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Updated: Aug 19, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
Overview of patency as an end point of thrombolytic therapy
1Department of Medicine, University of Utah, Salt Lake City.
Insights
Maintaining coronary blood flow (patency) is key for treating acute myocardial infarction with thrombolytic therapy. Early patency achievement with agents like alteplase, especially with heparin, shows promise but requires further assessment beyond 90 minutes.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Thrombolytic therapy aims to restore coronary blood flow in acute myocardial infarction.
- Coronary patency is crucial for therapeutic benefit, with spontaneous rates around 33%.
Purpose of the Study:
- To evaluate the effectiveness of different thrombolytic agents in achieving and maintaining coronary patency.
- To compare early and late patency rates among thrombolytic therapies.
Main Methods:
- Review of studies assessing coronary patency after thrombolytic administration.
- Comparison of patency rates at 90 minutes and >24 hours post-therapy.
- Evaluation of the impact of concurrent heparin use.
Main Results:
- Alteplase and anistreplase show higher early patency than streptokinase.
- Concurrent heparin improves alteplase patency rates, preventing decline.
- No significant difference in patency exists among agents when assessed >24 hours.
Conclusions:
- Early patency assessment at 90 minutes may not fully differentiate thrombolytic efficacy.
- The overall reperfusion profile is a better indicator of therapeutic benefit.
- Advanced intravenous thrombolytic regimens are being developed for rapid and sustained coronary patency.
Abstract:
Underlying the use of thrombolytic therapy is the hypothesis that reestablishment and maintenance of coronary blood flow (coronary patency) are the primary mechanisms of therapeutic benefit in patients with acute myocardial infarction. Early achievement and maintenance of adequate coronary blood flow (patency) in the infarct-related artery are the primary goals of thrombolytic therapy. One third of patients may achieve spontaneous patency within a few days following acute myocardial infarction. When antithrombotic therapy (i.e., heparin) is administered, this rate increases to greater than 50%, but patency is achieved only gradually and mortality reductions comparable to thrombolytic therapy are not achieved. After administration of a thrombolytic agent, early (90-minute) patency rates are greater with alteplase or anistreplase than with streptokinase. However, patency rates for alteplase decline by 10-30% if intravenous heparin is not given concurrently. When patency is assessed greater than 24 hours following thrombolytic therapy, no significant difference exists among the agents. A single angiographic observation of the artery at 90 minutes, although useful, may be inadequate to distinguish among the beneficial clinical effects of different thrombolytic regimens. The overall reperfusion or patency profile is probably a better basis for assessing relative benefits. Intravenous thrombolytic regimens that are increasingly effective in rapidly achieving and maintaining coronary patency are now available and in further development.
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