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1.5 testa achieva whole body scanner

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The 1.5-Tesla Achieva whole-body scanner is a magnetic resonance imaging (MRI) system developed by Philips. It is designed to provide high-quality imaging of the entire human body. The system utilizes a 1.5-Tesla superconducting magnet to generate the magnetic field necessary for MRI scanning.

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Lab products found in correlation

Mr extended work space 2, by Philips (2 mentions) 16 element phased array cardiac coil, by Philips (1 mentions)

Close spelling variants of this product

Achieva (844 citations) Achieva scanner (536 citations) Achieva whole-body scanner (39 citations) 1.5 Achieva (2 citations)

2 protocols using 1.5 testa achieva whole body scanner

1

Cardiac MRI Imaging Protocol for Volumetric Analysis

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Cardiac magnetic resonance (CMR) examinations were conducted with a Philips 1.5-Testa Achieva whole-body scanner (Philips Healthcare) equipped with a 16-element phased-array cardiac coil [39 (link)]. The imaging protocol always included a standard segmented cine steady-state free-precession (SSFP) sequence to provide high-quality anatomical references. The imaging parameters for the SSFP sequence were as follows: 280 × 280 mm field of view, 8 mm slice thickness with no gap, 3 ms repetition time, 1.50 ms echo time, 60° flip angle, 30 cardiac phases, 1.7 × 1.7 mm voxel size, and a single excitation. CMR images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare, Best, The Netherlands) by two observers experienced in CMR analysis and blinded concerning time-point allocation and patient identification.
Gómez-Vecino A., Corchado-Cobos R., Blanco-Gómez A., García-Sancha N., Castillo-Lluva S., Martín-García A., Mendiburu-Eliçabe M., Prieto C., Ruiz-Pinto S., Pita G., Velasco-Ruiz A., Patino-Alonso C., Galindo-Villardón P., Vera-Pedrosa M.L., Jalife J., Mao J.H., Macías de Plasencia G., Castellanos-Martín A., Sáez-Freire M.D., Fraile-Martín S., Rodrigues-Teixeira T., García-Macías C., Galvis-Jiménez J.M., García-Sánchez A., Isidoro-García M., Fuentes M., García-Cenador M.B., García-Criado F.J., García-Hernández J.L., Hernández-García M.Á., Cruz-Hernández J.J., Rodríguez-Sánchez C.A., García-Sancho A.M., Pérez-López E., Pérez-Martínez A., Gutiérrez-Larraya F., Cartón A.J., García-Sáenz J.Á., Patiño-García A., Martín M., Alonso-Gordoa T., Vulsteke C., Croes L., Hatse S., Van Brussel T., Lambrechts D., Wildiers H., Chang H., Holgado-Madruga M., González-Neira A., Sánchez P.L, & Pérez Losada J. (2023). Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk. Cells, 12(15), 1956.
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2

Cardiac MRI Imaging Protocol for Clinical Research

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Cardiac magnetic resonance (CMR) examinations were conducted with a Philips 1.5-Testa Achieva whole-body scanner (Philips Healthcare) equipped with a 16-element phased-array cardiac coil and fully installed and managed by the Cardiology Department at the University Hospital of Salamanca (Barreiro-Perez et al. 2018 (link)). The imaging protocol always included a standard segmented cine steady-state free-precession (SSFP) sequence to provide high-quality anatomical references. The imaging parameters for the SSFP sequence were: 280 × 280 mm field of view, 8 mm slice thickness with no gap, 3 ms repetition time, 1.50 ms echo time, 60° flip angle, 30 cardiac phases, 1.7 × 1.7 mm voxel size and a single excitation. CMR images were analyzed using dedicated software (MR Extended Work Space 2.6, Philips Healthcare, Netherlands) by two observers experienced in CMR analysis and blinded concerning time-point allocation and patient identification.
Gómez-Vecino A., Corchado-Cobos R., Blanco-Gómez A., García-Sancha N., Castillo-Lluva S., Martín-García A., Mendiburu-Eliçabe M., Prieto C., Ruiz-Pinto S., Pita G., Velasco-Ruiz A., Patino-Alonso C., Galindo-Villardón P., Vera-Pedrosa M.L., Jalife J., Mao J.H., de Plasencia G.M., Castellanos-Martín A., Freire M.D., Fraile-Martín S., Rodrigues-Teixeira T., García-Macías C., Galvis-Jiménez J.M., García-Sánchez A., Isidoro-García M., Fuentes M., García-Cenador M.B., García-Criado F.J., García J.L., Hernández-García M.Á., Hernández J.J., Rodríguez-Sánchez C.A., Martín-Ruiz A., Pérez-López E., Pérez-Martínez A., Gutiérrez-Larraya F., Cartón A.J., García-Sáenz J.Á., Patiño-García A., Martín M., Gordoa T.A., Vulsteke C., Croes L., Hatse S., Brussel T.V., Lambrechts D., Wildiers H., Hang C., Holgado-Madruga M., González-Neira A., Sánchez P.L, & Losada J.P. (2023). Intermediate molecular phenotypes to identify genetic markers of anthracycline-induced cardiotoxicity risk. bioRxiv.
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