Literature DB >> 10608001

Novel Antithrombotic Strategies for the Treatment of Coronary Artery Thrombosis: A Critical Appraisal.

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Abstract

Large-scale clinical trials have demonstrated that treatment of patients with acute myocardial infarction and unstable angina with antithrombotic agents significantly improves outcome. Despite the proven benefit of current therapies, there is a widespread perception that outcome could be enhanced further with novel antithrombotic agents. Enthusiasm for novel antithrombotic strategies has been stimulated by recent advances in the understanding of the mechanisms responsible for coronary artery thrombosis, which has led to the development of diverse inhibitors of platelet function and coagulation factors. In experimental models of coronary artery thrombosis, aspirin and heparin have been ineffective in preventing recurrent thrombosis after coronary thrombolysis and in preventing the progression of thrombosis in response to strong thrombogenic stimuli. In contrast, inhibitors of the platelet fibrinogen receptor, direct-acting thrombin inhibitors, and inhibitors of coagulation factors that promote elaboration of thrombin have been shown to be effective in attenuating arterial thrombosis in a variety of experimental preparations. Initial clinical trials with these agents have also documented efficacy in attenuating thrombotic events in patients treated with coronary thrombolysis and in those with unstable angina. However, optimal doses of novel antithrombotic agents, the degree to which combination antiplatelet and anticoagulant therapies are needed, and the risk/benefit ratio associated with specific novel antithrombotic drugs are still relatively undefined. With regard to the latter, it is possible that the large-scale clinical trials now in progress may show an increase in bleeding complications with novel anticoagulants compared with conventional therapy. Nonetheless, there are considerable data that suggest that treatment with aspirin and heparin is not completely effective in preventing the progression of thrombosis or its recurrence after interventions in high-risk subgroups of patients with coronary artery thrombosis and unstable coronary artery disease. Accordingly, continued investigation of a large variety of antithrombotic agents, both currently available and in development, should improve the treatment of high-risk patients with coronary disease if regimens with appropriate efficacy but without serious hemorrhagic effects can be designed.

Entities:  

Year:  1995        PMID: 10608001     DOI: 10.1007/bf01060733

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  133 in total

1.  Inhibition of thrombus formation by activated recombinant protein C in a primate model of arterial thrombosis.

Authors:  A Gruber; S R Hanson; A B Kelly; B S Yan; N Bang; J H Griffin; L A Harker
Journal:  Circulation       Date:  1990-08       Impact factor: 29.690

Review 2.  Surface-dependent reactions of the vitamin K-dependent enzyme complexes.

Authors:  K G Mann; M E Nesheim; W R Church; P Haley; S Krishnaswamy
Journal:  Blood       Date:  1990-07-01       Impact factor: 22.113

3.  Importance of continued activation of thrombin reflected by fibrinopeptide A to the efficacy of thrombolysis.

Authors:  P R Eisenberg; L Sherman; M Rich; D Schwartz; K Schechtman; E M Geltman; B E Sobel; A S Jaffe
Journal:  J Am Coll Cardiol       Date:  1986-06       Impact factor: 24.094

4.  Inhibition of platelet-dependent thrombus formation by human activated protein C in a primate model.

Authors:  A Gruber; J H Griffin; L A Harker; S R Hanson
Journal:  Blood       Date:  1989-02-15       Impact factor: 22.113

5.  Selective immobilization of alpha-thrombin by surface-bound fibrin.

Authors:  G D Wilner; M P Danitz; M S Mudd; K H Hsieh; J W Fenton
Journal:  J Lab Clin Med       Date:  1981-03

6.  Pharmacodynamic study of F(ab')2 fragments of murine monoclonal antibody 7E3 directed against human platelet glycoprotein IIb/IIIa in patients with unstable angina pectoris.

Authors:  H K Gold; L W Gimple; T Yasuda; R C Leinbach; W Werner; R Holt; R Jordan; H Berger; D Collen; B S Coller
Journal:  J Clin Invest       Date:  1990-08       Impact factor: 14.808

7.  Comparison of invasive and conservative strategies after treatment with intravenous tissue plasminogen activator in acute myocardial infarction. Results of the thrombolysis in myocardial infarction (TIMI) phase II trial.

Authors: 
Journal:  N Engl J Med       Date:  1989-03-09       Impact factor: 91.245

8.  Paradoxic elevation of fibrinopeptide A after streptokinase: evidence for continued thrombosis despite intense fibrinolysis.

Authors:  P R Eisenberg; L A Sherman; A S Jaffe
Journal:  J Am Coll Cardiol       Date:  1987-09       Impact factor: 24.094

9.  Prevention of arterial reocclusion after thrombolysis with recombinant lipoprotein-associated coagulation inhibitor.

Authors:  E J Haskel; S R Torr; K C Day; M O Palmier; T C Wun; B E Sobel; D R Abendschein
Journal:  Circulation       Date:  1991-08       Impact factor: 29.690

10.  Coronary angioscopy in patients with unstable angina pectoris.

Authors:  C T Sherman; F Litvack; W Grundfest; M Lee; A Hickey; A Chaux; R Kass; C Blanche; J Matloff; L Morgenstern
Journal:  N Engl J Med       Date:  1986-10-09       Impact factor: 91.245

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