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Achieva system

Manufactured by Siemens

The Achieva System is a medical imaging device designed for diagnostic and research purposes. It is capable of performing magnetic resonance imaging (MRI) scans to provide detailed images of the body's internal structures. The core function of the Achieva System is to generate high-quality MRI data that can be used by healthcare professionals and researchers for analysis and clinical decision-making.

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2 protocols using achieva system

1

Brain Imaging with 3T MRI Scanners

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Images of the brain were acquired using a 3 Tesla (3T) Philips Achieva System with an 8-channel head-receiver coil or a 3T Siemens Prisma using a 20-channel head-neck coil. Structural T1-weighted images and T2-weighted fluid attenuated inversion recovery (FLAIR) images were reviewed by a staff neuroradiologist.
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2

Multiparametric MRI Evaluation of Testicular Lesions

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MRI explorations were initially performed on a 1.5 Tesla Philips Healthcare Achieva™ system (11/42) (Best, The Netherlands), a 1.5 Tesla Siemens Healthcare Magnetom Aera™ system (21/42) or a 3 Tesla Siemens Healthcare Skyra™ system (10/42) (Erlangen, Germany). The imaging protocol included axial, coronal, and sagittal T2 turbo spin echo, axial T1 turbo spin echo, diffusion MRI with two B-values (0–800 for the first exams, 50–1000 for the next exams), and dynamic T1 contrast-enhanced sequences that were acquired in the axial plane. We collected the following data: T2WI lesion shape (round or oval-shaped nodule versus focal area with irregular boundaries); number of lesions on T2WI (1; 2; >2); T2WI, T1WI and DWI signal (hyposignal; isosignal; hypersignal); apparent diffusion coefficient (ADC) values in the ADC map of the lesion and the normal testis parenchyma using the manual region of interest; enhancement of the nodule compared with that of the normal contralateral parenchyma (hypoperfusion; isoperfusion; hyperperfusion); time–signal-intensity curve type (15) (if available); and the size of the hypo- or hyperperfused area compared to the T2WI lesion, after intravenous injection of gadolinium chelates (Dotarem™, gadoteric acid, 0.2 mL per kg body weight, Guerbet SA, Aulnay-sous-Bois, France).
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