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Achieva quasar dual scanner

Manufactured by Philips

The Achieva Quasar Dual scanner is a magnetic resonance imaging (MRI) system developed by Philips. It is designed to provide high-quality images for diagnostic purposes. The scanner utilizes dual-energy imaging technology to capture images at different energy levels, allowing for enhanced visualization of various tissues and structures within the body. The core function of the Achieva Quasar Dual scanner is to facilitate medical imaging and diagnosis through the acquisition of detailed and informative MRI scans.

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2 protocols using achieva quasar dual scanner

1

Longitudinal Brain Imaging Across Scanners

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The participants were scanned using a 3-T Intera Quasar scanner initially, followed by a 3-T Achieva Quasar Dual scanner, both manufactured by Philips Medical Systems, Best, The Netherlands. There was no alteration in acquisition parameters for T1-weighted sequences for both the scanners: TR = 6.39 ms, TE = 2.9 ms, flip angle = 8°, matrix size = 256 × 256, FOV = 256 × 256 × 190, and slice thickness = 1 mm with no gap between; yielding 1 × 1 × 1 mm3 isotropic voxels. The use of different scanners was due to reasons beyond investigator’s control and any systematic bias arising from the scanner change is unlikely given that participant recruitment was random. In fact, there were no significant differences in cortical features found between the two scanners in the Sydney MAS cohort (18 (link)). Even though there were some cohort differences across the two scanners (at age scan: scanner 1 = 77.9, scanner 2 = 79.0, p = 0.003; years of education: scanner 1 = 11.4, scanner 2 = 12.2, p = 0.013; male/female ratio: scanner 1 = 125/160, scanner 2 = 120/137, p = ns; the final selection of subjects in Section 2.2 are part of this larger cohort), previous studies have suggested that when vendor, field strength, and acquisition parameters remained unchanged, data collected during scanner upgrades could be pooled (19 (link)).
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2

Multi-center MRI Data Processing

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Magnetic resonance imaging data were obtained from 3 different centers. In Sydney, a Phillips 1.5T Gyroscan scanner (Philips Medical Systems, Best, The Netherlands) was initially used (n=118) and was later replaced by a Philips 3T Achieva Quasar Dual scanner (n=35). In Melbourne, a 1.5T Siemens Magnetom Avanto scanner (n=152) and in Brisbane, a 1.5T Siemens Sonata (n=107; Siemens Medical Solutions, Malvern, PA) of similar upgrades and years of manufacture were used. Acquisition protocols of resolution and slice thickness were matched between the centers. Five volunteers were scanned at the 3 centers and a 3D phantom was used to correct for geometric distortions. 14 (link) Twin pairs were always scanned on the same scanner and were scanned either on the same day or within a few weeks of each other.
Three dimensional T1-weighted scans and T2-weighted fluid-attenuated inversion recovery sequence scans were used for data analysis and an automated extraction of WMH was performed (Materials in the online-only Data Supplement). Extracted WMH was then classified into different brain regions and DWMH, PWMH, and false WMH clusters.
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