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Updated: Aug 17, 2026

Ferric Chloride-induced Murine Thrombosis Models
Published on: September 5, 2016
Antiplatelet therapy from clinical trials to clinical practice
Shereif H Rezkalla1, Michele Benz
1Department of Cardiology, Marshfield Clinic, Marshfield, Wisconsin 54449, USA. rekalla.shereif@marshfieldclinic.org
Insights
Antiplatelet therapy, including aspirin and clopidogrel, is crucial for managing acute ischemic syndromes caused by blood clots. Aspirin is recommended for most patients, with clopidogrel offering additional benefits in severe cases.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Acute ischemic syndromes frequently result from platelet-rich clots at sites of coronary artery disease.
- Antiplatelet therapy is a fundamental treatment strategy for these conditions.
Purpose of the Study:
- To outline the current recommendations for antiplatelet therapy in acute ischemic syndromes.
- To detail the roles of aspirin, clopidogrel, and glycoprotein IIb/IIIa inhibitors.
Main Methods:
- Review of current clinical guidelines and evidence for antiplatelet agents.
- Analysis of therapeutic benefits and indications for aspirin, clopidogrel, and glycoprotein IIb/IIIa inhibitors.
Main Results:
- Aspirin (160-325 mg daily) is recommended for nearly all patients.
- Adding clopidogrel (75 mg daily) to aspirin benefits patients with severe disease for up to one year.
- Intravenous glycoprotein IIb/IIIa inhibitors are beneficial with coronary intervention, not medical therapy alone.
Conclusions:
- Aspirin is a foundational antiplatelet agent for acute ischemic syndromes.
- Combination therapy with aspirin and clopidogrel offers enhanced protection in specific patient groups.
- The role of glycoprotein IIb/IIIa inhibitors is limited to interventional procedures.
Abstract:
A platelet-rich clot at the site of severe coronary stenosis, plaque erosion, or a recent plaque rupture is the common etiology of acute ischemic syndromes. Thus, antiplatelet therapy is the cornerstone in the management of these conditions. Aspirin in a dose ranging from 160 to 325 mg once daily should be administered to virtually all patients. In patients with severe disease, particularly those who have no acute angiography, clopidogrel (Plavix, Bristol-Myers Squibb/Sanofi Pharmaceuticals) in a dose of 75 mg once daily should add to the benefit of aspirin for up to a year after the event. Clopidogrel also is an alternative to aspirin where a true aspirin allergy exists. Intravenous platelet glycoprotein IIb/IIIa receptor inhibitors demonstrated a robust benefit when used in conjunction with coronary intervention and thus far have no role in medical therapy alone. Oral platelet glycoprotein IIb/IIIa receptor inhibitors are of no clinical value.
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