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双推注瑞替普酶(重组纤溶酶原激活剂)与前负荷加速阿替普酶(重组组织型纤溶酶原激活剂)用于急性心肌梗死患者冠状动脉溶栓的随机对照比较。RAPID II研究组。

Randomized comparison of coronary thrombolysis achieved with double-bolus reteplase (recombinant plasminogen activator) and front-loaded, accelerated alteplase (recombinant tissue plasminogen activator) in patients with acute myocardial infarction. The RAPID II Investigators.

作者信息

Bode C, Smalling R W, Berg G, Burnett C, Lorch G, Kalbfleisch J M, Chernoff R, Christie L G, Feldman R L, Seals A A, Weaver W D

机构信息

Medizinische Klinik III (Kardiologie), Universität Heidelberg, Germany.

出版信息

Circulation. 1996 Sep 1;94(5):891-8. doi: 10.1161/01.cir.94.5.891.

Abstract

BACKGROUND

The therapeutic benefit of thrombolytic therapy has been shown to correlate directly with completeness (TIMI grade 3 flow) and speed of reperfusion of the infarct-related coronary artery. The purpose of the RAPID II study was to determine whether a double-bolus regimen of reteplase, a recently developed deletion mutant of wild-type tissue plasminogen activator, could improve 90-minute coronary artery patency rates achieved with the most successful standard regimen, an "accelerated" front-loaded infusion of alteplase.

METHODS AND RESULTS

Three hundred twenty-four patients with acute myocardial infarction were randomized to receive (along with intravenous heparin and aspirin) either a 10 plus 10 megaunits double bolus of reteplase or front-loaded alteplase. The primary end point of "patency at 90 minutes, graded according to the TIMI classification" was centrally assessed in a blinded fashion. Infarctrelated coronary artery patency (TIMI grade 2 or 3) and complete patency (TIMI grade 3) at 90 minutes after the start of thrombolytic therapy were significantly higher in the reteplase-treated patients (TIMI grade 2 or 3: 83.4% versus 73.3% for front-loaded alteplase-treated patients, P = .03; TIMI grade 3: 59.9% versus 45.2%, P = .01). At 60 minutes, the incidence of both, patency and complete patency, was also significantly higher in reteplase-treated patients (reteplase versus alteplase, TIMI grade 2 or 3: 81.8% versus 66.1%, P = .01; TIMI grade 3: 51.2% versus 37.4%, P < .03). Reteplase-treated patients required fewer acute additional coronary interventions (13.6% versus 26.5%, P < .01), and 35-day mortality was 4.1% for reteplase and 8.4% for alteplase (P = NS). There were no significant differences between reteplase and alteplase in bleedings requiring a transfusion (12.4% versus 9.7%) or hemorrhagic stroke (1.2% versus 1.9%).

CONCLUSIONS

Reteplase, when given as a double bolus of 10 plus 10 megaunits to patients with acute myocardial infarction, achieves significantly higher rates of early reperfusion of the infarct-related coronary artery and requires significantly fewer acute coronary interventions than front-loaded alteplase without an apparent increased risk of complications.

摘要

背景

溶栓治疗的疗效已被证明与梗死相关冠状动脉再灌注的完全程度(TIMI 3级血流)和速度直接相关。RAPID II研究的目的是确定瑞替普酶(一种最近开发的野生型组织纤溶酶原激活剂的缺失突变体)的双推注方案是否能提高最成功的标准方案(阿替普酶“加速”前端负荷输注)所达到的90分钟冠状动脉通畅率。

方法与结果

324例急性心肌梗死患者被随机分组,接受(联合静脉注射肝素和阿司匹林)10 + 10兆单位瑞替普酶双推注或前端负荷阿替普酶治疗。“90分钟时的通畅情况,根据TIMI分类分级”这一主要终点以盲法进行集中评估。溶栓治疗开始后90分钟时,瑞替普酶治疗组患者梗死相关冠状动脉通畅(TIMI 2级或3级)和完全通畅(TIMI 3级)的比例显著更高(TIMI 2级或3级:瑞替普酶治疗组为83.4%,前端负荷阿替普酶治疗组为73.3%,P = 0.03;TIMI 3级:59.9%对45.2%,P = 0.01)。在60分钟时,瑞替普酶治疗组患者通畅和完全通畅的发生率也显著更高(瑞替普酶组对阿替普酶组,TIMI 2级或3级:81.8%对66.1%,P = 0.01;TIMI 3级:51.2%对37.4%,P < 0.03)。瑞替普酶治疗组患者需要的急性额外冠状动脉干预较少(13.6%对26.5%,P < 0.01),35天死亡率瑞替普酶组为4.1%,阿替普酶组为8.4%(P = 无显著差异)。瑞替普酶组和阿替普酶组在需要输血的出血(12.4%对9.7%)或出血性卒中(1.2%对1.9%)方面无显著差异。

结论

对于急性心肌梗死患者,给予10 + 10兆单位双推注的瑞替普酶,梗死相关冠状动脉早期再灌注率显著更高,且与前端负荷阿替普酶相比,所需的急性冠状动脉干预显著更少,而并发症风险无明显增加。

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