Treatment
Antiplatelet Therapy (Aspirin, Clopidogrel)
Antiplatelet medications reduce the ability of platelets to aggregate and form clots in arteries, which is the mechanism behind most heart attacks and ischemic strokes. The two most commonly used agents are aspirin (a COX-1 inhibitor) and the P2Y12 inhibitors — clopidogrel, ticagrelor, and prasugrel. Single antiplatelet therapy is standard for many patients with established cardiovascular disease, while dual antiplatelet therapy (aspirin plus a P2Y12 inhibitor) is required after stent placement or acute coronary syndrome for a defined period. Dr. Kedan tailors agent selection and duration to your specific risk profile, prior procedures, and bleeding considerations.
What This Treatment Approach Includes
- Indication-specific decision: primary prevention vs secondary prevention vs post-stent
- Selection between aspirin, clopidogrel, ticagrelor, and prasugrel based on scenario
- Duration planning for dual antiplatelet therapy after stenting or acute coronary syndrome
- Bleeding risk assessment and gastrointestinal protection when warranted
- Periprocedural management — when to hold, when to bridge, when to resume
- Coordination with anticoagulation when both are required ("triple therapy" decisions)
- Surveillance for bleeding and reevaluation as risk profile changes
How It Works
Aspirin irreversibly inhibits cyclooxygenase-1 (COX-1) in platelets, blocking thromboxane A2 production and reducing platelet aggregation for the lifespan of the platelet (about 7 to 10 days). P2Y12 inhibitors block the adenosine diphosphate receptor on the platelet surface, preventing the conformational change required for stable platelet activation. Combining the two classes (DAPT) provides additive inhibition during the period when arterial healing or stent endothelialization is most vulnerable to thrombosis.
Who This Is For
- Established coronary artery disease, prior heart attack, or prior coronary intervention
- Ischemic stroke or transient ischemic attack of atherothrombotic origin
- Peripheral artery disease with symptoms or prior revascularization
- After coronary stenting — required dual antiplatelet therapy for a defined period
- Acute coronary syndrome treated medically or with PCI
- Selected high-risk primary prevention scenarios after careful risk-benefit discussion
- Carotid disease following revascularization
Monitoring and Follow-Up
Antiplatelet therapy does not require routine laboratory monitoring, but ongoing assessment focuses on bleeding signs, drug interactions, and changes in risk profile that might shift the duration plan. After stenting or acute coronary syndrome, the duration of dual therapy is decided in advance and revisited at scheduled intervals — sometimes shortened for bleeding risk, sometimes extended for ongoing ischemic risk. Direct access to Dr. Kedan allows real-time decisions when surgery, dental work, or new bleeding arises.
How Cardiolucent Manages This
Antiplatelet duration after stenting and acute coronary syndrome is one of the most frequent points of confusion when care is fragmented between cardiology, primary care, and proceduralists. Dr. Kedan personally tracks the indication, the start date, the planned duration, and the post-DAPT plan — and coordinates with your surgeon when procedures arise mid-course. Extended visits also allow shared decision-making about bleeding risk and protective strategies when both antiplatelet and anticoagulant therapy are required.
Common Questions
Frequently Asked Questions
Why do I need an antiplatelet medication?
Is aspirin still recommended for primary prevention?
What is dual antiplatelet therapy (DAPT) and how long does it last?
What is the difference between clopidogrel, ticagrelor, and prasugrel?
What about combining antiplatelet and anticoagulant therapy?
What bleeding signs should I take seriously?
What about surgery or dental work?
Do these drugs interact with anything?
Can I stop antiplatelet therapy if I feel fine?
How do I start antiplatelet therapy with Dr. Kedan?
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