• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

急性心肌梗死单次静脉推注组织型纤溶酶原激活剂的有效性和安全性。组织型纤溶酶原激活剂推注剂量递增研究(BEST)研究者。

Effectiveness and safety of a single intravenous bolus injection of tissue-type plasminogen activator in acute myocardial infarction. Bolus Dose-Escalation Study of Tissue-Type Plasminogen Activator (BEST) Investigators.

作者信息

Hackett D, Andreotti F, Haider A W, Brunelli C, Shahi M, Fussell A, Buller N, Foale R, Lipkin D, Caponnetto S

机构信息

Department of Medicine, Royal Postgraduate Medical School, Hammersmith Hospital, United Kingdom.

出版信息

Am J Cardiol. 1992 Jun 1;69(17):1393-8. doi: 10.1016/0002-9149(92)90888-6.

DOI:10.1016/0002-9149(92)90888-6
PMID:1590225
Abstract

The efficacy of multiple intravenous bolus injections of tissue-type plasminogen activator (t-PA) in inducing rapid coronary recanalization in patients with acute myocardial infarction was previously demonstrated. In this Bolus Dose-Escalation Study of Tissue-Type Plasminogen Activator (BEST), the efficacy of 3 different doses of a single rapid intravenous bolus injection of t-PA (dute-plase, Wellcome Foundation, London) in inducing coronary patency (Thrombolysis In Myocardial Infarction perfusion grade 2 or 3) in 64 patients with acute myocardial infarction presenting less than 6 hours after onset of symptoms was investigated. At 60 minutes after administration of t-PA, the infarct-related coronary artery was patent in 9 of 17 patients (53%; 95% confidence interval [CI] 28 to 77%) after 0.3 MU/kg, in 14 of 23 (61%; 95% CI 39 to 80%) after 0.45 MU/kg and in 10 of 14 (71%; 95% CI 42 to 92%) after 0.6 MU/kg. At 90 minutes after t-PA, coronary patency was present in 9 of 17 cases (53%; 95% CI 28 to 77%) after 0.3 MU/kg, in 12 of 24 (50%; 95% CI 29 to 71%) after 0.45 MU/kg and in 10 of 13 (77%; 95% CI 46 to 95%) after 0.6 MU/kg. One patient in each dose group had a silent reoccluded infarct-related artery by 24 hours, and there were 2 clinical reinfarctions before discharge. No major bleeding events were observed. There were 5 hospital deaths, all unrelated to t-PA. A single intravenous bolus injection of 0.6 MU/kg of t-PA appears to be effective in inducing rapid coronary patency and to be safe in patients with acute myocardial infarction.

摘要

先前已证明,多次静脉推注组织型纤溶酶原激活剂(t-PA)对急性心肌梗死患者诱导冠状动脉快速再通有效。在这项组织型纤溶酶原激活剂推注剂量递增研究(BEST)中,研究了单次快速静脉推注3种不同剂量的t-PA(都替普酶,威康信托基金会,伦敦)对64例症状发作后不到6小时的急性心肌梗死患者诱导冠状动脉通畅(心肌梗死溶栓灌注2级或3级)的效果。在给予t-PA后60分钟,0.3MU/kg剂量组17例患者中有9例(53%;95%置信区间[CI]28%至77%)梗死相关冠状动脉通畅,0.45MU/kg剂量组23例中有14例(61%;95%CI 39%至80%)通畅,0.6MU/kg剂量组14例中有10例(71%;95%CI 42%至92%)通畅。在给予t-PA后90分钟,0.3MU/kg剂量组17例中有9例(53%;95%CI 28%至77%)冠状动脉通畅,0.45MU/kg剂量组24例中有12例(50%;95%CI 29%至71%)通畅,0.6MU/kg剂量组13例中有10例(77%;95%CI 46%至95%)通畅。各剂量组均有1例患者在24小时时梗死相关动脉无症状性再闭塞,出院前有2例临床再梗死。未观察到重大出血事件。有5例住院死亡,均与t-PA无关。单次静脉推注0.6MU/kg的t-PA似乎对诱导冠状动脉快速通畅有效,且对急性心肌梗死患者安全。

相似文献

1
Effectiveness and safety of a single intravenous bolus injection of tissue-type plasminogen activator in acute myocardial infarction. Bolus Dose-Escalation Study of Tissue-Type Plasminogen Activator (BEST) Investigators.急性心肌梗死单次静脉推注组织型纤溶酶原激活剂的有效性和安全性。组织型纤溶酶原激活剂推注剂量递增研究(BEST)研究者。
Am J Cardiol. 1992 Jun 1;69(17):1393-8. doi: 10.1016/0002-9149(92)90888-6.
2
More rapid, complete, and stable coronary thrombolysis with bolus administration of reteplase compared with alteplase infusion in acute myocardial infarction. RAPID Investigators.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。
Circulation. 1995 Jun 1;91(11):2725-32. doi: 10.1161/01.cir.91.11.2725.
3
Open, noncontrolled dose-finding study with a novel recombinant plasminogen activator (BM 06.022) given as a double bolus in patients with acute myocardial infarction.
Am J Cardiol. 1993 Sep 1;72(7):518-24. doi: 10.1016/0002-9149(93)90345-d.
4
Effectiveness of multiple bolus administration of tissue-type plasminogen activator in acute myocardial infarction.组织型纤溶酶原激活剂多次静脉推注治疗急性心肌梗死的疗效
Am J Cardiol. 1990 May 1;65(16):1051-6. doi: 10.1016/0002-9149(90)90313-p.
5
Efficacy of 100 mg of double-bolus alteplase in achieving complete perfusion in the treatment of acute myocardial infarction.
J Am Coll Cardiol. 1994 Jan;23(1):6-10. doi: 10.1016/0735-1097(94)90495-2.
6
Sixty-minute alteplase protocol: a new accelerated recombinant tissue-type plasminogen activator regimen for thrombolysis in acute myocardial infarction.60分钟阿替普酶方案:一种用于急性心肌梗死溶栓的新型加速重组组织型纤溶酶原激活剂方案。
J Am Coll Cardiol. 1997 Dec;30(7):1611-7. doi: 10.1016/s0735-1097(97)00370-7.
7
A prospective, randomized, double-blind multicenter trial of a single bolus injection of the novel modified t-PA E6010 in the treatment of acute myocardial infarction: comparison with native t-PA. E6010 Study Group.
J Am Coll Cardiol. 1997 Jun;29(7):1447-53. doi: 10.1016/s0735-1097(97)00074-0.
8
Clot-selective coronary thrombolysis with low-dose synergistic combinations of single-chain urokinase-type plasminogen activator and recombinant tissue-type plasminogen activator. The Pro-Urokinase for Myocardial Infarction Study Group.单链尿激酶型纤溶酶原激活剂与重组组织型纤溶酶原激活剂低剂量协同组合的凝块选择性冠状动脉溶栓治疗。心肌梗死尿激酶原研究组。
Am J Cardiol. 1991 Dec 15;68(17):1564-9. doi: 10.1016/0002-9149(91)90310-h.
9
Dose finding with a novel recombinant plasminogen activator (BM 06.022) in patients with acute myocardial infarction: results of the German Recombinant Plasminogen Activator Study. A study of the Arbeitsgemeinschaft Leitender Kardiologischer Krankenhausärzte (ALKK).新型重组纤溶酶原激活剂(BM 06.022)用于急性心肌梗死患者的剂量探索:德国重组纤溶酶原激活剂研究结果。一项由德国心脏病医院主任医师协会(ALKK)开展的研究。
J Am Coll Cardiol. 1994 Jul;24(1):55-60. doi: 10.1016/0735-1097(94)90541-x.
10
Coronary recanalization rate after intravenous bolus of alteplase in acute myocardial infarction.急性心肌梗死患者静脉推注阿替普酶后的冠状动脉再通率。
Am J Cardiol. 1991 Jul 15;68(2):161-5. doi: 10.1016/0002-9149(91)90737-6.