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Magnetom skyra system

Manufactured by Siemens
Sourced in Germany

The Magnetom Skyra system is a magnetic resonance imaging (MRI) scanner designed and manufactured by Siemens. It is a high-field MRI system that utilizes a 3 Tesla superconducting magnet to generate a strong magnetic field for imaging the human body. The Magnetom Skyra is capable of performing a wide range of MRI examinations, including neurological, musculoskeletal, cardiovascular, and abdominal imaging.

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12 protocols using magnetom skyra system

1

Optimizing MRCP Imaging for IPMN Diagnosis

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For the IPMN group, MRI examinations were performed using a 1.5 T scanner (Magnetom Avanto Systems, Siemens Healthineers). T2-weighted MRCP three-dimensional (3D) images were acquired through sampling perfection with application-optimized contrast using different flip angle evolution (SPACE). Imaging relied on a repetition time (TR) of 2500 ms and an echo time (TE) of 700 ms, as well as a slice thickness (ST) of 1 mm with a trigged breathing technique.
For the control group, MRI examinations were performed using a 1.5 T scanner (Magnetom Avanto Systems) or a 3 T scanner (Magnetom Skyra Systems, Siemens Healthineers). For the 1.5 T scanner, T2-weighted MRCP 3D images were acquired through SPACE (TR/TE = 4000–4700/705 ms, ST 1.3 mm) with a trigged breathing technique. On the 3 T scanner, T2-weighted MRCP 3D images were acquired through SPACE (TR/TE = 3000–4600/700 ms, ST 1.3 mm) with a trigged breathing technique.
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2

Standardizing MRI Sequence Descriptions

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We also analyzed challenges associated with the heterogeneity of protocols (protocol trees) and assessed the similarity between different protocol trees on protocol and sequence level. Therefore, we computed the overlap coefficient for different protocol trees (for all body regions) and the sequences used within the protocols. However, since the sequence name can be adapted individually, it is not suitable for the objective characterization of a protocol step, i.e., the parameterized MRI sequence. Therefore, different strategies were recently developed to categorize and standardize MRI sequence descriptions, which can be used as a meaningful, standardized feature for machine learning applications [11 , 37 , 38 ]. We used a heuristic rule–based approach [11 ] that generates a standardized sequence name based on the MR acquisition parameters of a sequence (e.g., TR, TE, imaging technique, imaging orientation). We show the effect and benefit of sequence name standardization on assessing sequence heterogeneity across different protocol trees.
We evaluated the protocols from three different MRI scanners of the same radiology practice. Two scanners (scanner 1 and 2) are located at the same site, and one scanner (scanner 3) is located at a different site. All MRI scanners are 3 T MAGNETOM Skyra systems (Siemens Healthcare, Erlangen, Germany) with the same software baseline.
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3

Diffusion Tensor Imaging of the Brain

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Studies were performed with a 3-Tesla scanner (Siemens MAGNETOM Skyra System, Siemens Healthcare, Erlangen, Germany). DTI data were acquired using a single shot echo-planar imaging (EPI) sequence (echo time [TE] = 91 ms; repetition time [TR] = 9900 ms; field-of-view [FOV]: 256 mm; slices: 72, slice thickness: 2 mm; slice gap: 0 mm; 30 gradient directions with b = 1000 s/mm2 and 1 with b = 0 s/mm2).
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4

Cardiac Magnetic Resonance Imaging Protocol

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All enrolled subjects underwent CMR on a 3.0T whole-body Siemens MAGNETOM Trio Tim system or a MAGNETOM Skyra system (Siemens Medical Solutions, Erlangen, Germany). A standard ECG-triggering device and breath-hold technique were used to monitor dynamic changes. Cine images such as a stack of short-axis views from the base to apical level and long-axis views (2-chamber, 3-chamber, 4-chamber), were acquired by applying an electrocardiogram-gated balanced steady-state free precession (SSFP) sequence. Typical acquisition parameters were as follows: temporal time = 39.34/40.35 ms, echo time = 1.22/1.20 ms, slice thickness = 8 mm, field of view = 240 × 300/288 × 360 mm2, matrix size = 208 × 174/192 × 162 pixels, flip angle = 40°/50°. A dose of 0.2 ml/kg gadobenate dimeglumine (MultiHance; Bracco, Milan, Italy) was intravenously injected at an injection rate of 2.5–3.0 mL/s, followed by a 20 mL saline flush. Late gadolinium enhancement (LGE) images were acquired by a phase-sensitive inversion recovery sequence at 10–15 min after contrast administration (acquisition parameters: TR/TE = 750/1.18; 512/1.24 ms; slice thickness = 8 mm, field of view = 240 × 300/288 × 360 mm2, matrix size = 256 × 162/ 256 × 125 pixels, and flip angle = 20°/40°).
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5

High-Resolution Diffusion Tensor Imaging Protocol

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The MR imaging scans were performed on a 3.0 Tesla Siemens Magnetom Skyra system. The diffusion tensor images (DTIs) were acquired and the parameters were: two b0 images and 60 images with b-value of 1000 s/mm; echo time (TE) 93.0 ms, repetition time (TR) 6800 ms, field of view (FOV) 230 mm × 230 mm × 150 mm, flip angle 90°, voxel size 1.8 mm × 1.8 mm × 3.0 mm, slices 50 and slice thickness 3.0 mm. All acquired images were inspected for significant scanning artifacts and gross brain abnormalities and none were observed in any participant.
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6

Breast MRI Acquisition Protocol for Tumor Characterization

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All the MR scans were performed using a 3.0T MAGNETOM Skyra system (Siemens Healthcare, Erlangen, Germany) with a 16-channel phased-array breast coil, with patients in the prone position. The breast MRI examinations included a transverse fat-suppressed T2-weighted (TR/TE, 3,570/69 ms) sequence and a transverse T1-weighted (TR/TE, 5.4/2.4 ms) sequence.
Before contrast injection, DWI was performed in the transverse plane covering both breasts at the position of the tumor using a single-shot echo-planar imaging sequence with the following parameters: TR/TE, 3,000/54 ms; flip angle, 90°; field of view, 340 × 150 – 280 mm2; matrix, 220 × 220; slice thickness, 6 mm; 3 b-values, 50, 400, and 800 s/mm2, with the number of averages 3, 4, and 5, respectively; rate 3 GRAPPA acceleration. The total acquisition time was 2:09 min.
DCE-MRI was performed using a 3D T1-weighted fat-suppressed, fast spoiled gradient-echo sequence (TR/TE 4.5/1.6 ms; flip angle, 10°; bandwidth, 380 Hz/Pixel) with one pre-contrast and five consecutive post-contrast dynamic series after a bolus injection of 0.1 mmol/L of gadopentetate dimeglumine (Magnevist; Bayer Schering Pharma, Berlin, Germany) per kilogram of body weight, injected at a rate of 1.5 mL/s. Image acquisition in the transverse plane lasted for 60 s per volumetric acquisition with slice thickness and was 1.5 mm with no gap and a matrix of 384 × 384.
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7

Brain Imaging Protocol for 3T MRI Scans

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Brain imaging was performed on a 3-T SIEMENS Magnetom Skyra System (Siemens, Erlangen, Germany) with a 20 channel head/neck coil. For functional scans, A T2*-weighted multiband gradient echo-planar imaging (EPI) sequence was used (TR = 700 ms, TE = 30 ms, flip angle = 55°, 48 axial slices, slice thickness = 3 mm, no gap, in-plane resolution 3x3 mm) (Feinberg et al., 2010). After the functional scanning session, a high resolution magnetization prepared rapid acquisition gradient echo (MPRAGE) T1-weighted sequence (TR = 2100 ms, TE = 4.6 ms, TI = 900 ms, flip angle = 8°, 192 contiguous slices, voxel resolution 1 mm³, FOV = 256x256x192 mm, iPAT factor of 2) was obtained in sagittal orientation. These anatomical scans were used to co-register the functional runs.
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8

Resting-State fMRI and Structural MRI Protocol

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All subjects were scanned with a 3-Tesla MRI scanner (MAGNETOM Skyra System, Siemens, Erlangen, Germany). Foam pads and the earplugs were used to minimize head motion and acoustic noise. The subjects were asked to stay still with their eyes closed and not think anything particular during the resting state scan. Functional images were collected using an echo-planar imaging sequence (repetition time [TR] =2510 ms, echo time [TE] =30 ms, flip angle = 90°, field of view [FOV] =240 mm × 240 mm, in-plane matrix = 80 × 80, slice thickness/gap = 3/0 mm). Additionally, subjects underwent structural imaging using a T1-weighted magnetization-prepared rapidly acquired gradient-echo sequence (176 slices, TR = 2300 ms, TE = 3.17 ms, TI = 900 ms, flip angle = 8°, FOV = 256 mm × 256 mm, in-plane matrix = 256 × 256, slice thickness/gap = 1/0 mm).
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9

High-resolution T1-weighted MRI Acquisition

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MRI scans were performed on a 3 Tesla Siemens Magnetom Skyra System with a 32-channel head coil. Anatomical T1 weighted (T1w) images were obtained with an in-house developed MP-RAGE sequence with 1 × 3z1 CAIPIRINHA and elliptical sampling95 (link): sagittal slice orientation, voxel size = 1 × 1 × 1 mm, field-of-view = 192 × 192 × 144 mm, TR = 2.5 s, TI = 1.1 s, TE = 5 ms, flip angle = 7°, total scan duration: 2 min 53 s.
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10

Anesthesia-Induced Tissue Fluid Changes

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MRI was performed to measure fluid accumulation in tissues during anesthesia in the pilot 1 experiment using a clinical 3 T Siemens Magnetom Skyra system. Animals were scanned immediately following anesthesia and again after 3 days in anesthesia. For each scan, axolotls were positioned head first in a prone position. A T2-weighted spin-echo sequence was acquired with the following parameters: repetition time = 1030 ms, echo time = 141 ms, excitation flip angle of 120°, four averages and an isotropic image resolution of 0.45 mm.
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