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Signa excite hdxt

Manufactured by GE Healthcare
Sourced in United States

The Signa Excite HDxt is a magnetic resonance imaging (MRI) system designed and manufactured by GE Healthcare. It is a high-field MRI system that utilizes a superconducting magnet to generate a strong magnetic field for imaging the body's internal structures and functions.

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32 protocols using signa excite hdxt

1

3T MRI Protocols for Brain Imaging

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MRI was performed at both the University of Fukui and Osaka University. At the University of Fukui, a 3-T MR scanner (Discovery MR 750; General Electric Medical Systems) was used for high-resolution T1-weighted anatomical MRI (repetition time = 6.38 ms, echo time = 1.99 ms, flip angle = 11°, field of view = 256 × 256 mm2, 256 × 256 matrix size, 172 slices, voxel dimensions = 1.0 × 1.0 × 1.0 mm3). At Osaka University, two kinds of 3-T MR scanners (Discovery MR 750w and Signa Excite HDxt; General Electric Medical Systems) were used for high-resolution T1-weighted anatomical MRI (repetition time = 880 ms, echo time = 0.016 ms, flip angle = 5°, field of view = 256 × 256 mm2, 256 × 256 matrix size, 480 slices, voxel dimensions = 0.94 × 0.94 × 0.94 mm3; and repetition time = 10.084 ms, echo time = 3.04 ms, flip angle = 18°, field of view = 512 × 512 mm2, 512 × 512 matrix size, 248 slices, voxel dimensions = 0.43 × 0.43 × 0.43 mm3).
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2

Functional MRI of Handwriting Motor Task

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Seven out of 22 subjects, who executed the two experimental sessions of the Experiment 2, during the INSIDE session were also examined by means of an fMRI test. MRI examination was performed on a 1.5 T MR system (Signa Excite HDxt, General Electric Healthcare, Waukesha, WI, USA) and included the following series covering the whole brain: axial FLAIR sequence (slice thickness = 5 mm; TR = 9002 ms; TE = 97.5 ms; inversion time = 2250 ms; flip angle = 90°; FOV = 240 mm × 240 mm; matrix = 512 × 512) to exclude incidental findings in the enrolled subjects; axial T2-weighted sequence (slice thickness = 5 mm; TR = 6300 ms; TE = 123.7 ms; FOV = 260 mm × 260 mm; matrix = 256 × 256) used as structural reference for the fMRI acquisition; T2-weighted single-shot EPI sequences (32 slices; slice thickness = 4 mm; gap = 0.5 mm; TR = 3000 ms; TE = 40 ms; FOV = 260 mm × 260 mm; matrix = 64 × 64) for fMRI. Particularly, each fMRI run included 63 brain volumes; the first 3 volumes were discarded because of non-steady magnetization. Within each run the subject performed the handwriting motor task (i.e., active task) alternatively with a rest condition (i.e., control), according to a block designed paradigm consisting of 30-sec active task periods alternating with 30-s control periods (10 brain volumes per block).
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3

Manganese-enhanced MRI for cancer models

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The pre-clinical MR imaging protocol was developed for an experimental mouse-dedicated volume coil with a diameter of 55 mm (linear birdcage transmit/receive coil, Flick Engineering Solutions BV-General Electric-Baio G.) applied to a clinical 3T MR system (Signa EXCITE®HDxT, GE, Milwaukee, USA). The MR protocol applied to these new cancer animal model experiments was as previously described [15 (link)].
As previously established [15 (link)], the manganese chloride solution (Sigma Chemical Co., St. Louis, MO, USA) was prepared (5 mM MnCl2 solution in 0.9% NaCl) and 180 μl per mouse were manually injected in the tail vein (corresponding to a dose range between 7.4 mg/kg in a 24 g mouse and 8.5 mg/kg in a 21 g mouse; animal weights were within the mentioned range). MR imaging was performed before and immediately after manganese administration was completed at the following time points 10, 30, 60 and 90 minutes, for the orthotopic cancer animal models (breast or prostate) and at 10, 30, 60, 90 minutes until 3 hours, for the metastatic cancer animal models (breast or prostate), in order to study the dynamics of manganese uptake per each metastatic lesion.
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4

Magnetic Resonance Imaging and Spectroscopy of Liver

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Patients were imaged using a 3T MRI system (Signa EXCITE HDxt, GE Healthcare, Waukesha, WI) in the supine position with an eight-channel torso phased-array coil centered over the liver. A dielectric pad was placed between the coil and the abdomen. Each examination included single voxel MRS, and the following CSE-MRI acquisitions: MRI-M, Hi-SNR MRI-M, MRI-C, and Hi-SNR MRI-C. MRI methods assumed monoexponential R2* signal decay and applied a 6peak fat spectral model derived from human triglyceride composition [16 (link)]. A rectangular field of view was adjusted depending on body habitus and breath-hold capacity. The Hi-SNR methods obtained larger voxels by decreasing the matrix size, avoiding parallel imaging, and for MRI-C, by also decreasing the receiver bandwidth. Depending on the specific imaging parameters for any given patient, this resulted in an estimated SNR increase 2.0–2.4-fold for MRI-M and 3.13.5-fold for MRI-C. Previous studies have suggested that Hi-SNR methods may estimate PDFF with higher precision than standard methods, especially in the low PDFF range relevant to splenic measurements [15 ]. Acquisition parameters are summarized in Table 1 and Table 2.
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5

Liver MRI Protocol for Hepatic Assessment

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Subjects were scanned in the supine position using a 3T MR scanner (SIGNA Excite HDxt; GE Medical Systems; Milwaukee, WI) using an eight-channel torso phased-array surface coil centered over the liver, with a dielectric pad placed over the abdomen. Two-dimensional noncontrast axial liver magnitude-based MRI was performed using a spoiled gradient-recalled-echo sequence. Low flip angle (108) was used with repetition times (TRs) of 100–300 msec to minimize T1 weighting.11 (link),15 (link)–17 (link) Six fractional-echo magnitude images were obtained at nominally in-phase (IP) and out-phase (OP) echo times (~1.15, 2.3, 3.45, 4.6, 5.75, and 6.9 msec) in a single 12–24-second breath-hold. Other imaging parameters were as follows: slice thickness 8–10 mm; 14–26 slices (default, 23) covering most, but preferably all of the liver; slice gap 0 mm; receiver bandwidth ±142 kHz; base matrix range from 160 to 288 frequency encoding steps, and from 128 to 224 phase encoding steps; and rectangular field of view adjusted to body habitus.
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6

Multimodal MRI Techniques for Brain Tumor

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All MRI examinations were performed within 7 days before surgery. The precontrast sequence consisted of axial T1-weighted image (T1WI), T2-weighted image (T2WI), DWI, and fluid-attenuated inversion recovery (FLAIR). Once the precontrast imaging was completed, 0.2 mL/kg gadolinium (Gd)-based MR contrast agent (gadoterate meglumine, MAGNESCOPE; Guerbet, Tokyo, Japan) at a rate of 3 mL/s was administered without preload by an MRI-compatible power injector (Spectris; Medrad, Pittsburgh, PA, USA) followed by a 30-mL bolus of saline flush. Postcontrast 3D T1WIs were obtained immediately after DSC-PWI. All patients were scanned on a 3T scanner (Signa Excite HDxt; GE Healthcare, Milwaukee, USA) with an 8-channel head coil. A DWI using spin echo (SE) echo-planar imaging (EPI) sequence was performed with TR/TE = 6,000/90 ms, FA = 90°, slice thickness = 5 mm, b = 0, 1,000, FOV = 240 mm, matrix = 128 × 128, 20 slices per 1 mm gap. A DSC-PWI using the gradient-echo EPI (GRE-EPI) sequence was performed with TR/TE = 2,000/21 ms, FA = 60°, matrix 96 × 128; FOV, 220 mm; slice thickness = 5 mm, 20 slices per 1 mm gap.
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7

Multimodal Imaging of Cervical Spine

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Subjects underwent T2-weighted imaging (T2WI), DTI, magnetisation transfer (MT) and T2*WI at 3T (GE Signa Excite HDxt) covering C1–C7, as previously described.14 (link) DTI, MT and T2*WI images were acquired with 13 axial slices from C1 to C7. T2WI was performed with a fast imaging employing steady-state acquisition cycled phases sequence with 0.8×0.8×0.8 mm3 isotropic resolution. DTI used spin echo single-shot echo planar imaging with three acquisitions averaged offline, b=800 s/mm2 in 25 directions, five images with b=0 s/mm2 and resolution of 1.25×1.25×5 mm3. MT used 2D spoiled gradient echo ±MT prepulse, with 1×1×5 mm3 voxels. T2*WI acquisition used multiecho recombined gradient echo with 3 echoes at 5, 10, 15 ms and resolution 0.6×0.6×4 mm3. Total imaging time was 30–35 min including patient positioning, slice prescription and second order localised shimming (prior to DTI).
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8

Cardiac MRI Imaging Protocol for Tissue Characterization

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All CMR exams were performed on a 1.5 Tesla field strength scanner (Signa Excite HDXt platform, General Electric Healthcare, Milwaukee, USA) using a dedicated 8-channel cardiac coil with technical parameters recommended by the manufacturer and optimized on a case-by-case basis via direct physician supervision. After localizing images were obtained, high-resolution T1-weighted spin-echo images were acquired in an axial plane through the ventricles, followed by corresponding fat-suppressed T1 spin-echo images. Double inversion recovery fast spin echo T1 images were acquired with and without fat saturation in the short axis plane. Cine balanced-steady state free precession (SSFP) cine images were obtained in short axis, and two-, three- and four-chamber planes. Late Gadolinium Enhancement (LGE) images were obtained in the short axis view after intravenous administration of 0.2 mmol/kg Magnevist (gadopentetate dimeglumine, Bayer Healthcare Pharmaceuticals, Germany) with a preparatory null time selected for optimal nulling of normal myocardium. All quantitative parameters were measured using balanced-SSFP cine sequences (short axis view).
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9

Hepatic Fat Quantification in Children

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All children were scanned on a single 3T scanner (GE, Signa EXCITE HDxt, GE Medical Systems, Milwaukee, WI) in supine position with an eight-channel torso phased-array coil centered over the liver. A dielectric pad was placed between the coil and the abdomen. Children were asked to fast for a minimum of four hours prior to the MR examination to reduce potential confounding effects of meals on fat quantification. No sedatives/anxiolytics were administered. Each MR examination included MRS and M-MRI fat quantification acquisitions.
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10

Neuroimaging of Brainstem Structures

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Using a 3T MRI unit (Signa Excite HDxt, GE healthcare, Milwaukee, Wisconsin), we obtained oblique T1-weighted oblique axial images perpendicular to the brainstem. The T1-weighted sequence was acquired with a 3D-spoiled GRASS sequence with magnetization transfer contrast: TR/TE = 38.4/2.4 ms, FA = 20 degrees, matrix size 480×320 in axial plane, FOV = 220 mm, and acquisition time = 3 min 25 s. A 40-mm slab thickness was used and images were reconstructed 40 slices with a slice thickness of 2 mm with in-slice zero-fill interpolation (ZIP2). We also obtained axial T2-weighted images of the whole brain to exclude coexisting disorders and any abnormal findings that might influence the signals for the SNc or LC. The T2-weighted image parameters are as follows: TR/TE = 4500/88 ms, FOV = 220 mm, Matrix = 512×256, 24 slices with slice thickness 5 mm, and 6 mm slice interval.
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