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Biograph mct truev

Manufactured by Siemens
Sourced in Germany

The Biograph mCT TrueV is a positron emission tomography (PET) and computed tomography (CT) imaging system designed for clinical and research applications. It combines high-resolution PET imaging with the anatomical detail of a multi-slice CT scanner, providing integrated imaging capabilities.

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3 protocols using biograph mct truev

1

Diagnostic Workup for Autoimmune Encephalitis

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We performed a retrospective database analysis as part of an internal audit to identify patients evaluated between 2003 and 2018 with definite diagnosis of AE according to Graus and colleagues’ Position Paper [3 (link)]. We identified 6 patients in whom potential differential diagnoses were excluded by adequate tests, and who underwent autoantibodies analysis, MRI and electroencephalogram (EEG). Additionally, an early brain FDG-PET study was performed in all cases within the first week from the onset of symptoms. A whole-body –FDG-PET scan was added to the paraneoplastic workup of AE screening for malignancy in three patients (cases 1, 2 and 5). Patients fasted for at least 4 h before the study. Forty minutes after the injection of 336.7 ± 72.7 MBq of 18Fluorine-fluorodeoxyglucose, a 20-min PET/CT scan was acquired. All patients were scanned in a Siemens Biograph mCT TrueV. Acquisition and reconstruction were performed with the standard protocol for brain studies, as previously described [20 (link)]. Informed consent was obtained from all individual participants included in the study. Additional informed consent was obtained from all individual participants from whom identifiable information is included in this article.
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2

PET/CT Imaging Protocol for FDG Uptake

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PET/CT images were obtained through Biograph mCT TrueV (Siemens Healthineers, Erlangen, Germany) and uMI 510 (Shanghai United Imaging Healthcare, Shanghai, China) according to the existing procedure guidelines, before and after May 1, 2017, respectively.21 (link)22 (link)23 (link) After measurement of fasting blood glucose, 3.7 MBq/kg of FDG was administered, and PET imaging was performed after 60 minutes. If necessary, delayed imaging was additionally obtained at 120 minutes. Image reconstruction was performed using three-dimensional ordered subset expectation maximization, point-spread function, and time-of-flight correction methods, and attenuation correction was achieved based on the low-dose CT images that were obtained concurrently.
At least one board-certified nuclear medicine specialist interpreted the imaging visually and semi-quantitatively using the maximum standardized uptake values (SUVmax) within the region of interest. The interpreters were informed of all clinical information and were unaware of the final diagnosis. Positive findings were defined as focal or diffuse area(s) of increased activity that were not explained by physiological uptakes. No cutoff values for the SUVmax were specified a priori.
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3

Optimized 90Y PET/CT Imaging Protocol

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The morning after the RE treatment, a 90Y PET/CT scan centered on the liver region (two beds, 10 min/bed) was performed using a Biograph mCT-TrueV (Siemens Medical Solutions), which combines a 64-slice CT with a 21.8 cm field of view time-of-flight PET scanner comprised by lutetium-based crystals (LSO) detector blocks [22 (link)]. The reconstruction protocol used (one iteration, 21 subsets, a 6-mm Gaussian filter and a 200 × 200 matrix) was previously optimized by Martí-Climent et al. [11 (link)].
Final TgV in 90Y PET/CT was defined using the multimodality reading software Syngo.via for MI (Siemens Healthneers) as previously described for 99mTc-MAA-SPECT/CT.
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