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Updated: Aug 15, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
[Advances in intracoronary thrombolysis treatment]
1Department of Internal Medicine, Kyoto University Hospital.
Insights
Intracoronary thrombolysis improves left ventricular function in myocardial infarction patients within 4 hours. Therapy up to 10 hours can preserve function, but percutaneous transluminal coronary angioplasty (PTCA) after thrombolysis is debated.
Area of Science:
- Cardiology
- Interventional Cardiology
Background:
- Acute myocardial infarction (AMI) requires timely reperfusion to preserve left ventricular function.
- Intracoronary thrombolysis is a primary treatment for AMI, aiming to restore blood flow.
- The role of adjunctive percutaneous transluminal coronary angioplasty (PTCA) after thrombolysis remains a subject of investigation.
Purpose of the Study:
- To evaluate the efficacy of intracoronary thrombolysis in patients with anterior myocardial infarction.
- To assess the impact of reperfusion timing on left ventricular function and infarct size.
- To investigate the benefits and risks of adding PTCA to thrombolytic therapy during the acute phase of myocardial infarction.
Main Methods:
- Retrospective analysis of 30 patients with anterior myocardial infarction treated with intracoronary thrombolysis.
- Assessment of left ventricular function and clinical outcomes based on reperfusion timing.
- Comparison of outcomes between thrombolytic therapy alone and combined thrombolysis with PTCA.
Main Results:
- Reperfusion within 4 hours significantly improved left ventricular function and clinical features.
- Intracoronary thrombolysis up to 10 hours post-onset was associated with preserved ventricular function.
- Early experiences suggested PTCA post-thrombolysis increased reinfarction risk, but improved techniques have reduced this tendency.
Conclusions:
- Early reperfusion, ideally within 4 hours, is crucial for optimal outcomes in anterior myocardial infarction.
- Intracoronary thrombolysis is beneficial up to 10 hours post-onset for preserving ventricular function.
- The addition of PTCA to acute thrombolytic therapy requires careful consideration due to evolving techniques and potential risks.
Abstract:
Based on the results of intracoronary thrombolysis in 30 patients with initial onset of anterior myocardial infarction, we concluded that: (1) left ventricular function and clinical features are markedly improved when reperfusion is accomplished within four hours after coronary artery occlusion; and (2) intracoronary thrombolysis therapy should be considered possible up to 10 hours after the onset of myocardial infarction to prevent expansion of infarct sizes and to preserve ventricular functions. Not infrequently, there is a significant stenosis at the site of initial occlusion after thrombolytic therapy, which results in an immediate reocclusion. Consequently, percutaneous transluminal coronary angioplasty (PTCA) is now widely performed after thrombolytic treatment to achieve more definite revascularization. Our early experiences showed that PTCA following thrombolytic treatment has an increased potential for reinfarction rather than added benefits for left ventricular functions. More recently, however, since our PTCA technique has been improved so as to achieve sufficient dilatation of the stenosed coronary artery, there has been less tendency to immediate reinfarction after the procedure for acute myocardial infarction. Whether PTCA should be added to thrombolytic therapy during the acute phase of myocardial infarction is controversial. The alternative is to wait until it can be performed on an elective basis. It is obvious that early revascularization is essential for preserving left ventricular functions after acute myocardial infarction. For this reason, thrombolytic agents such as tissue plasminogen activator and plasminogen proactivator, which can be administered intravenously, are being intensively sought using molecular biological techniques. The ideal thrombolytic agents should have more fibrin-specific properties with longer half-lives than currently-available substances. However, so far none of these novel agents, have been studied in patients.
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