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Discovery dst

Manufactured by GE Healthcare
Sourced in United States

The Discovery DST is a laboratory equipment product from GE Healthcare. It is designed to perform diagnostic testing and screening procedures. The core function of the Discovery DST is to provide accurate and reliable results for various medical and scientific applications.

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2 protocols using discovery dst

1

Quantitative PET Myocardial Perfusion Imaging

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All patients underwent clinically indicated PET MPI using 13N-ammonia acquired at rest and during pharmacological stress (adenosine infused at 0.14 mg⋅kg−1⋅min−1 over 6 minutes or single bolus injection of 400 mcg of regadenosone) according to clinical routine. All data were acquired in list-mode on a PET/CT scanner (Discovery DST, Discovery MI or Discovery VCT, all GE Healthcare, Waukesha, WI, USA) as previously reported.16 (link) In brief, a body mass index-adapted dose of 13N-ammonia (i.e., 400-1200 Megabecquerels) was injected and the datasets were reconstructed using ordered subset expectation maximum (OSEM, VUE Point HD or VUE Point FX with 2 iterations and 16 subsets), and a 5 mm Hanning filter and standard decay, scatter and sensitivity corrections (voxel size 2.34, 2.34, 2.80-3.27) were applied. Low-dose unenhanced computed tomography was used for attenuation correction. Dynamic datasets were reconstructed from the first 7 minutes of acquisition and consisted of 9 frames of 10 seconds duration, 6 frames of 15 seconds, 3 frames of 20 seconds, 2 frames of 30 seconds and 1 frame of 120 seconds. MBF at rest (corrected for the rate-pressure-product) and during stress and MFR was calculated using commercially available software (QPET 2017.7 Cedars-Sinai Medical Center, Los Angeles, CA, USA). Static datasets were reconstructed from the following 10 minutes of the acquisition.
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2

PET/CT Imaging Protocol for 18F-FDG Uptake

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All studies were performed with a PET/CT scanner (Discovery 600 and Discovery DST, GE Healthcare, Milwaukee, WI), consisting of a PET scanner and a multidetector CT scanner, which allows the acquisition of co-registered CT and PET images from the same patient in 1 session. Patients fasted for at least 6 hours before the intravenous administration of 3.7 MBq/kg of 18F-FDG; patients’ blood glucose levels had to be above 170 mg/dL. All patients were orally hydrated (500 mL of water) during the FDG uptake period and were asked to empty their bladder before positioning for the scan. The combined examination was started about approximately 60 minutes after the FDG injection. CT was acquired first, during shallow breathing, with 140 kV, 60 mA, and 3.75 mm of slice thickness. No oral contrast or intravenous contrast was used for the CT component of the examination. PET was acquired in 3D mode with 3 minutes in each bed position; PET images were reconstructed with an iterative algorithm (ordered subset expectation maximization–OSEM), attenuation, random, and scatter correction. Attenuation correction was performed on the basis of CT scan data.
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