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Ancrod causes rapid thrombolysis in patients with acute stroke.

Abstract
Clot lysis is desirable in patients with thrombi in arteries and arterioles by a safe rapidly-acting thrombolytic agent. Ancrod cleaves fibrinogen; the resulting circulating ancrod-fibrin stimulates fibrinolysis. Ancrod action and effect were studied in 20 patients with acute developing stroke in a double-blind, placebo-controlled study. Patients were randomly assigned to one of two treatment groups, and received either normal saline or ancrod 0.5 mu/kg in normal saline administered as a constant-rate intravenous infusion over 6 hours. Subsequent doses of ancrod (or saline placebo) were determined daily thereafter for a total treatment period of 7 days. Neither bleeding nor re-thrombosis occurred within the 90 day follow-up period. That ancrod acted rapidly was shown by a significant decrease in functional plasminogen activator inhibitor (PA-I) within 60 minutes, and by significant elevations of fibrin(ogen) degradation products (FDP) and D-dimer within 3 and 4 hours. The biological effect of fibrinolysis in ancrod infused patients was demonstrated by a greater improvement in stroke score when compared to those infused with saline.
AuthorsV E Pollak, P Glas-Greenwalt, C P Olinger, N K Wadhwa, S A Myre
JournalThe American journal of the medical sciences (Am J Med Sci) Vol. 299 Issue 5 Pg. 319-25 (May 1990) ISSN: 0002-9629 [Print] United States
PMID2186630 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Fibrin Fibrinogen Degradation Products
  • Plasminogen Inactivators
  • Protein C
  • alpha-2-Antiplasmin
  • Fibrinogen
  • Plasminogen
  • Ancrod
  • Plasminogen Activators
Topics
  • Acute Disease
  • Adult
  • Aged
  • Aged, 80 and over
  • Ancrod (therapeutic use)
  • Cerebrovascular Disorders (blood, drug therapy)
  • Double-Blind Method
  • Fibrin Fibrinogen Degradation Products (analysis)
  • Fibrinogen (analysis)
  • Fibrinolysis (drug effects)
  • Humans
  • Intracranial Embolism and Thrombosis (blood, drug therapy)
  • Middle Aged
  • Pilot Projects
  • Plasminogen (analysis)
  • Plasminogen Activators (analysis)
  • Plasminogen Inactivators (analysis)
  • Protein C (analysis)
  • Randomized Controlled Trials as Topic
  • Time Factors
  • alpha-2-Antiplasmin (analysis)

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