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Updated: Aug 10, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
Combination therapy for acute myocardial infarction: glycoprotein IIb/IIIa inhibitors plus thrombolysis
1Cardiovascular Division, Brigham and Women's Hospital, Boston, MA 02115, USA.
Insights
Combining glycoprotein IIb/IIIa receptor inhibitors with reduced-dose thrombolytic therapy shows promise for improving early artery patency in acute myocardial infarction (MI) patients without increasing bleeding risk.
Area of Science:
- Cardiology
- Pharmacology
- Emergency Medicine
Background:
- Thrombolytic therapy is crucial for acute ST-segment elevation myocardial infarction (MI).
- Newer thrombolytic agents have not improved early reperfusion rates.
- Aspirin is an effective adjunctive agent in acute MI management.
Purpose of the Study:
- To investigate the efficacy of combining platelet glycoprotein (GP) IIb/IIIa receptor inhibitors with thrombolytic agents.
- To determine if this combination enhances platelet inhibition and clinical outcomes in acute MI.
- To evaluate improved angiographic and clinical efficacy compared to standard thrombolytic therapy.
Main Methods:
- Review of emerging experimental and clinical data.
- Analysis of findings from the Thrombolysis in Myocardial Infarction (TIMI)-14 trial.
- Focus on combining GP IIb/IIIa receptor inhibition with reduced-dose thrombolytic therapy.
Main Results:
- Combining GP IIb/IIIa receptor inhibition with reduced-dose thrombolytic therapy improves early infarct-related artery patency.
- This combination strategy does not appear to increase bleeding risk.
- Emerging data suggest enhanced platelet inhibition and clinical efficacy.
Conclusions:
- There is a strong clinical and physiologic rationale for combining GP IIb/IIIa receptor inhibitors with reduced-dose fibrinolytic agents in acute MI.
- Clinical investigation is focusing on this combined approach for acute ST-segment elevation MI.
- This strategy holds potential for improving treatment efficacy in acute myocardial infarction.
Abstract:
Although thrombolytic therapy has been a major advance in the treatment of acute ST-segment elevation myocardial infarction (MI), new thrombolytic agents have been unable to improve early reperfusion. Because aspirin has been shown to be a very effective adjunctive agent in patients with acute MI, it has been hypothesized that the use of platelet glycoprotein (GP) IIb/IIIa receptor inhibitors combined with thrombolytic agents would lead to more effective platelet inhibition and improved angiographic and clinical efficacy. Emerging experimental and clinical data, including the Thrombolysis in Myocardial Infarction (TIMI)-14 trial, suggest that combining GP IIb/IIIa receptor inhibition with reduced-dose thrombolytic therapy improves early infarct-related artery patency without increasing bleeding risk. Thus, given the strong clinical and physiologic rationale, clinical investigation in patients with acute ST-segment elevation MI is currently focused on combining GP IIb/IIIa receptor inhibitors with reduced-dose fibrinolytic agents in acute MI.
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