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与急性心肌梗死中阿替普酶静脉输注相比,瑞替普酶大剂量推注可实现更快速、完全和稳定的冠状动脉溶栓。RAPID研究组。

More rapid, complete, and stable coronary thrombolysis with bolus administration of reteplase compared with alteplase infusion in acute myocardial infarction. RAPID Investigators.

作者信息

Smalling R W, Bode C, Kalbfleisch J, Sen S, Limbourg P, Forycki F, Habib G, Feldman R, Hohnloser S, Seals A

机构信息

Division of Cardiology, University of Texas Medical School at Houston 77030, USA.

出版信息

Circulation. 1995 Jun 1;91(11):2725-32. doi: 10.1161/01.cir.91.11.2725.

Abstract

BACKGROUND

Early restoration and maintenance of normal (TIMI 3) blood flow during acute myocardial infarction is critical for optimal preservation of left ventricular function and survival. Recombinant plasminogen activator (r-PA, reteplase) is a nonglycosylated deletion mutant of wild-type tissue-type plasminogen activator (TPA) that has been shown to achieve more rapid and complete thrombolysis compared with other plasminogen activators in animal models.

METHODS AND RESULTS

The RAPID Trial was designed to test the hypothesis that bolus administration of one or more dosage regimens of r-PA was superior to standard-dose alteplase (TPA) in achieving infarct-related artery patency 90 minutes after initiation of treatment. Six hundred six patients with acute myocardial infarction were randomized to one of four treatment arms: (1) TPA 100 mg i.v. over 3 hours, (2) r-PA as a 15-MU single bolus, (3) r-PA as a 10-MU bolus followed by 5 MU 30 minutes later, or (4) r-PA as a 10-MU bolus followed by 10 MU 30 minutes later. Coronary arteriography was performed at 30, 60, and 90 minutes after initiation of treatment and at hospital discharge. The 10 + 10-MU r-PA group achieved better 90-minute and 5- to 14-day TIMI 3 flow (63% [CI, 55% to 71%] versus 49% [41% to 57%], P = .019, and 88% [82% to 94%] versus 71% [63% to 79%], P < .001, respectively) than the TPA group. The TIMI 3 flow in the 10 + 10-MU r-PA group at 60 minutes was equivalent to that in the TPA group at 90 minutes (51 versus 49%). Global ejection fraction and regional wall motion in the 10 + 10-MU r-PA group were superior to those of the TPA group at hospital discharge (53 +/- 1.3% versus 49 +/- 1.3%, P = .034; -2.19 +/- 0.12 versus -2.61 +/- 0.13 SD per chord, P = .02, respectively). The 15-MU and 10 + 5-MU r-PA patency and left ventricular function results were similar to those of the TPA and inferior to those of the 10 + 10-MU r-PA group. Bleeding complications were similar between the groups.

CONCLUSIONS

r-PA given as a double bolus of 10 + 10 MU achieves more rapid, complete, and sustained thrombolysis of the infarct-related artery than standard-dose TPA, without an apparent increased risk of complications. This was associated with improved global and regional left ventricular function at hospital discharge.

摘要

背景

急性心肌梗死期间尽早恢复并维持正常(TIMI 3级)血流对于最佳地保留左心室功能及提高生存率至关重要。重组纤溶酶原激活剂(r-PA,瑞替普酶)是野生型组织型纤溶酶原激活剂(TPA)的非糖基化缺失突变体,在动物模型中已显示与其他纤溶酶原激活剂相比,它能实现更快速、更完全的溶栓。

方法与结果

RAPID试验旨在检验以下假设:在治疗开始后90分钟,推注一种或多种剂量方案的r-PA在实现梗死相关动脉通畅方面优于标准剂量的阿替普酶(TPA)。606例急性心肌梗死患者被随机分为四个治疗组之一:(1)3小时内静脉注射100 mg TPA;(2)单次推注15 MU r-PA;(3)先推注10 MU r-PA,30分钟后再推注5 MU;(4)先推注10 MU r-PA,30分钟后再推注10 MU。在治疗开始后30、60和90分钟以及出院时进行冠状动脉造影。与TPA组相比,10 + 10 MU r-PA组在90分钟时以及5至14天时TIMI 3级血流情况更好(分别为63% [可信区间,55%至71%] 对49% [41%至57%],P = 0.019;88% [82%至94%] 对71% [63%至79%],P < 0.001)。10 + 10 MU r-PA组在60分钟时的TIMI 3级血流与TPA组在90分钟时相当(51%对49%)。出院时,10 + 10 MU r-PA组的整体射血分数和节段性室壁运动优于TPA组(分别为53 ± 1.3%对49 ± 1.3%,P = 0.034;每节段-2.19 ± 0.12对-2.61 ± 0.13标准差,P = 0.02)。15 MU和10 + 5 MU r-PA组的血管通畅情况及左心室功能结果与TPA组相似,且不如10 + 10 MU r-PA组。各组间出血并发症相似。

结论

给予10 + 10 MU双推注剂量的r-PA比标准剂量的TPA能更快速、完全且持续地溶解梗死相关动脉血栓,且并发症风险无明显增加。这与出院时整体及局部左心室功能改善相关。

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