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29 protocols using ge discovery 710

1

Multimodal PET/CT Imaging Protocol

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The PET/CT scanners are state‐of‐the art scanners from GE (GE Discovery 710 and GE Discovery MI, Hospital South West Jutland; GE Discovery MI, Odense University Hospital) and Siemens (Siemens Biograph mCT Flow 64 and Siemens Biograph Vision 600 Edge, Hospital Lillebaelt). All patients will have a CECT (according to local guidelines for contrast administration) as performed clinically in these patients in each department. The [18F]PSMA‐1007‐PET/CT scans will be performed 60 min post injection of the tracer, and Na[18F]F‐PET/CT 30 min post tracer injection.
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2

PET/CT Imaging Protocol for Fasting Patients

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Patients were asked to fast for a minimum of six hours prior to scanning. All scans were acquired at the Institute of Nuclear Medicine, University College London Hospitals, on either a Discovery VCT (140 kV, 80 mA, 0.8 s) or Discovery 710 PET/CT (120 kV, 170 mA, 0.8 s) (GE Healthcare). Patients were injected with a target activity of 250 MBq and an uptake time of 30–45 min. Scans were acquired for 15 min per bed (slice thickness: 3.27 mm) and reconstructed (3 iterations, 20 subsets, post-filtering: Hanning, 4 mm). Time-of-flight imaging was used for those scans acquired on the GE Discovery 710. Reconstructed images were exported as DICOM files, and converted to NifTi format for further pre-processing.
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3

Comparison of Four PET/CT Systems

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Four PET/CT systems equipped with both ToF and PSF capabilities from three major vendors (General Electric (GE), Siemens and Philips) were selected for this study. Systems included were the Siemens Biograph mCT (Siemens system 1), the Siemens Biograph mCT Flow (Siemens system 2), the GE Discovery 710 (GE system) and the Philips Ingenuity TF 128 (Philips system). The equipment was calibrated in accordance with the corresponding manufacturer’s instructions. In addition, all systems were participating and accredited in the EANM/EARL 18F–FDG PET/CT accreditation program. Detailed specifications for the systems can be found in supplemental Table 1 and references [47 (link)–51 ].
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4

Quantitative 68Ga-DOTATATE PET/CT Imaging

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Available 68Ga-DOTATATE PET/CT and PET/MR scans were reviewed by a nuclear medicine physician and radiologist (GBJ) and a Krenning score was applied. Briefly, Krenning score is a qualitative measure of relative uptake of 68Ga-DOTATATE in tumors versus the physiologic uptake in the internal organs of the liver and spleen, with a Krenning score of 1 being negative and tumor activity far below liver activity, a Krenning score of 2 being mildly positive with activity slightly less than liver, a Krenning score of 3 being positive with activity higher than liver, and a Krenning score of 4 being very positive with activity above spleen. Scans were performed on GE Discovery 710, GE Discovery MI and Siemens Vision 600 PET/CT or GE Signa PET/MR scanners. Uptake was 60 minutes plus or minus 5 minutes in all patients, and the injected dose was 5.2 mCi 68Ga-DOTATATE IV +/- 10% IV.
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5

Rubidium-82 Cardiac PET-MPI Protocol

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Rest and pharmacological stress PET-MPI studies utilizing [82Rb]Cl were performed with a Biograph 64 PET/CT scanner (Siemens Healthcare, Erlangen, Germany) or GE Discovery 710 (GE Healthcare, Waukesha, Wisconsin) scanners. Directly prior to the injection of weight-based dose of 925–1,850 MBq (25–50 mCi) of [82Rb]Cl, a 6-min rest list-mode acquisition was initiated. Regadenoson was utilized to induce pharmacological stress, and a 6-min stress list-mode acquisition was initiated at the same time along with the [82Rb]Cl infusion of the same dose as for the rest scan. As previously detailed, before each rest and stress PET scanning, a low-dose CT scan was obtained for attenuation correction [11 (link)].
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6

Multimodal Imaging of Amyloid and Tau

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T1-weighted magnetic resonance imaging (MRI) scans were acquired on a GE Discovery MR750 (Wisconsin), Siemens Trio or Prisma (Pittsburgh), GE SIGNA (Cambridge), and GE Discovery MR750 (Barrow). MRI images were processed using FreeSurfer v5.3.0 for region of interest (ROI) definition. Positron emission tomography (PET) scans were performed on a Siemens ECAT HR + scanner (Wisconsin/Pittsburgh), Siemens 4-ring Biograph mCT (Pittsburgh), GE SIGNA (Cambridge), and GE Discovery 710 (Barrow). A target dose of 15 mCi of [C-11]Pittsburgh Compound-B (PiB) was injected intravenously, and PET scans were used to measure Aβ acquired 50–70 min post-injection (four 5-minute frames). Following completion of the PiB scan, a target dose of 10 mCi of [F-18]AV-1451 was injected intravenously, and PET scans were used to measure neurofibrillary tau acquired 80–100 min post-injection (four 5-minute frames). Using the Statistical Parametric Mapping 12 software (SPM12), PET frames were re-aligned to correct for motion and averaged to form a 3D image.
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7

FDG-PET/CT Imaging Protocol for Bladder Cancer Staging

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The Department of Medical Imaging and Physiology at Skåne University Hospital in Lund/Malmö, Kristianstad County Hospital, and Växjö County Hospital, Sweden, conducted the FDG-PET/CT scans. The systems used were Philips Gemini TF (Philips Medical Systems, Cleveland, OH), GE Discovery 690 (GE Healthcare, Milwaukee, WI, USA), GE Discovery 710 (GE Healthcare, Milwaukee, WI, USA) or GE Discovery MI (GE Healthcare, Milwaukee, WI, USA). To decrease the concentration of FDG in the urinary tract, a diuretic (intravenous furosemide 20 mg) was administrated at the same time as 18F-FDG (4 MBq/kg), and imaging was performed 120 min after radiopharmaceutical administration (Anjos et al. 2007 (link)). The patients were scanned from the inguinal region to the base of the skull. CT images were acquired for attenuation correction and anatomic correlation of the PET images. A diagnostic CT with intravenous and oral contrast or a low-dose CT without contrast was performed. A low-dose CT was chosen in 51/157 (32%) of the patients when a previous diagnostic CT was performed within 4 weeks of the FDG-PET/CT scan, and thus, no direct comparison between the CT and FDG-PET/CT was feasible. Instead, the outcome measure preoperative lymph node stage in the current study was derived from a reassessment and visual analyses by one nuclear medicine physician and one radiologist at the MDT prior to RC.
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8

PET-CT Imaging of 18F-FDG Biodistribution

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Following a 6-h fast, up to 400 MBq 18F-FDG was administered intravenously if blood glucose was <10 mmol/L. At 60 +/- 5 min post-injection, imaging was acquired from skull vertex to feet at 3.5 min per bed position with an axial field of view of 15.7 cm and an 11-slice overlap between bed positions, using a GE Discovery 710 PET-CT scanner (GE Healthcare, Chicago, US). A low-dose CT scan (140 kV, mA 15-100, noise index 40, 0.5 s rotation time, and 40 mm collimation) was performed at the start of imaging to provide attenuation correction and an anatomical reference. PET image reconstruction included scanner-based corrections for radiotracer decay, scatter, randoms, and dead-time. Emission sinograms were reconstructed with an ordered subset expectation maximisation algorithm (2 iterations, 24 subsets).
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9

PET/CT Imaging Protocol for 18F-FDG Acquisition

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18F-FDG PET images were acquired on four PET/CT scanners at the University of Wisconsin-Madison: GE Discovery 710, GE Discovery STE, GE Discovery IQ, and GE Discovery MI (General Electric, Waukesha, WI). Our institutional PET imaging protocol required that patients fast for 6 h prior to injection of the radiotracer and have a blood glucose level below 200 mg dl−1 at the time of the scan. Patients were also required to hold diabetic medication for 6 h prior to radiotracer injection. On the GE Discovery IQ, patients were injected with 259 ± 52 MBq of 18F-FDG. On all other scanners, patients were injected with a weight-based dose of 5.2 MBq per kilogram (minimum 370 MBq) of 18F-FDG. Scans were acquired 60 ± 10 min post-injection. A low-dose CT was acquired for attenuation correction. Following reconstruction, images were normalized by patient weight and injected dose to compute Standardized Uptake Values (SUV).
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10

Whole-Body 18F-FDG PET/CT Protocol

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All patients underwent whole-body
18F-FDG PET/CT in the Department of Nuclear Medicine, the Hospital 108. PET/CT scan was performed, using GE Discovery 710 (GE Healthcare, Milwaukee, Wisconsin, United States), according to the European Association of Nuclear Medicine guidelines, version 2.0.
24 (link)
Patients should be fasted at least 4 hours, and blood sugar was measured before injection of
18F-FDG. The PET/CT study schedule was postponed when glucose level higher than 11 mmol/L (about 200 mg/dL). Afterward, the patients rested in the waiting room before intravenous injection of 2.5 MBq/kg body weight (±10%) of
18F-FDG. The parameters of the low dose CT scan were as follows: 120 kVp, modulated milliampere-seconds (mAs), the helical slice thickness of 3.75 mm, and 0.5 s/rotation. PET images were reconstructed using an iterative algorithm with attenuation correction with CT.
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