Erschienen in:
01.08.2014 | Original Paper
Microvascular obstruction in patients with non-ST-elevation myocardial infarction: a contrast-enhanced cardiac magnetic resonance study
verfasst von:
Elena Guerra, Martin Hadamitzky, Gjin Ndrepepa, Corinna Bauer, Tareq Ibrahim, Ilka Ott, Karl-Ludwig Laugwitz, Heribert Schunkert, Adnan Kastrati
Erschienen in:
The International Journal of Cardiovascular Imaging
|
Ausgabe 6/2014
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Abstract
The aim of the study was to assess the frequency and predictive factors of microvascular obstruction (MVO) in patients with non-ST-segment elevation myocardial infarction (NSTEMI). This study included 190 consecutive patients with NSTEMI who underwent percutaneous coronary intervention (PCI) within 24 h after admission and cardiac magnetic resonance (CMR) imaging, 4.1 days after angiography. MVO was defined using the CMR criteria. MVO was detected 26 of 190 patients (13.8 %). Patients with MVO had higher peak high-sensitivity troponin T, creatine-kinase and creatine kinase-myocardial band levels and higher proportions of those with baseline thrombolysis in myocardial infarction (TIMI) flow grade 0–1, absence of collateral circulation, post-PCI TIMI flow grade <3, myocardial blush grade <3 and angiographic no-reflow than patients without MVO. Patients with MVO had larger initial area at risk [median (25th–75th percentiles), 23.9 % (17.4–33.9 %) vs. 16.1 % (7.8–27.7 %), P = 0.018] and infarct size [11.4 % (6.6–19.2 %) vs. 1.4 % (0–4.7 %) of the left ventricle, P < 0.001] than patients without MVO. In multivariable analysis, the culprit lesion localization in the circumflex coronary artery [adjusted odds ratio (OR) 13.71, 95 % confidence interval 2.91–64.58, P < 0.001] and the infarct size [adjusted OR 3.37 (1.80–6.29), P < 0.001, for each 5 % of the left ventricle] were independently associated with the increased risk for MVO. In patients with NSTEMI undergoing early PCI, the MVO defined by CMR imaging was present in 13.8 % of the patients. The localization of culprit lesion in the circumflex coronary artery and larger infarct size were independently associated with the increased risk for MVO.