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3.0 tesla mri scanner

Manufactured by GE Healthcare
Sourced in United States

The 3.0 Tesla MRI scanner is a medical imaging device that uses a powerful magnetic field and radio waves to generate high-resolution images of the human body. It is capable of producing detailed, three-dimensional images of internal structures, including organs, soft tissues, and bones. The 3.0 Tesla MRI scanner is designed to provide healthcare professionals with the information they need to make accurate diagnoses and develop effective treatment plans.

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3 protocols using 3.0 tesla mri scanner

1

MRI and PET Imaging in Animal Study

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Structural brain images (T1-weighted) were acquired using a 3.0 Tesla MRI scanner (GE Medical Systems, Milwaukee, WI) one day prior to the first fWBI fraction, and within two weeks prior to euthanasia. For one animal requiring additional diagnostic imaging, a multi-slice computed tomography (CT) scanner (GE Healthcare, Milwaukee, WI) was used to provide axial, noncontrast anatomic images with 5 mm slice thickness. Animals also received PET scans [data reported previously (9 (link))]. Anesthesia for imaging procedures was as for irradiation.
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2

High-Resolution Brain Imaging Protocol

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High-resolution T1-weighted anatomic scans were acquired on a GE 3.0 Tesla MRI scanner before the overnight sleep recording (BRAVO; TR = 6.70 ms; TE = 2.93 ms; TI = 450 ms; flip angle = 12°; FOV = 256 mm; acquisition voxel size = 1 × 1 × 1 mm).
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3

Cardiac MRI Evaluation of PCI Patients

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CMR was performed with a 3.0 Tesla MRI scanner (General Electric, Waukesha, WI, United States) (Morgan et al., 2018 (link)) both before and 3 months after PCI. CMR included 4 pulse sequences. Specifically, Cine-CMR was performed with a steady-state free precession pulse sequence. Images were acquired in contiguous LV short axis and standard (2-, 3- and 4-chamber) long axis orientations (Figure 2A). SP-CMR was assessed in accordance with established methods previously validated by members of our group (Klem et al., 2006 (link); Heitner et al., 2019 (link)). In brief, pharmacologic stress was induced with regadenoson (0.4 mg), during which gadolinium was infused (0.1 mmol/kg) and LV short axis images (4–5, evenly distributed from base-apex) were acquired using a gradient echo pulse sequence (Figure 2B). Perfusion CMR was repeated 5-min thereafter under baseline (non-stress) conditions. Myocardial infarction (LGE-CMR) was assessed using an inversion recovery pulse sequence, which was acquired 10–30 min post-gadolinium (0.2 mmol/kg) infusion and acquired in spatial orientations matched to Cine-CMR (Figure 2C). CSPAMM in contiguous LV short and long axis slices (8 mm tag spacing, 10 mm slice thickness, no gap) was performed to measure myocardial deformation and strain (Figure 2D).
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