Third-generation thrombolytic drugs

被引:119
|
作者
Verstraete, M [1 ]
机构
[1] Univ Leuven, Ctr Mol & Vasc Biol, B-3000 Louvain, Belgium
来源
AMERICAN JOURNAL OF MEDICINE | 2000年 / 109卷 / 01期
关键词
D O I
10.1016/S0002-9343(00)00380-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several third-generation thrombolytic agents have been developed. They are either conjugates of plasminogen activators with monoclonal antibodies against fibrin, platelets, or thrombomodulin; mutants, variants, and hybrids of alteplase and prourokinase (amediplase); or new molecules of animal (vampire bat) or bacterial (Staphylococcus aureus) origin. These variations may lengthen the drug's half-life, increase resistance to plasma protease inhibitors, or cause more selective binding to fibrin. Compared with the second-generation agent (alteplase), third-generation thrombolytic agents such as monteplase, tenecteplase, reteplase, lanoteplase, pamiteplase, and staphylokinase result in a greater angiographic patency rate in patients with acute myocardial infarction, although, thus far, mortality rates have been similar for those few drugs that have been studied in large-scale trials. Bleeding risk, however, may be greater. Am J Med. 2000;109:52-58. (C) 2000 by Excerpta Medica, Inc.
引用
收藏
页码:52 / 58
页数:7
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