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3 t magnetom skyra

Manufactured by Siemens
Sourced in Germany, United States

The Siemens 3 T Magnetom Skyra is a magnetic resonance imaging (MRI) system. It is a 3 Tesla (3 T) superconducting MRI scanner designed for clinical imaging applications. The Magnetom Skyra provides high-field MRI capabilities for advanced imaging techniques.

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2 protocols using 3 t magnetom skyra

1

Multimodal Imaging Workflow for Prostate Cancer

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Planning CT and MRI scans were performed the same day, with as short a time as possible between scans. Patients were positioned within the scanners on a couch with a flat insert to mimic a radiotherapy couch top. CT scans were performed with patients supine with knee and footstock immobilisation on a Big Bore 16 slice scanner (Philips, Amsterdam, Netherlands), 30 min after drinking 500 mL of water and emptying their rectum (using micro-enema). Scans 2 mm wide were acquired with the Clarity TPUS probe (Elekta, Stockholm, Sweden) [11] (link), [12] (link), [13] (link) in position. To replicate this on the MRI scanner, patients were scanned in the same position with a ‘dummy’ probe constructed of compatible materials in position. At this stage patients had received three to four months of Luteinizing hormone-releasing hormone (LHRH) agonist therapy.
A Siemens 3 T Magnetom Skyra (Siemens Healthineers, Erlangen, Germany) was used for the MRI scans. Multi-parametric sequences were used to determine the location/presence of DILs within the prostate (a combination of anatomical and functional MRI sequences) as recommended in the ESUR prostate MRI guidelines 2012 [14] (link) and elsewhere including the FLAME study [6] (link).
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2

Cardiac MRI Criteria for Acute Myocarditis

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Two different cardiac magnetic resonance (CMR) scanners were used during our study: the Philips Achieva 1.5T (Philips Medical Systems, Best, Netherlands) until the end of September 2016 and Siemens 3T MAGNETOM Skyra (Siemens Medical Solutions USA, Inc, Malvern, PA) since.
Diagnostic CMR criteria for acute myocarditis were the Lake Louise Consensus Criteria defined by the presence of at least 2 of the following criteria: regional or global myocardial signal intensity increase in T2-weighted images, increased global myocardial early gadolinium enhancement ratio between myocardium and skeletal muscle in gadolinium-enhanced T1-weighted images, and nonischemic regional distribution in inversion recovery-prepared gadolinium-enhanced T1-weighted images (late gadolinium enhancement).31 (link) Most recent mapping techniques were not available during the study because of the lack of local validation of these techniques for clinical use during the study period.
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