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链激酶与阿替普酶治疗大面积肺栓塞的疗效比较:一项评估右心血流动力学及肺血管阻塞情况的随机试验

Streptokinase vs alteplase in massive pulmonary embolism. A randomized trial assessing right heart haemodynamics and pulmonary vascular obstruction.

作者信息

Meneveau N, Schiele F, Vuillemenot A, Valette B, Grollier G, Bernard Y, Bassand J P

机构信息

Department de Cardiologie, Hopital Universitaire Saint-Jacques, Besançon, France.

出版信息

Eur Heart J. 1997 Jul;18(7):1141-8. doi: 10.1093/oxfordjournals.eurheartj.a015410.

Abstract

OBJECTIVE

The aim of the study was to test the efficacy of recombinant tissue plasminogen activator and streptokinase in massive pulmonary embolism, the primary endpoints being haemodynamic improvement and thrombus lysis, and the secondary endpoints efficacy and safety.

DESIGN

Fifty patients with massive pulmonary embolism were randomly allocated either to a 100 mg 2 h infusion of recombinant tissue plasminogen activator followed by a 20 IU.kg-1.h-1 infusion of heparin, or to a 100,000 IU.h-1 12 h infusion of streptokinase after a initial bolus of 250,000 IU over 15 min, followed by heparin infusion of 10 IU.kg-1.h-1. Total pulmonary resistance and right ventricular ejection fraction were monitored over a 12 h period. Pulmonary vascular obstruction was assessed at 24 to 48 h and 10 days after thrombolytic therapy.

RESULTS

Thrombolysis occurred more rapidly with recombinant tissue plasminogen activator than with streptokinase, but without any significant difference in terms of right heart haemodynamics at 12 h or in improvement of pulmonary vascular obstruction at 24-48 h or at 10 days. There was no significant difference in bleeding complication rates and no patients suffered intracranial haemorrhage.

CONCLUSION

These results proved that, when the full dose of streptokinase has been given over 12 h, its efficacy is as good as that of 2 h of recombinant tissue plasminogen. A further trial aimed at comparing recombinant tissue plasminogen activator and streptokinase infused over a 2 h period is needed to determine whether a similar efficacy can be obtained.

摘要

目的

本研究旨在测试重组组织型纤溶酶原激活剂和链激酶在大面积肺栓塞中的疗效,主要终点为血流动力学改善和血栓溶解,次要终点为疗效和安全性。

设计

50例大面积肺栓塞患者被随机分配,一组接受100mg重组组织型纤溶酶原激活剂2小时输注,随后以20IU.kg-1.h-1输注肝素;另一组在15分钟内静脉推注250,000IU链激酶后,接受100,000IU.h-1链激酶12小时输注,随后以10IU.kg-1.h-1输注肝素。在12小时内监测总肺阻力和右心室射血分数。在溶栓治疗后24至48小时以及10天时评估肺血管阻塞情况。

结果

重组组织型纤溶酶原激活剂引起的溶栓比链激酶更快,但在12小时时右心血流动力学或在24 - 48小时或10天时肺血管阻塞改善方面无显著差异。出血并发症发生率无显著差异,且无患者发生颅内出血。

结论

这些结果证明,当链激酶在12小时内给予全剂量时,其疗效与2小时的重组组织型纤溶酶原激活剂相当。需要进一步进行试验,比较2小时输注的重组组织型纤溶酶原激活剂和链激酶,以确定是否能获得相似疗效。

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