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Achieva quasar dual

Manufactured by Philips

The Achieva Quasar Dual is a magnetic resonance imaging (MRI) system developed by Philips. It is designed to provide high-quality imaging of the human body. The system utilizes dual-channel radiofrequency (RF) technology to acquire data, enabling efficient and reliable image acquisition.

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12 protocols using achieva quasar dual

1

MRI-Based Carotid Plaque Vulnerability Assessment

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Three days before CAS, magnetic resonance (MR) examinations, including 3D-T1 gradient echo (GRE) carotid plaque imaging, were performed on all patients after diagnostic angiography. No ischemic events, such as transient ischemic attack or stroke, occurred between pre-procedural MR examinations and CAS. MR imaging was performed using a 3.0-T MR imaging system (Achieva Quasar Dual, Philips Medical Systems, Best, The Netherlands).
3D-T1 GRE carotid plaque imaging was performed in the coronal plane with null blood conditions (effective inversion time, 600 ms; TR/TE, 5.0/2.3 ms) and the water excitation technique to suppress fat signals. Other scanning parameters were as follows: FOV, 260 mm; voxel size, 0.68×0.68×1.00 mm; flip angle, 13°; partitions, 56 partitions covering 70 mm around the carotid bifurcation; and data acquisition time, 4 min 2 s.
MR images were reviewed by a neurointerventionalist blinded to the clinical data. Regions of interest were drawn manually on a workstation around the carotid plaque and the adjacent sternocleidomastoid muscle (SCM) with coronal 3D-T1TFE images that detected the largest carotid plaque segment. The signal intensity ratio (SIR) was defined as the signal intensity of the carotid plaque divided by the signal intensity of SCM, being >1.8 for vulnerable plaques and ≤1.8 for stable plaques, as previously described [14] (link).
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2

Functional MRI Acquisition Protocol

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Scanning was conducted using a 3 T MRI scanner (Achieva Quasar Dual, Philips). Blood oxygenation level-dependent (BOLD) T2*-weighted MR signals were measured using a gradient echo-planar imaging sequence. Forty 3-mm-thick contiguous slices covering the entire brain were acquired (repetition time [TR] = 2,500 ms, echo time = 30 ms, flip angle = 85°, field of view = 192 mm2, and scan matrix = 64 × 64). Excluding the first two “dummy” volumes to stabilize the T1-saturation effect, 388 volumes were acquired in each fMRI session.
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3

Cardiac MRI Imaging Protocol

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All studies were performed on a clinical 3 T CMR scanner (Achieva Quasar Dual; Philips Healthcare, Best, The Netherlands) equipped with a dedicated cardiac software package and a 32-element cardiac phased-array coil (16 posterior elements, 16 anterior elements); a 4-lead vector electrocardiogram (ECG) was used for cardiac gating. In all patients, double-angulated scout images were obtained to plan cardiac axis views, and retrospective ECG gated cine imaging was performed using a segmented balanced steady state free precession (bSSFP) sequence in continuous short-axis views, spanning the entire left ventricle (LV) from base to apex. Ten minutes after the injection of 0.2 mmol/kg gadopentetate dimeglumine (Magnevist; Bayer Healthcare, Berline, Germany), we acquired three-dimensional (3D) IR sequences that spanned the LV from the base to the apex, selecting the myocardium null TI values from the TI scout images. The imaging parameters were: repetition time/echo time, 3.4/1.6 ms; TI, 300–400 ms; flip angle, 15°; field-of-view, 350 mm × 350 mm; pixel size, 1.6 mm × 2.3 mm; slice thickness, 10.0 mm; sensitivity encoding (SENSE) factor, 2.4.
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4

Functional Neuroimaging Protocol for Brain Analysis

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Thirty-three gradient-echo images (echo time  = 25 ms, flip angle  = 78°, slice thickness  = 3 mm, slice gap  = 1 mm, field of view  = 200 mm, matrix size  = 64×64) covering the whole brain were acquired at a repetition time of 2000 ms using an echo planar sequence and a 3-T magnetic resonance scanner (Achieva Quasar Dual, Philips Medical Systems; Best, The Netherlands).
For each subject, data were acquired in two scanning sessions. Excluding the first two “dummy” volumes for stabilization of the T1-saturation effect, 404 volumes were acquired in each fMRI session. The following preprocessing procedures were performed using Statistical Parametric Mapping (SPM8) software (Wellcome Department of Imaging Neuroscience; London, UK) implemented in MATLAB R2009b (MathWorks; Natick, MA, USA) for whole brain analysis: correction for head motion, adjustment of acquisition timing across slices, spatial normalization using the MNI template, and smoothing using a Gaussian kernel with a full width at a half-maximum of 5 mm.
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5

fMRI Protocol for Brain Imaging

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For fMRI measurements, gradient echo T2*-weighted echo-planar images with blood oxygenation level-dependent (BOLD) contrast were obtained using 3.0 Tesla MRI scanner (Achieva Quasar Dual, Philips, The Netherlands) with the participants in a supine position. The participant was instructed not to move their head and body, except for the right index finger, left index finger, right foot, or mouth throughout the experiment.
Whole-brain volumes were collected in 40 axial slices (repetition time (TR) = 2500 ms; echo time (TE) = 25 ms; flip angle (FA) = 81°, field of view (FOV) = 192 mm, matrix size = 64 × 64; slice thickness = 3 mm; interslice gap = 1 mm; voxel size = 3 × 3 × 4 mm). The initial 3 scans of each participant were dummy scans to equilibrate the state of magnetization and were discarded from the time-series data. Thus, we collected 455 or 475 scans during the fMRI measurement. In addition, high resolution T1-weighed structural MR images (TR = shortest; TE = shortest; FOV = 240 mm; matrix size = 240 × 240; 162 sagittal slices of 1-mm thickness) were also acquired.
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6

Whole-brain fMRI Time-course Acquisition

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A time-course series of 442 volumes was acquired using T2*-weighted gradient-echo echo-planar imaging (EPI) sequences and a 3-Tesla MR scanner (Achieva Quasar Dual, Philips Medical Systems, Best, The Netherlands). Each volume consisted of 41 transaxial slices covering the entire cerebrum (echo time = 30 ms; flip angle = 85°; slice thickness = 2.5 mm; gap = 0.5 mm; field of view = 192 mm; 64 × 64 matrix; voxel dimension = 3.0 × 3.0 mm) and a repetition time of 2500 ms.
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7

Functional Brain Imaging Acquisition Protocol

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Scanning was conducted using a 3 T MRI scanner (Achieva Quasar Dual, Philips). Blood oxygenation leveldependent T2*-weighted MR signals were measured using a gradient echo-planar imaging (EPI) sequence. Forty-three 2.5-mm-thick contiguous slices (0.5 mm gap) covering the entire brain were acquired (repetition time [TR] = 2,500 ms, echo time [TE] = 30 ms, flip angle = 85°, field of view [FOV] = 192 mm 2 , and scan matrix = 64 × 64). Excluding the first two "dummy" volumes to stabilize the T1-saturation effect, 295 volumes were acquired in each fMRI session.
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8

Functional MRI Neuroimaging Protocol

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All MRI data were collected using a 3-T MRI scanner (Achieva Quasar Dual, Philips Medical Systems, Best, Netherlands). To obtain functional images of blood oxygenation level-dependent T2*-weighted MR signals, 40 transaxial images covering the entire brain were obtained using a gradient echo-planar imaging (EPI) sequence [repetition time (TR) = 2,500 ms; echo time (TE) = 30 ms; slide thickness = 3 mm; gap = 0 mm; flip angle (FA) = 85°; field of view (FOV) = 192 mm2; and scan matrix = 64 × 64]. High-resolution T1-weighted structural MR images were also obtained from each participant.
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9

Multimodal MRI Acquisition and Analysis Protocol

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All MRI data were acquired using a 3T MRI scanner (Achieva Quasar Dual; Philips Medical Systems, Best, The Netherlands). We performed fluid-attenuated inversion recovery (FLAIR) imaging. A magnetization-prepared rapid acquisition gradient-echo (MPRAGE) sequence was collected as a high resolution, three-dimensional structural image. Diffusion-weighted imaging (DWI) with 32 non-collinear directions was acquired using a single-shot spin-echo echo-planar imaging sequence. Echo-planar images were acquired using a b value of 1,000 s/mm2 along 32 isotropic diffusion gradients in the anterior-posterior phase-encoding direction. Each DWI acquisition was completed with a b = 0 image. We also acquired standard and reverse phase-encoded blipped images with no diffusion weighting (blip-up and blip-down) to correct for magnetic susceptibility-induced distortions related to the echo-planar image acquisitions. Within ~1 year of shunting, the second MRI scan was performed on each participant. The acquisition parameters of FLAIR, MPRAGE, and DWI are presented in Table 2. Periventricular hyperintensity and deep white matter hyperintensity evaluations using the Fazekas scale (36 (link)) and Evans' index based on axial FLAIR imaging were conducted by an experienced neuroradiologist (JK).
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10

Functional MRI Acquisition Protocol

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Functional neuroimaging data were acquired with a 3.0 Tesla MRI scanner (Philips Achieva Quasar Dual, Philips Medical Systems, Best, The Netherlands) using a gradient echo planar image (EPI) sequence ([TE] = 30 ms, field of view [FOV] = 192 mm, flip angle [FA] = 70°, slice thickness = 5 mm, slice gap = 0 mm). Thirty-two axial slices spanning the entire brain were obtained every 2 s. After the attainment of functional imaging, T1-weighted anatomical images were also acquired from each participant.
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