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Updated: Aug 20, 2026

A Hydrogel Construct and Fibrin-based Glue Approach to Deliver Therapeutics in a Murine Myocardial Infarction Model.
Published on: June 14, 2015
A marriage of enhancement: fibrinolysis and conjunctive therapy
Robert C Welsh1, Paul W Armstrong
1The University of Alberta, Department of Medicine, Division of Cardiology, Edmonton, AB T6G 2H7 Canada.
Insights
Pharmacologic reperfusion using fibrinolytics and adjunctive therapies like anticoagulants and antiplatelets improves outcomes for ST-elevation myocardial infarction patients. Novel agents are crucial for comprehensive treatment and enhanced survival.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute ST-segment elevation myocardial infarction (STEMI) requires prompt reperfusion.
- Fibrinolytic monotherapy alone is insufficient for optimal patient outcomes.
Purpose of the Study:
- To review pharmacologic reperfusion strategies for STEMI.
- To discuss the role of various antithrombotic and antiplatelet agents.
Main Methods:
- Review of current literature on pharmacologic reperfusion in STEMI.
- Discussion of unfractionated heparin, enoxaparin, direct thrombin inhibitors, aspirin, and glycoprotein IIb/IIIa inhibitors.
Main Results:
- Combination therapy with fibrinolytics and antiplatelet/antithrombotic agents is necessary.
- Glycoprotein IIb/IIIa inhibitors show promise but have risks in the elderly.
- Facilitated percutaneous coronary intervention is a potential future strategy.
Conclusions:
- Optimal STEMI reperfusion requires a multifaceted pharmacologic approach.
- Future research should focus on novel antiplatelet, antithrombin, and anti-inflammatory agents.
Abstract:
Pharmacologic reperfusion of patients with acute ST segment elevation myocardial infarction is designed to achieve prompt high-quality reperfusion, prevent recurrent ischemia and reinfarction, maintain long-term patency, and to enhance patient survival and quality of life. Because monotherapy with fibrinolytics is by itself unable to achieve all of these objectives, antithrombotic, anti-platelet, and other novel agents are required. We discuss herein the role of unfractionated and enoxaparin, the potential added value of direct thrombin inhibitors, and the importance of aspirin. Despite the promise of glycoprotein IIb/IIIa inhibitors, risks associated with intracranial hemorrhage in the elderly have led to restraint in their application to broad populations. Facilitation of urgent percutaneous coronary intervention with combination reduced-dose fibrinolytic and glycoprotein IIb/IIIa inhibitors remains a promising potential future path. The future is likely to emphasize greater application of the already effective therapies at our disposal and the development of novel anti-platelet and anti-thrombin agents as well as those directed toward inflammation.
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