分级 3 的比例(79.8%、77.7%和 76.6%)、心肌灌注分级 2/3(85.6%、79.5%和 86.4%)的术后无显著差异。

结论

与无预处理相比,经导管室给予阿昔单抗单独治疗,特别是联合半剂量瑞替普酶治疗,IRA 在基础冠状动脉造影时的通畅率更高。然而,辅助治疗对术后血管造影和微循环变量没有影响。

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