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急性心肌梗死中替奈普酶与加速型阿替普酶对比:心肌梗死溶栓治疗(TIMI)10B试验结果。心肌梗死溶栓治疗(TIMI)10B研究组

TNK-tissue plasminogen activator compared with front-loaded alteplase in acute myocardial infarction: results of the TIMI 10B trial. Thrombolysis in Myocardial Infarction (TIMI) 10B Investigators.

作者信息

Cannon C P, Gibson C M, McCabe C H, Adgey A A, Schweiger M J, Sequeira R F, Grollier G, Giugliano R P, Frey M, Mueller H S, Steingart R M, Weaver W D, Van de Werf F, Braunwald E

机构信息

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Mass 02115, USA.

出版信息

Circulation. 1998;98(25):2805-14. doi: 10.1161/01.cir.98.25.2805.

Abstract

BACKGROUND

Bolus thrombolytic therapy is a simplified means of administering thrombolysis that facilitates rapid time to treatment. TNK-tissue plasminogen activator (TNK-tPA) is a highly fibrin-specific single-bolus thrombolytic agent.

METHODS AND RESULTS

In TIMI 10B, 886 patients with acute ST-elevation myocardial infarction presenting within 12 hours were randomized to receive either a single bolus of 30 or 50 mg TNK-tPA or front-loaded tPA and underwent immediate coronary angiography. The 50-mg dose was discontinued early because of increased intracranial hemorrhage and was replaced by a 40-mg dose, and heparin doses were decreased. TNK-tPA 40 mg and tPA produced similar rates of TIMI grade 3 flow at 90 minutes (62.8% versus 62.7%, respectively, P=NS); the rate for the 30-mg dose was significantly lower (54.3%, P=0.035) and was 65. 8% for the 50-mg dose (P=NS). A prespecified analysis of weight-based TNK-tPA dosing using median TIMI frame count demonstrated a dose response (P=0.001). Similar dose responses were observed for serious bleeding and intracranial hemorrhage, but significantly lower rates were observed for both TNK-tPA and tPA after the heparin doses were lowered and titration of the heparin was started at 6 hours.

CONCLUSIONS

TNK-tPA, given as a single 40-mg bolus, achieved rates of TIMI grade 3 flow similar to those of the 90-minute bolus and infusion of tPA. Weight-adjusting TNK-tPA appears to be important in achieving optimal reperfusion; reduced heparin dosing appears to improve safety for both agents. Together with the safety results from the parallel Assessment of the Safety of a New Thrombolytic: TNK-tPA (ASSENT I) trial, an appropriate dose of this single-bolus thrombolytic agent has been identified for phase III testing.

摘要

背景

大剂量溶栓疗法是一种简化的溶栓给药方式,可缩短治疗时间。替奈普酶(TNK - tPA)是一种高度纤维蛋白特异性的单次大剂量溶栓剂。

方法与结果

在心肌梗死溶栓试验(TIMI)10B研究中,886例在12小时内出现急性ST段抬高型心肌梗死的患者被随机分为接受30mg或50mg单次大剂量TNK - tPA或先静脉推注后静脉滴注tPA治疗,并立即进行冠状动脉造影。由于颅内出血增加,50mg剂量提前停用,改为40mg剂量,并降低了肝素剂量。40mg TNK - tPA和tPA在90分钟时TIMI 3级血流的发生率相似(分别为62.8%和62.7%,P = 无显著性差异);30mg剂量的发生率显著较低(54.3%,P = 0.035),50mg剂量的发生率为65.8%(P = 无显著性差异)。使用中位TIMI帧数对基于体重的TNK - tPA给药进行的预设分析显示出剂量反应(P = 0.001)。在严重出血和颅内出血方面观察到类似的剂量反应,但在降低肝素剂量并于6小时开始调整肝素剂量后,TNK - tPA和tPA的发生率均显著降低。

结论

单次静脉推注40mg TNK - tPA达到TIMI 3级血流的发生率与90分钟静脉推注及静脉滴注tPA相似。调整TNK - tPA的体重剂量对于实现最佳再灌注似乎很重要;降低肝素剂量似乎可提高两种药物的安全性。结合平行的新型溶栓剂安全性评估:TNK - tPA(ASSENT I)试验的安全性结果,已确定该单次大剂量溶栓剂的合适剂量用于III期试验。

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