Sixty-four-MSCT in the characterization of porcine acute and subacute myocardial infarction: Determination of transmurality in comparison to magnetic resonance imaging and histopathology

• Published in: European journal of radiology 2007-05, Vol.62 (2), p.235-246
• Main Authors: Brodoefel, H, Klumpp, B, Reimann, A, Fenchel, M, Heuschmid, M, Miller, S, Schroeder, S, Claussen, C, Scheule, A.M, Kopp, A.F
• Format: Article
• Language: English
• Subjects: Analysis of Variance; Animals; Biological and medical sciences; Cardiology. Vascular system; Coloring Agents; Contrast Media; Coronary heart disease; Disease Models, Animal; Gadolinium DTPA; Heart; Heart Ventricles - diagnostic imaging; Heart Ventricles - pathology; Image Enhancement; Magnetic Resonance Imaging; Medical sciences; MRI; MSCT; Myocardial Infarction - diagnostic imaging; Myocardial Infarction - pathology; Myocardial viability; Myocarditis. Cardiomyopathies; Observer Variation; Porcine model; Radiology; Reproducibility of Results; Research Design; Sensitivity and Specificity; Swine; Tetrazolium Salts; Tomography, X-Ray Computed; Transmural extent
• ISSN: 0720-048X; 1872-7727
• DOI: 10.1016/j.ejrad.2006.11.031

Abstract Objective The aim of this study was to assess the accuracy of MSCT in characterizing myocardial infarction (MI) and, thereby, determine the extent of early perfusion defect (ED), microvascular obstruction (MO) and transmural depth of late enhancement (LE) in comparison to MRI and histology. Materials and methods Seven pigs were studied with MSCT (Somatom Sensation 64) and MRI (Magnetom Sonata) a median 1 and 21 days following temporary occlusion of a diagonal branch and creation of small reperfused infarction. For depiction of ED, CT images were acquired in the early arterial phase and following 35 s; LE and MO were evaluated on images obtained at 3, 5, 10 and 15 min. Thereby, a bolus/low-flow contrast injection protocol was used. Triphenyltetrazolium-chloride (TTC) stain and histology were obtained. Volumes of enhancement patterns were assessed as percentage of the ventricle and compared by Bland–Altman analysis. Segmental co-localization and graded transmurality was evaluated with weighted-kappa-test. Results Close spatial agreement was observed for MRI–MO and MSCT–MO (bias = 0.55; CI = −1.49 to 2.60 at 5 min MSCT), TTC and MSCT–LE (bias = −1.28; CI = −3.76 to 1.19) or MRI–LE and MSCT–LE (bias = −0.79; CI = −4.19 to 2.60). There was good segmental co-localization for MO (weighted kappa = 0.93) and high agreement for transmural extent of TTC, MRI–LE and MSCT–LE (weighted kappa = 0.84 TTC versus MSCT; 0.86 MRI versus MSCT). Arterial and 35 s ED significantly underestimated infarct size and showed poor segmental or transmural agreement (weighted kappa = 0.33; 0.44). Conclusions MSCT late-scans not only reliably depict size of MO and LE in acute or subacute infarct phases but, moreover, allow for accurate determination of LE transmurality.