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Biograph 64 pet ct

Manufactured by Siemens
Sourced in Germany

The Biograph 64 PET/CT is a medical imaging system that combines positron emission tomography (PET) and computed tomography (CT) technologies. It is designed to provide high-quality imaging for clinical and research applications.

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12 protocols using biograph 64 pet ct

1

Comparative 18F-FDG PET Brain Imaging Protocol

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All subjects were asked to fast for at least 6 h but had free access to water prior to imaging. All patients underwent 18F-FDG PET at least 12 h after the cessation of oral antiparkinsonian medications. The American subjects were scanned on a GE Advance Tomograph (General Electric, Milwaukee, WI) in three-dimensional (3D) mode (Ma et al., 2007 (link)). Following a transmission scan, a PET scan was acquired over 35-45 min after an intravenous injection of 18F-FDG (5-10 mCi) and reconstructed with the 3D reprojection method. The Chinese subjects were scanned with a Siemens Biograph 64 PET/CT (Siemens, Munich, Germany) in 3D mode (Wu et al., 2013 (link)). After a CT transmission scan for attenuation correction, a PET scan was acquired over 45-55 min post-injection and reconstructed with the ordered subset expectation maximization method. All studies in patients and normal subjects were performed in a resting state in a quiet and dimly lit room. Only relative brain glucose metabolism was measured without arterial blood sampling as in any routine clinical imaging protocol.
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2

FDG-PET Imaging of Glucose Metabolism

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Patients underwent a FDG-PET study and neuropsychological evaluation within 3 months. Before FDG PET imaging, the patients were asked to fast for at least 6 h, but had free access to water. Before injection of the radiopharmaceutical agent, blood glucose was checked and confirmed to be <120 mg/dl in all cases. PET scans were performed with a Siemens Biograph 64 PET/CT (Siemens, Germany) in three-dimensional (3D) mode. A CT transmission scan was first performed for attenuation correction. The scan was started 45 min after an intravenous bolus injection of 185 MBq of FDG and lasted for 10 min. Hanning filters were used during image reconstruction with filtered-backprojection, giving a transaxial and axial cut-off frequency of 0.5. As no arterial blood sampling was taken in this clinical imaging protocol, we could not measure absolute glucose metabolism in our subjects. Instead, we used radioactivity count images to measure changes in relative regional glucose metabolism. All studies in patients and normal individuals were performed in a resting state in a quiet and dimly lit room.
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3

Resting-State 18F-FDG PET Imaging

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All subjects were asked to fast for at least 6 h but had free access to water, and antiparkinsonian medications in patients were withheld for at least 12 h before PET imaging. The USA site used a GE Advance tomograph (Milwaukee, WI). A PET transmission scan was first performed for attenuation correction with a 10-min emission scan acquired in 3D mode between 35 and 45 min after intravenous bolus injection of 18F-FDG (~185 MBq). The Chinese site used a Siemens Biograph 64 PET/CT (Munich, Germany). Following a short CT scan, a 10-min PET scan was started 45-min post-injection. Only relative glucose metabolic activity was measured as no arterial blood sampling was taken in this clinical imaging protocol. All studies in patients and NL controls were performed in a resting state in a quiet and dimly lit room.
Images were processed by Statistical Parametric Mapping (SPM5) software (Wellcome Department of Imaging Neurosciences, Institute of Neurology, London, UK) implemented in Matlab 7.4.0 (Mathworks Inc, Sherborn, MA). All scans were spatially normalized into a standard brain space and smoothened by a Gaussian filter of 10-mm FWHM over a 3D space to increase the signal to noise ratio for statistical analysis.
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4

PET Imaging of Alzheimer's Disease

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Based on the preclinical findings, we enrolled AD patients and healthy control subjects in performing a PET study after the injection of [18F]DRKXH1. The present study aimed to evaluate the effectiveness of [18F]DRKXH1 in distinguishing AD patients from healthy individuals. This study complied with the Declaration of Helsinki and was approved by the Ethics Committee Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine (approval no. XHEC-F-2019–120). All subjects signed informed consent before participation in the study.
The AD patients were recruited, examined, and diagnosed by qualified attending neurologists. All physicians abided by the uniform diagnostic criteria, including detailed medical history and mini-mental state examination (MMSE).
All subjects underwent a PET assessment at 45 min after intravenous bolus injection of [18F]DRKXH1(370 MBq). Siemens Biograph 64PET/CT (Erlangen, Germany) was used for three-dimensional (3D) scanning. Before PET scanning, a low dose CT transmission scan was performed, and attenuation correction was performed. The image reconstruction was carried out by ordered subset expectation maximization 3D (OSEM 3D) method.
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5

PET Imaging of Dopamine Transporter and Glucose Metabolism in Parkinson's Disease

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One week before or after the neuropsychological assessments, all patients underwent 11C-CFT PET and then underwent 18F-FDG PET on the following day. No anti-parkinsonian medications were administered to the patients within 12 h prior to PET imaging. To prepare for 18F-FDG PET, subjects were additionally required to fast for at least 6 h before the PET scan. The patients underwent a Siemens Biograph 64 PET/CT (Siemens, Munich, Germany) in 3D mode. A low-dose CT transmission scan was performed for attenuation correction. Then, PET scanning was acquired during the interval of 60–75 min after 350–400 MBq of 11C-CFT was intravenously injected. For 18F-FDG, a 10-min PET scan was acquired at 45 min post injection (150–200 MBq). Image reconstruction was obtained by the ordered subset expectation maximization 3D (OSEM 3D) method. All patients were placed in a quiet, dimly lit room to rest.
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6

PET/CT Imaging Protocol for 18F-FDG Uptake

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Whole body PET/CT images were obtained using a PET/CT scanner Biograph 64 PET/CT (Siemens Healthcare Sector, Erlangen, Germany) as previously reported (Stecco et al., 2016 (link)). Patients fasted for at least 6 h before tracer injection. After injection of 2.22∼4.44 MBq/kg of 18F-FDG, PET images were obtained after an approximately 60-min uptake period with the patient’s arms raised to cover the orbitomeatal line to the proximal third of the femurs. After obtaining a scout view (120-140 kVp, 30 mAs), the PET protocol comprised five to six bed positions (3 min each) depending on the patients height. Three-dimensional image reconstructions were acquired using the iterative reconstruction algorithms. The duration of PET/CT acquisition was approximately 20 min.
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7

Quantifying Myocardial Fatty Acid Uptake

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For this particular subanalysis, PET images from study 3 were obtained using a Siemens Biograph 64 PET/CT with a 21.8-cm axial field of view (Siemens). Patients were placed with the heart in the field of view, and a low-dose CT scan was obtained for attenuation and anatomic localization purposes. [11C]Palmitate was injected as a bolus (283 ± 65 MBq) and a 50-minute list mode scan (frame structure 6 × 5 seconds, 6 × 10 seconds, 3 × 20 seconds, 5 × 30 seconds, 5 × 60 seconds, 8 × 150 seconds, 4 × 300 seconds) was performed. Data were reconstructed using a 3D iterative algorithm with a 168 × 168 matrix size, 3 iterations, 21 subsets, and a 5-mm Gaussian postfilter.
The [11C]palmitate corrected for metabolites from study 2 was then used in cardiac image analysis to compare the values of myocardial fatty acid uptake (MFAU) using 2 differently corrected input functions; (1) image-derived input function (IDIF)16 (link) with hematocrit correction and individual [11C] metabolite correction and (2) IDIF with hematocrit correction and population-based [11C] metabolite correction. For both approaches, the metabolite-corrected plasma activity curve was calculated by fitting a Hill-function to the metabolite data.
Analysis of MFAU was done by a 3-tissue compartmental model17 (link) using in-house developed software. The kinetic model and equations are depicted in supplementary Figure 1.
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8

Dynamic PET/CT Imaging of Myocardial Uptake

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Eight scans, 5 control and 3 injury pigs, were performed using a Siemens Biograph 64 PET/CT. Following administration of 185 MBq of 18F-TPP+ as a single intravenous bolus, scanning was performed over 120 minutes in list mode. CT angiography was performed for anatomic reference. List mode data were framed as a dynamic series of 12x3, 9x5, 7x10, 15x30 second frames. PET/CT data were reconstructed using a filtered back projection algorithm with CT-based attenuation correction to yield a radioactivity concentration map in units of Bq/cc with 83 slices and a voxel size of 2.14x2.14x3 mm3. fECS was measured in 3 injury pigs with CT scanning using a bolus plus infusion iodinated contrast protocol [36 (link)].
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9

Multimodal Imaging of Phantom and Cadavers

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The phantom with hydrogel packing underwent CT imaging with a Siemens SOMATOM® sliding gantry CT (Siemens AG; Berlin and Munich, Germany) using 1.5 mm slice thickness. For the cadaver studies, scanning was performed on a Siemens Biograph 64 PET/CT using 1.5 mm slice thickness for CT imaging. Cadavers were then transferred to a 1.5 T Siemens Avanto MRI with T2 sequencing obtained with 2.0 mm slice thickness.
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10

Multimodal Neuroimaging Protocol for Brain Analysis

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MRI scans were performed using a 3-T General Electric Signa scanner (GE, USA). Resting-state fMRI was obtained with the following parameters: TR = 2,000 ms, TE = 35 ms, flip angle = 90°, slice number = 45, field of view (FOV) = 240 × 240 mm, voxel size = 3.3 × 3.3 × 4.0 mm3, 240 time points (8 min). During the scanning, subjects were instructed to keep still with their eyes closed but not to fall asleep. High-resolution 3D T1-weighted anatomical images in the sagittal orientation were acquired with a magnetization-prepared rapid gradient-echo sequence (repetition time = 2,300 ms, echo time = 2.98 ms, flip angle = 9°, FOV = 256 × 256 mm2, matrix size = 256 × 256, slice thickness = 1 mm, without interslice gap, voxel size = 1 × 1 × 1 mm3 and 176 slices).
PET scans were performed with a Siemens Biograph 64 PET/CT (Siemens, Germany) in 3D mode. First, these subjects were still and resting in a room that was quiet and had dim lighting. Then an intravenous bolus injection of 185 MBq of FDG was administered. CT transmission scan was performed to allow attenuation correction. Next, The PET scan was started 45 min after the injection and lasted 10 min. Hanning filters were used with filtered-back projection for image reconstruction, resulting in a transaxial and axial cut-off frequency of 0.5. Additional technical details on the scanner were reported elsewhere (13 (link), 14 (link)).
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