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From Philips Medical Systems;
Philips continues to expand the frontiers of utra high field MRI with the introduction of the new Intera Achieva 3.0T™. Its powerful future-safe platform shares all the advantages of the Achieva family and covers applications throughout the whole body.
Device Information and Specification
CLINICAL APPLICATION
Whole body
CONFIGURATION
Short bore compact
SE, Modified-SE, IR (T1, T2, PD), STIR, FLAIR, SPIR, FFE, T1- FFE, T2- FFE, Balanced FFE, TFE, Balanced TFE, Dynamic, Keyhole, 3D, Multi Chunk 3D, Multi Stack 3D, K Space Shutter, MTC, TSE, Dual IR, DRIVE, EPI, Cine, 2DMSS, DAVE, Mixed Mode; Angiography: Inflow MRA, TONE, PCA, CE MRA
128 x 128, 256 x 256,512 x 512,1024 x 1024 (64 for Bold img)
Variable in 1% increments
Lum.: 120 cd/m2; contrast: 150:1
Variable (op. param. depend.)
POWER REQUIREMENTS
380/400 V
Passive and dynamic, 1st order std./2nd opt.
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(IR) Inversion recovery is an MRI technique, which can be incorporated into MR imaging, wherein the nuclear magnetization is inverted at a time on the order of T1 before the regular imaging pulse-gradient sequences. The resulting partial relaxation of the spins in the di fferent structures being imaged can be used to produce an image that depends strongly on T1. This may bring out di fferences in the appearance of structures with di fferent T1 relaxation times. Note that this does not directly produce an image of T1. T1 in a given region can be calculated from the change in the MR signal from the region due to the inversion pulse compared to the signal with no inversion pulse or an inversion pulse with a di fferent inversion time. This sequence involves successive 180° and 90° pulses. The inversion recovery sequence is specified in terms of three parameters, inversion time (TI), repetition time (TR) and echo time (TE). See also Inversion Recovery Sequence and FLAIR. | | | | | | • View the DATABASE results for 'Inversion Recovery' (42).
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( MRI) Magnetic resonance imaging is a noninvasive medical imaging technique that uses the interaction between radio frequency pulses, a strong magnetic field and body tissue to obtain images of slices/planes from inside the body. These magnets generate fields from approx. 2000 times up to 30000 times stronger than that of the Earth. The use of nuclear magnetic resonance principles produces extremely detailed pictures of the body tissue without the need for x-ray exposure and gives diagnostic information of various organs.
Measured are mobile hydrogen nuclei (protons are the hydrogen atoms of water, the 'H' in H 20), the majority of elements in the body. Only a small part of them contribute to the measured signal, caused by their di fferent alignment in the magnetic field. Protons are capable of absorbing energy if exposed to short radio wave pulses (electromagnetic energy) at their resonance frequency. After the absorption of this energy, the nuclei release this energy so that they return to their initial state of equilibrium.
This transmission of energy by the nuclei as they return to their initial state is what is observed as the MRI signal. The subtle di ffering characteristic of that signal from di fferent tissues combined with complex mathematical formulas analyzed on modern computers is what enables MRI imaging to distinguish between various organs. Any imaging plane, or slice, can be projected, and then stored or printed.
The measured signal intensity depends jointly on the spin density and the relaxation times ( T1 time and T2 time), with their relative importance depending on the particular imaging technique and choice of interpulse times. Any motion such as blood flow, respiration, etc. also a ffects the image brightness.
Magnetic resonance imaging is particularly sensitive in assessing anatomical structures, organs and soft tissues for the detection and diagnosis of a broad range of pathological conditions. MRI pictures can provide contrast between benign and pathological tissues and may be used to stage cancers as well as to evaluate the response to treatment of malignancies. The need for biopsy or exploratory surgery can be eliminated in some cases, and can result in earlier diagnosis of many diseases. See also MRI History and Functional Magnetic Resonance Imaging (fMRI). | | | | | | • View the DATABASE results for 'Magnetic Resonance Imaging MRI' (9).
| | | • View the NEWS results for 'Magnetic Resonance Imaging MRI' (222).
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Drug Information and Specification T1, Predominantly positive enhancement PHARMACOKINETIC Intravascular, extracellular, renal excretion DOSAGE 0.1-0.3 mmol/kg / 0.2-0.6 mL/kg PREPARATION Finished product INDICATION Neuro/whole body DEVELOPMENT STAGE For sale PRESENTATION Vials of 5, 10, 15, 20 and 100 mL bulk package
Pre-filled syringes of 10, 15 and 20 mL 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 Magnevist® for sale Turkey Magnevist®, Magnograf for sale Australia Magnevist® for sale | | | | • View the DATABASE results for 'Magnevist®' (7).
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Quick Overview
NAME
Moire fringes, moire
DESCRIPTION
Superimposed signals of different phases
A moiré pattern is an interference pattern created for example when two grids are overlaid at an angle, or when they have slightly di fferent mesh sizes. The human visual system creates an imaginary pattern of roughly horizontal dark and light bands, the moiré pattern that appears to be superimposed on the lines.
In MRI, the appearance of moiré fringes can be caused by a variety of reasons e.g., inhomogeneity of the main magnetic field caused by a defect shielding ( interference with RF pulses), interferences produced by aliasing, and interferences of echoes from di fferent excitation modes (with di fferent echo times).
Image Guidance
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