Key words: acute myocardial infarction, fibrinolysis, primary percutaneous coronary intervention Myocardial reperfusion treatment for ST-elevation acute myocardial infarction (AMI) has made great strides since the 1980s when, for the first time, its effectiveness was shown without any doubt. While the issue of pharmacologic versus mechanical reperfusion dominated the 1990s, more fundamental issues of reperfusion have emerged as the framework on which the effectiveness of any reperfusion treatment should be judged. First and foremost is the issue of complete optimal myocardial reperfusion. Its achievement appears to be surprisingly low even after the most modern reperfusion treatment, and clearly needs to be improved. 1 Thrombolysis alone reaches a plateau of 57% of normal epicardial flow (Thrombolysis in Myocardial Infarction [TIMI 3 flow]). It has been shown that of patients with TIMI 3 flow, 23% have no real myocardial perfusion; thus, patients with true myocardial reperfusion constitute 44% of the initial population. If we also count those patients with intermittent reperfusion and reocclusion, we end up with final complete, optimal myocardial reperfusion in only 25% of patients treated. Given the almost linear relationship of myocardial tissue flow with outcome, the great need for improving reperfusion therapy becomes apparent.The plateau in lowering mortality-slightly over 6% on the average in the fibrinolytic trials that have been reported so far-has been directly associated with the plateau achieved in TIMI 3 flow. The next logical step in improving the outcome of fibrinolytic therapy was an effort to improve the percentage of TIMI 3 flow by enhancing fibrinolytic therapy. 2 However, in the Global Utilization of Streptokinase and t-PA for Occluded coronary arteries-V (GUSTO V) and the Assessment of the Safety and Efficacy of a New Thrombolytic regimen-3 (ASSENT 3) trials, the combination of fibrinolytics with glycoprotein (GP) IIb/IIIa inhibitors did not lead to lower mortality. 3,4 Enhanced fibrinolysis still remains an open issue.Primary percutaneous coronary intervention (PCI) for AMI has evolved over the last 20 years in parallel to fibrinolysis. Today there are 23 randomized trials of primary PCI versus fibrinolytics, with a total of 7,739 patients enrolled.In the first-generation trials, plain balloon angioplasty was compared with fibrinolytics. In a recent meta-analysis of 11 such trials, primary percutaneous transluminal coronary angioplasty (PTCA) was better than fibrinolytics with regard to mortality (4.3 vs. 6.9%, p < 0.02), mortality/infarct recurrence (D/re-MI) (7.0 vs. 12.9%, p < 0.001), and intracranial hemorrhage (ICH) (0.07 vs. 1.08%, p < 0.001). The TIMI 3 flow achieved with primary PTCA was significantly higher than that achieved with fibrinolytics. These results held for 6 months after the acute event. 5 In the second phase, stents were introduced in an effort to decrease MI recurrence and restenosis post PTCA. In the first large stent-in AMI trial, the Stent Primary Angioplasty for My...