Why the study?
Do glycoprotein IIb/IIIa integrin receptor antagonists improve outcomes in patients with acute coronary syndromes and during percutaneous interventions?
Do glycoprotein IIb/IIIa integrin receptor antagonists improve outcomes in patients with acute coronary syndromes and during percutaneous interventions?
Intravenous glycoprotein IIb/IIIa inhibitors provide clinical benefit in acute coronary syndromes and PCI, particularly in high-risk patients, whereas oral formulations increase mortality.
Supports selective IV GP IIb/IIIa use in ACS/PCI; leaves open optimal agent choice amid evolving therapies.
The glycoprotein IIb/IIIa integrin receptor binds fibrinogen and is therefore a final common pathway responsible for platelet aggregation. One antibody (abciximab) and two synthetic compounds (tirofiban and eptifibatide) are clinically available to antagonize the function of this receptor. Several large-scale studies have documented the benefit of these compounds in acute coronary syndromes and during percutaneous interventions. Current data suggest that abciximab is the preferred drug in the catheterization laboratory, whereas the other compounds reduce risk for patients with unstable angina before coronary interventions are performed. The highest benefit is achieved in diabetic patients and in patients with elevated troponins. Adverse reactions are rare, and bleeding complications are minor when weight-adjusted heparin is given. Oral compounds have been associated with excess mortality, precluding their clinical use.
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Christian W. Hamm (2003) studied this question.
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