Hematology· Topic 6.4 Platelet disorders· 6.4.2

Antiplatelet agents

Antiplatelet agents block platelet activation and aggregation to prevent arterial thrombosis. Aspirin irreversibly inhibits cyclooxygenase-1, and P2Y12 inhibitors such as clopidogrel, ticagrelor, and prasugrel block adenosine diphosphate-driven platelet activation. Aspirin 81 mg daily anchors secondary prevention, and dual antiplatelet therapy with aspirin plus a P2Y12 inhibitor is first-line after acute coronary syndrome or coronary stenting.

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What this article covers

  • Overview

    What they are: antiplatelet agents block platelet activation, adhesion, or aggregation to prevent arterial thrombus, distinct from anticoagulants, which act on the coagulation cascade instead.

  • Epidemiology

    Population exposure: aspirin and P2Y12 inhibitors are among the most prescribed cardiovascular drugs.

  • Risk factors

    Bleeding risk: advanced age, female sex, anemia, low body weight, chronic kidney disease, diabetes, and concomitant glucocorticoid, NSAID, or anticoagulant use.

  • Pathophysiology

    Arterial hemostasis: collagen exposure triggers platelet adhesion via glycoprotein Ib binding von Willebrand factor, then activation with release of adenosine diphosphate (ADP) and thromboxane A2…

  • Clinical features

    Intended effect: prolonged bleeding time, not routinely measured since platelet reactivity assays have not improved outcomes when used to guide therapy.

  • Differential diagnosis

    Aspirin versus clopidogrel monotherapy: aspirin is preferred first-line, but clopidogrel replaces it when there is true aspirin intolerance or allergy.

  • Diagnosis

    Indication established by: starting an antiplatelet agent is confirmed by a defined atherothrombotic indication, acute coronary syndrome, coronary stenting, ischemic stroke or high-risk TIA, or…

  • Management

    First-line, aspirin: 162 to 325 mg PO load in acute coronary syndrome, then 81 mg PO daily indefinitely; low-dose aspirin (75 to 162 mg daily) matches high-dose aspirin for preventing myocardial infarction with less bleeding.

  • Complications

    Gastrointestinal bleeding: the most common serious complication, more frequent with DAPT than monotherapy and with concomitant NSAID or anticoagulant use.

  • Prognosis

    Secondary prevention benefit: aspirin lowers myocardial infarction and cardiovascular death risk in established coronary artery disease.

  • Prevention

    Cap ticagrelor's co-administered aspirin at 81 mg (75 to 100 mg) daily: higher aspirin doses reduce ticagrelor's efficacy, a boxed warning.

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