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43 protocols using biograph truepoint 64

1

Whole-Body [18F]FDG-PET/CT Protocol

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[18F]FDG-PET/CT was performed, covering the anatomy from the superior orbital rim to the upper thigh, using a 64-row multi-detector hybrid PET/CT device (Biograph TruePoint 64; Siemens, Erlangen, Germany). For PET, this scanner offers an axial field-of-view of 216 mm, a sensitivity of 7.6 cps/kBq, and a transaxial resolution of 4–5 mm. After patients had fasted for five hours, PET was performed 45–60 min after an intravenous administration of a mean of 300 MBq of [F18]FDG, with 3-min/bed position, four iterations, and 21 subsets, a 5-mm slice thickness, and a168x168 matrix, using the point-spread function (PSF)-based reconstruction algorithm TrueX. Venous-phase CE-CT was used for attenuation correction, and was obtained after the intravenous injection of 100 ml of a tri-iodinated, non-ionic contrast medium at a rate of 2 ml/s; a tube current of 120 mA; a tube voltage of 230kV; a collimation of 24x1.2 mm; a 3 mm slice thickness with a 2-mm increment; and a 512x512 matrix.
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2

Multimodal Imaging for Patient Studies

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All patient studies were performed using a fully-integrated PET/MRI system (Siemens Biograph mMR, Siemens Healthcare, Erlangen, Germany) (Delso et al., 2011 (link)). For the purpose of obtaining a reference low-dose CT image of the head, whole-body PET/CT systems were used (Biograph TruePoint 40 and Biograph TruePoint 64, Siemens Healthcare) (Jakoby et al., 2009 ).
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3

PET/CT Dual-Time Acquisition Protocol

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All exams were performed on the same Biograph TruePoint™ 64 PET/CT system (Siemens healthineers®, Erlangen, Germany) after injection of 3 MBq/Kg of 18FDG (Curium®, Saclay, France).
Dual-time acquisition consisted of an initial whole-body acquisition (2 min 30 per step) in dorsal decubitus with arms raised (wbPET) ~1 h after tracer injection, followed by a 1-step acquisition (5 min) centered on the head and neck area with arms down (headPET).
PET images were reconstructed with an iterative OSEM 3D method and corrected for random coincidences, scatter and attenuation using the CT scan. The reconstructed images parameters were as follows: wbPET (cutting thickness = 5 mm; matrix = 1682; voxel size = 4.1 × 4.1 × 5 mm) and headPET (cutting thickness = 3 mm; matrix = 2562; voxel size = 2.7 × 2.7 × 3 mm).
All PET data were anonymized and then analyzed blindly by 2 nuclear medicine physicians to assess inter-observer reproducibility (MM, RA).
To assess intra-observer reproducibility, a second analysis by the most experienced operator was performed 3 months later on a third of the randomly selected cohort.
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4

PET/CT Imaging of [11C]Acetate Uptake

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[11C]acetate was prepared according to a well-established method [27 (link)]. All PET/CT scans were obtained using combined PET/CT scanner (Siemens Biograph TruePoint 64). According to the routine protocol all patients were asked to fast for at least 6 h before the examination and then received an intra-venous injection of [11C]acetate of 8 MBq/kg of body weight. After 20 min patients were scanned from thorax and abdomen. PET images were reconstructed using the TruX algorithm, with four iterations per 21 subsets, a 5-mm-slice thickness and a 168 × 168 matrix. Helical CT acquisitions were performed with 4 D care dose protocol and the following parameters: a tube current of 230 effective mAs, a tube voltage of 120 kVp, a collimation of 24 × 1.2 mm, a pitch of 0.813, and a scanning time of 0.5 s per rotation. For review, the CT images were reconstructed with a section thickness of 5 mm in 3-mm increments.
PET, non-enhanced CT and fused PET/CT images were generated and reviewed on the computer by a specialized physician, and co-registered images were displayed on special workstation system using Hybrid Viewer (HERMES Medical solutions, Stockholm, Sweden).
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5

PET-CT Imaging of Cervical Cancer

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Patients fasted for six hours prior to intravenous injection of 4 MBq/kg 18FDG (with a maximum of 400 MBq). Blood glucose levels were checked before injection, levels <10 mmol/L were accepted. One hour after injection a PET-scan was performed from head to proximal thighs, combined with a low-dose CT using a Biograph TruePoint 64 PET/CT scanner (Siemens medical Solutions, Knoxville, TN, USA), slice thickness 5 mm. All patients were scanned using the same scanner. An extra scan of the cervix area was performed after emptying of the urinary bladder. The CT scans were performed without administration of contrast agent.
Maximum standard uptake value (SUVmax) adjusted for patient weight before and after emptying of the urinary bladder was calculated for the cervix. FDG uptake in nodal areas of the parametria, groins, para-iliacs and para-aortics was reported as well as asymmetrical uptake. FDG uptake in pre-sacral and other more uncommon nodal areas and in other organs was also reported.
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6

PSMA-11 PET/CT Imaging Protocol

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PSMA 11 PET/CT was performed from the vertex to the upper thighs using a 64-row, multidetector hybrid system (Biograph TruePoint 64; Siemens, Erlangen, Germany), with an axial FoV of 216 mm, a PET sensitivity of 7.6 cps/kBq, and a transaxial PET resolution of 4–5 mm (full-width at half-maximum). PET was performed 60 min after intravenous administration of 2 MBq/kg body weight 68Ga-PSMAHBED-CC conjugate 11 with 4 min per bed position, four iterations/21 subsets, slice thickness 5 mm and matrix size 168 × 168, using the point-spread function-based reconstruction algorithm TrueX. CT maps were used for PET attenuation correction. Venous-phase contrast-enhanced CT was performed after intravenous injection of 100 ml of a tri-iodinated, non-ionic contrast medium at a rate of 2 ml/s, with tube voltage 120 kV, tube current 230 mAs, collimation 24 × 1.2 mm, slice thickness 3 mm at a 2-mm increment, and matrix size 512 × 512.
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7

Multimodal Imaging for Patient Studies

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All patient studies were performed using a fully-integrated PET/MRI system (Siemens Biograph mMR, Siemens Healthcare, Erlangen, Germany) (Delso et al., 2011 (link)). For the purpose of obtaining a reference low-dose CT image of the head, whole-body PET/CT systems were used (Biograph TruePoint 40 and Biograph TruePoint 64, Siemens Healthcare) (Jakoby et al., 2009 ).
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8

Amyloid-PET Imaging Acquisition and Analysis

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Amyloid-PET scans were obtained with a Biograph Truepoint 64 PET/CT scanner (Siemens, Erlangen, Germany). All patients underwent PET scanning at rest after intravenous injection of 370 MBq. Amyloid-PET data were first qualitatively analysed by a trained physiologist using a binary method of interpretation for relating “positive” or “negative” scans to neuropathologically defined categories of Aβ plaque density. Structural MRI was also acquired, and FLAIR-weighted images and PET images were co-registered to individual volumetric T1-weighted images. After PET/MRI co-registration, ImcCalc of Statistical Parametric Mapping (SPM12, Wellcome Department of Cognitive Neurology, London, UK) was used to derive standardised uptake value (SUV) PET maps as SUV = AC/(radiotracer dose/BW). AC represents activity concentration in a given voxel [kBq/ml], radiotracer dose is the injected tracer dose corrected for residual activity in the syringe [MBq] and BW is the body weight [kg]. SUV maps were calculated in the grey matter (GM) of anterior cingulate gyrus, frontal lobe, parietal lobe, posterior cingulate gyrus, precuneus, temporal lobe, and of the average of these six regions (GM mean). The whole cerebellum was the reference region for the SUV relative ratio (SUVR). For the GM mean, we applied the validated threshold for amyloid-PET SUVR (1.11) [24 (link), 25 (link)].
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9

11C-PiB PET Imaging of Amyloid-Beta in Alzheimer's Disease

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PET images were acquired using either a Siemens Biograph 40 or Biograph TruePoint 64 PET/CT scanner (Siemens Healthcare, Erlangen, Germany) and the tracer 11C-PiB-PET, which binds with affinity to Aβ. Both baseline and follow-up scans were acquired on the same scanner. 11C-PIB was administered as a bolus with a mean activity of 421 MBq (183-754 MBq) per injection, with image acquisition 40–70 minutes after injection as 6 × 5-minute frames. The time window 40- to 70-minute postinjection was used because it provides stability and an effective contrast between healthy subjects and patients with AD [54] (link).
Default random, scatter, and dead time correction and low-dose CT-based attenuation correction were applied (120 kVp, 40 mA) for all images. Image reconstruction was performed using a 2D ordered-subsets expectation maximization algorithm with 6 iterations and 16 subsets and filtered with a 5-mm (full-width, half-maximum) gaussian filter.
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10

PET/CT Imaging Protocol for F-FDG Uptake

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All patients fasted for 6 h before undergoing 18F-FDG-PET/CT, which involved the injection of 4.44 MBq/kg of 18F-FDG. In all cases, the fasting serum glucose level was below 180 mg/dL. The studies were performed in a 64-slice PET/CT scanner (Biograph TruePoint 64; Siemens Medical Solutions, Knoxville, TN, USA) 60 min after radiotracer injection. The CT parameters included 5 mm axial reconstruction, with a tube voltage of 120 kV or automatic tube voltage selection (CARE Dose 4D; Siemens Healthcare, Forchheim, Germany). The PET images were acquired from the head to upper thighs in three-dimensional mode with 90 s/bed position, without contrast administration.
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