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Qmass MR is a software suite for quantitative cardiovascular magnetic resonance (CMR) image analysis. It provides tools for the analysis and evaluation of CMR images, enabling the measurement and assessment of various cardiac parameters.

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4 protocols using qmass mr

1

Cardiac MRI Volumetric Analysis

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MRI studies were performed using a 1.5-Tesla MRI scanner (Philips Medical Systems, Best, the Netherlands) with 5-element cardiac synergy coil and vector electrocardiographic gating as previously described. 12 (link) To determine LV end-systolic volumes and LV end-diastolic volumes and to calculate LV ejection fractions, previously validated software (QMass MR; Medis Medical Imaging Systems, Leiden, the Netherlands) was used. Scans were analyzed by an observer blinded to all clinical data.
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2

Cardiac MRI Assessment of Aortic Valve and Aortic Root

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Images were analysed with commercial software (Qmass MR, Medis Medical Imaging Systems, Leiden, the Netherlands) by an experienced, observer-blinded to the patients’ profile (KMJ). LV volumes, ejection fraction, and compacted mass were calculated as previously described [12 ]. Published sex-specific normal values were used to assess the normalization of LV parameters [13 (link)]. Three-chamber and LV outflow tract cine images were used for aortic annulus assessment. The average diameter of the annulus was calculated from minimal and maximal annulus diameters. Anatomical aortic valve area (AVA) planimetry was performed at the systolic frame (largest aortic valve opening) after careful confirmation of the correct imaging plane. Maximum cross-sectional measurements of the aortic root, STJ, and ascending aorta were performed. From phase-contrast images, forward and backward flow through the aortic valve was measured. Regurgitant volume and regurgitant fraction were calculated. In order to minimize phase offset errors background correction was applied with the region of interest in the stationary tissue (pectoralis muscle).
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3

Comprehensive Cardiac MRI Protocol

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Patient scanning was performed with a 3.0-T or a 1.5-T system (Tim Trio and Aera, Siemens, Erlangen, Germany). Detailed imaging information was reported previously[9 (link),10 (link)]. All patients underwent standard cine imaging for acquisition of left and right ventricular mass and function, along with LGE imaging in matching slice locations. Patients were further categorized if the left ventricular end-diastolic volume index (LVEDVi) was enlarged in comparison to reference values[18 ], and LVEF was ≤50%. LGE presence was quantified visually and the extent of enhancement was quantified by using the full width half maximum signal intensity (FWHM) threshold cut-off and expressed as a percent of the LV myocardium[19 (link)]. From 2007, T2w inversion recovery images were included into the protocol and myocardial oedema was evaluated by assessing the ratio of the signal intensity in the LV myocardium compared to the skeletal muscle (musculus pectoralis major or minor). Since 2009, patients also underwent acquisition of T1 mapping and ECV calculations. Image analysis was performed with MASS v15 and QMASS MR (Medis Medical Imaging Systems, Leiden, the Netherlands).
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4

Magnetic Resonance Imaging of Left Ventricular Non-Compaction

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All CMR examinations were performed on a 1.5T clinical scanner (Signa HDxt, GE Healthcare, Milwaukee, WI) with standard acquisition methods to acquire cine and delayed enhancement images. Images were analyzed with commercial software (Qmass MR, Medis Medical Imaging Systems, Leiden, the Netherlands) by an experienced observer blinded to the patients' profile. The 17-segment model of LV segmentation was used26 (link) and the presence of any degree of trabeculation/non-compaction was assessed in every LV segment. A segment was considered as non-compacted if a distinct two-layered appearance of trabeculated and compacted myocardium could be visually identified. For the segment with the most pronounced trabeculations, the maximal ratio of non-compacted to compacted myocardium (NC/C) was calculated. According to generally accepted CMR criteria proposed by Petersen et al.,13 (link) NC/C ratio greater than 2.3:1 was considered diagnostic for LVNC. Subjects that failed to meet these criteria but were otherwise suspected of having LVNC were labeled as having LVHT. Details regarding imaging protocol and data analysis are provided in the Supplementary Appendix.
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