Key result
GP IIb/IIIa inhibitors improve prognosis in STEMI but carry bleeding risks, and their indications have been reduced by the routine use of clopidogrel and bivalirudin.
Why the study?
What is the risk/benefit profile of GP IIb/IIIa inhibitors in STEMI patients undergoing revascularization?
What is the risk/benefit profile of GP IIb/IIIa inhibitors in STEMI patients undergoing revascularization?
This review evaluates the risk/benefit profile of GP IIb/IIIa inhibitors in STEMI patients undergoing revascularization in the context of newer antithrombotic therapies.
May support narrower GP IIb/IIIa use in STEMI; leaves open optimal selection criteria with current P2Y12 inhibitors.
Glycoprotein (GP) IIb receptor plays a central role on platelets activation and its blockage has been a matter of interest since the beginning of percutaneous revascularization. After first promising trials, GP IIb inhibitors (GPI) have been widely used in cath labs for about a decade, significantly improving prognosis for patients with STSegment Elevation Myocardial Infarction (STEMI). However, their utilization isn't exempt from risks, mainly in form of bleeding disorders, which can negatively affect patients' outcome. Moreover, routinary administration of thyenopiridines like clopidogrel and the introduction of new anticoagulants like bivalirudin significantly reduced indications for GPI. In this review, a risk/benefit evaluation GP IIb inhibitors is presented and their indications for STEMI patients addressed to revascularization are discussed according to recent advances reported in literature.
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Musumeci et al. (2012) conducted a review in ST-Segment Elevation Myocardial Infarction (STEMI). Glycoprotein (GP) IIb/IIIa inhibitors was evaluated. GP IIb/IIIa inhibitors improve prognosis in STEMI but carry bleeding risks, and their indications have been reduced by the routine use of clopidogrel and bivalirudin.
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