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Absorption Mode
 
Component of the signal that yields in a symmetric, positive-valued line shape.
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Specific Absorption Rate
 
(SAR) The Specific Absorption Rate is defined as the RF power absorbed per unit of mass of an object, and is measured in watts per kilogram (W/kg).
The SAR describes the potential for heating of the patient's tissue due to the application of the RF energy necessary to produce the MR signal. Inhomogeneity of the RF field leads to a local exposure where most of the absorbed energy is applied to one body region rather than the entire person, leading to the concept of a local SAR. Hot spots may occur in the exposed tissue, to avoid or at least minimize effects of such theoretical complications, the frequency and the power of the radio frequency irradiation should be kept at the lowest possible level. Averaging over the whole body leads to the global SAR.
It increases with field strength, radio frequency power and duty cycle, transmitter-coil type and body size. The doubling of the field strength from 1.5 Tesla (1.5T) to 3 Tesla (3T) leads to a quadrupling of SAR. In high and ultrahigh fields, some of the multiple echo, multiple-slice pulse sequences may create a higher SAR than recommended by the agencies. SAR can be reduced by lower flip angle and longer repetition times, which could potentially affect image contrast.
Normally no threatening increase in temperature could be shown. Even in high magnetic fields, the local temperature increases not more than 1°C. 2.1°C is the highest measured increase in skin temperature. Eddy currents may heat up implants and thus may cause local heating.

FDA SAR limits:
Whole body: 4W/kg/15-minute exposure averaged;
Head: 3W/kg/10-minute exposure averaged;
Head or torso: 8W/kg/5 minute exposure per gram of tissue;
Extremities: 12W/kg/5 minute exposure per gram of tissue.

IEC (International Electrotechnical Commission) SAR limits of some European countries:
All limits are averaged over 6 minutes.
Level 0 (normal operating mode): Whole body 2W/kg; Head 3.2W/kg; Head or Torso (local) 10W/kg; Extremities (local) 20W/kg;
Level I (first level controlled operating mode): Whole body 4W/kg; Head 3.2W/kg; Head or Torso (local) 10W/kg; Extremities (local) 20W/kg;
Level II (second level controlled operating mode): All values are over Level I values.
(For more details: IEC 60601-2-33 (2002))

In most countries standard MRI systems are limited to a maximum SAR of 4 W/kg, so most scanning in level II is impossible.
For Level I, in addition to routine monitoring, particular caution must be exercised for patients who are sensitive to temperature increases or to RF energy.
For Japan different SAR limits are valid.
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Further Reading:
  Basics:
SED Guidance
Saturday, 1 January 2022   by www.mriphysics.scot.nhs.uk    
On the estimation of the worst-case implant-induced RF-heating in multi-channel MRI.
Thursday, 2 March 2017   by www.ncbi.nlm.nih.gov    
What MRI Sequences Produce the Highest Specific Absorption Rate (SAR), and Is There Something We Should Be Doing to Reduce the SAR During Standard Examinations?
Thursday, 16 April 2015   by www.ajronline.org    
Evaluation of Specific Absorption Rate as a Dosimeter of MRI-Related Implant Heating
2004   by www.imrser.org    
  News & More:
Specific Absorption Rate and Specific Energy Dose: Comparison of 1.5-T versus 3.0-T Fetal MRI
Tuesday, 7 April 2020   by pubs.rsna.org    
MRI in Patients with Implanted Devices: Current Controversies
Monday, 1 August 2016   by www.acc.org    
Commission delays electromagnetic fields legislation
Monday, 29 October 2007   by cordis.europa.eu:80    
Accounting for biological aggregation in heating and imaging of magnetic nanoparticles
Tuesday, 2 September 2014   by www.ecnmag.com    
Guidance for Industry and FDA Staff, Criteria for Significant Risk Investigations of Magnetic Resonance Diagnostic Devices
Monday, 14 July 2003   by www.fda.gov    
MRI Resources 
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Absorbed Dose
 
This dose means the RF power absorbed per unit of mass of an object, and is measured in watts per kilogram (W/kg).
The absorbed dose is dependent on the duty cycle and transmitter-coil type and increases with field strength, radio frequency power and and body size.
The specific absorption rate (SAR) describes the potential for heating of the patient's tissue due to the application of the RF energy necessary to produce the MR signal.

See also Specific Absorption Rate, MRI Safety, and MRI Risks.
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• View the DATABASE results for 'Absorbed Dose' (2).Open this link in a new window

 
Further Reading:
  Basics:
Commission delays electromagnetic fields legislation
Monday, 29 October 2007   by cordis.europa.eu:80    
Physics of MRI Safety
   by www.aapm.org    
  News & More:
SED Guidance
Saturday, 1 January 2022   by www.mriphysics.scot.nhs.uk    
Specific Absorption Rate and Specific Energy Dose: Comparison of 1.5-T versus 3.0-T Fetal MRI
Tuesday, 7 April 2020   by pubs.rsna.org    
Evaluation of Absorbed Dose by MRI Read-Out
Saturday, 18 November 2017   by www.jstage.jst.go.jp    
Searchterm 'Absorption' was also found in the following services: 
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Duty Cycle
 
Duty cycle is the time during which the gradient system can be run at maximum power. The duty cycle is based on the total time and includes the cool down phase. The duty cycle on the RF pulse during MRI is restricted based on the specific absorption rate (SAR) limit.
SAR limits restrict radio frequency heating effects. The specific absorption rate increases with field strength, radio frequency power and duty cycle, type of the transmitter coil and body size. The especially in high and ultrahigh magnetic fields, important SAR issue can be readily addressed by reducing the RF duty cycle due to longer repetition times (TR) and the use of parallel imaging techniques. A TR longer than the minimum needed provides time for the tissue to cool down, but for the cost of a longer scan time. A parallel imaging technique reduces the RF exposure and the scan time.

See also High Field MRI.
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Gastrointestinal Superparamagnetic Contrast AgentsInfoSheet: - Contrast Agents - 
Intro, Overview, 
Characteristics, 
Types of, 
etc.MRI Resource Directory:
 - Contrast Agents -
 
Gastrointestinal (GI) superparamagnetic contrast agents are used in MRI to improve the visualization of e.g., the intestinal tract, the pancreas (see MRCP), etc. Disadvantages are susceptibility artifacts e.g., dependent on delayed imaging or large volumes resulting in artifacts in the colon and distal small bowel loops related to higher concentration of the particles and absorption of the fluid.
Different types of MRI gastrointestinal superparamagnetic contrast agents:
Magnetite albumin microsphere

Usually gastrointestinal superparamagnetic contrast media consist of small iron oxide crystals (ferrites), which produce a signal reduction in the stomach and bowel after oral administration. The T2 shortening caused by these particles is produced from the local magnetic field inhomogeneities associated with the large magnetic moments of superparamagnetic particles. Ferrites are iron oxides of the general formula Fe203.MO, where M is a divalent metal ion and may be mixed with Fe3O4 in different preparations. Ferrites can produce symptoms of nausea after oral administration, as well as flatulence and a transient rise in serum iron. Embedding in inert substances reduce side effects by decreasing the absorption and interaction with body tissues. Combining these contrast materials with polymers such as polyethylene glycol or cellulose, or with sugars such as dextrose, results in improved T1 and/or T2 relaxivity compared with that of the contrast agent alone.

See also Negative Oral Contrast Agents, Gastrointestinal Diamagnetic Contrast Agents, Relaxivity, and Combination Oral Contrast Agents.
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Further Reading:
  Basics:
Negative GI Contrast Agents
   by www.mritutor.org    
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