A new hypothesis with implications for the treatment of sepsishas recently been tested the hypothesis that part ofthe pathophysiology of sepsis is caused by unrestricted or inappropriatecoagulation in the microcirculation. Three agents that blockcoagulation at different stages have now been evaluated in large,multicenter trials as adjunctive therapy for sepsis. Neitherantithrombin III nor tissue-factor-pathway inhibitor was effectivein patients with severe sepsis or septic shock.1,2 In contrast,treatment with activated protein C (drotrecogin alfa [activated])was associated with a significant reduction in 28-day mortality.Of the patients who received activated protein C, 24.7 percent. . . [Full Text of this Article]
The Two Phases of the Activated Protein C Trial
Subgroups and Restriction to Use in High-Risk Patients
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