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Interleaved Image Acquisition
 
The joint collection of data for two or more separate images such that a subset of k-space samples for the second image is acquired immediately after that for the first image. This method avoids misregistration between the two images and allows for accurate subtraction of the two images.
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Liver ImagingForum -
related threadsMRI Resource Directory:
 - Liver Imaging -
 
Liver imaging can be performed with sonography, computed tomography (CT) and magnetic resonance imaging (MRI). Ultrasound is, caused by the easy access, still the first-line imaging method of choice; CT and MRI are applied whenever ultrasound imaging yields vague results. Indications are the characterization of metastases and primary liver tumors e.g., benign lesions such as focal nodular hyperplasia (FNH), adenoma, hemangioma and malignant lesions (cancer) such as hepatocellular carcinomas (HCC). The decision, which medical imaging modality is more suitable, MRI or CT, is dependent on the different factors. CT is less costly and more widely available; modern multislice scanners provide high spatial resolution and short scan times but has the disadvantage of radiation exposure.
With the introduction of high performance MR systems and advanced sequences the image quality of MRI for the liver has gained substantially. Fast spin echo or single shot techniques, often combined with fat suppression, are the most common T2 weighted sequences used in liver MRI procedures. Spoiled gradient echo sequences are used as ideal T1 weighted sequences for evaluating of the liver. The repetition time (TR) can be sufficiently long to acquire enough sections covering the entire liver in one pass, and to provide good signal to noise. The TE should be the shortest in phase echo time (TE), which provides strong T1 weighting, minimizes magnetic susceptibility effects, and permits acquisition within one breath hold to cover the whole liver. A flip angle of 80° provides good T1 weighting and less of power deposition and tissue saturation than a larger flip angle that would provide comparable T1 weighting.
Liver MRI is very dependent on the administration of contrast agents, especially when detection and characterization of focal lesions are the issues. Liver MRI combined with MRCP is useful to evaluate patients with hepatic and biliary disease.
Gadolinium chelates are typical non-specific extracellular agents diffusing rapidly to the extravascular space of tissues being cleared by glomerular filtration at the kidney. These characteristics are somewhat problematic when a large organ with a huge interstitial space like the liver is imaged. These agents provide a small temporal imaging window (seconds), after which they begin to diffuse to the interstitial space not only of healthy liver cells but also of lesions, reducing the contrast gradient necessary for easy lesion detection. Dynamic MRI with multiple phases after i.v. contrast media (Gd chelates), with arterial, portal and late phase images (similar to CT) provides additional information.
An additional advantage of MRI is the availability of liver-specific contrast agents (see also Hepatobiliary Contrast Agents). Gd-EOB-DTPA (gadoxetate disodium, Gadolinium ethoxybenzyl dimeglumine, EOVIST Injection, brand name in other countries is Primovist) is a gadolinium-based MRI contrast agent approved by the FDA for the detection and characterization of known or suspected focal liver lesions.
Gd-EOB-DTPA provides dynamic phases after intravenous injection, similarly to non-specific gadolinium chelates, and distributes into the hepatocytes and bile ducts during the hepatobiliary phase. It has up to 50% hepatobiliary excretion in the normal liver.
Since ferumoxides are not eliminated by the kidney, they possess long plasmatic half-lives, allowing circulation for several minutes in the vascular space. The uptake process is dependent on the total size of the particle being quicker for larger particles with a size of the range of 150 nm (called superparamagnetic iron oxide). The smaller ones, possessing a total particle size in the order of 30 nm, are called ultrasmall superparamagnetic iron oxide particles and they suffer a slower uptake by RES cells. Intracellular contrast agents used in liver MRI are primarily targeted to the normal liver parenchyma and not to pathological cells. Currently, iron oxide based MRI contrast agents are not marketed.
Beyond contrast enhanced MRI, the detection of fatty liver disease and iron overload has clinical significance due to the potential for evolution into cirrhosis and hepatocellular carcinoma. Imaging-based liver fat quantification (see also Dixon) provides noninvasively information about fat metabolism; chemical shift imaging or T2*-weighted imaging allow the quantification of hepatic iron concentration.

See also Abdominal Imaging, Primovistâ„¢, Liver Acquisition with Volume Acquisition (LAVA), T1W High Resolution Isotropic Volume Examination (THRIVE) and Bolus Injection.

For Ultrasound Imaging (USI) see Liver Sonography at Medical-Ultrasound-Imaging.com.
 
Images, Movies, Sliders:
 Anatomic Imaging of the Liver  Open this link in a new window
      

 MRI Liver T2 TSE  Open this link in a new window
    
 
Radiology-tip.comradAbdomen CT,  Biliary Contrast Agents
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Medical-Ultrasound-Imaging.comLiver Sonography,  Vascular Ultrasound Contrast Agents
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• View the DATABASE results for 'Liver Imaging' (13).Open this link in a new window


• View the NEWS results for 'Liver Imaging' (10).Open this link in a new window.
 
Further Reading:
  Basics:
Comparison of liver scintigraphy and the liver-spleen contrast in Gd-EOB-DTPA-enhanced MRI on liver function tests
Thursday, 18 November 2021   by www.nature.com    
Liver Imaging Today
Friday, 1 February 2013   by www.healthcare.siemens.it    
Elastography: A Useful Method in Depicting Liver Hardness
Thursday, 15 April 2010   by www.sciencedaily.com    
Iron overload: accuracy of in-phase and out-of-phase MRI as a quick method to evaluate liver iron load in haematological malignancies and chronic liver disease
Friday, 1 June 2012   by www.ncbi.nlm.nih.gov    
  News & More:
Utility and impact of magnetic resonance elastography in the clinical course and management of chronic liver disease
Saturday, 20 January 2024   by www.nature.com    
Even early forms of liver disease affect heart health, Cedars-Sinai study finds
Thursday, 8 December 2022   by www.eurekalert.org    
For monitoring purposes, AI-aided MRI does what liver biopsy does with less risk, lower cost
Wednesday, 28 September 2022   by radiologybusiness.com    
Perspectum: High Liver Fat (Hepatic Steatosis) Linked to Increased Risk of Hospitalization in COVID-19 Patients With Obesity
Monday, 29 March 2021   by www.businesswire.com    
EMA's final opinion confirms restrictions on use of linear gadolinium agents in body scans
Friday, 21 July 2017   by www.ema.europa.eu    
T2-Weighted Liver MRI Using the MultiVane Technique at 3T: Comparison with Conventional T2-Weighted MRI
Friday, 16 October 2015   by www.ncbi.nlm.nih.gov    
EORTC study aims to qualify ADC as predictive imaging biomarker in preoperative regimens
Monday, 4 January 2016   by www.eurekalert.org    
MRI effectively measures hemochromatosis iron burden
Saturday, 3 October 2015   by medicalxpress.com    
Total body iron balance: Liver MRI better than biopsy
Sunday, 15 March 2015   by www.eurekalert.org    
MRI Resources 
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MAGNETOM ESSENZA
 
www.healthcare.siemens.com/magnetic-resonance-imaging/0-35-to-1-5t-mri-scanner/magnetom-essenza/ From Siemens Medical Systems;
Received FDA clearance in 2007.
The MAGNETOM Essenza is designed to combine high system performance with simple installation and power requirements to provide optimal operating costs for limited budgets. The standard system has up to 25 integrated coil elements and 8 independent radio frequency channels. Tim allows the combination of up to 4 different coils that reduce patient and coil repositioning.
The 1.5 Tesla system is designated for a complete range of clinical applications, including neurology, orthopedics, body imaging, angiography, cardiology, breast imaging, oncology and pediatric MRI.
Device Information and Specification
CLINICAL APPLICATION
Whole body
CONFIGURATION
Ultra-short bore
Head, spine, torso/ body coil, neurovascular, cardiac, neck, and multi-purpose flex coils. Peripheral vascular, breast, shoulder, knee, wrist, foot//ankle, TMJ optional.
CHANNELS (min. / max. configuration)
8, 16
Chemical shift imaging and single volume spectroscopy
IMAGING TECHNIQUES
iPAT, mSENSE and GRAPPA (image, k-space), noncontrast angiography, radial motion compensation
MINIMUM TR
3-D GRE: 1.58 (256 matrix)
MINIMUM TE
3-D GRE: 0.5 (256 matrix)
FOV
0.5 - 45 cm
BORE DIAMETER
or W x H
At isocenter: 60 cm
TABLE CAPACITY
200 kg
MAGNET WEIGHT (gantry included)
4350 kg in operation
DIMENSION H*W*D (gantry included)
145 x 226 x 216 cm
5-GAUSS FRINGE FIELD
2.5 m / 4.0 m
CRYOGEN USE
Zero boil off rate, approx. 10 years
COOLING SYSTEM
Water; single cryogen, 2 stage refrigeration
up to 100 T/m/s
30 mT/m, 300 msec to 10 mT/m
Passive, active; first order standard second order optional
POWER REQUIREMENTS
380 / 400 / 420 / 440 / 460 / 480 V, 3-phase + ground; 45 kVA
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MAGNETOM Prisma
 
www.healthcare.siemens.com/magnetic-resonance-imaging/3t-mri-scanner/magnetom-prisma From Siemens Medical Systems; Received FDA clearance in 2013.
The MAGNETOM Prisma is the 3T PowerPack for exploration that offers most demanding clinical and research challenges of today and the future. The latest parallel transmit technology, TimTX TrueShape, enables zooming into specific body regions for enhanced image quality. Furthermore, the Tim 4G integrated coil technology offers remarkable imaging flexibility and supports complex examinations across the whole body.
Onsite upgrades to the MAGNETOM Prisma for customers who have already installed the 3 Tesla MAGNETOM Trio are possible.
Device Information and Specification
CLINICAL APPLICATION
Whole Body
CONFIGURATION
Ultra-short bore
3 Tesla
Head, spine, torso/ body coil, neurovascular, cardiac, neck, shoulder, knee, wrist, foot//ankle and multi-purpose flex coils. Peripheral vascular, breast, shoulder.
CHANNELS (min. / max. configuration)
64, 128
IMAGING TECHNIQUES
iPAT, mSENSE and GRAPPA (image, k-space), noncontrast angiography, radial motion compensation, Dixon
FOV
0.5 - 50 cm
BORE DIAMETER
or W x H
At isocenter: L-R 60 cm
TABLE CAPACITY
250 kg
MAGNET WEIGHT (gantry included)
13000 kg
DIMENSION H*W*D (gantry included)
173 x 230 x 222 cm
5-GAUSS FRINGE FIELD
2.6 m / 4.6 m
CRYOGEN USE
Zero boil off rate, refill approx. 10 years
COOLING SYSTEM
Water
up to 200 T/m/s
MAX. AMPLITUDE
80 mT/m
Passive, active; first order, second order
POWER REQUIREMENTS
380 / 400 / 420 / 440 / 460 / 480 V, 3-phase + ground;
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MAGNETOM Spectra
 
www.healthcare.siemens.com/magnetic-resonance-imaging/3t-mri-scanner/magnetom-spectra From Siemens Medical Systems;
Received FDA clearance in 2012.
The MAGNETOM Spectra is a cost-optimized high field MRI system with Tim 4G and Dot technologies. The system consumes less energy compared to other 3 Tesla scanners. The magnet-cooling helium is contained in a closed loop, which prevents the gas from escaping and reduces the need for refills. TimTX includes innovative techniques in the radio frequency excitation hardware as well as new application and processing features enabling uniform RF distribution in all body regions.
Device Information and Specification
CLINICAL APPLICATION
Whole Body
CONFIGURATION
Short bore
3 Tesla
Head, spine, torso/ body coil, neurovascular, neck and multi-purpose flex coils. Peripheral vascular, breast, shoulder, knee, wrist, foot//ankle, endorectal optional.
CHANNELS
24
Chemical shift imaging, single voxel spectroscopy
IMAGING TECHNIQUES
iPAT, mSENSE and GRAPPA (image, k-space), noncontrast angiography, radial motion compensation
FOV
0.5 - 45 cm
BORE DIAMETER
or W x H
At isocenter: L-R 60 cm
TABLE CAPACITY
200 kg
MAGNET WEIGHT
7200 kg
DIMENSION H*W*D (gantry included)
173 x 231 x 219 cm
5-GAUSS FRINGE FIELD
2.6 m / 4.6 m
CRYOGEN USE
Zero boil off rate, approx. 10 years
COOLING SYSTEM
Water; single cryogen, 2 stage refrigeration
up to 125 T/m/s
MAX. AMPLITUDE
33 mT/m
Passive, active; first order standard, second order optional
POWER REQUIREMENTS
380 / 400 / 420 / 440 / 460 / 480 V, 3-phase + ground; connection value with chiller 100 kvA /without chiller 60 kVA
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