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Biograph 64 hd pet ct

Manufactured by Siemens
Sourced in Germany

The Biograph 64 HD PET/CT is a medical imaging system that combines positron emission tomography (PET) and computed tomography (CT) capabilities. It is designed to provide high-resolution, three-dimensional images of the body's internal structures and functions.

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10 protocols using biograph 64 hd pet ct

1

FDG-PET Brain Imaging Protocol

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The Eclipse RD cyclotron (Siemens AG, Germany) and FDG synthesis device (Siemens ExploraFDG4, Germany) were used to synthesize 18F-FDG, and the resulting radiochemical purity was >95%. All of the subjects were asked to fast at least 6 h before the exam, rested for 15 min in a dark, quiet environment, and received intravenous FDG 0.15 mCi/kg via the cubital vein. Afterward, the subjects continued to rest for 40–50 min and then underwent head PET scans for 3 min. The PET scanner used was a Siemens Biograph 64 HD PET/CT (Siemens AG, Germany), and the spatial resolution of the scanner is 4.2 mm full width at half maximum (FWHM) in axial, sagittal or coronal plane. The PET scan used the 3-dimensional (3D) mode.
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2

FDG-PET Imaging of Temporal Lobe Epilepsy

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All participants fasted for at least 6 h before receiving the injection of 0.07 mCi (2.59 MBq) (Alavi et al., 1986 (link)). F‐FDG per body weight intravenously in an awake and resting state with eyes closed. PET image acquisition was started approximately 60 min after the injection (mean time of 59 min with ranges from 47 to 79 min). The mean scanning time after the FDG injection was not different between the TLE patients with and without HS (59 vs. 56 min, p = 0.665). The PET scanner was a Siemens Biograph 64 HD PET/CT (Siemens AG, Germany). All participants were scanned once, which lasted about 25 min (3.5 min/bed, 7~8 bed/subjects), and the 18F‐FDG‐PET image was reconstructed with ordered-subset expectation maximization (OSEM) iterative reconstruction algorithm in a 168 × 168 matrix with a pixel size of 3.4 mm.
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3

Synthesis and PET Imaging of [11C]-MET

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11C-MET was synthesized by the GE Healthcare-Tracerlab-FXc 11C radiolabelling module semi-automatically. 11C-CO2 was produced by SIEMENS RDS III cyclotron, and homo-cysteine was used as the precursor. The radiochemical purity of the obtained sterile product was higher than 95%. All patients had fasted for at least 4 h before imaging. At 10–15 min after an intravenous bonus injection of 11C-MET (370–550 MBq), a static PET scan was subsequently collected for 20 min with a Siemens Biograph 64 HD PET/CT (Siemens, Erlangen, Germany) in 3-dimensional (3D) mode. PET images were reconstructed using the filter back projection (FBP) with Gaussian filter (FWHM 3.5 mm) and a 256*256 matrix, providing 64 contiguous transaxial slices of 5 mm-thick spacing. Attenuation correction was performed using a low-dose CT (150 mAs, 120 kV, Acq. 64*0.6 mm) before the emission scan.
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4

PET/CT Imaging Protocol for Neurological Disorders

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The scanning equipment used is Siemens Biograph 64 HD PET/CT (Siemens, Erlangen, Germany)

In preparation before scanning, all subjects should fast over 6 hours and withdrew anti-Parkinsonian and antipsychotics drugs for more than 12 hours before clinical assessment and each imaging acquisition. And other drugs that may affect glucose metabolism also need to withdrew over 12 h before the 18F-FDG PET imaging

The acquisition protocols of PET imaging are shown in Table 2.

Acquisition for patients was performed in a resting state in a quiet and dimly lit room to avoid sensory, auditory, and motor stimulation to the patient.
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5

PET Imaging of Dopaminergic Neurotransmission

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All patients stopped taking anti-parkinsonian medications (if used) at least 12 h before PET imaging and received an intravenous injection of the [11C]CFT (370 MBq). A 15-min three-dimensional emission scan was acquired one hour after the injection using the Biograph™ 64 HD PET/CT (Siemens Healthcare, Erlangen, Germany). The low-dose computed tomography was employed for the attenuation correction before the emission scan. PET images were then reconstructed using the three-dimensional ordered subset expectation maximization algorithm after the corrections for scatter, dead time and random coincidences. After that, the SPM5 software (Wellcome Department of Imaging Neuroscience, Institute of Neurology, London, UK), implemented in Matlab 7.4.0 (Mathworks Inc, Sherborn, MA), was utilized to spatially normalize these PET images into the Montreal Neurological Institute (MNI) brain space as previously described in [24 (link), 25 (link)]. Individual MRI scans were not used for image preprocessing since these scans were performed in the routine clinical workup but not acquired according to a standardized protocol [25 (link)]. Finally, a three-dimensional Gaussian filter (10 mm full width at half maximum (FWHM)) was involved to smoothen the normalized PET images.
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6

18F-FDG PET Imaging in Parkinson's Disease

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Before PET scanning, all participants were required to fast for at least six hours, but had free access to water. The PD patients withheld their medication for at least 12 h. PET scans were performed with a Siemens Biograph 64 HD PET/CT (Siemens, Germany) in three-dimensional (3D) mode. Emission data was recorded for ten minutes at 60 min after intravenous injection of 185 ± 25 MBq of 18F-FDG (Wu et al., 2013 (link)). In addition, a low-dose CT transmission scan was carried out for attenuation correction. Data were reconstructed using 3D-ordered subset expectation maximization and corrected for random coincidences, scatter, and radioactive decay. All studies in the patient and HC subjects were conducted in a dimly lit room with minimal background noise.
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7

18F-FET PET Imaging Protocol for Brain

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All patients had fasted for at least 4 hours before imaging. 20 minutes after an intravenous bonus injection of 18F-FET (370 ± 30 MBq), a static PET scan was collected for 20 minutes with a Siemens Biograph 64 HD PET/CT (Siemens, Erlangen, Germany) in 3-dimensional (3D) mode for 50 patients in this cohort. 8 patients underwent dynamic 18F-FET PET scanning lasted longer than 40 minutes after the tracer injection; 20–40 minutes images were reconstructed for diagnosis and analysis. Attenuation correction was performed using a low-dose CT (tube current 150mAs, voltage 120kV, Acq. 64*0.6mm, convolution kernel H30s, slice thickness 5mm, interslice gap 1.5mm) before the emission scan. After acquisition, the PET images were reconstructed by filtered back projection algorithm with Gaussian filter and full-width-at-half-maximum at the center of the field of view of 3.5mm). The reconstructed brain PET image matrix size was 168*168 with voxel size of 2.04*2.04mm. And the reconstructed brain CT image matrix size was 512*512 with voxel size of 0.59*0.59 mm.
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8

PET-CT Imaging Protocol for Glioma Characterization

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18F-FDG PET/CT was performed using integrated PET-CT scanner (Siemens Biograph 64HD PET/CT, Siemens, Germany). During the procedure, the subjects were fixed, and attenuation correction was applied with a low-dose CT (150 mAs, 120 kV, Acq. 64 × 0.6 mm). Following corrections for scatter, dead time, and random coincidences, PET images were reconstructed by 3D filtered back projection and a Gaussian Filter (FWHM 3.5 mm), providing 64 continuous trans-axial slices of 5-mm-thick spacing. PET-CT images were interpreted by experienced radiologists. The FDG uptake was normalized using the standardized uptake value (SUV) by dividing the radioactivity (kBq/mL) in the brain by the radioactivity injected per gram of body weight. The background area is defined in the symmetrical cerebellar cortex. SUVmax was used as the reference measurement and was determined by considering the tumor uptake given by the maximum pixel value within the gliomas [26 (link)].
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9

Resting-State 18F-FDG PET Imaging

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All subjects underwent 18F-FDG PET examination at resting state. PET scans were performed with a Siemens Biograph 64 HD PET/CT (Siemens, Germany) in three-dimensional (3D) mode. All subjects were fasted for at least 6 h before scanning. After intravenous injection of 185 MBq 18F-FDG, the PET scan was started after a 45-min rest in a quiet and dimly lit environment. Prior to the PET scan, a low-dose CT transmission scan was performed for attenuation correction. The PET scan was performed in 3D mode for 10 min. All PET data were reconstructed using a 3D ordered subset expectation maximization algorithm and corrected for random coupling, scattering, and radioactive decay.
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10

PET Imaging of Cerebral Glucose Metabolism

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All subjects were scanned with a Siemens Biograph 64 HD PET/CT (Siemens, Erlangen, Germany) in 3dimensional (3D) mode. 9,23 A CT transmission scan was performed for photon attenuation correction. 11 C-CFT PET imaging: a PET scan was subsequently acquired over 60 to 80 minutes after an intravenous injection of CFT (350-400 MBq) and reconstructed with the ordered subset expectation maximization method. 18 F-FDG PET imaging: a PET scan was acquired over 45 to 55 minutes postinjection (150-200 MBq) and reconstructed with the ordered subset expectation maximization method. Acquisition for individual patient was performed in a resting state in a quiet and dimly lit room. 18 F-FDG image was used as a relative measure of regional cerebral metabolic rate of glucose (rCMRglc).
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