Key result
Enhanced plasminogen activators and conjunctive antiplatelet or antithrombotic agents accelerated clot lysis and reduced reocclusion in animal models of thrombosis.
Experimental models suggest that combining enhanced plasminogen activators with targeted antiplatelet or antithrombotic agents improves thrombolysis, though human bleeding risks remain a concern.
May enhance thrombolysis in models but should not change practice; leaves open human translation pending safety trials.
New approaches to further improve thrombolytic therapy include strategies to enhance the fibrinolytic potency of plasminogen activators and to improve conjunctive antiplatelet or antithrombotic agents. The fibrinolytic potency of plasminogen activators may be enhanced by the construction of mutant and chimeric molecules and of antibody-targeted plasminogen activators. Antiplatelet strategies include the use of platelet glycoprotein llb/llla receptor blocking agents, thromboxane synthase inhibitors, and endoperoxide receptor antagonists. Antithrombotic strategies include the use of more selective thrombin inhibitors and inhibitors of tissue factor or of factor Xa. Several of these conjunctive strategies were shown to contribute to the prevention of platelet-rich arterial thrombosis, the acceleration of clot lysis with thrombolytic agents, and the reduction of reocclusion in animal models of thrombosis. The safety of these strategies in humans, particularly with respect to the bleeding risk that may be associated with the use of more potent antiplatelet or antithrombotic agents, will require careful evaluation.
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Lijnen et al. (1993) conducted a review in Thrombosis. Enhanced plasminogen activators and conjunctive antiplatelet or antithrombotic agents was evaluated. Enhanced plasminogen activators and conjunctive antiplatelet or antithrombotic agents accelerated clot lysis and reduced reocclusion in animal models of thrombosis.
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