Thromb Haemost 2003; 90(04): 642-653
DOI: 10.1160/TH02-11-0270
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Drotrecogin alfa (activated) (recombinant human activated protein C) reduces host coagulopathy response in patients with severe sepsis

Jean-François Dhainaut
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
S. Betty Yan
2   Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA
,
Benjamin D. Margolis
3   Intensive Care Unit, West Suburban Hospital, Oak Park, Illinois, USA
,
José A. Lorente
4   Unidad de Cuidados Intensivos, Hospital Universitario De Getafe, Madrid, Spain
,
James A. Russell
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
Ross C. Freebairn
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
Herbert D. Spapen
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
Hanno Riess
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
Bruce Basson
2   Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA
,
Gerald Johnson III
2   Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana, USA
,
Gary T. Kinasewitz
1   Service de Reanimation Medicale, Centre Hospitalo-Universitaire Cochin Port-Royal, AP-HP, Paris V University, Paris, France
,
for the PROWESS Sepsis Study Group› Author Affiliations

Financial support: This study was supported by Eli Lilly and Company, Indianapolis, IN.
Further Information

Publication History

Received 20 November 2002

Accepted after resubmission 09 June 2003

Publication Date:
05 December 2017 (online)

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Summary

Drotrecogin alfa (activated) improved survival in patients with severe sepsis in PROWESS, a double-blind, study of 1690 adult patients randomized to drotrecogin alfa (activated) at 24 μg/kg/h (N=850) or placebo (N=840) infused for 96 hours. Pharmacodynamic effects of drotrecogin alfa (activated) were assessed with 15 prospectively defined systemic biomarkers of hemostasis, inflammation and endothelial injury. The last-observation-carried-forward (LOCF) method of imputation for missing observations was the prospectively defined statistical method. The results were also analyzed with only the observed values without imputation for missing data (repeated measures analysis). With both statistical methods, drotrecogin alfa (activated)-treated patients demonstrated antithrombotic (reduced markers of thrombin generation and accelerated normalization of anticoagulant factor, protein C and fibrinolytic factors) and anticoagulant (prolonged PT and APTT) effects compared with placebo. A profibrinolytic (reduction in plasminogen activator inhibitor-1) effect was significant only with the LOCF imputation method in observed case and percent change from baseline analyses. An anti-inflammatory (reduction in interleukin-6) effect was significant only with the LOCF imputation method in change from baseline and percent change from baseline analyses. Drotrecogin alfa (activated) is a new and promising agent for treatment of patients with severe sepsis. The extensive analysis of systemic biomarkers confirms the previously published antithrombotic effects. However, the present results using different statistical methods do not provide a strong basis for systemic anti-inflammatory or pro-fibrinolytic effects. These latter two effects may occur at the local or cellular level. The systemic biomarkers reported here might not be the most appropriate approach to demonstrate these potential effects of drotrecogin alfa (activated).

* PROWESS, recombinant human activated protein C Worldwide Evaluation in Severe Sepsis. Additional institutions and investigators participating in the PROWESS Study Group are listed in Bernard et al. (1).