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Mr extended work space 2

Manufactured by Philips
Sourced in Netherlands

The Philips MR Extended Work Space 2.6 is a magnetic resonance imaging (MRI) system component that provides an extended patient-accessible space within the imaging system. It allows for increased patient comfort and accommodates a wider range of patient sizes and conditions during MRI procedures. The core function of this product is to enhance the physical workspace of the MRI system without elaborating on its intended use.

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9 protocols using mr extended work space 2

1

Cardiac MRI Imaging Protocol for Volumetric Analysis

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Cardiac magnetic resonance (CMR) examinations were conducted with a Philips 1.5-Testa Achieva whole-body scanner (Philips Healthcare) equipped with a 16-element phased-array cardiac coil [39 (link)]. The imaging protocol always included a standard segmented cine steady-state free-precession (SSFP) sequence to provide high-quality anatomical references. The imaging parameters for the SSFP sequence were as follows: 280 × 280 mm field of view, 8 mm slice thickness with no gap, 3 ms repetition time, 1.50 ms echo time, 60° flip angle, 30 cardiac phases, 1.7 × 1.7 mm voxel size, and a single excitation. CMR images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare, Best, The Netherlands) by two observers experienced in CMR analysis and blinded concerning time-point allocation and patient identification.
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2

Cardiac Perfusion Imaging with Doxorubicin

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All CMR exams were performed before doxorubicin administration, using a 3 Tesla Philips Achieva Tx whole-body scanner (Philips Healthcare, Best, the Netherlands) equipped with a 32-element phased-array cardiac coil. Imaging studies were performed under the same anaesthesia used for doxorubicin administration. Cardiac quantitative perfusion was estimated using dynamic acquisition with dual-saturation recovery (TS=20, 80 ms) during gadolinium-based contrast administration (0.1 mmol/kg), as previously described.12 (link) After perfusion map generation, regions of interest were analysed in the infused and remote areas using dedicated software (MR Extended Work Space 2.6, Philips Healthcare).
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3

Cardiac MRI Imaging Protocol for Infarct Assessment

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CMR examinations were conducted with a Philips 3-Tesla Achieva Tx whole body scanner (Philips Healthcare) equipped with a 32-element phased-array cardiac coil. The imaging protocol included an steady-state free-precession sequence to provide high-quality anatomic references, and assessment of LV mass and wall thickness; a T2W-STIR sequence to assess the extent of edema and IMH; a T2-gradient-spin-echo mapping sequence10 (link),16 (link); and a T1-weighted inversion recovery turbo field echo sequence to assess IS and MVO. CMR images were similarly analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare; and QMassMR 7.6, Medis) by 2 observers experienced in CMR analysis and blinded to group allocation.
Detailed information about MDCT and CMR imaging protocol and parameters, and imaging analysis, can be found in the online-only Data Supplement Methods.
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4

MDCT Imaging for Myocardial Infarction

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All MDCT studies were performed on a 64-slice CT scanner (Brilliance CT 64, Philips Healthcare) after intravenous administration of 60 mL of 400 mgI/mL iomeprol (Iomeron 400, Bracco Imaging).21 (link) MDCT images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare). MaR and remote areas were visually identified based on contrast enhancement differences, manually delineated, and expressed as a percentage of LV area.
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5

Quantifying Myocardial Ischemia Area in Pigs

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After coronary artery occlusion, pigs were moved to the MDCT suite. In all cases, pigs were back in the catheterization laboratory within 15 min of ischemia onset. Arterial phase MDCT studies were performed in a 64-slice CT scanner (Brilliance CT 64; Philips Healthcare, Cleveland, OH) after intravenous administration of iodinated contrast medium. MDCT images were evaluated with dedicated software (MR Extended Work Space 2.6; Philips Healthcare, Best, The Netherlands) by two observers blinded to ischemia duration protocol and treatment allocation. Short-axis orientation images were obtained from volumetric CT images by multiplanar reconstruction. The region negative for contrast enhancement corresponds to the territory supplied by the occluded vessel (AAR) and was identified based on contrast enhancement differences vs the remote myocardium. The AAR was manually delineated and expressed as a percentage of LV area.
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6

Cardiac T2 Relaxation Mapping

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CMR images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare, The Netherlands). T2-maps were automatically generated on the acquisition scanner by fitting the SI of all echo times to a monoexponential decay curve at each pixel with a maximum likelihood expectation maximization algorithm. T2 relaxation maps were quantitatively analyzed by placing a wide transmural region of interest (ROI) at the ischemic and remote areas of the corresponding slice in all studies. The masking was defined in the first echo image to improve the contrast between the cardiac muscle and the cavity. Higher T2 values in this interface can be found due to slow flow artifact; therefore, ROIs were carefully placed avoiding those areas from the analysis to minimize contamination on the reported T2 values. Hypointense areas suggestive of microvascular obstruction or hemorrhage were included in the ROI for T2 quantification purposes.
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7

Comprehensive Cardiac MRI Protocol for Myocardial Infarction Assessment

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All CMR studies were performed with patients under anesthesia, maintained by continuous intravenous infusion of midazolam, in a 3‐T Achieva Tx whole‐body scanner (Philips Healthcare, Best, The Netherlands) equipped with a 32‐element phased‐array cardiac coil. The protocol included (1) a standard segmented cine steady‐state free‐precession sequence to provide high‐quality anatomical references and to determine left ventricular end‐diastolic wall thickness (EDWT), left ventricular end‐diastolic volume (LVEDV), left ventricular end‐systolic volume (LVESV), and left ventricular ejection fraction (LVEF); (2) a late gadolinium‐enhanced sequence to assess infarct size; and (3) a dynamic acquisition with dual‐saturation technique during gadolinium‐based contrast administration to determine absolute myocardial perfusion.23, 24 CMR images were processed with a commercial analysis software (QMass MR 7.5 Medis, Leiden, the Netherlands and MR Extended Work Space 2.6, Philips Healthcare) and were analyzed by 2 independent blinded experienced investigators as previously described.23, 24, 25
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8

MDCT Imaging Protocol for Myocardial Area at Risk

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Arterial phase MDCT studies were performed on a 64-slice computed tomographic-scanner (Brilliance CT 64; Philips Healthcare, Cleveland, OH) after intravenous administration of iodinated contrast media.19 (link) MDCT images were analyzed using dedicated software (MR Extended Work Space 2.6; Philips Healthcare, Best, The Netherlands) by 2 observers blinded to group allocation. Short axes orientation were obtained from volumetric computed tomographic images by multiplanar reconstruction using equivalent anatomic coordinates used for T2-weighted short-tau triple inversion-recovery (T2W-STIR) planning acquisition. MaR and remote areas were visually identified based on contrast enhancement differences, manually delineated, and expressed as a percentage of left ventricle (LV) area.
Detailed information about imaging MDCT protocol and analysis is shown in the Online Data Supplement.
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9

Cardiac MRI Imaging Protocol for Clinical Research

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Cardiac magnetic resonance (CMR) examinations were conducted with a Philips 1.5-Testa Achieva whole-body scanner (Philips Healthcare) equipped with a 16-element phased-array cardiac coil and fully installed and managed by the Cardiology Department at the University Hospital of Salamanca (Barreiro-Perez et al. 2018 (link)). The imaging protocol always included a standard segmented cine steady-state free-precession (SSFP) sequence to provide high-quality anatomical references. The imaging parameters for the SSFP sequence were: 280 × 280 mm field of view, 8 mm slice thickness with no gap, 3 ms repetition time, 1.50 ms echo time, 60° flip angle, 30 cardiac phases, 1.7 × 1.7 mm voxel size and a single excitation. CMR images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare, Netherlands) by two observers experienced in CMR analysis and blinded concerning time-point allocation and patient identification.
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