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Systemic effects of BRL 26921 during thrombolytic treatment of acute myocardial infarction.

Abstract
The effects of BRL 26921, an active-site acylated streptokinase-plasminogen complex, on the fibrinolytic and coagulation systems were studied in 13 patients treated for acute myocardial infarction with a short intravenous infusion of 30 mg of the new drug. In 12/13 patients (92%) significant changes were observed in the concentrations of fibrinogen, fibrin(ogen) degradation products, plasminogen, alpha 2-antiplasmin and F VIII:C; all changes indicating a substantial degree of systemic fibrinolysis. In only one patient were no signs of systemic activation of the fibrinolytic system observed. The therapeutic efficacy of the drug was 85% in this study.
AuthorsJ J Hoffmann, F J Van Rey, J J Bonnier
JournalThrombosis research (Thromb Res) Vol. 37 Issue 5 Pg. 567-72 (Mar 01 1985) ISSN: 0049-3848 [Print] United States
PMID3920779 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Fibrin Fibrinogen Degradation Products
  • Fibrinolytic Agents
  • alpha-2-Antiplasmin
  • Anistreplase
  • Factor VIII
  • Fibrinogen
  • Plasminogen
  • Streptokinase
Topics
  • Adult
  • Aged
  • Anistreplase
  • Factor VIII (analysis)
  • Female
  • Fibrin Fibrinogen Degradation Products (analysis)
  • Fibrinogen (analysis)
  • Fibrinolytic Agents (therapeutic use)
  • Humans
  • Male
  • Middle Aged
  • Myocardial Infarction (drug therapy)
  • Plasminogen (therapeutic use)
  • Streptokinase (therapeutic use)
  • alpha-2-Antiplasmin (analysis)

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