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Biograph 40 mct pet ct scanner

Manufactured by Siemens
Sourced in United States

The Biograph 40 mCT PET/CT scanner is a medical imaging device designed for positron emission tomography (PET) and computed tomography (CT) scans. It combines these two imaging modalities to provide comprehensive information about the body's structure and function. The device is capable of acquiring high-quality images to assist healthcare professionals in the diagnosis and monitoring of various medical conditions.

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4 protocols using biograph 40 mct pet ct scanner

1

PET/CT Imaging of Prostate Cancer with 68Ga-PSMA-11

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A mean activity of 68Ga-PSMA-11 of 120 ± 19 MBq was administered intravenously, followed by a 500 mL infusion of NaCl 0.9%. No diuretics were applied. The mean time between injection and PET acquisition was approximately 60 min according to standard procedures for prostate cancer imaging [22 (link)]. PET/CT datasets were acquired on a Biograph 40 mCT PET/CT scanner (Siemens Medical Solutions, Knoxville, TN, USA) (acquisition time: 3 min/bed position; extended FOV: 21.4 cm (TrueV), slice thickness: 3.0 mm) with EANM Research Ltd. accreditation. A standard LD spiral CT was acquired for attenuation correction and anatomical localization using an X-ray tube voltage of 120 keV and a modulation of the tube current applying CARE Dose4D with a reference tube current of 50 mAs. CT images were reconstructed as a 512 × 512 matrix with an increment of 3 mm and a slice thickness of 5.0 mm. The PET images were iteratively reconstructed using the three-dimensional OSEM (ordered-subset expectation maximization) algorithm with 3 iterations, 24 subsets, and with Gaussian filtering to a transaxial resolution of 5 mm at full-width at half-maximum (FWHM). Attenuation correction was performed using the low-dose non-enhanced CT data.
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2

Amplitude-based Respiratory Gating in PET/CT

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A Biograph 40 mCT PET/CT scanner with an extended field of view (TrueV) was used (Siemens Healthcare). This scanner is accredited by the Research 4 Life initiative for quantitative PET/ CT imaging (16) . The PET images were acquired using an optimized, amplitude-based respiratory gating algorithm (HD• Chest) that was integrated in the PET/CT software. Respiratory gating was performed on bed positions covering the thorax and upper abdomen. Gated and nongated bed positions were acquired during free breathing for 6 and 2 min, respectively. Respiratory gating was performed with a duty cycle of 35%, providing a good balance between image quality and motion rejection (7) . The longer acquisition time for the gated bed positions (thorax and upper abdomen) than for the nongated ones led to images with similar statistical quality after gating. The respiratory signal was acquired using a respiratory gating system with a pressure sensor integrated in an elastic belt placed around the patient's abdomen (AZ-733V Electronics; Anzai Medical Co, Ltd.).
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3

PET Imaging of Prostate Cancer with [68Ga]Ga-PSMA-11

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For PET imaging, a mean activity of 127 ± 18 MBq [68Ga]Ga-PSMA-11 was applied, followed by a 500 mL infusion of NaCl 0.9%. In accordance with standard procedures for prostate cancer imaging [31 (link)], the time between injection and PET acquisition was 64 ± 9 min. All PET/CT scans were performed using a Biograph mCT 40 PET/CT scanner (Siemens Medical Solutions, Knoxville, TN, USA) 18F-accredited by European Association of Nuclear Medicine (EANM) Research Ltd. With respect to 68Ga, inhouse phantom measurements were also routinely performed to allow valid PET quantification. The PET acquisition was conducted from vertex to proximal femur with a 3 min acquisition time per bed position (extended field of view: 21.4 cm). CT data was acquired in low-dose technique using an X-ray tube voltage of 120 keV and a modulation of the tube current by applying ‘CARE Dose4D’ with a maximal tube current time product of 30 mAs. The PET data sets were reconstructed using an iterative 3D OSEM (ordered subset expectation maximization) algorithm (3 iterations, 24 subsets) with Gaussian filtering and slice thickness of 5 mm. Random correction, decay correction, scatter attenuation and attenuation correction were applied.
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4

Comparative PET Imaging with 18F-DCFPyL and 18F-PSMA-1007

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Imaging was performed on 2 different days to minimize the effects of possible competitive interactions of the radiotracers. The first 6 patients were imaged with 18 F-DCFPyL and then 48 h later with 18 F-PSMA-1007. The next 6 patients were examined with 18 F-PSMA-1007 and then 48 h later with 18 F-DCFPyL. The patients fasted for at least 4 h before injection of the radiotracer. For both tracers, the injected activities were 240-260 MBq and imaging began 2 h after injection.
All scans were obtained on a Biograph mCT 40 PET/CT scanner (Siemens). For both tracers, an unenhanced CT scan was obtained, followed by PET scans from thighs to vertex. CT parameters were adjusted for patient weight (120 keV, 40-150 mAs), with a section width of 5 mm and a pitch of 0.8. Vertex to mid-thigh PET imaging was performed in 3-dimensional mode at 3 min per bed position. CT data were used for attenuation correction. Images were reconstructed with an ordered-subset expectation-maximization iterative reconstruction algorithm (4 iterations, 8 subsets). A gaussian filter of 5.0 mm in full width at half maximum was applied.
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