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Updated: Aug 7, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
High-dose, brief intravenous streptokinase early in acute myocardial infarction
Insights
High-dose, short-duration intravenous streptokinase effectively dissolves coronary clots in early myocardial infarction, restoring blood flow without significant bleeding. This approach offers a promising alternative for treating heart attacks.
Area of Science:
- Cardiology
- Interventional Cardiology
- Thrombolytic Therapy
Background:
- Myocardial infarction (MI) is typically caused by acute coronary thrombus formation.
- Intracoronary thrombolysis shows promise but faces challenges in application.
- Intravenous thrombolysis offers potential for wider use if effective and safe.
Purpose of the Study:
- To evaluate the efficacy and safety of high-dose, brief-duration intravenous streptokinase for early reperfusion in acute myocardial infarction.
- To determine if intravenous streptokinase can lyse coronary clots and restore blood flow without causing significant bleeding.
Main Methods:
- Systemic intravenous infusion of high-dose streptokinase (850,000 IU) within 6 hours of symptom onset.
- Angiographic assessment to confirm coronary clot lysis and reperfusion.
- Monitoring for bleeding complications and assessment of left ventricular function.
Main Results:
- Coronary clot lysis and reperfusion were achieved in 6 of 13 patients within 1 hour of infusion.
- Previous studies reported reperfusion in 11/21 and 24/39 patients with similar regimens.
- No serious bleeding complications were observed across studies; improved left ventricular function noted in reperfused patients.
Conclusions:
- Brief-duration, high-dose intravenous streptokinase can rapidly achieve intracoronary clot lysis and coronary reperfusion in early myocardial infarction.
- This method appears safe, with a low incidence of serious bleeding.
- Intravenous streptokinase represents a viable early treatment strategy for acute myocardial infarction.
Abstract:
An acute thrombus at the proximal border of a high-grade atherosclerotic obstruction is the usual cause of myocardial infarction. Although intracoronary thrombolysis is potentially an exciting new therapy for reducing the extent of myocardial infarction by lysing coronary clot, a number of major difficulties limit its widespread application. It is a complex procedure requiring intracoronary visualization and infusion within a few hours of onset of symptoms. Since intravenous streptokinase could be widely applied if effective, we and others have wondered whether high-dose, brief-duration intravenous streptokinase infusion given early in myocardial infarction would lyse coronary clots without bleeding. To date we have treated 13 patients within 6 hours of onset of symptoms and with ECG and angiographic evidence of typical myocardial infarction caused by coronary clot. Clot lysis and angiographically proved coronary reperfusion were achieved in 6 patients within 1 hour of starting a systemic intravenous infusion of 850,000 IU of streptokinase. Schroeder et al., in Berlin, West Germany, achieved angiographically proved coronary reperfusion in 11 of 21 patients with acute myocardial infarction following a 30-minute intravenous streptokinase infusion of 500,000 IU. Neuhaus et al., in Göttinen, West Germany, achieved angiographically proved coronary reperfusion in 24 of 39 similar patients within 48 minutes by intravenous infusion of 1,700,000 IU of streptokinase. In these three studies, no serious bleeding occured; left ventricular function was improved in patients who achieved coronary reperfusion. We conclude that rapid intracoronary clot lysis and coronary reperfusion can be achieved early in myocardial infarction by brief-duration systemic intravenous infusion of high-dose streptokinase without a high incidence of serious bleeding.
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