Coagulation inhibition for sepsis

被引:15
作者
Key, NS
Ely, EW
机构
[1] Univ Minnesota, Sch Med, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN USA
关键词
D O I
10.1097/00062752-200209000-00005
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Following on the heels of multiple failed clinical trials of adjunctive therapeutic agents in sepsis, the positive outcome of a recent phase III study using activated protein C (APC) has led to a renewed optimism in targeted biotherapies for this syndrome. A growing body of data (both preclinical and clinical) suggests that the protection against death afforded by APC cannot be solely explained by its antithrombotic activity but rather is likely explained by its associated anti-inflammatory and profibrinolytic effects. Although a recent phase III study failed to demonstrate any protective effect of another important antithrombotic molecule, antithrombin, it is premature to conclude that the benefit observed with APC is unique among inhibitors of the coagulation system. The result of a third phase III study examining the effect of tissue factor pathway inhibitor (TFPI) in sepsis is currently awaited, and the possibility that other antithrombotic agents-and combinations thereof-have a place in the therapeutic armamentarium will undoubtedly be the topic of future studies. Curr Opin Hematol 2002, 9:416-421 (C) 2002 Lippincott Williams Wilkins, Inc.
引用
收藏
页码:416 / 421
页数:6
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