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From Hitachi Medical Systems America, Inc.;
the AIRIS made its debut in 1995. Hitachi followed up with the AIRIS II system, which has proven equally successfully. 'All told, Hitachi has installed more than 1,000 MRI systems in the U.S., holding more than 17 percent of the total U.S. MRI installed base, and more than half of the installed base of open MR systems,' says Antonio Garcia, Frost and Sullivan industry research analyst.
Now Altaire employs a blend of innovative Hitachi features called VOSI™ technology, optimizing each sub-system's performance in concert with the
other sub-systems, to give the seamless mix of high-field performance
and the patient comfort, especially for claustrophobic patients, of open MR systems.
Device Information and Specification
CLINICAL APPLICATION
Whole body
DualQuad T/R Body Coil, MA Head, MA C-Spine, MA Shoulder, MA Wrist, MA CTL Spine, MA Knee, MA TMJ, MA Flex Body (3 sizes), Neck, small and large Extremity, PVA (WIP), Breast (WIP), Neurovascular (WIP), Cardiac (WIP) and MA Foot//Ankle (WIP)
SE, GE, GR, IR, FIR, STIR, ss-FSE, FSE, DE-FSE/FIR, FLAIR, ss/ms-EPI, ss/ms EPI- DWI, SSP, MTC, SE/GE-EPI, MRCP, SARGE, RSSG, TRSG, BASG, Angiography: CE, PC, 2D/3D TOF
IMAGING MODES
Single, multislice, volume study
TR
SE: 30 - 10,000msec GE: 3.6 - 10,000msec IR: 50 - 16,700msec FSE: 200 - 16,7000msec
TE
SE : 8 - 250msec IR: 5.2 -7,680msec GE: 1.8 - 2,000 msec FSE: 5.2 - 7,680
0.05 sec/image (256 x 256)
2D: 2 - 100 mm; 3D: 0.5 - 5 mm
Level Range: -2,000 to +4,000
COOLING SYSTEM TYPE
Water-cooled
3.1 m lateral, 3.6 m vertical
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With this method irregular RR intervals in cardiac gating during cardiovascular imaging are rejected and then repeated to improve the image quality, whereby the cardiac frequency is used as a basis of the normal heart rate.
The RR interval window determines the percentage variation of the heart rate. Variations of the acquired data outside the window are rejected and not used in the image reconstruction. Also one interval after the arrhytmic beat will be rejected.
Arrhythmia rejection may be inappropriate for patients with certain pathologies, because if the RR interval is constant long, short, long, - all intervals would be rejected. Also a disadvantage is the time consume, but in some cases this function is mandatory, e.g. for diverse retrospective triggered sequences. | | | | | Further Reading: | | Basics:
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An image artifact is a structure not normally present but visible as a result of a limitation or malfunction in the hardware or software of the MRI device, or in other cases a consequence of environmental influences as heat or humidity or it can be caused by the human body (blood flow, implants etc.). The knowledge of MRI artifacts (brit. artefacts) and noise producing factors is important for continuing maintenance of high image quality. Artifacts may be very noticeable or just a few pixels out of balance but can give confusing artifactual appearances with pathology that may be misdiagnosed.
Changes in patient position, different pulse sequences, metallic artifacts, or other imaging variables can cause image distortions, which can be reduced by the operator; artifacts due to the MR system may require a service engineer.
Many types of artifacts may occur in magnetic resonance imaging. Artifacts in magnetic resonance imaging are typically classified as to their basic principles, e.g.:
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Physiologic (motion, flow)
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Hardware (electromagnetic spikes, ringing)
Several techniques are developed to reduce these artifacts (e.g. respiratory compensation, cardiac gating, eddy current compensation) but sometimes these effects can also be exploited, e.g. for flow measurements.
See also the related poll result: ' Most outages of your scanning system are caused by failure of'
| | | | • View the DATABASE results for 'Artifact' (166).
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From Aurora Imaging Technology, Inc.;
The Aurora® 1.5T Dedicated Breast MRI System with Bilateral SpiralRODEO™ is the first and only FDA approved MRI device designed specifically for breast imaging. The Aurora System, which is already in clinical use at a growing number of leading breast care centers in the US, Europe, got in December 2006 also the approval from the State Food and Drug Administration of the People's Republic of China (SFDA).
'Some of the proprietary and distinguishing features of the Aurora System include: 1) an ellipsoid magnetic shim that provides coverage of both breasts, the chest wall and bilateral axillary lymph nodes; 2) a precision gradient coil with the high linearity required for high resolution spiral reconstruction;; 3) a patient-handling table that provides patient comfort and procedural utility; 4) a fully integrated Interventional System for MRI guided biopsy and localization; and 5) the user-friendly AuroraCAD™ computer-aided image display system designed to improve the accuracy and efficiency of diagnostic interpretations.'
Device Information and Specification
CONFIGURATION
Short bore compact
TE
From 5 ms for RODEO Plus to over 80 ms, 120 ms for T2 sequences
Around 0.02 sec for a 256x256 image, 12.4 sec for a 512 x 512 x 32 multislice set
20 - 36 cm, max. elliptical 36 x 44 cm
POWER REQUIREMENTS
150A/120V-208Y/3 Phase//60 Hz/5 Wire
| | | | • View the DATABASE results for 'Aurora® 1.5T Dedicated Breast MRI System' (2).
| | | • View the NEWS results for 'Aurora® 1.5T Dedicated Breast MRI System' (3).
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| | | | • View the DATABASE results for 'B-Value' (5).
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