mr safety
DESCRIPTION
MR Safety. Bioeffects. Static Magnetic Fields Varying Magnetic Fields RF Exposure, Acoustic Noise, SAR Implants Missile Effect Pregnancy Pediatric. MR-Related Injuries. Missile Effect/Projectile injury Dislodged ferromagnetic implants Burns Failure of internal/external devices - PowerPoint PPT PresentationTRANSCRIPT
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MR Safety
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Bioeffects
Static Magnetic Fields Varying Magnetic Fields RF Exposure, Acoustic Noise, SAR Implants Missile Effect Pregnancy Pediatric
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MR-Related Injuries
Missile Effect/Projectile injury Dislodged ferromagnetic implants Burns Failure of internal/external devices Failure of patient support systems Acoustic injury Contrast agent adverse effects Cryogen handling related injuries
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Relative Proportions
Reported 2005, injuries occurred over 10 year span
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Reported Deaths 9 deaths out of 389 reported events
3 due to pacemaker failure
2 due to insulin pump failure
Remaining 4 due to Projectile Implant disturbance Asphyxiation (due to cryogenic mishap during
install) Escaped He gas displaces O2
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Static Fields No deleterious bioeffects have been shown for typical
clinical magnet strengths
ECG traces have shown enhanced T wave amplitude
Very high magnet strengths (4 T +) anecdotal reports Dizziness/nausea Disorientation Metallic taste When moving through field
Mild sensory effects Visual sensations (magnetophosphenes)
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Bioeffects Studied
Alterations in cell growth/morphology DNA structure & gene expression Pre- & post-natal reproduction & development Visual functions Animal Behavior Visual response to photic stimulation Nerve bioelectric activity Cardiovascular dynamics, hematological indices Physiological regulation & circadian rhythms Immune response
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Study Results
Often contradictory
Cannot be reliably reproduced
Data based on animal models Cannot be readily extrapolated to humans
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Varying Fields Gradient switching
Rapidly oscillating magnetic fields Induces current in conductors Produces loud banging
Earplugs necessary
Very high gradient fields Magnetophosphenes Peripheral nerve stimulation Most likely with EPI sequences
Most common effect is heating Epicardial or retained intracardiac pacer wires More often heating attributable to RF fields
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RF Fields Major cause of tissue heating
Ferromagnetic implants esp. susceptible
Temperatures < 42° C body does a good job of self regulation FDA limits core temperature rise to 1° C
Specific Absorption Rate (SAR) Watts/Kg Measured by MR
Enter correct patient’s weight! FDA limits
ECG gating studies requires MRI compatible leads Otherwise skin burns could result
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Limiting SAR SAR depends on:
[Magnetic field strength]² [Flip angle]² Size of patient Duty cycle of RF pulses
Minimize heat deposition by: Controlling flip angle ↑ repetition time ↓ # of sections ↑ echo spacing in FSE ↓ # echoes in FSE ↓ refocusing flip angle in FSE
To reduce SAR:
Decrease Power & Duty Cycle of RF Pulses
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Issue Parameter Variables Specified ValueStatic magnetic Field
Magnetic Field B0Maximum strength 3.0 T
Inadvertent exposure
Maximum 0.0005 T
Changing magnetic Field Axial gradients
Τ > 120μs < 20 T/s12μs < Τ < 120μs < 2400/Τ T/s
Τ < 12μs < 200T/sTransverse gradients <3x axial gradients
System < 6 T/sRF Power Deposition
Temperature
Core of body < 18º CMaximum head < 38º CMaximum trunk < 39º CMaximum extremities < 40º C
SAR
Whole body (average) < 4W/kgHead (average) < 3W/kgHead or torso per gram
< 8W/kg
Extremities per gram < 12W/kgAcoustic noise Levels
Peak pressure 200 PaAverage pressure 105 dBA
FDA Limits
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Projectiles
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Wheelchair
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Office Chair
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Firearms
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O2 Tank
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Bed
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Floor Polisher
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Other Metal Objects
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Screening Options
Written screening form
Verbal screening
Screening devices Hand-held magnets Metal detectors CAUTION
Device sensitivity may not guarantee no metal present
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Portable Item Labels
MR SafeWholly nonmetallic itemsComposition known
Not MR SafeClearly ferromagnetic
MR ConditionalNo/negligible attractive forces observed
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Screening Form
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Form Cont’d
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Implants & Prostheses
Intracranial Vascular clips Intravascular coils, filters, stents Extra-cranial vascular clips Vascular access ports Heart valves Dental devices & materials Penile implants Otologic implants Ocular implants Intra-occular ferrous foreign bodies Bullets, pellets & shrapnel Orthopedic implants, materials & devices Halo vest & other similar externally applied devices
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Electrically, Magnetically, orMechanically-Activated or Electrically Conductive Implants
Cardiac pacemakers May be possible to scan assuming:
Non-dependent pacer patient Clinically fit to scan Radiologist, cardiologist, rep from pacer company present Or Newer MR safer pacemaker implanted
Cochlear implants Tissue expanders Ocular prostheses Dental implants Neurostimulators Bone growth stimulators Implantable cardiac defibrillators Implantable drug infusion pumps
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Safety Zones
Zone 1General Public
Zone 2Interface between public & strictly controlled access areas
Zone 3Access strictly controlled by MR personnelSerious injury could result from interaction between ferromagnetic materials & static/time-varying magnetic fields
Zone 4Magnet roomWithin Zone 3
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Personnel Definitions
Non-MR personnel Patients Visitors Facility staff
Not undergone formal training in MR Safety in previous 12 months
Level 1 personnel Passed minimal safety education efforts MR department office staff Patient aides
Level 2 personnel More extensively trained/educated in broader aspects of MR safety issues MR techs Radiologists Radiology department nursing staff
Level 1 & 2 may move about in all zones
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Quench Superconducting magnet suddenly becomes resistive
Wires formerly offering no resistance to large currents suddenly have resistance
Rapidly heat
Liquid He quickly boils Converts to gaseous state Rapidly expands
Typical cryostat volume ~1500 Liters Produces 1 million liters of gas
Rapid expansion causes large ↑ in volume Large ↑ in pressure
May have to break control room window to allow entry if venting fails
Must be vented to outside
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Magnet Quench
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Vented Inside
Case in which stack was unable to handle amount of venting gases during a quench while patient was being scanned
Room filled with cloud of escaped gases & condensed water vapors
Pressure increased to the point where door could not be opened
After breaking glass, patient was removed
Damaged stack
Separated ceiling & walls
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Installation Planning
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Before Installing Is floor strong enough? What is the delivery path for magnet? Evaluate possible electromagnetic interference
Moving metal-cars, elevators Evaluate vibrations Examine fringe field extent vs. planned controlled
areas Within 5 gauss line, posted & controlled access Within 1 gauss line exclude sensitive equipment
CT scanners CRTs
If not possible, add magnetic shielding Consider adding Ferrous metal detectors Sound penetration into adjacent areas
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RF Shielding
Walls, floors & ceilings covered with copper sheeting
Door perimeter lined with continuous pneumatic RF sealStainless steel frame/hinges
View window includes wire mesh
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FDA recommends limiting personnel access to 5 gauss line
Fringe Fields
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Active ShieldingFringe field: Any field outside magnet boreActive shielding ensures fringe field contained w/in magnet room
1 documented case fringe field fatality (torque on ferromagnetic aneurism clip)
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Pregnancy To date no deleterious effects seen in fetus
Single Shot FSE sequences can be used
Pregnant healthcare workers No restrictions Should not remain in magnet room however
Pregnant patients No restrictions on scans
Many facilities prefer to delay scan until after 1st trimester Written consent Review on case-by-case basis
Use of contrast agents should not routinely be used Agents do cross placental barrier & enter amniotic fluid Ingested by fetus, passed via urinary tract & re-ingested
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ACR White PaperEstablish, Implement, & Maintain Current MR Safety Policies & Procedures1. All clinical & research MR sites, irrespective of magnet format / field strength, including
installations for diagnostic, research, interventional, and/or surgical applications, should maintain MR safety policies.
2. These PAP should also be reviewed concurrently w/ introduction of any significant changes in safety parameters of MR environment of site (e.g., adding faster / stronger gradient capabilities or higher RF duty cycle studies) & updated as needed. In this review process, national & international standards & recommendations should be taken into consideration prior to establishing local guidelines, PAP.
3. Each site will name an MR medical director whose responsibilities will include ensuring that MR safe practice guidelines are established & maintained as current & appropriate for the site. It is the responsibility of site’s administration to ensure that PAP that result from these guidelines are implemented & adhered to at all times by all of the site’s personnel.
4. Procedures should be in place to ensure that any & all adverse events, MR safety incidents, or “near incidents” that occur in the MR site are reported to the medical director in a timely fashion (e.g., within 24 hours or 1 business day of their occurrence) & used in continuous quality improvement efforts. It should be stressed that the FDA states that it is incumbent upon the sites to also report adverse events & incidents to them via their MedWatch program. The ACR supports this requirement & feels that it is in the ultimate best interest of all MR practitioners to create & maintain this consolidated database of such events to help us all learn about them & how to better avoid them in future
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FDA Recommendation
‘If non-ionizing imaging (like sonography) is sub-optimal, or if the information to be gained by MR would have required more invasive testing (like radiography, CT, angiography to name a few), MRI is acceptable.’
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Pediatric
Special consideration mainly due to: Sedation Monitoring
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EndMRI Safety