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Ingenia 3.0t scanner

Manufactured by Philips
Sourced in Netherlands

The Ingenia 3.0T scanner is a magnetic resonance imaging (MRI) system developed by Philips. It is designed to provide high-quality, high-resolution images of the body. The Ingenia 3.0T scanner operates at a magnetic field strength of 3 Tesla, which enables it to capture detailed anatomical information. The system is capable of performing a variety of MRI examinations.

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21 protocols using ingenia 3.0t scanner

1

MRI Examination of Laryngeal Anatomy

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MRI examination was performed using a Philips Ingenia 3.0T scanner (Philips Healthcare, Best, The Netherlands) with dedicated head–neck 20-channel parallel imaging array coils. The patients were imaged in the supine position and asked to breathe quietly and refrain from swallowing and coughing during the scanning. Axial images were captured parallel to the plane of the true vocal cords; coronal images were obtained perpendicular to this plane. The MRI protocol employed is specified in Table 1.
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2

Resting-state fMRI Acquisition Protocol

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An Ingenia 3.0 T scanner (Philips, Amsterdam, The Netherlands) was used to collect all rs-fMRI data. Scanning was conducted while patients remained awake and still with their eyes closed using the following settings: repetition time/echo time (TR/TE) 2,000/30 ms; 36 slices; 90° flip angle; 220 mm × 220 mm field of view; 3 mm slice thickness; and 1 mm pitch (34 (link)).
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3

Comprehensive MRI Brain Imaging Protocol

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Because all animals were clinical patients, anesthetic protocols were selected on a case-by-case basis by clinicians of the anesthesiology service. Animals in general anesthesia were scanned in the same 3.0 Tesla MR System (Philips Ingenia 3.0 T scanner, Philips AG Healthcare, Zurich Switzerland) and images of the brain were acquired from the olfactory lobes to at least the second cervical vertebrae. All patients were scanned in dorsal recumbency.
The standard brain protocol includes, additionally to the diffusion-weighted imaging (DWI) sequence, at least T2-weighted (T2W), FLAIR, and T1-weighted (T1W) pre- and post-contrast and susceptibility-weighted sequences [T2 FFE (from 2015 until July 2017) and SWIp sequence (from August 2017) for canine patients, and T2 FFE for all feline patients]. The protocols for canine and feline patients are reported in Table 1. Contrast medium was injected manually, always after the DW sequence, in all patients (gadoteric acid, DOTAREM® Guerbet GmbH, 0.2 mL/kg, IV), followed by saline solution (0.9% NaCl, 5 mL, IV).
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4

Resting-state fMRI Data Acquisition

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The resting-state fMRI data were collected using a Philips Ingenia 3.0T scanner at the First Hospital of Jilin University. During this process, each participant was required to avoid head movement and close their eyes without thinking or falling asleep. It took 8 min for each scan of the 240 functional volumes to acquire the fMRI data. The specific parameters were as follows: repetition time (TR) = 2000 ms; echo time (TE) = 30 ms; flip angle (FA) = 90°; field-of-view (FOV), 224 × 224 × 138 mm3; matrix size, 64 × 63 mm2; slice thickness = 3.5 mm, and 33 slices. All original image files were available for subsequent analysis.
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5

Resting-state fMRI Imaging Protocol

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Scanning was performed using an Ingenia 3.0 T scanner (Philips, Amsterdam, Netherlands) with an 8-channel phase-array head coil at the Shanghai Public Health Clinical Center. For the resting-state scan, subjects were instructed to stay awake and to remain as still as possible while keeping their eyes closed. Resting-state fMRI images were acquired via an echo-planar imaging sequence (echo time = 25 ms, repetition time = 2,000 ms, flip angle = 75°, field of view = 224 × 224 mm, axial slices = 34, slice thickness = 4 mm, and voxel size = 1.0 × 1.0 × 1.0 mm, 200 time points). T1-weighted structural images were obtained on a sagittal orientation employing a magnetization-prepared rapid gradient-echo sequence (echo time = 3.8 ms, repetition time = 1,900 ms, flip angle = 8°, field of view = 240 × 240 mm, 170 slices per slab, voxel size = 1.0 × 1.0 × 1.0 mm, and matrix = 256 × 256).
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6

Multimodal MRI Acquisition Protocol

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All experiments were performed on a Philips Ingenia 3.0T scanner (Philips, Eindhoven, Netherlands), equipped with a 32-channel head coil. All the images were collected through a same MRI machine to keep homogeneity of images. Head motion was minimized using foam padding, and scanner noise were reduced using a pair of earplugs. Resting-state functional imaging was obtained using a gradient-echo echo-planar imaging (GRE-EPI) sequence, and the imaging parameters were as follows: repetition time (TR) = 2000 ms, flip angle (FA) = 90°, echo time (TE) = 30 ms, matrix = 64 × 64, thickness = 4.0 mm, voxel size = 3 × 3 × 3 mm, field of view = 192 × 192 mm, number of slices = 35, and gap = 0 mm. The scan process totally continued for 8 min and 7 s, and subjects received an instruction to keep still during the whole procedure. The three-dimensional T1-weighted sagittal imaging were acquired by turbo fast echo sequence: TR = 9.8 ms, FA = 8°, TE = 4.6 ms, matrix = 256 × 256, thickness = 1.0 mm, voxel size = 1 × 1 × 1 mm, field of view = 256 × 256 mm, number of slices = 192, and gap = 0 mm. The three-dimensional FLAIR sagittal imaging was acquired by the following sequence: TR = 4,500 ms, FA = 90°, TE = 344 ms, matrix = 272 × 272, thickness = 1.0 mm, number of slices = 200, and gap = 0 mm.
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7

Cervical Spine MRI Acquisition Protocol

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Magnetic resonance images were acquired with a Philips Ingenia 3.0 T scanner (Philips Health Care, Best, the Netherlands) using the built in phased-array posterior coil, a 32-channel head coil and an anterior flexible coil placed adjacent to the head coil. The participants were imaged in the supine, headfirst position. A 3D gradient-echo Dixon sequence was used with out-of-phase and in-phase echo times of 3.66 ms and 7.24 ms respectively. The echo times were chosen to enable the production of high-resolution images. The repetition time, TR, was 10 ms and the flip angle was 10° with a total acquisition time of 9.07 minutes. The images covered cervical segmental levels C2-C7 and were angled so that the in-plane images were parallel to each disc space and perpendicular to the long axis of the cervical musculature. The acquired image resolution was 0.75×0.75×0.75 mm3. Phase sensitive reconstruction was used to acquire fat and water separated image [34 , 35 ].
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8

Lumbar MRI Classification for Spinal Disorders

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In this study, lumbar MR Images and clinical diagnosis reports were collected from the Medical Imaging Department of Xi’an Number 3 Hospital, which is a large-scale grade 3A general hospital in Xi’an, China. The sagittal and axial T2-weighted lumbar MR images of 500 patients were acquired by using a Philips Ingenia 3.0T scanner and exported in the Digital Imaging and Communications in Medicine (DICOM) format. The main diagnosis was based on axial images, as they display the morphology of IVDs more clearly than other images. For each subject, midsagittal images were used to locate IVDs in axial images. A total of 3555 axial images were used in this study. These images were labeled as normal disk, disk bulge, and disk herniation according to diagnosis reports and rechecked by an experienced radiologist, as shown in Table 1. Examples of midsagittal lumbar images and axial images of normal disks, disk bulge, and disk herniation are shown in Figure 1.
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9

Cervical Spinal Cord DTI Protocol

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All MRI data were acquired on a Philips Ingenia 3.0T scanner (Philips, Best, the Netherlands) with a 16‐channel head–neck coil. For each patient, MRI scans were performed three times: at the preoperative stage, and at the 3 and 6 months follow‐up stages. The single‐shot echo‐planar‐imaging‐based sequence was used to acquire the axial diffusion‐weighted images with three b values (b = 0, 1000, and 2000 s/mm2) and 32 diffusion directions. The reduced field of view (FOV) technique, outer volume suppression, was used to reduce the image distortion along the phase‐encoding direction. The imaging parameters were: FOV = 160 × 60 mm2, in‐plane resolution = 1.5 × 1.5 mm2, SENSE factor = 2, partial Fourier factor = 0.75, and TE/TR = 77/4500 ms. Seventeen slices were acquired with 4‐mm thickness and a 2‐mm gap to cover the vertebral levels from C2 to C7, with the central slice located between C4 and C5. The total scan time for the DTI sequence was 5 min. In addition, conventional MRI images including sagittal T1‐, T2‐weighted, and axial T2‐weighted images were obtained for structural imaging.
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10

Resting-State fMRI Acquisition Protocol

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An Ingenia 3.0 T scanner (Philips, Amsterdam, Netherlands) equipped with a standard head coil was used to perform rs-fMRI scanning for all study participants. Scanning was conducted while participants remained still while lying down with their heads fixed in place with a belt. Foam padding and earplugs were used to mitigate scanner-related noise and head movements. Participants were directed to remain awake and not think about anything specific. rs-fMRI scans were performed with the following settings: repetition time = 2,000 ms, echo time = 25 ms, 36 axial slices, slice thickness = 3 mm, gap = 1 mm, 90° flip angle, field of view = 220 mm × 220 mm. The duration of rs-fMRI scanning for each participant was 8 min, with 240 volumes being obtained per participant.
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