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Ge discovery ls pet ct scanner

Manufactured by GE Healthcare
Sourced in United States

The GE Discovery LS PET/CT scanner is a medical imaging device that combines positron emission tomography (PET) and computed tomography (CT) technologies. It is designed to capture detailed images of the body's anatomy and metabolism for diagnostic and treatment planning purposes.

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2 protocols using ge discovery ls pet ct scanner

1

PET/CT Imaging Protocol for Cancer Evaluation

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18F-FDG PET/CT scans were performed on a Biograph mCTx scanner (Siemens, Erlangen, Germany) in nine patients, and the remaining two were scanned using a GE Discovery LS PET/CT scanner (GE Healthcare, Waukesha, WI, USA). All patients were instructed to fast for at least 6 h, and blood glucose level was monitored to ensure the level within normal limits (<7.0 mmol/L). Approximately 60 min after the intravenous injection of 144–467 MBq (3.9–12.6 mCi, 150 μCi/kg) of 18F-FDG, whole-body PET/CT scan was performed according to the guidelines for tumor imaging with PET/CT 1.0 (20 ). 18F-FDG with a radiochemical purity >95% was manufactured automatically using the tracer synthesis system of a Tracerlab FXF-N (GE Healthcare, Waukesha, WI, USA; Beijing PET Biotechnology Co., Ltd., China). The corresponding low-dose CT was acquired at 80 mA and 140 kV (GE Healthcare) or automatic mA (Siemens). The acquired CT and PET images were sent to a Xeleris or MMWP workstation for registration and fusion. Lesions with focally increased 18F-FDG uptake exceeding that of the surrounding normal tissues were considered positive lesions. The region of interest (ROI) was drawn along the margin of the lesion on the PET image, and the maximum standardized uptake value (SUVmax) was measured.
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2

FDG PET/CT Imaging Protocol for Various Patient Groups

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For Group 1, FDG PET/CT scans were performed after a 4-h or overnight fast (6 hours for patients undergoing sedation/anesthesia). First, the patients were given intravenous injections of 5.6 MBq (0.15 mCi)/kg 18F- FDG (maximum 444 MBq [12 mCi]). Approximately 1 h later, after the patient voided, image acquisition began with a non-contrast CT scan for attenuation correction and lesion localization followed by emission imaging using a GE Discovery LS PET CT scanner. Then, images from the top of the head through the feet were acquired at 5 minutes per bed position using 2D acquisition.
For Groups 2 and 3, a GE Discovery 690 PET/CT system was used, with images acquired at 3 minutes per bed position in 3D mode. Patients were maintained in a warm 24°C temperature-controlled environment for one hour prior to injection. Group 3 patients aged 8 years or older received oral propranolol one hour prior to injection (Group 3a). Promptly after receiving propranolol, the patients were escorted to an uptake room, where they remained at rest for an hour during the warming period, and for an additional hour following 18F-FDG administration.
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