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Discovery st scanner

Manufactured by GE Healthcare
Sourced in United States

The Discovery ST scanner is a medical imaging device produced by GE Healthcare. It is designed to capture high-quality, cross-sectional images of the body's internal structures through the use of computed tomography (CT) technology. The core function of the Discovery ST scanner is to provide healthcare professionals with detailed visualizations that can aid in the diagnosis and monitoring of various medical conditions.

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17 protocols using discovery st scanner

1

Whole-Body FDG PET/CT Imaging Protocol

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After fasting for at least 6 hours, patients were administered 5 MBq/kg of FDG intravenously. The blood glucose level at the time of injection of FDG was <150 mg/dL in all patients. Patients were instructed to rest comfortably for 60 minutes and to urinate before scanning. Whole-body PET/CT images were obtained with a Discovery ST scanner (GE Healthcare, Milwaukee, WI). Seven or 8 frames (3 min/frame) of emission PET data were acquired in 3-dimensional (3D) mode after a non-contrast CT scan from the base of the skull to the upper thigh (120 kV, 30–100 mA in the AutomA mode; section width = 3.75 mm). Emission PET images were reconstructed using an iterative method (ordered-subsets expectation maximization with 2 iterations and 20 subsets, field of view = 600 mm, slice thickness = 3.27 mm) and attenuation corrected with non-contrast CT.
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2

Standardized PET/CT Imaging Protocol

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All patients fasted for 6 h before 18F-FDG administration, and the patients’ blood glucose level was checked to ensure it was below 200 mg/dl. PET/CT scans were performed using a Biograph mCT Scanner (Siemens Healthcare, Henkestr, Germany) in 65 patients, and a Discovery ST Scanner (GE Healthcare, Waukesha, USA) in 11 patients. Total body scan was conducted 60 min after the 18F-FDG injection (0.1 mCi/kg or 3.7 MBq/kg body weight). CT scans of the whole body from skull to mid-thigh were obtained without contrast enhancement in an arm-up position for attenuation correction and fusion (80–200 mAs, 120 kVp, 3 mm slice thickness for the Biograph mCT Scanner; and automatic tube current, 140 kVp, 3.75 mm slice thickness for the Discovery ST Scanner) and were reconstructed in a 512 × 512 matrix. The subsequent PET scan was conducted in six to eight bed positions with acquisition time of 2 to 3 min per bed position. The PET images were reconstructed with a slice thickness of 2 mm for the Biograph mCT Scanner or 3.25mm for the Discovery ST Scanner, using the Ordered Subsets Expectation Maximization (OSEM) iterative reconstruction method. Counter correction and cross-calibration of the two scanners were conducted periodically to ensure an optimal quantitative accuracy, and no significant difference at SUV quantitation was observed between the two scanners.
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3

Quantitative PET/CT Imaging Protocol

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The patients were required to fast for at least four hours prior to examination. Upon admission, the patients’ body weight was measured and blood glucose level was recorded. Then, 6 MBq/kg of 18F-FDG (range: 285-460 MBq) was intravenously injected, and PET/CT imaging was performed on the dedicated GE® Discovery ST Scanner, equipped with PET and eight-slice CT units. Image acquisition was performed with a whole-body field of view (vertex to mid-thigh), 45-60 min after the injection.
CT transmission images for attenuation correction were captured with exposure factors of 120 kVp, 80 mA, and 0.8 s for all examinations; no intravenous CT contrast was administered. Emission PET images were obtained in a two-dimensional mode at the rate of four min per bed position with a three-slice overlap between consecutive bed positions.
Transaxial PET data were reconstructed using filtered back-projection. The CT data for PET were reconstructed to axial slices with a thickness of 3.3 mm. The images were reviewed on GE Advantage Workstation (version 4.2) by two experienced nuclear medicine physicians. Positive uptakes on PET images were based on non-physiological uptakes greater than liver or SUVmax>2.5, corrected for body weight.
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4

Whole-body 18F-FDG PET/CT Imaging Protocol

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Whole-body 18F-FDG PET/CT was performed in the supine position on a Discovery ST scanner (GE Healthcare). Patients fasted for at least 6 hours before each received 5 MBq/kg of FDG intravenously with a blood glucose level <150 mg/dL. Non-enhanced, low-dose CT scans were obtained from the base of the skull to the upper thigh (120 kV, 30–100 mA in the Automa mode, section width=3.75 mm). After CT scanning, seven or eight frames (3 minutes/frame) of emission PET data were acquired in the 3D mode. PET images were reconstructed using an iterative method (ordered-subsets expectation maximization with two iterations and 20 subsets; FOV=600 mm; slice thickness=3.27 mm) with attenuation correction using nonenhanced CT.
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5

FDG-PET Imaging in Amnestic MCI

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Fifteen patients with aMCI received FDG-PET. PET/CT data were acquired on a Discovery ST scanner (General Electric Medical Systems, USA). After fasting for at least 4 h, patients received 300 MBq of FDG intravenously. We checked serum glucose-levels in all subjects prior to FDG injection, and the subjects whose glucose-level exceeds 150 mg/dl were excluded. All subjects were instructed to rest comfortably for 30 min with their eyes closed and ears unplugged and then image acquisition was started. To reduce head movement during scanning, the patients were positioned and maintained using an individually molded head holder. They first had a CT scan (tube-rotation time of 1 s per revolution, 120 kV, 70 mA, 5.0 mm per rotation and an acquisition time of 11.8 s for a scan length of 150.42 mm). Subsequently, one frame (8 min per frame) of emission PET data was acquired in a three-dimensional mode. PET images were reconstructed by iterative reconstruction (ordered subsets expectation maximization, with one iteration and 32 subsets), using the CT images for attenuation correction. Also, the random correction by singles and model-based scatter correction were applied.
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6

Brain PET/CT Imaging of Amyloid

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All iNPH and AD subjects underwent 18F-florbetaben PET. Brain PET/computed tomography (CT) images were obtained with a Discovery ST scanner (GE Healthcare, Milwaukee, WI, USA). An average of 300 MBq of 18F-florbetaben was injected intravenously, and scanning was initiated 90 min later. A noncontrast brain CT scan was performed in the automatic mode (120 kV, 30–100 mA, and section width=3.75 mm) for attenuation correction, and was immediately followed by PET imaging in the three-dimensional mode for 20 min. Motion artifacts were minimized by immobilizing the subject's head in a head holder. PET images were obtained by iterative reconstruction using an ordered subset expectation maximization algorithm with 4 iterations and 21 subsets.
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7

Whole-body PET/CT Imaging Protocol

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After fasting for at least 6 hours, patients were administered 5 MBq/kg of FDG intravenously. The blood glucose level at the time of injection of FDG was <150 mg/dL in all patients. Patients were instructed to rest comfortably for 60 minutes and to urinate before scanning. Whole-body PET/CT images were obtained with a Discovery ST scanner (GE Healthcare, Milwaukee, WI). Seven or 8 frames (3 minutes/frame) of emission PET data were acquired in 3-dimensional (3D) mode after a noncontrast CT scan from the base of the skull to the upper thigh (120 kV, 30–100 mA in the AutomA mode; section width = 3.75 mm). Emission PET images were reconstructed using an iterative method (ordered-subsets expectation maximization with 2 iterations and 20 subsets, field of view = 600 mm, slice thickness = 3.27 mm) and attenuation corrected with noncontrast CT.
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8

Standardized FDG-PET/CT and PET/MR Protocols

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FDG-PET/CT was performed using a Discovery MI scanner (GE Healthcare, Waukesha, WI), Discovery 690 Standard scanner (GE Healthcare), Discovery VCT scanner (GE Healthcare), or Discovery ST scanner (GE Healthcare). FDG-PET/MR was performed using a 3 T PET/MR scanner (Signa PET/MR, GE Healthcare). According to our institution’s protocol, a standardized dose of 3.5 MBq of [18F]FDG per kg body weight (PET/CT) or 3.0 MBq per kg body weight (PET/MR) was injected until 2017, and from 2017 on, BMI-adapted body weight–dependent dosage protocols were used24 (link). The CT included of a standardized protocol of high-resolution axial volume acquisition (0.6–1.0 mm) with reconstructions in the coronal and sagittal plane in the bone and soft tissue kernel with contrast enhancement of the sinonasal and neck region. For the sinonasal and neck MR, dedicated regionalized T2-weighted and T1-weighted pulse sequences with and without gadolinium-based contrast agent and with and without fat suppression were used23 (link).
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9

Standardized PET/CT Imaging Protocol

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After fasting for least 6 hours, patients were administered 370 MBq of 18F-FDG intravenously. All patients were instructed to rest comfortably for 60 minutes and to urinate before scanning. Whole-body PET/CT images were obtained with a discovery ST scanner (GE Healthcare, Milwaukee, WI, USA). Seven to eight frames (3 min/frame) of emission PET data were acquired in three-dimensional mode after a non-contrast CT scan from the base of the skull to the upper thigh (tube rotation time of 1 second per revolution, 120 kV, 60 mA, 7.5 mm per rotation, and an acquisition time of 60.9 second for a scan length of 867 mm). Emission PET images were reconstructed using an iterative method (ordered-subsets expectation maximization with two iterations and 30 subsets, field of view = 600 mm, slice thickness = 3.27 mm) and attenuation-corrected with non-contrast CT.
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10

FDG-PET/CT Imaging Protocol for Lesion Analysis

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All procedures performed in studies involving human participants were done in accordance with the ethical standards of the institutional and national research committees and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all subjects. FDG-PET/CT scans were performed on a GE Discovery ST scanner. The dose of FDG was 0.15 mCi/kg, all patients fasted for at least 6 h, serum glucose prior to scanning was less than 250 mg/dl, and scans were performed approximately 60 min after dose administration. The standardized uptake value maximum (SUVmax) was obtained by defining a region of interest (ROI) that encompassed the lesion, calculating the standardized uptake value (SUV) = (activity concentration in tissue)/(injected activity/body weight), and obtaining the maximum SUV in the ROI.
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