Why the study?
Does facilitated percutaneous coronary intervention improve outcomes in patients with acute myocardial infarction?
Does facilitated percutaneous coronary intervention improve outcomes in patients with acute myocardial infarction?
Facilitated PCI with combination pharmacological therapy improves initial infarct-related artery patency but increases bleeding risk, highlighting the need for ongoing trials to establish its clinical utility.
Bleeding risk warrants caution with facilitated PCI; leaves open net clinical benefit pending randomized trials.
Facilitated percutaneous coronary intervention (PCI) refers to a strategy of immediate PCI following the administration of pharmacological therapies in acute myocardial infarction. It has evolved primarily from the time delays (due to geography or logistics) in getting acute myocardial infarction patients to the catheterization laboratory and the associated irreversible loss of myocardial muscle that occurs as door-to-balloon time increases. Facilitated PCI provides an opportunity to start treating many of these patients before they reach the catheterization laboratory and provides an ability to open the infarct-related artery before PCI, which is associated with better outcomes for AMI patients. Pharmacological strategies before PCI include: thrombolytic therapy, glycoprotein IIb/IIIa inhibitor alone, or a combination of thrombolytic therapy plus glycoprotein IIb/IIIa inhibitor. Initial results of angiographic studies show better patency with the latter strategy but at the expense of higher bleeding event rates. Ongoing trials are evaluating different combinations of thrombolytic and glycoprotein IIb/IIIa inhibitor therapy.
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Kelly et al. (2004) studied this question.
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