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Twinspeed

Manufactured by GE Healthcare
Sourced in United States

The Twinspeed is a laboratory centrifuge system designed for efficient sample processing. It features two independently controlled rotors that can operate simultaneously at different speeds, enabling parallel processing of multiple sample types. The Twinspeed is a versatile and high-performance equipment aimed at enhancing productivity in laboratory settings.

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17 protocols using twinspeed

1

MRI Protocol for Neuroimaging Assessments

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MRI was performed on 1 of 2 systems: a 3‐T General Electric system (General Electric Medical Systems) or, for patients in whom cardiovascular devices or coils had been implanted, a 1.5‐T General Electric Twinspeed magnetic resonance scanner. MRI methods using the 1.5‐T scanner have previously been described.20, 21 Subjects were scanned without the use of sedation. The T1‐weighted acquisition used a 3‐dimensional spoiled gradient recalled steady state sequence with the following parameters: repetition time/echo time=7/2.8 ms; flip angle=8°; and voxel size=1 mm3 isotropic. The susceptibility sensitive T2‐weighted acquisition consisted of multiplanar gradient recalled axial sequences with repetition time/echo time=600/40 ms; flip angle=30°; slice thickness=5 mm (with 1‐mm gap); and voxel size=0.8594×0.8594×6 mm3 chosen to maintain a streamlined total scan time.
Brain MRI results were read by a single blinded neuroradiologist (R.L.R.). Images were assessed by visual inspection to rate the quality of data and to identify abnormalities. Abnormalities were classified by origin (acquired or developmental), type (infarction, mineralization, iron deposition, myelination delay, ventriculomegaly, or abnormal T2‐weighted signal hyperintensity), extent (focal or diffuse), and anatomic location.
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2

Pelvic MRI Protocol for Comprehensive Evaluation

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All patients underwent MRI with a 1.5 T clinical MR imaging system (Twinspeed, GE Medical Systems, Milwaukee, WI, USA), using a pelvic phased-array coil. The imaging protocol involved axial non-contrast T1 weighted imaging (T1WI) (TR/TE range, 400–600/10–14 ms) and axial T2 weighted imaging (T2WI) (TR/TE range, 4000–6000/100–120 ms) performed with a chemical shift-selective fat saturation pulse using the following parameters: slice thickness, 6 mm; gap, 1 mm; field of view (FOV), 32–42 cm; matrix, 256 × 256; and number of excitation, 2. Sagittal T1WI and T2WI (TR/TE, 3000–6000/100–110 ms) fast spin-echo imaging without chemical shift-selective fat saturation pulse was also performed, as well as postcontrast enhanced axial and sagittal T1WI with the same parameters, apart from a slice thickness of 5–7 mm. DWI was acquired in the axial plane prior to administration of contrast medium using a single-shot echo-planar imaging sequence (TR/TE effective range, 8000–10,000/70–100; slice thickness/intersection gap, 6/1 mm; FOV, 32 to 42 cm; matrix, 128 × 128; number of excitation, 2). A b-value of 0 and 1000 s/mm2 was also used in three orthogonal (Z, Y, and X) directions.
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3

Comparative MRI of Hepatic Contrast Agents

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Gd-DO3A-butrol and Gd-EOB-DTPA enhanced MRIs were acquired using standard institutional clinical liver imaging protocols. Delayed 3D axial T1 imaging was performed with 10-min post-intravenous injection of Gd-DO3A-butrol (0.1ml/kg body mass up to 10ml at 1.0mmol/ml) and 20-min post-intravenous injection of Gd-EOB-DTPA (10ml of 0.25mmol/ml). Scans were performed on 1.5-T (GE Twinspeed™, TR, 4.5; TE, 2.2; flip angle, 15; slice thickness, 5mm; spacing, 2.5mm; FOV, 380mm; matrix, 320×192) or 3.0-T (Philips Achieva™, TR, 3.0; TE, 1.4; flip angle, 10; slice thickness, 3mm; spacing, 1.5mm, FOV, 380; matrix, 250×250) magnets with an eight-channel body phased array coil covering the entire liver. Further details are given elsewhere (9 (link), 10 (link)). Gd-DTPA enhanced MRI were acquired using delayed 3D axial T1 imaging at 5-min post-intravenous injection of Gd-DTPA (10-20mL of 0.5mmol/mL), on 1.5-T (Siemens SymphonyTim™, TR, 4.3; TE, 1.4; flip angle, 18; slice thickness, 2.5mm; spacing, 1.25mm; matrix, 320×132) or 1.5-T (Siemens TrioTim™, TR, 3.5; TE, 1.3; flip angle, 11; slice thickness, 2mm; spacing, 1.125mm, matrix, 320x144) magnets with a phased array coil covering the liver.
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4

Structural MRI Acquisition Protocol for SLE

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Magnetic resonance imaging images acquisition was performed by an experienced neuroradiologist. MRI sequences were performed on all subjects with a 1.5T clinical MRI scanner manufactured by General Electric Company (Twin speed; Milwaukee, WI, USA) equipped with a birdcage head coil. Supportive foam pads were used to minimize head motion. A rapid sagittal localizer scan was acquired to confirm alignment. Normal T1 and T2 MRI scans were taken to exclude obvious structural abnormalities. In the 98 SLE patients, nine patients were excluded due to brain structural abnormities identified by T1- and T2-weighted MRI (local infarction or ischemia). Data from the remaining 89 patients were included in this study. 11 subjects from the HC group were also excluded due to local ischemia, and thus 84 HC subjects were included in the study. A set of three-dimensional volumetric structural MRI scans was taken on each subject using a fast spoiled gradient echo sequence with the following parameters: repetition time/echo time = 10.5/2 ms, matrix size = 256 × 256, thickness = 1.8 mm with no interslice gap, field of view = 240 mm, and flip angle = 15°. Resolution = 0.94 mm× 0.94 mm× 0.9 mm. Whole brain images were acquired in axial planes parallel to the anterior commissure-posterior commissure line, yielding 172 continuous slices of 0.9 mm thick.
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5

Standardized MRI Acquisition Protocol

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All MR images were obtained by an experienced neuroradiologist using a 1.5T MRI scanner (TwinSpeed; GE Medical Systems, Milwaukee, WI, USA) with cage head coils for MRI data acquisition. Subjects were placed in a supine position and advised to be relaxed, to be motionless, to have their eyes closed during the scan. Foam support pads were used to reduce head movement. Conventional T1-weighted image (T1WI) and T2-weighted image (T2WI) plain scanning was performed first to exclude obvious structural abnormalities. The scanning parameters were as follows: axial T1WI: echo time (TE) = 8.9 ms, repetition time (TR) = 2,056.9 ms, layer thickness = 5 mm, layer spacing = 6 mm, and turning angle = 90°; T2WI: TR = 12,000 ms, TE = 88.4 ms, layer thickness = 6 mm, layer spacing = 6 mm, and turning angle = 90°. No subjects were excluded for the presence of abnormal brain structure; 3D-MRI uses 3D-T1-weighted fast phase disturbance gradient echo sequence (3D-T1-fspgr sequence), and the parameters were as follows: TR = 10.5 ms, TE = 2 ms, inversion time = 350 ms, layer thickness = 1.8 mm and no layer interval, scanning matrix = 256, turning angle = 15°, field of view = 240 mm, spatial resolution = 0.94 mm × 0.94 mm × 0.9 mm, and layer number = 172; scanning range covers the whole brain.
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6

Multimodal MRI Imaging Protocol for Longitudinal Brain Assessment

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DSC MRI was performed at baseline, one week and one month following treatment. Structural MRIs were performed every two months thereafter. MRI brain sequences were performed on a 1.5 T GE Twinspeed (General Electric, Mississauga, Canada) and included a DWI (7000 ms/min [TR/TE], FOV of 24 cm, matrix 128×128, section thickness of 5 mm with no gap); a FLAIR image (8000/120/200 [TR/TE/TI], FOV 24 cm, matrix 320×224, ST 5, 1 mm gap); a sagittal T1 FLAIR image (2200/24/750 [TR/TE/TI], FOV 24 cm, matrix 224×320, NEX 2, ST 5 mm, 1 mm spacing); a 3D T1 SPGRE (8.5/4.2, FA 20, FOV 22 cm, matrix 270×270, NEX 2) and a DSC study (1700/31.5/90, FOV 24 cm; section thickness 5 mm; matrix 128×128; no gap). Gadovist 0.1 mL/kg, 1 mmol/l concentration was injected at 5 mL/s for the DSC study. The DSC study was followed by a post-gadolinium 3D T1FSPGRE with similar parameters to pre-gadolinium sequence.
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7

Functional MRI Brain Connectivity Analysis

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The MRI scans for all subjects were conducted by a highly experienced radiologist, utilizing the same 1.5 T MRI scanner manufactured by General Electric (Twinspeed; GE Medical Systems, Milwaukee, WI, USA). Initially, plain scanning including routine T1-weighted image and T2-weighted image was conducted to rule out any intracranial organic lesions. An echo planner imaging sequence scan was used with the following parameters: repetition time = 2000 ms, echo time = 40 ms, thickness = 5 mm with an interslice gap of 1 mm, field of view = 240 mm × 240 mm, matrix size = 64 × 64, flip angle = 90°, number of excitation = 2.00, number of layers = 24, time point = 160. The total fMRI scan time was 320 s.
The rs-fMRI data was preprocessed on a DPARSF software based on the MatlabR2016a platform. As per the Anatomical Automatic Labeling template from MNI, the gray matter in each subject's brain was segmented into 116 regions. Among these, the initial 90 regions corresponded to the brain's gray matter, while the remaining 26 regions represented the gray matter of the cerebellum. The rs-fMRI data processing toolkit REST V1.8 was used to extract the mean ReHo value, mean ALFF value, and mean fALFF value of each region.
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8

Multimodal Brain Imaging Protocol

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Imaging was performed using a 1.5-T (Twinspeed; General Electric) clinical MRI scanner. DWI and PWI series were acquired colocalized over the entire brain with a superior to inferior coverage of 14 cm. Typical imaging parameters for the spin-echo DWI echo-planar series included either 40–3.5-mm- or 20–7-mm-thick contiguous axial oblique sections with b = 0 and b = 1000 seconds/mm2, trace or isotropically weighted, TR/TE = 6000–7000/72–90 ms, acquisition matrix of 64 × 64–128 × 128, and FOV= 22 cm field of view. Typical imaging parameters for the gradient-recalled PWI echoplanar series included 20 contiguous axial oblique slices with single-dose gadolinium contrast injection of 0.1 mmol/kg through a power injector using 25 to 40 phase measurements TR/TE = 2000 to 2200/45 ms, acquisition matrix of 64x64 – 128x128, 20 7-mm slice thickness and FOV = 22-cm field of view. The intracranial 3D time-of-flight (TOF) MRA was acquired in the region of the Circle of Willis with parameters as follows: TR/TE = 39/6.9 ms, flip-angle = 25°; FOV = 24 x 18 cm; matrix of 224 x 160 for an in-plane resolution of approximately 1 mm, reconstructed to 92 axial images, 1.6 mm thick with a 0.8 mm overlap.
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9

CMR Protocol for Repaired Tetralogy of Fallot

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The CMR protocol used for patients with repaired TOF has been previously published [23 (link)]. Briefly, studies were performed with a 1.5-T whole body scanner (Achieva, Phillips Healthcare Systems, Best, the Netherlands or TwinSpeed, GE Healthcare, Milwaukee, Wisconsin, USA) using surface coils selected based on patient size. The scanner manufacturer was different for the pre- and post-PVR CMR study in 4 patients. Imaging included breath-hold, electrocardiographically-gated, balanced steady-state free precession cine CMR acquisitions in 4-chamber and short-axis planes. A total of 12−14 slices were obtained in the short-axis plane to completely cover both ventricles. In all views, 30 images per cardiac cycle were acquired which yielded a temporal resolution of 20–40 ms, depending on heart rate. Ventricular volumes and blood flow were measured using commercially available software (QMASS and QFLOW, Medis, Leiden, the Netherlands) [23 (link)].
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10

Multimodal MRI Neuroimaging Protocol

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MR imaging was performed using either 1.5 T (Twinspeed, General Electric) or 3.0 T (Achieva, Philips) clinical scanners, depending on hospital site. Typical sequences have been described.12, 13 The diffusion‐weighted imaging (DWI) was a spin‐echo planar series. The perfusion‐weighted imaging (PWI) was a dynamic gradient‐echo series with single‐dose gadolinium contrast injection of 0.1 mmol/kg of gadolinium (gadolinium‐DTPA; Magnevist; Bayer Schering Pharma) through a power injector using 25–40 phase measurements. The mean transit time (MTT) maps were calculated as the first moment of the time concentration curves divided by the zeroth moment with no arterial input correction or deconvolution. Only MTT maps were used for the perfusion assessments. The DWI, FLAIR, and PWI series were acquired co‐localized over the entire brain with a superior to inferior coverage of 14 cm. The magnetic resonance angiography (MRA) was an intracranial 3D time‐of‐flight (TOF) centered in the region of the Circle of Willis. The detailed imaging protocol parameters are found in Table S1.
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