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. 2019 Sep 22;25:7115–7125. doi: 10.12659/MSM.915830

Table 1.

Classification of myocardial infarction [4].

Type 1: Spontaneous MI
Related to atherosclerotic plaque rupture, ulceration, fissuring, erosion, or dissection leading to intraluminal thrombus in one or more coronary arteries leading to ischemia and resultant myocyte necrosis
Type 2: MI secondary to oxygen supply and demand mismatch/ischemia imbalance
Ischemia imbalance leading to myocyte necrosis and is resultant from a condition other than CAD
Type 3: MI secondary to sudden cardiac death (biomarker values unavailable)
Cardiac death associated with symptoms and ECG findings suggestive of ischemia in the absence of cardiac biomarkers
Type 4a: MI secondary to percutaneous coronary intervention (PCI)
PCI-associated MI defined arbitrarily as an elevation in cTn >5×99th percentile of the upper limit of normal with normal baseline values or a rise of cTn values >20% of previously elevated baseline values that are stable or falling in association with the presence of at least one of the following: symptoms suggestive of cardiac ischemia, new ischemic ECG findings or new LBBB, angiographic loss of patency of a major coronary vessel or a side branch or persistent slow- or no-flow or embolization, or imaging demonstrating new loss of viable myocardium or new regional wall motion abnormality
Type 4b: MI secondary to stent thrombosis
MI associated with stent thrombosis as detected by coronary angiography or autopsy with a combination of myocardial ischemia and rise and/or fall of cardiac biomarkers with at least one value ≥99th percentile of the upper limit of normal
Type 5: MI secondary to coronary artery bypass grafting (CABG)
MI associated with CABG defined arbitrarily as an elevation in cardiac biomarker levels >10×99th percentile of the upper limit of normal in patients with normal baseline values in addition to at least one of the following: new pathological Q waves or new LBBB, new graft or new native coronary artery occlusion, or imaging demonstrating new loss of viable myocardium or new regional wall motion abnormality