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Biograph 16 scanner

Manufactured by Siemens
Sourced in Germany

The Biograph 16 scanner is a medical imaging device manufactured by Siemens. It is designed to capture high-quality images of the human body using computed tomography (CT) technology. The scanner has a 16-slice configuration, allowing it to obtain multiple cross-sectional images simultaneously. This device is used by healthcare professionals for diagnostic purposes.

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6 protocols using biograph 16 scanner

1

Ga-68 DOTATOC PET/CT Imaging Protocol

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PET/CT examinations were performed on a Biograph 16 scanner (Siemens AG, Germany). Ga-68 DOTATOC was prepared as described by Zhernesekov et al.28 (link) The mean Ga-68 DOTATOC activity administered per patient was 112.5 MBq (median, 106 MBq; range, 66–200 MBq). The PET scan was acquired at approx. 1 hour after administration in 5 – 6 bed positions using a 168 × 168 acquisition matrix. Iterative reconstruction was performed with a scatter correction using the ordered subset expectation maximization technique (OSEM) with 5 iterations and 8 subsets. The transaxial field of view (FOV) was 585 mm and the axial FOV 162 mm. Non-contrast CT or venous phase CT was used for attenuation correction. For the triphasic CT protocol, 80–100 ml Ultravist 370 (Bayer Schering, Germany) was administered, using bolus tracking for acquisition of an arterial phase (approx. 24s delay), a portal venous phase (approx. 45s delay) for an upper abdominal scan with 16 × 0.75 mm slice thickness, and a venous phase (approx. 70s delay) for an upper abdominal scan with 16 × 1.5 mm slice thickness. PET/CT was performed with a triphasic CT protocol in 40 patients, a venous phase alone in 4 patients, and unenhanced CT in 8 patients. The CT dose parameters were: 230 effective mAs and 120 kV.
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2

Preoperative [18F]FDG-PET/CT Imaging Protocol

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All patients underwent preoperative [18F]FDG-PET/CT scanning using a Biograph 16 scanner (Siemens Medical Solutions, Erlangen, Germany). The Biograph 16 consists of a 16-slice CT detector and a Lu2SiO5[Ce] crystal block, which were periodically inspected four times a year. The PET scanner field of view had an 830-mm ring diameter and a 162-mm axial length. The patient was fasting for 6 h prior to the examination34 (link). The injected activity was 3 MBq/kg of [18F]FDG, and PET scans were acquired from the parietal to the proximal thigh at 2 min on bed position, 60 min after injection. PET images were reconstructed using iterative reconstruction (iterations: 2, subsets: 8). Noise reduction was performed by smoothing the images with a Gaussian filter (full width at half maximum, 5 mm). Whole-body CT scans were acquired with patients in the supine position, from the parietal to the proximal thigh (120 kVp; 100 mA in auto mA mode). All data were subjected to attenuation correction based on CT data. The scatter correction followed a single-scatter simulation method.
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3

Multimodal Brain Imaging Protocol

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All participants underwent amyloid PET with 11C-PiB and tau PET with 18F-THK 5351, using a Siemens/Biograph 16 scanner in three-dimensional (3D) mode. For each patient, the two scans were performed within 2 weeks. MRI was also performed on all participants.
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4

Radiotherapy Planning and PET/CT Imaging

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Before the initiation of the treatment, patients underwent a planning CT scan (GE medical systems, USA). Planning CT images were imported into a radiotherapy planning system (Oncentra® External Beam, Elekta, Sweden) for delineation of regions of interest (ROIs) such as gross tumor volume (GTV), lymph nodes, lungs, heart, thoracic vertebrae, and esophagus. Patients also underwent at most three 18F-FDG PET/CT examinations using a Biograph 16-scanner (Siemens, Germany); prior to radiotherapy, at mid-therapy (after median delivery of 9 Gy (range 6 to 18 Gy), and six weeks after completion of radiotherapy. All patients fasted for at least 6 h prior to intravenous administration of 18F-FDG. The amount of 18F-FDG administered was 377 MBq (range; 263–445 MBq) irrespective of patients’ body weight. Patients included in this study had blood glucose level <11 mmol/L when imaged.
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5

Multimodal Brain PET Imaging Protocols

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FACBC-PET and MET-PET were performed in accordance with previously reported procedures (4 (link), 7 (link), 8 ). All the patients underwent MET- and FACBC-PET using the Biograph-16 scanner (lutetium oxyorthosilicate detector, LSO; Siemens, Bonn, Germany). FACBC was manufactured in accordance with Good Manufacturing Practices for investigational drugs and was supplied at a dose of 185 MBq per 2 ml (at the time of assay) by Nihon Medi-Physics Co., Ltd. (Tokyo, Japan) according to previously reported methods (8 , 10 (link)).
Patients fasted for at least 4 h and then were treated with 2 ml of FACBC (mean dose of radioactivity: 235.5±35.2 MBq, range: 211.2–268.1 MBq) or MET (4 MBq/kg) by intravenous injection, followed by a flush with physiological saline. Emission scans of the brain were performed for a total of 10 min, after either 19 min of FACBC administration, or 20 min of MET administration. Axial and trans-axial PET resolutions in Biograph-16 were 5.5 and 5.9 mm (full width at half maximum), respectively. Emission scans were reconstructed to a matrix of 336×336 and attenuation and scatter correction were performed; voxel size was 1.02×1.02×2.00 mm.
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6

Fasting FDG PET/CT Imaging During Mindfulness

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All participants fasted for 6 h before being scanned using a Siemens/Biograph 16 scanner in three-dimensional mode. Imaging was then performed 30 min after intravenous injection of 5 MBq/kg18F-FDG during normal consciousness and mindfulness of breathing in Anapanasati meditation. The level of plasma glucose was determined prior to the18F-FDG PET/CT study. The plasma glucose level of < 200 mg/dl was considered as acceptable for all patients. Image acquisition was performed for 10 min per bed position, matrix size = 256 × 256, zoom = 1, and a Gaussian filter of full-width at half-maximum (FWHM) =2.0. Image reconstruction was performed using the ordered subset expectation maximization (OSEM) with four iterations and eight subsets.
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