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采用急性ST段抬高型心肌梗死新策略缩小差距:大剂量溶栓、糖蛋白IIb/IIIa抑制剂、联合治疗、经皮冠状动脉介入治疗以及“易化”经皮冠状动脉介入治疗

Bridging the gap with new strategies in acute ST elevation myocardial infarction: bolus thrombolysis, glycoprotein IIb/IIIa inhibitors, combination therapy, percutaneous coronary intervention, and "facilitated" PCI.

作者信息

Cannon C P

机构信息

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

出版信息

J Thromb Thrombolysis. 2000 Apr;9(3):235-41. doi: 10.1023/a:1018714627681.

DOI:10.1023/a:1018714627681
PMID:10728022
Abstract

Achieving early reperfusion with thrombolytic agents or primary percutaneous coronary intervention (PCI) in patients with acute myocardial infarction (AMI) is the cornerstone of current therapy. Two advances in pharmacologic therapy are: (1) bolus thrombolysis, which simplifies therapy, reduces door-to-needle time, and reduces the potential for medication errors, and (2) Low-dose fibrinolytic therapy combined with a glycoprotein (GP) IIb/IIIa inhibitor which can achieve higher rates of reperfusion than fibrinolytic therapy alone. In addition, the IIb/IIIa inhibitor as part of the reperfusion regimen will support any acute-phase interventions that are performed. The combination of fibrinolytic therapy and GP IIb/IIIa inhibition to "facilitate" PCI is being examined in TIMI-14, SPEED, and GUSTO IV. Early findings in the SPEED trial have shown promising results with "facilitated" PCI when patency is achieved before PCI is attempted. Results of these trials will further define the role of combination therapy in facilitating mechanical interventions.

摘要

在急性心肌梗死(AMI)患者中,使用溶栓药物或直接经皮冠状动脉介入治疗(PCI)实现早期再灌注是当前治疗的基石。药物治疗方面的两项进展是:(1)推注溶栓,这简化了治疗,减少了门到针的时间,并降低了用药错误的可能性;(2)低剂量纤维蛋白溶解疗法联合糖蛋白(GP)IIb/IIIa抑制剂,与单独使用纤维蛋白溶解疗法相比,可实现更高的再灌注率。此外,作为再灌注方案一部分的IIb/IIIa抑制剂将支持进行的任何急性期干预。纤维蛋白溶解疗法与GP IIb/IIIa抑制联合以“促进”PCI正在TIMI-14、SPEED和GUSTO IV试验中进行研究。SPEED试验的早期结果表明,在尝试PCI之前实现血管通畅时,“促进”PCI有令人鼓舞的结果。这些试验的结果将进一步明确联合治疗在促进机械干预中的作用。

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