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3.0 t mr scanner

Manufactured by Philips
Sourced in Netherlands

The 3.0 T MR scanner is a medical imaging device manufactured by Philips. It is designed to produce high-resolution magnetic resonance imaging (MRI) scans of the human body. The 3.0 T MR scanner utilizes a powerful 3 Tesla magnetic field to generate detailed images of the internal structures and tissues.

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24 protocols using 3.0 t mr scanner

1

Carotid and Brain MRI Protocol

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The patients who participated in the present study underwent carotid and brain MRI on 3.0T MR scanner (Achieva TX, Philips Healthcare, Best, The Netherlands) with 8-channel carotid coil. The carotid MRI protocol included three-dimensional time-of flight, T1-weighted, T2-weighted, and Magnetization Prepared Gradient Recalled Echo imaging sequences. The imaging parameters are detailed in Table 1. The localization of the carotid plaque imaging is centered to the bifurcation of the carotid artery index, which is defined as arteries responsible for the symptoms. A routine brain imaging protocol, including T1-weighted, fluid attenuated inversion recovery and diffusion weighted imaging sequences, was used to assess the cerebral infarct.
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2

Multimodal MRI and Genomic Analysis

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All patients underwent conventional MRI examination using a 3.0T MR scanner (Philips Medical Systems Nederland BV) equipped with an eight-channel head and neck coil. The conventional MRI sequences collected were: sagittal, coronal, and axial T2-weighted and T1-weighted images, fluid-attenuated inversion recovery sequence (FLAIR) images, diffusion-weighted images (DWI) and apparent diffusion coefficient (ADC) and T1-weighted enhanced images. All the results were confirmed by experienced imaging doctors in Shandong Provincial Hospital affiliated to Shandong University. A total of 71 patients underwent the gene detection technique, using amplification refractory mutation system-polymerase chain reaction (ARMS-PCR) and next-generation sequencing technology (NGS). Of those, 43 patients had gene mutations, including epidermal growth factor receptor (EGFR) gene mutations and anaplastic lymphoma kinase (ALK) gene mutations.
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3

Rectal MRI Imaging Protocol

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All rectal MRIs were performed using a 3.0T MR scanner (Philips Ingenia, the Netherlands) with the patient in the supine position. To reduce colonic motility, 20 mg of anisodamine was injected intramuscularly 30 min before the MRI scan. All patients underwent the standard rectal MRI protocol including sagittal, axial, oblique axial, and coronal T2WI and DWI. DWI images were obtained with two b-factors (0 and 1,000 s/mm2), a repetition time (TR) of 2,800 ms, an echo time (TE) of 70 ms, a field of view (FOV) of 340 mm× 340 mm, a matrix of 256 × 256, a thickness of 4.0 mm, and a gap of 1.0 mm. Apparent diffusion coefficient maps were generated automatically and included both b-values. High-resolution T2WI images were obtained using turbo spin-echo with a TR of 3,500 ms, a TE of 100 ms, a FOV of 180 mm× 180 mm, an echo train length of 24, a matrix of 288 × 256, a thickness of 3.0 mm, and a gap of 0.3 mm.
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4

Breast Cancer MRI Imaging Protocol

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All patients underwent MRI using a 3.0 T MR scanner (Philips Medical Systems, Achieva, Best, The Netherlands) in the prone position, using a four-channel breast array coil.
All MR images were acquired using the following sequences: an axial DWI sequence, a fat-suppressed T2-weighted sagittal sequence, and an axial T1-weighted sequence. Finally, an axial dynamic contrast-enhanced MRI (DCE-MRI) was performed with three-dimensional (3D) T1-weighted fast spoiled gradient-echo sequences before and after injection of a contrast agent (0.1 mmol/kg body weight Gd-DPTA, Bayer Healthcare, Magnevist, Germany). For DWI, images were acquired with a single shot spin-echo-planar sequence, using the following parameters: repetition time/echo time (TR/TE), 2,681/82 ms; field of view, 230×240 mm; matrix, 224×224; slice thickness, 3 mm; 40 slices with 0 mm gap; number of excitation (NEX), 3; b-values, 0 and 800 sec/mm2.
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5

Resting-State fMRI Imaging Protocol

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Resting-state scans, as part of a fixed imaging protocol, were acquired on a Philips 3.0-T MR-scanner at all scanning sites. During the RS-fMRI scan, participants were asked to keep their eyes closed, lie as still as possible and to stay awake. Duration of the RS-fMRI scan was 7.51 min. See appendix A, section A.2 for details regarding the scan parameters.
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6

Multimodal MRI for Intracranial and Carotid Arteries

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MR imaging was performed on a Philips 3.0T MR scanner (Achieva TX, Philips Healthcare, Best, the Netherlands) with a custom‐designed 36‐channel neurovascular coil.10 Joint MR vessel wall imaging for intracranial and extracranial carotid arteries was performed for all the patients. The MR imaging parameters were as follows: 3D MERGE: fast field echo (FFE), repeat time (TR)/echo time (TE) 9.2/4.3 msec, flip angle 6°, field of view (FOV) 4 × 16 × 25 cm3, and spatial resolution 0.8 × 0.8 × 0.8 mm3; T2‐VISTA: turbo spin echo, TR/TE 2500/278 msec, flip angle 90°, FOV 4 × 16 × 25 cm3, and spatial resolution 0.8 × 0.8 × 0.8 mm3; and Simultaneous Non‐contrast Angiography and intraPlaque hemorrhage (SNAP): FFE, TR/TE 9.9/4.8 msec, flip angle 11/5°, FOV 4 × 16 × 25 cm3, and spatial resolution 0.8 × 0.8 × 0.8 mm3. Specifically, the intracranial arteries were also imaged with 3D time‐of‐flight angiography with the following parameters: FFE, TR/TE 25/3.5 msec, FOV 4.5 × 20 × 20 cm3, and spatial resolution 0.7 × 0.7 × 1.4 mm3.
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7

Automated Structural Brain Imaging Analysis

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MR images were acquired using a 3.0-T MR scanner (Philips Healthcare, Eindhoven, Netherlands). T1-weighted anatomical MR images were obtained with a repetition time of 9.9 ms, an echo time of 4.6 ms, a flip angle of 8°, and a voxel size of 1.0×1.0×0.5 mm3. To obtain local cortical thickness measurements for each subject, all T1 volume scans were processed using the CIVET pipeline (version 2.1.0) developed at the Montreal Neurological Institute (MNI) for fully automated structural image analysis.22 (link) Cortical thickness was calculated as the Euclidean distance between the linked vertices of the inner and outer surfaces. We extracted the regional cortical thickness value using automated anatomical labeling parcellation23 (link) and calculated a composite value for the cingulate, frontal, parietal, temporal, and occipital cortices by averaging each constituent region. We calculated intracranial volume by measuring the total volume of the voxels within the brain mask using the FSL bet algorithm (FMRI software library package, http://www.fmrib.ox.ac.uk/fsl).24 (link) To measure hippocampal volume, we used an automated hippocampus segmentation method using a graph cut algorithm combined with atlas-based segmentation and morphological opening.
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8

Multimodal Imaging of Thoracic Vasculature

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Patient-specific raw CTV images were obtained using a 256-slice spiral CT scanner (Philips Medical Systems, Netherlands); the CTV data consisted of 231 slices acquired before ligation (512 × 512 pixels, 0.625 mm slice thickness) in Digital Imaging and Communications in Medicine format. Iodinated non-ionic contrast material was applied to display the lumens of the TS, SS, jugular vein, and large MEV on CTV images.
The patient underwent MRV and a 4D flow scan with a 3.0 T MR scanner (Philips, Ingenia, Netherlands). All visualization, assessment and interpretation of 4D flow data were performed using dedicated GT Flow 2.2.15 software (GyroTools, Switzerland).
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9

Stroke Patients MRI Protocols

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The structural MR images analysed in the present study were from scans carried out as part of a routine clinical investigation of the patients' strokes. All included patients underwent conventional MRI of the brain without contrast administration on a 1.5 T MR scanner (Philips Medical Systems, Best, The Netherlands) with the sequences sagittal T2‐weighted images (SE, TR/TE 4240/100 ms), axial fluid‐attenuated inversion recovery (FLAIR) (IR, TR/TE 11 000/140 ms), axial T2‐weighted fast field echo (FFE) (TR/TE 699/23 ms, flip angle 18°), DW imaging (b = 0 ms, b = 1000 ms, TR/TE 2751/83 ms, flip angle 90°, acquisition matrix 128, slice thickness 5 mm, slice distance 6 mm) or on a 3.0 T MR scanner (Philips Medical Systems) with the sequences sagittal T2‐weighted images (SE, TR/TE 3000/80 ms), axial FLAIR (TR/TE 12 000/140 ms), axial T2‐weighted FFE (TR/TE 504/16 ms), DW imaging (b = 0 ms, b = 1000 ms, TR/TE 2255/55 ms, flip angle 90°, acquisition matrix 140, slice thickness 5 mm, slice distance 6 mm).
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10

Whole Brain 3D T1-weighted MRI

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Anatomical whole brain scans were obtained using a 3.0T MR scanner (Philips Achieva). Isotropic structural 3D T1-weighted images were acquired using a sagittal fast field echo sequence (repetition time = 7.9 ms, echo time = 4.5 ms, flip angle = 8°, 1 mm × 1 mm × 1 mm voxels).
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