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Ge discovery st pet

Manufactured by GE Healthcare

The GE Discovery ST PET is a positron emission tomography (PET) scanner. It is designed to acquire high-quality images of the body's metabolic and functional processes.

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2 protocols using ge discovery st pet

1

FDG-PET/CT Imaging Protocol for Metabolic Evaluation

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FDG-PET scans were acquired after the patient had fasted for 6 hours and had a confirmed blood glucose of lower than 200 mg/dl. 18F-FDG 3.5 MBq/kg body weight was administered via intravenous injection. The PET/CT was acquired using a (GE Discovery ST PET/CT, GE Health Care, Waukesha, WI) 45 minutes after FDG administration. The CT portion was performed during quiet breathing with the following parameters: kVp 120, automated tube current modulation with mA range 10–180, noise index 18, tube rotation time 0.8 sec., pitch 1.75, 50 cm field of view with 3.75mm slice thickness from the eyes to mid-thigh. Iodinated contrast was not administered. PET data was acquired following the CT. PET images were acquired in 3D mode and iteratively reconstructed by using 21 subsets and 4 iterations. The attenuation correction images fused with the CT Image data were displayed in axial, coronal, and sagittal views.
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2

4D CT Imaging Protocol for Respiratory Motion

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All 4D CT images were acquired in cine mode on a GE Discovery ST PET/CT scanner (GE Medical Systems, Waukesha, WI) with a 500 ms tube rotation time; the CT component is an 8‐slice LightSpeed CT. A real‐time processing monitor (RPM; Varian Associates, Palo Alto, CA) served as an external surrogate for organ motion, which provided a respiratory trace of relative abdominal height versus time.
Cine 4D CT acquires images in beam‐width steps that correspond to fixed couch positions to cover the superior–inferior scan extent. Acquiring images for at least 1 breathing cycle per couch position ensures data sufficiency; therefore, the acquisition time per couch position (cine duration) was based on the patient's average breathing cycle plus 1 s for all but the oversampling method. This yields several multislice image segments (8×2.5mm axial images) per couch position. Images from all acquisition methods were reconstructed using 360° of data every 350 ms following the first 500 ms rotation at each couch position. Acquisitions were obtained at 120 kVp, with a 100 mA tube current for clinical acquisitions and a dose‐sparing 50 mA for experimental acquisitions. Each acquisition was processed to yield a final 4D CT with a set of ten 3D CT volumes, each representing a component breathing phase.
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