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Discovery 690

Manufactured by Siemens
Sourced in Germany

The Discovery 690 is a laboratory equipment designed for scientific research and analysis. It is a versatile and reliable instrument that provides accurate and consistent results. The core function of the Discovery 690 is to perform various analytical and measurement tasks, enabling researchers and scientists to gather and analyze data effectively.

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4 protocols using discovery 690

1

FDG-PET Imaging Protocol Standardization

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FDG was purchased commercially. All FDG-PET images were created using either a 3-dimensional GE Discovery 690 PET/CT scanner or a Siemens ECAT EXACT HR+ PET scanner. Each subject fasted for at least 6 h, resulting in a plasma glucose level less than 120 mg/dl (6.7 mM) at the time of the tracer administration. All patients were injected i.v. with a dose of 142 ± 8 MBq FDG as a slow bolus while sitting quietly in a room with a low noise level and dimmed light. A static emission frame was acquired from 30 to 60 min p.i. for the Siemens ECAT EXACT HR+ PET scanner, respectively from 30 to 45 min p.i. for the Discovery 690 PET/DT. For attenuation correction, a transmission scan with external 68Ge-sources (Siemens) or a low-dose CT was performed before the static acquisition. PET data were reconstructed iteratively (GE) or with filtered back-projection (Siemens).
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2

Radiolabeling and PET/CT Imaging Protocols

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Radiolabeling and administration of 68Ga-PSMA-11 and 18F-PSMA-1007 were performed according to previously reported radiosynthesis and administration procedures [16 (link),17 (link)]. Immediately after injection of the tracer, 20 mg of furosemide was administered intravenously. Patients were asked to empty the bladder prior to the scan. PET/CT scans were acquired 60 min after tracer injection using an iodine-containing contrast agent (Ultravist 300, Bayer Pharma AG, Berlin, Germany; or Imeron 300, Bracco, Konstanz; Germany 2.5 mL/s) during the portal venous phase. For reconstruction, the TrueX algorithm (3 iterations, 21 subsets; Biograph 64, Siemens Healthineers, Erlangen, Germany) or the VUE Point FX algorithm (2 iterations, 36 subsets; Discovery 690) was used with an axial 168 x 168 matrix. Phantom studies based on the National Electrical Manufacturers Association NU2-2001 standard were conducted to allow valid pooling of results between different scanners. Mean injected activity was 213.1 ± 49.7 MBq in pre- and 212.6 ± 45.1 MBq in post-therapeutic PET.
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3

Staging and Restaging GEP NET Patients

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All GEP NET patients underwent [68Ga]DOTATOC PET/CT with the same scanner at different institutions (GE Discovery ST, Discovery ST, and Discovery 690; Siemens Biograph Horizon; Philips Gemini GXL 16) before and after complete PRRT for staging and restaging purposes following the current guidelines [22 (link)]. [68Ga]DOTATOC PET/CT images were acquired 60 min after an administered [68Ga]DOTATOC dose of 2 MBq/kg and co-registered with low-dose CT. The PET scans were validated for proper quantification and quality.
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4

FDG-PET Imaging Protocol for Neuro-Oncology

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FDG was purchased commercially. FDG-PET images were acquired using a 3-dimensional GE Discovery 690 PET/CT scanner or a Siemens ECAT EXACT HR+ PET scanner. All patients fasted for at least six hours, and had a plasma glucose level <120 mg/dl (6.7 mM) at time of tracer administration, when a dose of 140 ± 7 MBq [18F]-FDG was injected as a slow intravenous bolus while the subject sat quietly in a room with dimmed light and low noise level. A static emission frame was acquired from 30 min to 45 min p.i. for the GE Discovery 690 PET/CT, or from 30 min to 60 min p.i. for the Siemens ECAT EXACT HR+ PET scanner. A low-dose CT scan (GE) or a transmission scan with external 68Ge-sources (Siemens) was performed prior to the static acquisition for attenuation correction. PET data were reconstructed iteratively (GE) or with filtered back-projection (Siemens).
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