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Updated: Aug 24, 2026

An In vitro System to Gauge the Thrombolytic Efficacy of Histotripsy and a Lytic Drug
Published on: June 4, 2021
Pharmacologic and clinical characteristics of thrombolytic agents
Steven R Deitcher1, Michael R Jaff
1Section of Hematology and Coagulation Medicine and Section of Vascular Medicine, Cleveland Clinic Foundation, Cleveland, OH, USA.
Insights
Newer plasminogen activators (PAs) for dissolving blood clots show no significant advantage over older agents like urokinase for peripheral vascular thrombosis. Current data suggest similar efficacy and safety profiles, questioning the benefits of newer thrombolytic therapies.
Area of Science:
- Vascular Medicine
- Pharmacology
- Thrombosis Research
Background:
- Arterial and venous thromboembolic events are life-threatening vascular diseases.
- Anticoagulant therapy is standard for preventing further clot formation.
- The fibrinolytic system plays a crucial role in natural clot resolution.
Purpose of the Study:
- To evaluate the efficacy and safety of newer plasminogen activator (PA) thrombolytic agents.
- To compare newer PAs with established agents like urokinase for peripheral vascular thrombosis.
- To assess the risk of bleeding associated with newer PA formulations.
Main Methods:
- Review of pharmacokinetic and pharmacodynamic properties of various PA thrombolytic agents.
- Analysis of clinical data comparing newer fibrin-specific PAs with urokinase.
- Evaluation of safety profiles, including bleeding risks like intracranial hemorrhage.
Main Results:
- Newer PAs, including fibrin-specific agents, have varying properties.
- Continuous infusions of newer PAs are used for peripheral vascular thromboses.
- Data do not compellingly show superior efficacy or safety of newer PAs over urokinase for peripheral thrombosis.
Conclusions:
- Current evidence does not support significantly greater efficacy or safety of newer PAs compared to urokinase for peripheral vascular thrombosis.
- The risk of bleeding, including intracranial hemorrhage, may increase with newer tissue-type plasminogen activator-based PAs.
- Further research may be needed to clarify the role and benefits of newer thrombolytic agents.
Abstract:
Arterial and venous thromboembolic events, including myocardial infarction, ischemic stroke, peripheral arterial thrombosis, deep venous thrombosis, and pulmonary embolism are common potentially life-, organ-, and limb-threatening vascular diseases. Anticoagulant therapy is recommended in these settings to prevent further thrombosis pending gradual clearance of the thrombotic occlusion by the endogenous fibrinolytic system. Recognition of the importance of the fibrinolytic system in thrombus resolution has resulted in the development of pharmacologic fibrinolytic (thrombolytic) agents to facilitate rapid restoration of vascular patency. Several plasminogen activator (PA) thrombolytic agents with different pharmacokinetic and pharmacodynamic properties have been developed to treat thrombotic disease. Newer PAs have been developed as "fibrin-specific", bolus-administration drugs to primarily treat acute coronary syndromes. Continuous infusions of these fibrin-specific PAs have become popular for the lysis relatively larger peripheral vascular thromboses. Loss infusion of newer tissue-type plasminogen activator-based PAs may result in an increased risk of bleeding, including intracranial hemorrhage. Currently available data fail to provide compelling evidence that newer PAs offer significantly greater efficacy and safety than well-established agents like urokinase when used to treat peripheral vascular thrombosis.
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