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ABLAVAR™ (formerly named Vasovist™) is a blood pool agent for magnetic resonance angiography ( MRA), which opens new medical imaging possibilities in the evaluation of aortoiliac occlusive disease (AIOD) in patients with suspected peripheral vascular disease.
ABLAVAR™ binds reversibly to blood albumin, providing imaging with high spatial resolution up to 1 hour after injection, due to its high relaxivity and to the long lasting increased signal intensity of blood.
As with other contrast media: the possibility of serious or life-threatening anaphylactic or anaphylactoid reactions, including cardiovascular, respiratory and/or cutaneous manifestations, should always be considered.
WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with acute or chronic severe renal insufficiency (glomerular filtration rate less than 30 mL/min/1.73m 2), or acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
See also Cardiovascular Imaging, Adverse Reaction, Molecular Imaging, and MRI Safety.
Drug Information and Specification
NAME OF COMPOUND
Diphenylcyclohexyl phosphodiester-Gd-DTPA, gadofosveset trisodium, MS-325
T1, predominantly positive enhancement
20-45 mmol-1sec-1, Bo=0,47T
PHARMACOKINETIC
Intravascular
CONCENTRATION
244 mg/mL, 0.25mmol/mL
DOSAGE
0.12 mL/kg, 0.03 mmol/kg
DEVELOPMENT STAGE
FDA approved
DO NOT RELY ON THE INFORMATION PROVIDED HERE, THEY ARE NOT A SUBSTITUTE FOR THE ACCOMPANYING
PACKAGE INSERT!
Distribution Information
TERRITORY
TRADE NAME
DEVELOPMENT STAGE
DISTRIBUTOR
USA, Canada, Australia
ABLAVAR™
Approved
| | | | • View the NEWS results for 'ABLAVAR™' (1).
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From Hitachi Medical Systems America Inc.;
the AIRIS II, an entry in the diagnostic category of open MR systems, was designed by Hitachi
Medical Systems America Inc. (Twinsburg, OH, USA) and Hitachi Medical Corp. (Tokyo) and is manufactured by the Tokyo branch. A 0.3 T field-strength magnet and phased array coils deliver high image quality without the need for a tunnel-type high-field system, thereby significantly improving patient comfort not only for claustrophobic patients.
Device Information and Specification
CLINICAL APPLICATION
Whole body
QD Head, MA Head and Neck, QD C-Spine, MA or QD Shoulder, MA CTL Spine, QD Knee, Neck, QD TMJ, QD Breast, QD Flex Body (4 sizes), Small and Large Extrem., QD Wrist, MA Foot and Ankle (WIP), PVA (WIP)
SE, GE, GR, IR, FIR, STIR, FSE, ss-FSE, FLAIR, EPI -DWI, SE-EPI, ms - EPI, SSP, MTC, SARGE, RSSG, TRSG, MRCP, Angiography: CE, 2D/3D TOF
IMAGING MODES
Single, multislice, volume study
TR
SE: 30 - 10,000msec GE: 20 - 10,000msec IR: 50 - 16,700msec FSE: 200 - 16,7000msec
TE
SE : 10 - 250msec IR: 10 -250msec GE: 5 - 50 msec FSE: 15 - 2,000
0.05 sec/image (256 x 256)
2D: 2 - 100 mm; 3D: 0.5 - 5 mm
Level Range: -2,000 to +4,000
POWER REQUIREMENTS
208/220/240 V, single phase
COOLING SYSTEM TYPE
Air-cooled
2.0 m lateral, 2.5 m vert./long
| | | | • View the DATABASE results for 'AIRIS II™' (2).
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Developed by GE Lunar; the ARTOSCAN™-M is designed specifically for in-office musculoskeletal imaging. ARTOSCAN-M's compact, modular design allows placing within a clinical environment, bringing MRI to the patient. Patients remain outside the magnet at all times during the examinations, enabling constant patient-technologist contact. ARTOSCAN-M requires no special RF room, magnetic shielding, special power supply or air conditioning.
The C-SCAN™ (also known as Artoscan C) is developed from the ARTOSCAN™ - M, with a new computer platform.
Device Information and Specification
CLINICAL APPLICATION
Dedicated extremity
SE, GE, IR, STIR, FSE, 3D CE, GE-STIR, 3D GE, ME, TME, HSE
SLICE THICKNESS
2D: 2 mm - 10 mm;
3D: 0.6 mm - 10 mm
4,096 gray lvls, 256 lvls in 3D
POWER REQUIREMENTS
100/110/200/220/230/240V
| | | | • View the DATABASE results for 'ARTOSCAN™ - M' (3).
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Quick Overview
Please note that there are different common names for this MRI artifact.
DESCRIPTION
Image wrap around
Aliasing is an artifact that occurs in MR images when the scanned body part is larger than field of view ( FOV). As a consequence of the acquired k-space frequencies not being sampled densely enough, whereby portions of the object outside of the desired FOV get mapped to an incorrect location inside the FOV. The cyclical property of the Fourier transform fills the missing data of the right side with data from behind the FOV of the left side and vice versa. This is caused by a too small number of samples acquired in, e.g. the frequency encoding direction, therefore the spectrums will overlap, resulting in a replication of the object in the x direction.
Aliasing in the frequency direction can be eliminated by twice as fast sampling of the signal or by applying frequency specific filters to the received signal.
A similar problem occurs in the phase encoding direction, where the phases of signal-bearing tissues outside of the FOV in the y-direction are a replication of the phases that are encoded within the FOV. Phase encoding gradients are scaled for the field of view only, therefore tissues outside the FOV do not get properly phase encoded relative to their actual position and 'wraps' into the opposite side of the image.
Image Guidance
| | | | • View the DATABASE results for 'Aliasing Artifact' (11).
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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
| | | | • View the DATABASE results for 'Altaire™' (2).
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