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MRI Magnetom Verio 3T Siemens

Overview
   
Delivering the most exciting equation in MRI

As a proven innovator Siemens is bringing 3T field strength, 70 cm Open Bore and Tim™ (Total imaging matrix) together in one powerful system. Invest in the MRI solution that helps to make you a leader, with the versatility to provide a wide range of clinical applications today and well into the future.


  • 3T + 70 cm + Tim: high performance and future security
  • TrueForm™ design: enhanced image quality for a wide range of applications
  • 70 cm Open Bore: accommodate more patients

Technical Specifications

MAGNETOM Verio, A Tim System is available in

Tim [102 x 8]
Tim [102 x 18]
Tim [102 x 32]

for studies ranging from clinical routine up to the most advanced research. Extraordinary image quality, unmatched iPAT performance, excellent workflow, and whole body imaging functionality up to 196 cm (6,4 ft.). It comes standard with a VQ-engine (45mT/m @ 200mT/m/s) — one of the strongest gradients in the industry. It offers an anatomical coverage of up to 50 cm FoV.

70 cm Open Bore design

    Unique 70 cm CT-like patient bore diameter accommodates 36% more patient volume
    Table accommodates up to 250 kg or 550 lbs patients


Tim

    Up to 102 seamlessly integrated coil elements with up to 32 RF channels.
    Up to 50 cm FoV. Whole Body imaging functionality up to 196 cm
    iPAT2. Unmatched PAT up to 16.


Compact and light-weight magnet

    The shortest 3T system on the market today at only 173 cm system length
    Light-weight magnet, only 6.3 tons
    Zero Helium boil-off
    TrueFormTM magnet design offers enhanced image quality

  • Footprint: Same as 1.5T system
  • Magnet Weight: 6 tons
  • System Length: 173 cm
  • Stray Field (0.5 mT): 4.7 m x 2.6 m
  • Total Installation Area: 33 m2 (1.5T footprint)
  • Gradient Power: 45mT/m @ 200mT/m/s with up to FoV 50 cm


Workflow Automation

PREPARATION > SCAN > PROCESSING > DIAGNOSIS

Examples are:

    Phoenix and PhoenixZIP
    AutoAlign
    Inline Technology


Computer
syngo speaking user interface.
syngo is the common software platform for all imaging modalities. Enhanced productivity with minimized user interactions per operation step. Based on a powerful Pentium 4 / approx. 3 GHz Panoramic Recon Image Processor reconstructing up to 8694 images per second (256 x 256, 25% recFoV) in combination with a Pentium 4 based Host Computer with two CPU's / approx. 3 GHz and 4 GB RAM capacity.

Cost Effective Siting

    33 m2 floor space only, similar to a 1.5T system
    No computer room required
    Just two electronic cabinets (water-cooled) that can conveniently be placed against the wall

Source: Medical Siemens

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Magnetic Resonance Angiography (MRA)

Magnetic Resonance Angiography. MRA is a generic name for different approaches and variations of vascular imaging by MRI. MRA refers to the computer-assisted generation of images (angiograms) by MRI created by the contrast of magnetically polarized flowing blood against a stationary magnetically saturated parenchyma. The resulting high-differential signal intensity creates a map that includes anatomic and physiological information. MRA techniques that avoid the risks and limitations of conventional invasive arteriographic methods are in development. Current techniques are based on inflow enhancement (time-of-flight methods) or rely on velocity-induced phase shifts (phase-contrast methods). Time-of-flight acquisitions emphasize vessel morphology, whereas phase-contrast methods provide additional information about velocity, direction of blood flow, and volume flow rates. Slice-by-slice (two-dimensional), volumetric (three-dimensional) acquisitions, or a combination of these allow greater flow sensitivity and/or spatial resolution.
The best images are obtained in normal vessels or those with minimal stenotic lesions, using multiple overlapping thin slabs or three-dimensional-phase contrast techniques that are widely available. Vessels with a large lumen give excellent signals that can be measured and used for MRA display.

Advanced degrees of arterial narrowing will be detected by MRA as luminal narrowing and by an overall drop-off in signal intensity due to associated turbulence as lesions become more severe. There is an inherent bias in interpretation of current MRA images to overestimate degree of stenosis. The image of the true stenotic lumen is reduced by a combination of factors: turbulence that causes countercurrent blood flow, decreasing or negating the signal; loss or absence of laminar flow that produces better signals than turbulent flow; and volume of flow too small to generate a signal. A small volume of blood moving through a tight stenosis produces little detectable signal; in the most severe stenoses or near- occlusions with scarce flow of blood, a signal may not be detected at all. In 16 studies that were not uniformly blinded in which MRA was compared with carotid angiography and reported in the English literature, the concurrence rate in depicting lesion size ranged from 39% to 98%36 (Classes II and III). Overestimation of degree of stenosis was frequently noted and accounted for most disagreements (Class II).36 37

A meta-analytic review of MRA pooled as a noninvasive test with carotid duplex ultrasonography and carotid Doppler ultrasonography compared with conventional carotid arteriography has shown sensitivities between 0.82 and 0.86, specificities at 0.98, and test-effectiveness measures at or exceeding 3.0 when predicting occlusion32 (Class II). At ≥70% stenosis of the extracranial ICA, these tests have sensitivities of 0.83 to 0.86, specificities of 0.89 to 0.94, and test-effectiveness measures approaching 3.032 (Class II). At 50% stenosis, sensitivity of all three noninvasive tests ranges from 0.85 to 0.93, with a specificity of 0.9232 (Class II).

There is satisfactory anatomic correlation with conventional arteriography, but MRA generally overrepresents arterial stenosis, especially in high-grade narrowing.38 39 40 41 42 Carotid atheromatous ulceration is not reliably visualized with MRA.43 Research concerning ways to reduce signal loss as a result of stenosis is ongoing; contrast media, for example, might sufficiently increase the signal of flowing blood through stenoses to improve specificity.44 MRA has the advantage of not being operator dependent.

In patients with vertebrobasilar ischemia, vascular imaging may identify the source vessel of ischemic attacks such as the subclavian artery, extracranial or intracranial vertebral arteries, basilar artery, or their branches. A specific surgical intervention analogous to carotid endarterectomy as a verified therapy in the posterior territory does not exist; therefore, precise imaging and measurement of vascular stenoses as obtained with conventional carotid arteriography has not reached the level of importance attained in carotid disease. In this setting a technique such as high-quality MRA that provides a vascular overview45 of the extracranial and intracranial circulations is acceptable for evaluation of vertebrobasilar ischemia. Various MRA techniques produce anatomic images of the vertebral and basilar arteries and their main branches, including the posterior inferior cerebellar, superior cerebellar, and posterior cerebral arteries; the anterior inferior cerebellar artery appears with less consistency. An associated overview of the carotid arteries and the main intracranial branches can be obtained at the same time. Depending on vascular tortuosity and field placement, some vessel segments may not be seen on MRA because of planar exclusion, not disease. In the special case of fibromuscular dysplasia, MRA lacks the capability to distinguish this condition from long segmental atherosclerosis or dissection and may not cover the entire vertebrobasilar and subclavian system.

The agreement of MRA with conventional carotid arteriography in evaluating intracerebral vascular pathology reaches a mean of only 62%36 (Classes II and III), which is less than with extracerebral carotid pathology.

MRA alone is often not sufficient for study and analysis of blood flow and blood vessel anatomy. When MRA is combined with duplex ultrasound, sensitivity and specificity improve but still result in misclassification of 3% of patients showing negative noninvasive test results but carotid stenosis ≥70% on carotid angiography. Misclassification occurs in 9% of patients with occlusion on noninvasive test results but some degree of luminal patency on carotid angiography32 (Class II). When MRA and duplex ultrasound findings agree, some practitioners suspend use of radiographic angiography, reserving this technique for disparate results46 (Class III). Overestimation of degree of carotid stenosis without concurrent conventional angiographic measurements could lead to an excessive number of surgical procedures.

In summary, the limitations of MRA are relative unavailability, high cost compared with other noninvasive tests, sensitivity and specificity insufficient to establish an indication for carotid endarterectomy, and claustrophobic reactions.

Exclusions: MRA is not indicated for patients with intraorbital or intracranial ferromagnetic fragments, aneurysm clips, otic or cochlear implants, old prosthetic heart valves, pacemakers, and neurostimulators, or when agitation and severe claustrophobia cannot be resolved.

Source: AHA Journal

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Diagnostic Criteria of Infarction in MRI of the Brain in Acute Stroke

Acute: Subtle low signal (hypointense) on T1, often difficult to see at this stage, and high signal (hyperintense) on spin density and/or T2-weighted and proton density-weighted images starting 8 h after onset; should follow vascular distribution. Mass effect maximal at 24 h, sometimes starting 2 h after onset, even in the absence of parenchymal signal changes. No parenchymal enhancement with paramagnetic contrast agent. Territorial intravascular paramagnetic contrast enhancement of "slow-flow" arteries in hyperacute infarcts; at 48 h, parenchymal and meningeal enhancement can be expected.

    Subacute (1 wk or older): Low signal on T1, high signal on T2-weighted images. Follows vascular distribution. Revascularization and blood-brain barrier breakdown may cause parenchymal enhancement with contrast agents.

    Old (several weeks to years): Low signal on T1, high signal on T2. Mass effect disappears after 1 mo. Loss of tissue with large infarcts. Parenchymal enhancement fades after several months.

Source: Strokecenter

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Hitachi Oasis 1.2Tesla

Most powerful patient-friendly 1.2T whole body high field open MRI system, using newest gradient and RF technology to provide unmatched image quality throughout all application areas.
Echelon - the new standard in 1.5 Tesla MRI

A fully featured, high-field performance MRI, incorporating state-of-the-art imaging tools which meet your current and future clinical demands.
specification
1.2 Tesla vertical field MRI
Two pillar asymmetric design
270° panoramic view
33mT/m 100T/m/s gradients
ZenithTM solenoid coils
8 channel system
Fully motorised patient table

Features
Highest field strength vertical magnetic field 1.2T open design
Highest patient active comfort technology (PACT)
Covers the following applications: neurology, vascular, body and orthopaedics
High Order Shim System (HOSS™) to enable high homogeneity even when the patient enters the gantry
SENTINEL™ remote assistance and monitoring for maximum uptime

Imaging
RADAR™ RADial Acquisition Regime
RAPID™ Rapid Acquisition through Parallel Imaging Design
TIGRE™
CHESS
BASG
PVA
Water Exitation
TRAQ™
FLUTE™
VASC™ ASL
VASC™ EPI
TOF
PC angiography
PrimeFSE
PrimeFIR
MRCP single shot
Single shot fast spin echo
Sliding MIP
Diffusion-weighted imaging (DWI)
Perfusion analysis
Perfusion CBF
Spectroscopy
DTI (diffusion tensor imaging)
GE IR with 3D isotropic imaging

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MRI Philips Ingenia 3.0T

Specification

Xtend Magnet System


Magnet weight
4600 kg
Open bore diameter
70 cm
Maximum FOV
55 cm
Typical homogeneity at 55 x 55 x 50 cm
= 5 ppm
Typical homogeneity at 50 x 50 x 45 cm
= 1.8 ppm
HeliumSave technology
Yes (Zero boil-off)
Cryogen boil-off rate 
0.0 l/hr*


Xtend Gradient

3.0T Omega HP    

Max. amplitude for each axis
45 mT/m
Max. slew rate for each axis
200 T/m/s


Resolution Parameters
3.0T Omega HP    

Max scan matrix
1024 (2048 optional)
Highest in-plane resolution
5 µm
Max. number of slices
1024


RF Transmit

Parallel RF transmission
Yes, MultiTransmit
RF control
Patient-adaptive. Fully flexible for each
source, real time feedback loop




dStream RF Receive

Number of independent receive channels
Channel Independent
Location of analog-to-digital converter (ADC)
Inside the coil

Signal chain form coil to reconstructor
Signal chain from coil electronics to connector
Digital
Signal chain from connector to magnet
Digital
Signal chain from magnet to reconstructor
Digital 


Patient Environment


Patient aperture
70 cm
Flare on both ends
Yes
Tunnel diameter at both ends
95 cm
Maximum weight capacity*
250 kg (550 lbs)
Patient transport system (optional)
FlexTrak
FlexTrak Mammo
Wireless patient physiological synchronization
Yes
Various acoustic noise reduction solutions
Yes

*for vertical and horizontal movement


dStream Workflow (FlexStream)

FlexCoverage posterior coil
Yes
FlexCoverage anterior coil (optional)
Yes
FlexConnect connectors
Yes
FlexTrak tabletop
Yes
FlexCaddy coil storage (optional)
Yes
FlexTrak patient transport system (optional)
Yes
FlexTrak Mammo mammography solution (optional)
Yes


SmartAssist Efficiency Assistance

SmartStart
Yes
SmartSelect
Yes
SmartExam (optional)
Yes
SmartLine (package dependent)
Yes
SmartLink (package dependent)
Yes


Site Planning

Total gantry installed weight
= 5800 kg
Minimum siting requirement
30 m2

Souce: Medical Philips

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Site Map

How Is MRI Used

In just a few decades, the use of magnetic resonance imaging (MRI) scanners has grown tremendously. Doctors may order MRI scans to help diagnose multiple sclerosis, brain tumors, torn ligaments, tendonitis, cancer and strokes, to name just a few.

Magnetic resonance imaging (MRI) is a noninvasive way to take pictures of the body.An MRI scan is the best way to see inside the human body without cutting it open.

Unlike x-rays and computed tomographic (CT) scans, which use radiation, MRI uses powerful magnets and radio waves. The MRI scanner contains the magnet. The magnetic field produced by an MRI is about 10 thousand times greater than the earth's.

The magnetic field forces hydrogen atoms in the body to line up in a certain way (similar to how the needle on a compass moves when you hold it near a magnet). When radio waves are sent toward the lined-up hydrogen atoms, they bounce back, and a computer records the signal. Different types of tissues send back different signals.

Single MRI images are called slices. The images can be stored on a computer or printed on film. One exam produces dozens or sometimes hundreds of images.

You may not be able to have an MRI if you have any of the following metallic objects in your body:
    Brain aneurysm clips
    Certain artificial heart valves
    Inner ear (cochlear) implants
    Recently placed artificial joints
    Some older types of vascular stents

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