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Oral Antiplatelet Therapy in Coronary Disease
Pedro Falcão Gonçalves1, Luiz Menezes Falcão
11Pneumology Department (Serviço de Pneumologia), Centro Hospitalar Lisboa Norte (CHLN), Lisboa, Portugal; and 2Faculty of Medicine, University of Lisbon, Lisbon, Portugal.
Insights
Newer antiplatelet agents like prasugrel and ticagrelor offer faster, more consistent inhibition of platelet activation for managing ischemic heart disease. These drugs target the P2Y12 receptor, improving treatment options for coronary artery disease.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Ischemic heart disease is a leading global cause of mortality.
- Platelet activation and aggregation are critical targets for therapeutic intervention.
- Current antiplatelet therapies include cyclooxygenase inhibitors and thienopyridines.
Purpose of the Study:
- To review recent literature and guidelines on oral antiplatelet agents for coronary disease management.
- To compare the efficacy and mechanisms of novel antiplatelet agents.
Main Methods:
- Literature review of recent scientific publications.
- Analysis of clinical guidelines and pharmacological data.
- Comparison of antiplatelet agent classes and specific drugs.
Main Results:
- Prasugrel, a novel thienopyridine, provides irreversible P2Y12 receptor inhibition with rapid onset.
- Ticagrelor, a cyclopentyl-triazolo-pyrimidine, offers reversible P2Y12 inhibition with fast and consistent action.
- Both prasugrel and ticagrelor represent advancements over older antiplatelet agents.
Conclusions:
- Novel oral antiplatelet agents, including prasugrel and ticagrelor, offer improved therapeutic profiles for ischemic heart disease.
- These agents provide faster and more consistent platelet inhibition compared to previous treatments.
- Understanding their mechanisms and guidelines is crucial for effective coronary disease management.
Abstract:
Ischemic heart disease is the major isolated cause of death worldwide, responsible for 7,249,000 deaths in 2008, 12.7% of deaths from any causes. The inhibition of platelet activation and aggregation is an important therapeutic target. Cyclooxygenase inhibitors and thienopyridines are currently the 2 most used pharmacological classes, but novel antiplatelet agents have currently an important role. The most recent thienopyridine, prasugrel, allows an irreversible inhibition of the P2Y12 platelet receptor associated to a faster and more consistent onset of action rather the previous antiplatelet agents of the same class. Cyclopentyl-triazolo-pyrimidines, a newer pharmacological class from which ticagrelor is an example, also act at the P2Y12 platelet receptor, and like prasugrel, ticagrelor inhibits platelet aggregation in a fast and consistent manner, however, in a reversible way. This article aims to conduct a review on the literature about the most recent information and guidelines on oral antiplatelet agents available for the management of coronary disease.
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