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What are the challenges of translating positive trial results in severe sepsis into clinical practice? A media roundtable debate, 18 March 2002, Brussels, Belgium.
Ball J.
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Drotrecogin alfa (activated) for severe sepsis.
[No authors listed]
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Wheeler A, Steingrub J, Schmidt GA, Sanchez P, Jacobi J, Linde-Zwirble W, Bates B, Qualy RL, Woodward B, Zeckel M.
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Vincent JL, Abraham E, Annane D, Bernard G, Rivers E, Van den Berghe G.
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Comparison of mechanisms after post-hoc analyses of the drotrecogin alfa (activated) and antithrombin III trials in severe sepsis.
Wiedermann CJ, Kaneider NC.
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Use of an integrated clinical trial database to evaluate the effect of timing of drotrecogin alfa (activated) treatment in severe sepsis.
Vincent JL, O'Brien J Jr, Wheeler A, Wittebole X, Garg R, Trzaskoma BL, Sundin DP.
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Lack of evidence for qualitative treatment by disease severity interactions in clinical studies of severe sepsis.
Macias WL, Nelson DR, Williams M, Garg R, Janes J, Sashegyi A.
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Recombinant human activated protein C for severe sepsis in neonates.
Kylat RI, Ohlsson A.
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Effect of factor V Leiden polymorphism in severe sepsis and on treatment with recombinant human activated protein C.
Yan SB, Nelson DR.
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Drotrecogin alfa (recombinant human activated protein C) for the treatment of severe sepsis.
McCoy C, Matthews SJ.
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Inflammation and coagulation: implications for the septic patient.
Dellinger RP.
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Selecting patients with severe sepsis for drotrecogin alfa (activated) therapy.
Sollet JP, Garber GE.
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From bench to bedside: a review of the clinical trial development plan of drotrecogin alfa (activated).
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Drotrecogin alfa (recombinant human activated protein C) in severe sepsis--a New Zealand viewpoint.
Liang J, Streat S, Torrance J, Sleigh J, Freebairn R, Ramsay M.
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