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

被引:113
作者
Dhainaut, JFO
Yan, SB
Margolis, BD
Lorente, JA
Russell, JA
Freebairn, RC
Spapen, HD
Riess, H
Basson, B
Johnson, G
Kinasewitz, GT
机构
[1] Univ Paris 05, Ctr Hosp Univ Cochin Port Royal, AP HP, Serv Animat Med, F-75679 Paris 14, France
[2] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[3] W Suburban Hosp, Intens Care Unit, Oak Pk, IL USA
[4] Hosp Univ De Getafe, Unidad Cuidados Intensivos, Madrid, Spain
[5] St Pauls Hosp, Vancouver, BC V6Z 1Y6, Canada
[6] Hawkes Bay Hosp, Intens Care Unit, Hastings, New Zealand
[7] Free Univ Brussels, Univ Hosp, Intens Care Unit, Brussels, Belgium
[8] Kinikum Klin Haematol & Onkol, Berlin, Germany
[9] Univ Oklahoma, Hlth Sci Ctr, Dept Physiol & Med Biophys, Oklahoma City, OK USA
[10] Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
关键词
Drotrecogin alfa (activated); activated protein C; coagulopathy; biomarkers; randomized controlled trial;
D O I
10.1160/TH02-11-0270
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 pg/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-I) 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).
引用
收藏
页码:642 / 653
页数:12
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