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Aw4.6 workstation

Manufactured by GE Healthcare
Sourced in United States

The AW4.6 workstation is a laboratory equipment product offered by GE Healthcare. It is designed to provide a comprehensive platform for image visualization, processing, and analysis. The core function of the AW4.6 workstation is to enable healthcare professionals to efficiently manage and interpret medical imaging data from various modalities.

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29 protocols using aw4.6 workstation

1

Quantifying CEST Contrast of Hydroxyl Metabolites

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All data were transferred to an AW4.6 Workstation (GE Healthcare) and analyzed using its Functool software. The raw data were first organized into the Z-spectrum. Then, the Z-spectrum was fitted on a pixel-by-pixel basis according to the procedure described previously (16 (link)21 (link)), and the B0 inhomogeneity map was created. The original Z-spectrum was then corrected for the B0 inhomogeneity effect through interpolation and centering of the Z-spectrum.
CEST contrast of hydroxyl metabolites was quantified at +1.2 ppm using interpolation method and MTR asymmetry analysis with respect to the water frequency (20 (link)).
MTRasymΔω=S(Δω)S0S(Δω)S0
Where S (Δω) and S (−Δω) were the signals at positive offset and its counterpart at negative offset, respectively.
The MT effect from immobile macromolecules was calculated at +15.6 ppm saturation offset (16 (link)).
MT=S0SsaturationS0
The cortical and medullary regions of interest (ROIs) were manually segmented based on the original saturated images at 15.6 ppm that showed the best contrast between the cortex and the medulla. The same ROIs were propagated to the reconstructed MTRasym(1.2ppm) and MTR maps, and parameter values for each kidney cortex and medulla were obtained.
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2

Multiplanar Tumor Imaging Analysis

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Three-dimensional (3D) multiplanar reconstruction (MPR) images were generated using GSI general post-processing software running on an AW4.6 workstation (GE Healthcare). The maximal tumor length (including both the tumor and surrounding regions of suspected invasion) was measured perpendicular to the middle sagittal line, and the distance from the layer containing the maximal tumor length to the front of the brain was also determined. In the image layer (0.625 mm thick) containing the maximal tumor length, circular regions of interest (ROIs; diameter, 0.5 mm) were positioned at the following regions: the center of the solid tumor; a region of liquefactive necrosis; a peripheral tumor region; and adjacent normal brain tissue. Every region positioned 3 ROIs, and the average monoenergetic CT values and iodine concentrations were calculated for these regions. Two specialists experienced in the analysis of spectral CT data recorded the tumor diameter, distances from the ROIs in the peritumoral and adjacent brain tissue regions to the tumor center, CT values and iodine concentrations in a blinded fashion.
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3

Measuring Cerebral Blood Flow Using CBF Plots

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The CBF plots were obtained using a GE AW 4.6 workstation and the FunctooI software. CBF = (Mean arterial pressure [MAP]-Intracranial pressure [ICP]) /Cerebrovascular resistance (CVR). The CBF values in the area of interest were measured. The regions of interest (ROI) of all patients included the bilateral basal ganglia, thalamus, corona radiata, frontal and parietal white matter and brain stem. ROI was approximately 50 square millimeters. In order to ensure the consistency and comparability of the ROI, the mirror copy ROI method was adopted for measuring each brain area. Each brain area was measured for three times and averaged. Attempts were made to ensure that all newborns had the same ROI and the same shape. The level of ROI was determined according to the anatomical mark, and the consistency of the level was ensured.
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4

Multiparametric MRI Evaluation of PI-RADS 3 Lesions

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According to PI-RADS version 2.1 (3), we screened the PI-RADS 3 lesions strictly located in TZ (Table 2). All the images were independently evaluated by two radiologists (JW. L., J.B.) with more than 10 years of experience in abdominal imaging diagnosis without knowing the clinical history, laboratory examination results, and other imaging examination results (such as ultrasound). In case of deviation in the results, an agreement was reached. (After PI-RADS Version 2.1 published in March 2019, we reevaluated prostate MRI of 113 patients between December 2018 and April 2019 according to PI-RADS Version 2.1)
Acquisition of quantitative data was carried out on GE AW 4.6 workstation. The two radiologists (KP. Z., JW. L.) depicted every region of interest (ROI) separately on related parameter maps of IVIM, stretched exponential model, and DKI. Nine ROIs with area of 50 mm2 were randomly drawn at the maximum 3 slices of each PI-RADS 3 lesion in TZ. The average value was recorded and used for data analysis. Detail showed in Figure 2.
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5

Diffusion Tensor Imaging in Anesthetized Rats

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SD rats were placed in a scanner in the supine position after being anesthetized. All experiments were conducted on a 3.0-Tesla MR scanner (Discovery 750, General Electric, USA) with a dedicated animal coil (WK601-1085, Magtron Inc., China). Conventional DTI scans were then performed. Subsequently, all data were transferred to the General Electric AW 4.6 workstation, and the following parameters were used: b value of 800 s mm − 2, TE of 60 ms, TR of 3000 ms, 98 × 48 matrix, FOV 8 × 4, slice thickness of 2 mm, and 17 diffusion gradient directions.
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6

Metabolic Changes in Epileptic Foci

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18F-FDG PET images were assessed by two experienced nuclear physicians using the GE AW 4.6 workstation, and we used a colorized scale to detect metabolic changes. The nuclear physicians were blinded to patients’ information, and divided the left and right hemispheres into ten lobes (frontal, parietal, occipital, temporal and insula lobe). Abnormal metabolic regions occurred when one hemisphere was metabolically altered from the opposite hemisphere. The presence of at least one abnormal metabolic region in 18F-FDG PET images was considered indicative of potential epileptic foci (Spencer, 1994 (link)).
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7

Standardized 18F-FDG PET/CT Imaging Protocol

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All patients were instructed to fast for at least 6 h and their blood glucose levels were kept lower than 7.4 mmol/l. Image acquisition was taken 45~60 min after intravenous administration of 5.6 MBq of 18F-FDG per kilogram of body weight. All scans were performed on a GE Healthcare Discovery STE system. First, a CT scan from the vertex of the skull to the upper thigh with the patient supine was performed, under the following conditions: 120KV, auto mA, pitch 1.75:1; collimation 16×3.75 mm; and rotation cycle, 0.5 s, for PET attenuation correction and anatomical location, without oral or intravenous contrast. Then, PET images covering the same area were acquired in three‐dimensional mode on the same scanner for 2.5 min per bed position, a total of 6-7 bed positions per patient. PET images were reconstructed using CT for attenuation correction with the ordered-subsets expectation maximization algorithm (2 iterations, 28 subsets) and an 8-mm gaussian filter using a 128×128 matrix. All images were reviewed on a picture-archiving and communication system (PACS) workstation (GE AW 4.6 workstation) displaying a maximum-intensity projection image (MIP) and multiplanar PET, CT, and PET/CT fusion images.
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8

Quantifying Fat Fraction and T2* in Iliac Bone Marrow

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All MR images were sent to AW4.6 workstation (GE Healthcare). Three observers (two radiologists and a clinician) evaluated the images. Reader 1 is Z.Z., a junior radiologist with 3 years of experience in musculoskeletal MRI. Reader 2 is W.W., a senior radiologist with 22 years of experience in musculoskeletal MRI. Reader 3 is B.Y., a hematologist with no experience in musculoskeletal MRI. The image datasets of patients and controls were anonymized and presented to the observers in a random order. The gender, age, and patient information were all blinded to the readers. Each reader performed the following evaluations independently. T1‐ and T2‐weighted images were used as references for FF and R2* quantification. Regions of interest (ROIs) were manually drawn in the IDEAL‐IQ sequence FF images and R2* images of the left posterior superior iliac spine in the largest level. Red bone marrow and puncture holes were excluded (Fig. 1). The system automatically calculated the FF and R2* mean values for the drawn regions.
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9

3D Reconstruction and Morphological Analysis of Left Atrial Appendage

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The GE AW4.6 Workstation was used to perform 3D reconstruction of the original CT images to obtain 3D images of the LAA and left atrium (LA). Then, a cutting tool was used to separate the LAA from the LA to obtain the LAA volume. According to the morphological characteristics of the LAA, it can be divided into chicken wing (there is an obvious fold at the proximal or middle part of the main lobe of the left atrial appendage) and non-chicken wing (other forms beside chicken wings) (Figs. 4 and 5).

The shape of the LAA. A, B Chicken-wing. CF Non-chicken wing

Left atrial appendage volume

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10

In Vitro T1 Relaxivity Evaluation of Gd-HA Nanoparticles

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In vitro T1 relaxivity of the produced NPs was assessed using an MRI scanner (GE Discovery, 3T, GE Medical System, USA) with an 8-channel phased-array coil at room temperature of 25 °C. Gd-HA NPs were diluted in dd H2O with various Gd(III) concentrations (0.0005–0.06 mM). Gd-DPTA-HA and clinically used MRI contrast agent Gd-DPTA were utilized as controls. To obtain T1-weighted images, the following parameters and sequences were employed: inversion time (TI) = 50, 100, 200, 500, 800, 1200, and 1500 ms; echo time (TE) = 8 ms; repetition time (TR) = 5000 ms; matrix dimensions = 128 × 256; bandwidth = ±125 kHz; number of excitations = 3; and echo train length = 8. Plots of 1/relaxation time (1/T1, s−1) versus Gd(III) concentration were constructed to obtain relaxivity values (r1) as their slopes. The images were analyzed on a pixel-by-pixel basis by performing a single exponential fit through the Research-T1 mapping module of a GE AW 4.6 Workstation.
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