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Biograph hirez 16 pet ct

Manufactured by Siemens
Sourced in Germany

The Biograph HiRez 16 PET/CT is a medical imaging system that combines positron emission tomography (PET) and computed tomography (CT) technologies. It is designed to capture high-resolution images of the body's internal structures and functions.

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4 protocols using biograph hirez 16 pet ct

1

Dynamic 13N-NH3 and 18F-FDG PET Imaging for CRT Evaluation

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All patients underwent resting dynamic 13N-NH3 and static 18F-FDG PET studies (Biograph HiRez 16 PET/CT, Siemens, Erlangen, Germany) 1 week before CRT implantation (except for one patient who underwent a 99mTc-tetrofosmin perfusion scintigraphy). A scout acquisition followed by a low-dose CT (80 kVp, 11 mAs) was performed for optimal patient positioning and subsequent CT-based attenuation correction of the PET emission data.
For 13N-NH3 PET, a 30-min dynamic list-mode acquisition was started together with a slow bolus intravenous administration of 10 MBq/kg 13N-NH3. In case of a 1-day protocol, the 13N-NH3 scan always preceded the 18F-FDG scan with a minimum interval of 60 min between tracer administrations.
18F-FDG PET scan was performed using the hyperinsulinemic euglycemic clamp technique in accordance with the method of Lewis et al. [11 (link)]. After reaching a steady-state plasma glucose level, 4.25 MBq/kg 18F-FDG was administered intravenously and a 40-min acquisition was performed approximately 45 min after tracer administration.
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2

Cardiac Metabolic Imaging Protocol

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All patients underwent resting 13 N-NH3 and gated 18 F-FDG PET studies (Biograph HiRez 16 PET/CT, Siemens, Erlangen, Germany) within 1 month before CRT implantation with a maximum 1 week time interval between both acquisitions. In case of a one-day protocol, 13 N-NH3 always preceded 18 F-FDG scan with a minimum 60 minute interval between tracer administrations. A scout acquisition followed by a low-dose CT (80 kVp, 11 mAs) was performed before each PET emission for optimal patient positioning and subsequent CT-based attenuation correction. All static PET images were reconstructed using ordered-subsets expectation maximization algorithms (4 iterations and 8 subsets), matrix size 256 x 256 and a 5.0 mm Gaussian filter.
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Neuroimaging Protocols for Alzheimer's Diagnosis

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ADNI FDG-PET images were retrieved from the ADNI Laboratory of Neuroimaging (LONI) database in a format under which images had already been preprocessed through coregistration, averaging, and standardization. The detailed procedure can be found at http://adni.loni.usc.edu/methods/pet-analysis/pre-processing/.
DongA University’s SPECT images were acquired as described previously45 (link). Patients were injected with 925 MBq of Tc-99m-HMPAO at resting state. Brain SPECT images were obtained from patients using a dual-head gamma camera (Multi-SPECT II, ICON, Siemens, USA) equipped with fan-beamcollimator.
HSC’s FDG-PET images were acquired using Siemens Biograph 16 HiRez PET/CT (Siemens Medical Solutions, Knoxville, TN) scanner. Patients were fasted for at least 6 hours before scanning. Patients were injected i.v. with 185 MBq of FDG and a 15-minute static image was acquired starting 40 minutes post-injection. A head CT scan was acquired for attenuation correction purposes.
Asan Medical Center’s FDG-PET images were acquired as described previously26 (link),39 (link). All subjects fasted for at least 6 h before scanning. A 5-min transmission scan using a 68Ge rotating pin source and a 15-min emission scan were acquired on the ECAT HR + scanner (Siemens Medical Systems, Hoffman Estate, IL, USA) at the Asan Medical Center, 40 min after intravenous injection of 370 MBq of FDG.
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FDG-PET Imaging Protocol for Neurological Disorders

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All participants were withdrawn from anti-PD medications for at least 12 hours and fasted for at least 6 hours before scanning. For the patients who were recruited from the Asan Medical Center (Table 1), a 5-minute transmission scan using a 68Ge rotating pin source and a 15-minute emission scan were acquired on an ECAT HR+ scanner (Siemens Medical Systems) at the Asan Medical Center, 40 minutes after i.v. injection of 370 MBq FDG (82 (link)). For the patients who were recruited from the Crescentwood Memory Clinic and Health Science Centre in Winnipeg (Table 2), all PET imaging data were acquired on a Siemens Biograph 16 HiRez PET/CT (Siemens Medical Solutions) scanner at the University of Manitoba. Patients were injected i.v. with 185 MBq FDG, and a 15-minute static image was acquired starting 40 minutes after injection. A head CT scan was acquired for attenuation correction purposes.
All FDG-PET image preprocessing was carried out using the standard procedure implemented in Statistical Parametric Mapping 12 (SPM) software (www.fil.ion.ucl.ac.uk/spm/). Images were spatially normalized by warping to the Montreal Neurological Institute (MNI) standard space using a PET template and then subsequently smoothed using an 8 mm Gaussian filter. For all images, FDG uptake was proportionally scaled using the whole-brain mean value.
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