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A Microfluidic Flow Chamber Model for Platelet Transfusion and Hemostasis Measures Platelet Deposition and Fibrin Formation in Real-time
Published on: February 14, 2017
Blood coagulation changes during effective thrombolysis using urokinase and heparin
This study shows a new urokinase dosage regimen effectively treats deep vein thrombosis by activating the fibrinolytic system. The regimen proved safe and controllable, with no observed side effects.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Pharmacology
Background:
- Deep vein thrombosis (DVT) is a serious condition requiring effective anticoagulation and thrombolytic therapy.
- Urokinase is a thrombolytic agent used to dissolve blood clots.
- Optimizing urokinase dosage is crucial for balancing efficacy and safety.
Purpose of the Study:
- To evaluate the efficacy and safety of a novel urokinase dosage regimen for deep vein thrombosis.
- To assess the impact of this regimen on the blood coagulation and fibrinolytic enzyme system.
Main Methods:
- Ten patients with deep vein thrombosis received a specific urokinase dosage regimen (loading dose 250,000 IU, maintenance 2,000 IU/kg/h) combined with heparin.
- Coagulation and fibrinolytic parameters were analyzed, including euglobulin clot lysis time, FDP, fibrinogen, plasminogen, alpha 2-macroglobulin, and factor VIII:C.
Main Results:
- The urokinase regimen significantly activated the fibrinolytic system, evidenced by shortened euglobulin clot lysis time and increased FDP.
- Fibrinogen levels decreased to 50-100 mg/dl within 12-36 hours.
- Significant reductions were observed in plasminogen (63%), alpha 2-macroglobulin (32%), and factor VIII:C (42%).
- The observed decrease in fibrinogen correlated well with plasminogen reduction and shortened lysis time.
Conclusions:
- The studied urokinase dosage regimen is effective and controllable for treating deep vein thrombosis.
- Plasma fibrinogenolytic activity can serve as a reliable indicator for assessing urokinase therapy adequacy and guiding dose adjustments.
- The regimen demonstrated a favorable safety profile with no relevant side reactions.
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