Monitoring of patients is sometimes necessary in the MR scanner. It is understood that the Medical Director of the MR site will be one whose education and experience in MR safety qualifies them for designation as Level Two MR Personnel. For example, “MR compatible up to 3.0 Tesla at gradient strengths of 400-gauss/cm,” or “MR safe tested up to 1.5 Tesla up to maximum static gradient fields experienced in an unshielded 1.5 Tesla [manufacturer name] whole body MR scanner tested 1.5 feet within the bore.”. Patients with asthma also seem to be more likely to have an adverse reaction to gadolinium. As part of the Zone III site restriction and equipment testing/clearing responsibilities, all sites should have ready access to a strong handheld magnet (≥1000-gauss). Zone IV: This area is synonymous with the MR scanner magnet room itself—i.e., the physical confines of the room within which the MR scanner itself is located. Fax copies of operative reports, physician statements, etc., are acceptable as long as a legible physician signature accompanies the requisite documentation. Non-MR personnel are not to be provided with independent Zone III access until such time as they undergo the proper education and training and become MR Personnel themselves. Conscious, non-emergent patients and research and volunteer subjects are to complete written MR safety screening questionnaires prior to their introduction into Zone III regions. The minimum sets of images required for each examination and the anatomy to be included on those images are listed in … Zone IV/MR magnet rooms should be clearly marked with a lighted sign and red light stating, “The Magnet is On.” Except for resistive systems, this sign/red light should be illuminated at all times and should be provided with a backup energy source to continue to remain illuminated for at least 24 hours in the event of a loss of power to the site. Specifically identified MR Personnel (typically—but not necessarily only—the MR Technologists) are to be charged with ensuring that this MR Safe Practice Guideline is strictly adhered to for the safety of the patients and other non-MR personnel, the health care personnel, and the equipment itself. This includes but is not limited to positioning patients, scanning, archiving, injecting contrast, entering the MR scan room in response to an emergency, etc. It is in Zone II that the answers to MR screening questions, patient histories, medical insurance questions, etc., are typically obtained. The site might consider assigning appropriately trained security personnel, who have been trained and designated as MR Personnel, to respond to such calls. All patients/volunteers should be offered and encouraged to use hearing protection prior to their undergoing any imaging in the MR scanners. Final determination of whether or not to scan any given patient with any given implant, foreign body, etc., is to be made by the Level Two designated attending MR radiologist, or the MR Medical Director, or specifically designated Level Two MR Personnel following criteria for acceptability for MR scanning predetermined by the Medical Director. By means of illustration only, the MR Technologists would be able to directly observe and control, via line of site or via video monitors, the entrances or access corridors to Zone IV regions from their normal positions when stationed at their desks in the scan control room. Category B: Anatomic Coverage and Imaging Planes Proper anatomic coverage and imaging planes are important components of clinical MRI exams. Phone or verbal histories and histories provided by a non-physician are not acceptable. Today's metal detectors cannot detect, for example, a 2 × 3 mm, potentially dangerous ferromagnetic metal fragment in the orbit, near the spinal cord, or heart, etc. All those not having successfully complied with these MR safety instruction guidelines shall be referred to henceforth as Non—MR Personnel. AJR Am J Roentgenol. For all device/object screening, all verification and positive identification should be in writing. If external devices/objects are demonstrated to be ferromagnetic and Non-MR safe/MR compatible, they may still, under specific circumstances, be brought into Zone III regions if, for example, they are deemed by MR Personnel to be necessary and appropriate for the care of the patient. Should a quench be performed, appropriately designated MR personnel still need to ensure that ALL non-MR personnel (including and especially emergently responding personnel) continue to be restricted from Zone III/IV regions until the designated MR Personnel have personally verified that the static field is either no longer detectable or at least sufficiently attenuated so as to no longer present a potential hazard to one moving by it with, for example, large ferromagnetic objects such as oxygen tanks, axes, etc. We wish to acknowledge the assistance and support provided by Jeffrey Hayden, ACR MRI Accreditation Program, and Tamar Whipple, ACR. al, ACR Guidance Document for Safe MR Practices: 2007, AJR 2007; 188:1:27. If the nonferromagnetic skin staples/SMS are within the volume to be RF irradiated for the requested MR study several precautions are recommended, as follows: Warn the patient and make sure that they are especially aware of the possibility that they may experience warmth or even burning along the skin staple/SMS distribution. If so then the above precautions should be followed in that case as well. Furthermore, all MR Technologists must be trained as Level Two MR Personnel during their orientation, prior to being permitted free access to Zone III. Barring availability of either pre-testing or prior MR imaging data of the clip in question, a risk/benefit assessment and review must be performed in each case individually. This program is appropriate for MR Safety for MRI Personnel – Level 2.Agenda ACR WHITE PAPER ON MAGNETIC RESONANCE (MR) SAFETY Combined Papers of 2002 and 2004 INTRODUCTION There are potential risks in the MR environment, not only for the patient,1,2 but also for the accompanying family members, attending health care professionals, and others who find themselves only occasionally or Although permitted to work in and around the MR environment, pregnant health care practitioners are requested not to remain within the MR scanner bore or Zone IV during actual data acquisition/scanning itself. CONTRAST AGENT SAFETY MR SAFE PRACTICES, K. MR SAFE PRACTICE GUIDELINES REGARDING MR SCANNING OF PATIENTS IN WHOM THERE ARE/MAY BE INTRACRANIAL ANEURYSM CLIPS, Original Research. Should they still wish to proceed with access to Zone IV and/or within the 5-gauss line, and should the attending radiologist deem it medically advisable that they do so (e.g., for the care of their child about to undergo an MR study), written informed consent should be provided by these accompanying Non—MR Personnel prior to their undergoing x-ray examination of their orbits. All patients with asthma, allergic respiratory histories, prior iodinated and/or gadolinium-based contrast reactions, etc., be followed more closely as they are at a demonstrably higher risk of adverse reaction. Sawyer-Glover A, Shellock FG. Patients in whom there are long electrically conductive leads such as Swan-Ganz thermodilution cardiac output capable catheters, Foley catheters with electrically conductive leads, etc., should be considered at risk for MR studies if the body coil is to be used for RF transmission over the region of the electrically conductive lead. There should be NO exceptions to this guideline. (2) Guidelines for Screening Patients For MR Procedures and Individuals for the MR Environment, Institute for Magnetic Resonance Safety, Education, and Research, www.imrser.org. Access to the MR scanner would then be based on that opinion. Don't believe it? Without hearing protection in place, MR imaging sequences that are not FDA approved should not be performed on patients/volunteers. Zone IV, by definition, will always be located within Zone III as it is the MR magnet and its associated magnetic field that generates the existence of Zone III itself. First, it offers a set of refinements to sections of the previously published ACR Guidance Documents on MR Safe Practice. Radiology Safety. Examples of such devices that need to be positively identified include fire extinguishers, oxygen tanks, aneurysm clips, etc. Types of patients needing extra caution: Patients with implanted or retained wires in anatomically and/or functionally sensitive areas (e.g., myocardium or epicardium, implanted electrodes in the brain) should be considered at higher risk especially from faster MR imaging sequences, such as echoplanar imaging (which may be used in such sequences as diffusion weighted imaging, functional imaging, perfusion weighted imaging, MR angiographic imaging, etc.). h��V]o�6�+|l2�C�H�`{I`i�9[y��1�ȁ� Ϳ�9$��n�}����~�{yye��R(�p�J�8z���$�%�l�)�Iϙ:TN�{W���7�z�i��������SS|X\���u�kg��i{������_�ƿ��r�����N%H�r���R�Yo��*���z[,fB� �������P�r&��)�W��D�&Q8��_,��o�U�vOI�����+���bQ?��l��p�?6���HS�o��^��8ߵ�|��|{B�. Case in point: A patient who went blind from interactions between the metallic foreign body in the retina and the spatial static fields of the MR scanner entered the magnet and underwent the entire MR examination without difficulty. Magmedix - Products for MRI Facilities, We have the largest selection of MRI Accessories on the Market. Cart 0. The most recent version will reflect these changes. It is the responsibility of the MR Medical Director of the site not only to identify the necessary training, but also to identify those individuals that qualify as Level Two MR Personnel. Download Acr Mri Wrist Protocol doc. MR Safety continues to evolve and in response, the ACR's Committee on MR safety created the ACR Manual on MR Safety with updates and critical new information which replaces all earlier versions of the ACR Guidance Document on MR Safe Practices. All implanted intracranial aneurysm clips that are documented in writing to be composed of titanium (either the commercially pure and/or the titanium alloy types) can be accepted for scanning without any other testing necessary. No empty responses will be accepted—each question MUST be answered definitively with a “Yes” or “No” or provide specific further information as requested. Prior contrast agent reaction issues [18]: Adverse events after intravenous injection of gadolinium seem to be more common in patients who had previous reactions to an MR contrast agent. Procedures should be in place to ensure that any and all adverse events, MR safety incidents, or “near incidents” that occur in the MR site are to be reported to the Medical Director of the MR site in a timely fashion (e.g., within 24 hours/one business day of their occurrence) and used in continuous quality improvement efforts. ACR Guidance Document for Safe MR Practices: 2007, MR Safety and the American College of Radiology White Paper, Review. The MR site is conceptually divided into four Zones (Fig. Zone III regions or at the very least the area within them wherein the static magnetic field's strength exceeds 5-gauss should be clearly marked and demarcated as being potentially hazardous. They should only be brought into Zone III regions if they are under the direct supervision of specifically designated either Level One or Level Two MR Personnel who are thoroughly familiar with the device, its function, and the reason supporting its introduction into the Zone III designated region. A written history of the clip itself having been appropriately tested for ferromagnetic properties (and description of the testing methodology used) prior to implantation by the operating surgeon is also considered acceptable if the testing follows the ASTM (American Society of Testing and Materials) established Deflection Test methodology. All areas of scars or deformities that might be anatomically indicative of an implant such as on the chest or spine region, etc., and whose origins are unknown and which may have been caused by ferromagnetic foreign bodies, implants, etc., should be subject to plain film radiography (if such recently obtained plain films or computer tomographic or magnetic resonance studies of such areas are not already available). As noted in section 5 introduction above, testing for the purpose of this labeling is to be accomplished by the site's MR personnel by exposing the metallic object to a handheld magnet (≥1000-gauss). Attendance should be repeated at least annually, and appropriate documentation should be provided. Patients with allergies also seemed to be at increased risk (∼2.0-3.7 times, compared with patients without allergies). When it is necessary that such electrically conductive leads directly contact the patient during imaging, consideration should be given to prophylactic application of cold compresses or ice packs to such areas. For resistive systems, the magnetic field of the MR scanner should be shut down as completely as possible and verified as such prior to permitting the emergency response personnel access to the magnet/Zone IV. The ACR Manual on MR Safety addresses numerous MR safety-related topics such as: The policies and procedures manual should be readily available to the MR professionals on site at all times of operation. It is also important to ensure that the patient's own tissues do not form large conductive loops. For more information about Corwin Health Physics, please visit our website http://www.corwinhp.com/index.php. The minimum sets of images required for each examination and the anatomy to be included on those images are listed in … HOWEVER, if the fire is in such a location where Zone III/IV needs to be entered for whatever reason by the firefighting and/or emergency response personnel and their firefighting and emergent equipment such as air canisters, crowbars, axes, defibrillators, etc., a decision to quench a super-conducting magnet at that point should be VERY seriously considered to protect the health and lives of the emergent responding personnel in such an emergency situation. Should it be determined that Non—MR Personnel wishing to accompany a patient into an MR scan room require their orbits to be cleared by plain film radiography, a radiologist must first discuss with the Non—MR Personnel that plain x-ray films of their orbits are required prior to permitting them access to the MR scan room. This potential for injury is greater on especially higher field whole-body scanners (e.g., 1 Tesla and above). A steel oxygen tank is never permitted inside of the MRI system room. It is intended that these MR Safe Practice Guidelines (and the policies and procedures to which they give rise) be reviewed and updated on a regular basis. The usage of metal detectors in MR environments is NOT recommended. However, it is acceptable to have them in a changing room or restroom not in visual contact in Zone III as long as personnel and the patient can verbally communicate with each other. 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