During the past decades, advances in percutaneous coronary intervention and antithrombotic therapy have improved the prognosis of patients with ST-segment-elevation myocardial infarction (STEMI).1 However, in a substantial number of STEMI patients, myocardial perfusion remains impaired despite successful recanalization of the infarct-related epicardial coronary artery, and this scenario has been shown to increase the risk of future cardiovascular events.2 Therefore, coronary microcirculation has been identified as an important determinant of outcome after STEMI.2 The potential causes and mechanisms of coronary microvascular dysfunction include pre-existing transient or permanent alterations, individual susceptibility, ischemic injury, reperfusion injury, and distal embolization of thrombotic material.2,3 The no-reflow phenomenon after percutaneous coronary intervention is the angiographic correlate for microvascular dysfunction and relies on reduced antegrade blood flow (thrombolysis in myocardial infarction flow grade and thrombolysis in myocardial infarction frame count) and impaired penetration of dye into the myocardium (myocardial blush grade and thrombolysis in myocardial infarction myocardial perfusion grade). Cardiac magnetic resonance (CMR) imaging enables the direct visualization and quantification of microvascular obstruction (MVO), which reflects myocardial damage resulting from microvascular dysfunction.
See Article by Durante et alIn this issue of Circulation: Cardiovascular Imaging, Durante et al 4 report results from a prospective single-center study on the diagnostic and prognostic utility of angiographic and CMR parameters of microvascular dysfunction in STEMI. The authors directly compared angiographic noreflow (defined as thrombolysis in myocardial infarction flow grade ≤2 and myocardial blush grade <2) with the assessment of structural myocardial changes in terms of MVO on CMR imaging in 88 STEMI patients. The occurrence of major adverse cardiovascular events consisting of death, nonfatal re-infarction, unplanned revascularization, admission for heart failure, and cardioverter-defibrillator implantation was evaluated at a median of 464 days after infarction. Although the study is obviously limited by its small sample size and the high exclusion rate (only 35% of the screened STEMI patients were enrolled), the authors report some interesting observations that are both reassuring and expand our current knowledge.First, the incidence of MVO on CMR imaging (67%) was higher than that of angiographic no-reflow (36%). 4 Variable incidences of microvascular dysfunction with different diagnostic tools have been reported and range from 10% using angiographic methods to 60% using imaging modalities (CMR and contrast echocardiography).2 This discrepancy might, in part, be explained by the fundamentally different concepts of assessing functional alterations of coronary blood flow and structural changes at the tissue level. Furthermore, microvascular dysfunction is thought to be a dynamic process involvin...