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Biograph 16hr

Manufactured by Siemens
Sourced in Germany

The Biograph 16HR is a diagnostic imaging system designed for high-resolution molecular imaging. It combines PET and CT technologies to provide detailed images of the body's metabolism and anatomy. The system's core function is to capture and integrate PET and CT data, enabling comprehensive medical evaluations.

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11 protocols using biograph 16hr

1

Standardized PET/CT Imaging Protocol

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PET/CT examinations were performed using a Biograph 16 HR (Siemens Healthineers, Erlangen, Germany) or a Biograph 64 system (Siemens Healthineers, Erlangen, Germany). All patients were required to fast and avoid strenuous exercise at least 6 hours before 18F-FDG injection, and the level of fasting blood glucose was no more than 11.0 mmol/L. Six or seven-bed positions were imaged from the base of the skull to the mid-thigh at approximately 60±5 minutes after intravenous injection of 3.7–7.4 MBq of 18F-FDG per kilogram of body weight. PET images were acquired for 2–3 minutes per bed position. The ordered-subset expectation maximization algorithm was used for all image reconstructions, incorporating a CT-based transmission map.
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2

Quantification of Metabolic Activity in CRC

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Images of PET/CT were acquired from 71 patients with CRC on a Siemens Biograph 16HR PET/CT scanner with a transaxial intrinsic spatial resolution of 4.1 mm. The quantification of metabolic activity was performed using the standardized uptake value (SUV) normalized to body weight, and the SUVmax for each lesion was calculated.
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3

PET/CT Imaging of HER2 Expression

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68Ga-HER2 affibody was produced in conformity with previous literature (17 (link)). Scanning was performed on a Siemens Biograph 16HR PET/CT scanner. Before administering 3.0 MBq/kg (0.08 mCi/kg) 68Ga-HER2 affibody intravenously, all patients were asked to fast for at least 4 h to reduce gastrointestinal uptake. Patients were requested to keep quiet before and after injection of the tracer. About 2 h after the administration, whole-body PET/CT scanning was initiated. The scanning began with low-dose CT (120 kV, 250–300 mA, pitch 3.6, and rotation time 0.5). A PET examination scan (16.2 cm axial field width, 2–3 min per table position) was obtained immediately after CT scanning. The attenuation-corrected PET data were reconstructed iteratively by the standardized ordered-subset expectation maximization (OSEM) technique and were reoriented in axial, sagittal, and coronal sections.
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4

Standardized PET/CT Imaging Protocol

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A Biograph 16 HR PET/CT scanner (Siemens Healthineers) was used in the single-center study. Briefly, patients were fasted for more than 6 h; and before imaging, their blood glucose levels needed to be less than 8 mmol/L. 18F-FDG (Sumitomo HM-12, pH 4–8, radioactive purity > 95%, radioactive concentration > 370 MBq/ml) was then intravenously injected at a dose of 3.7 MBq/kg; the image acquisition was started 1 h later. CT image scan was preformed (tube voltage 120 kV, tube current 50 mAs, rotational speed 0.5 s/r, FOV 812 mm × 812 mm, 512 × 512 matrix, slice thickness 4 mm) from the vertex to the proximal legs. Low-dose CT was used for attenuation correction, and a standard B19f soft-tissue reconstruction kernel was used for CT images. Consequently, PET image scans (8-bed positions at 2.5 min each, FOV 812 mm × 812 mm, 144 × 144 matrix, slice thickness 4 mm) were acquired from the vertex to the proximal legs with correction for dead time, scatter, and decay. PET images were iteratively reconstructed in 3D mode using ordered subset expectation maximization (2 iterations, 24 subsets, and Gaussian filtering). CT and PET images were reconstructed at a slice thickness of 2.0 mm and an increment of 1.0 mm.
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5

PET/CT Imaging for Chemoradiotherapy Evaluation

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Patients underwent PET/CT scans both before CRT (pre-CRT) and after receiving 20 fractions of radiation doses (mid-CRT). PET/CT scans were obtained with a BIOGRAPH 16HR (Siemens Molecular Imaging, Knoxville, TN) with an axial field of view of 16.2 cm. All images were composed of 128 × 128 pixels with voxel dimensions of 4 × 4 × 4 mm. Patients fasted for at least 6 h before the administration of 0.2 mCi/kg or 7.4 MBq/kg body weight of 18F-FDG, which was produced onsite using Siemens Cyclotron (Eclipse ST 111, Siemens/CTI, Knoxville, TN), and they then rested for approximately 60 (range, 55–75) minutes before the PET scan. The 16-slice CT process was performed for attenuation correction with an X-ray tube voltage and current peak of 120 kV and 120 mA, respectively, a slice thickness of 5 mm, and a spacing of 4 mm. The images were reconstructed using a three-dimensional ordered subset expectation maximization algorithm and attenuation correction derived from the CT data.
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6

PET/CT Imaging and Quantitative Analysis

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18F-FDG PET/CT (Biograph 16HR; Siemens, Germany) examinations were acquired after fasting for 6 h and 60–75 min after intravenous injection of 18F-FDG (3.70–5.55 MBq/kg weight). The blood glucose level was below 120 mg/dl in all included patients before tracer injection. All patients had normal tidal breathing during PET and CT scans. Patients underwent low-dose CT scans (120–140 kV, 65 mA and 5.0 mm slice), followed by PET scans with six to eight bed positions (2 min per bed positions) per patient based on the height. The PET images were reconstructed with attenuation corrected CT using the ordered subset expectation maximization (OSEM) algorithm. Then, all dates were transferred in DICOM format to the Beth Israel PET/CT viewer plugin for FIJI and displayed as axial, coronal, and sagittal images. The SUVmax, SUVmean, MTV, and TLG of all lesions were delineated semiautomatically by the Beth Israel PET/CT viewer plugin for FIJI (http://sourceforge.net/projects/bifijiplugins/) (ImageJ distribution) (13 (link)).
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7

Comparative Evaluation of PET/CT Scanners

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In this study, non-time of flight (TOF) 18F-FDG PET/CT scans were performed using a whole-body PET/CT scanner (Biograph mCT, Siemens Medical Systems, Erlangen, Germany) and a regular PET/CT scanner (Biogragh 16 HR, Siemens Medical Systems, Erlangen, Germany). Before 18F-FDG administration, all the patients received glucose level test and the blood glucose levels should be less than 140 mg/dL. Then, patients fasted for at least 6 h before the injection of 18F-FDG (7.4 MBq/kg) and image acquisition was started 1 hour afterward.
For Siemens Biograph mCT PET/CT scanner, a spiral CT scan with a standardized protocol including 120 kV, 140 mA, and a 3-mm slice thickness was conducted followed by a PET scan. And then, for PET scanning, the acquisition time was 3 minutes per bed position and PET image datasets were reconstructed iteratively with CT data for attenuation correction. While for Siemens biograph 16HR PET/CT scanning, CT scanning was first acquired using a low-dose technique (120 kV, 140 mA, 5 mm slice thickness), and PET scan was obtained immediately after the CT scan (2–3 minutes/bed) with gaussian-filter iterative reconstruction method (iterations 4; subsets 8; image size 168).
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8

PET/CT Imaging Protocol for 18F-FDG

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PET/CT scans were performed using a Biograph 16 HR (Siemens Healthineers, Erlangen, Germany) or a Biograph 64 system (Siemens Healthineers, Erlangen, Germany). All patients were inquired to fast and avoid strenuous exercise at least 6 h before 18F-FDG injection, and the level of fasting blood glucose was no more than 7.0 mmol/L. Images were acquired approximately 60 ± 5 min after intravenous injection of 3.7 MBq of 18F-FDG per kilogram of body weight. Six or seven-bed positions were imaged from the base of the skull to the mid-thigh. PET images were obtained for 2–3 min per bed position. All image reconstructions were performed with the ordered-subset expectation maximization algorithm, incorporating a CT-based transmission map. PET images were reconstructed at 200 × 200 pixels using a Gaussian filter of 5.0 mm full width at half maximum value.
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9

PET-CT Imaging of 18F-FDG Uptake

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18F-FDG was produced by an RDS Eclipse ST medical cyclotron (Siemens Healthiness, Knoxville, TN, USA) and an Explore FDG4 synthesis module.18F-FDG radiochemical purity was >95%. Blood glucose levels of all patients were less than 7.78 mmol/L. Patients fasted for at least 6 hours prior to injection. After intravenous administration of 18F-FDG (3.7 MBq/kg), all patients laid in a bed for one hour and imaged by a Biograph 16HR PET/CT scanner (Siemens Medical Systems, Erlangen, Germany). First, an unenhanced low-dose whole-body CT scan was performed from head to the top of the thighs (tube voltage, 120 kV; tube current, 80–250 mA; rotation time, 0.5 s; helical pitch 3.6; slice thickness, 5 mm; matrix, 512×512). Images were performed for attenuation correction. Then, whole-body PET scan was acquired over the same extent at three minutes per bed position for a total of 6–7 bed positions. PET data were reconstructed using iterative protocols with gaussian-filter iterative method (iterations, 4; subsets, 8). The PET and CT images were imported into the Siemens workstation for analysis.
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10

18F-FDG PET/CT Imaging Protocol

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18F-FDG PET/CT scans were performed with a whole-body PET/CT scanner (Biograph 16 HR; Siemens Medical Systems, Erlangen, Germany). Patients fasted for at least 6 hours, and blood glucose levels had to be <140 mg/dL before the injection of 18F-FDG (3.7 MBq/kg). Scanning was started approximately 1 hour later. CT images were acquired first, with a low-dose technique (120 kV, 140 mA, 5-mm slice thickness), and then positron emission tomography (PET) scanning with the following parameters: 2–3 min/bed with Gaussian-filter iterative reconstruction method (iterations 4; subsets 8; image size 168) for the reconstruction. Two experienced nuclear medicine physicians evaluated the PET/CT images, and the tumor parameters were measured using a computer platform (Syngo; Siemens, Knoxville, TN, USA), including maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV40%, MTV2.5), and total lesion glycolysis (TLG40%, TLG2.5), according to published articles (18 (link)).
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