Abstract
RF electromagnetic wave exposure during MRI scans induces heat and occasionally causes burn injuries to patients. Among all the types of physical injuries that have occurred during MRI examinations, RF burn injuries are the most common ones. The number of RF burn injuries increases as the static magnetic field of MRI systems increases because higher RFs lead to higher heating. The commonly believed mechanisms of RF burn injuries are the formation of a conductive loop by the patient’s posture or cables, such as an electrocardiogram lead; however, the mechanisms of RF burn injuries that occur at the contact points, such as the bore wall and the elbow, remain unclear. A comprehensive understanding of RF heating is needed to address effective countermeasures against all RF burn injuries for safe MRI examinations. In this review, we summarize the occurrence of RF burn injury cases by categorizing RF burn injuries reported worldwide in recent decades. Safety standards and regulations governing RF heating that occurs during MRI examinations are presented, along with their theoretical and physiological backgrounds. The experimental assessment techniques for RF heating are then reviewed, and the development of numerical simulation techniques is explained. In addition, a comprehensive theoretical interpretation of RF burn injuries is presented. By including the results of recent experimental and numerical simulation studies on RF heating, this review describes the progress achieved in understanding RF heating from the standpoint of MRI burn injury prevention.
Keywords: magnetic resonance safety, numerical simulation, radiofrequency burn, radiofrequency heating, specific absorption rate
Introduction
MRI is a widely used, versatile contrast-, and radiation-free imaging modality. However, because of MRI-specific hardware characteristics, i.e., a strong static magnetic field, a fast-switching gradient magnetic field, and a RF field, accidents that harm patients can occur. The static magnetic field exerts displacement force1 and torque2 on the magnetic objects. It has been reported that a ferromagnetic gas cylinder was magnetically attracted to the scanner, causing a fatal accident.3,4 If the time-varying magnetic field (dB/dt) and its duration are sufficient to produce an action potential across a cell, the fast-switching gradient magnetic field (which has improved new imaging techniques, such as diffusion tensor imaging5) stimulates the peripheral nerves6–8 or causes heating of implantable medical devices.9 The RF field heats the human body (in conjunction with or without the use of medical devices) and occasionally leads to RF burn injuries.10 The frequency of these accidents is increasing with the increasing static magnetic field strength of MRI systems owing to stronger attractive displacement forces, the advent of new imaging techniques, and higher RF frequencies. Therefore, MR safety has been a concern as a medical safety issue, e.g., screening for projectile ferromagnetic objects at the walk-in stage and checking the MRI compatibility of implantable medical devices.1,2,11–14
Several reports have surveyed accidents that occurred during MRI examinations. In the United Kingdom, the Medicines and Healthcare Products Regulatory Agency (MHRA) reported that 308 MRI accidents occurred from 1993 to 201415, and in the United States, the Food and Drug Administration (FDA) reported that 1548 MRI accidents occurred from 2008 to 2017.16 Among these accidents, RF burn injuries were the most common, accounting for 42% and 55% of all the accidents reported by the MHRA15 and FDA,16 respectively. In addition, a survey in Japan revealed that RF burn injuries had occurred in 12% of 1319 hospitals.17 The number of RF burn injuries has increased in recent decades; the FDA reported 419 cases in 1997–200918 and 849 cases in 2008–2017.16 This tendency may be related to the prevalence of 3T MRI because the RF heating is theoretically proportional to the square of the static magnetic field strength of MRI; the heating sensation experienced by patients increases with the increase in strength of the static magnetic field.19 Moreover, with the development of ≥ 7T MRI systems, the risk of RF burn injuries would increase. Thus, to ensure MRI safety, it is necessary to address the problem of RF burn injuries.
Focusing on RF heating during MRI examinations, this review summarize the occurrence of RF burn injuries by categorizing the RF burn injuries reported worldwide in recent decades. Safety standards and regulations governing RF heating during MRI examinations are presented, along with their theoretical and physiological backgrounds. The experimental assessment techniques used for RF heating are reviewed, and the development of numerical simulation techniques is explained. In particular, the electromagnetic characteristics of RF burn injury cases are discussed with numerical simulations, and a recent theoretical interpretation of RF burn injuries is discussed. By including the results of recent experimental and numerical simulation studies on RF heating, this review describes the progress achieved in understanding RF heating from the standpoint of MRI burn injury prevention.
RF Burn Injuries
RF burn injuries (Fig. 1) are the most common MRI-related accidents, accounting for approximately half of all such accidents.15,16 The numbers of RF burn injuries surveyed in the United States, the United Kingdom, and Japan are presented in Table 1, where RF burn occurrences are categorized as “contact with an object,” “skin-to-skin contact,” or “bore contact”.16 Some RF burn injuries were not clearly reported—particularly in surveys conducted in the United States and the United Kingdom; excluding these cases, it has been shown that RF burn injuries occur most frequently when a human body contacts an object, for example, the MR coil, monitor lead and electrode, tattoo, makeup, or dermal patch. This is followed by skin-to-skin contact, e.g., the inner thighs or calves, and bore contacts by the body’s extremities. All three countries exhibited this tendency of frequent RF burn injuries at contact points, indicating that “contact” on a human body is the key feature of RF burn injuries.
Table 1.
Occurrence | US16 | UK15 | Japan17 |
---|---|---|---|
Contact with an object | 257 (51%) | 53 (58%) | 79 (56%) |
Skin-to-skin contact | 147 (29%) | 39 (42%) | 49 (33%) |
Bore contact | 97 (19%) | 0 (0%) | 12 (9%) |
Subtotal | 501 | 92 | 140 |
Unclear | 348 | 39 | 9 |
Total | 849 | 131 | 149 |
Surveyed duration | 2008–2017 | 1993–2014 | Unknown–2010 |
Data from the United Kingdom and Japan were reclassified according to the categories of the United States. The percentage in parentheses shows the proportion (per subtotal) of the number of cases in each category for each country.
During an MRI scan, an RF field is applied to the conductive human body, inducing eddy currents, which leads to Joule heating. From this fundamental knowledge of electromagnetic properties, it has been determined that conductive loop formation via skin–skin contact20,21 or body–conductive object contact, such as a conductive wire or cable attached to the patient’s skin,22,23 is a potential cause of RF burn injuries. When a closed loop is formed on the patient’s body, it is commonly believed that the eddy currents concentrate at the skin–skin or body–conductive object contact points and induce significant local heating,24 which may be intensified, in particular, for a resonant conductive loop.25 This basic mechanism qualitatively explains the occurrence of RF burn injuries related to “skin-to-skin contact” and, in some instances, “contact with an object.”15–17 Another potential mechanism of RF burn injuries is the antenna effect; the resonant length of a conductive wire functions as an antenna for induced RF electric fields, and the resonant current in the wire generates a large amount of heat.25,26 RF burn injuries resulting from “contact with an object” that do not form a closed loop, such as an RF burn injury occurring at a contact point with an unlooped electrocardiogram cable, have been explained by the antenna effect.24 In addition, safety concerns have been raised regarding patients with large tattoos, which may function as antennas.27
Although conductive loop formation and the antenna effect qualitatively explain the mechanism of RF burn injuries, the mechanism of such injuries that occur at contact points without forming a loop or an antenna remains unknown; for example, when the human body contacts the bore, no loop is formed. Electromagnetically induced heat is proportional to the square of the electric field strength; Delfino et al. suggested that bore-contact RF burn injuries result from the strong electric field16 near the capacitors of the RF transmit body coil.28–30 Thus far, the mechanisms of RF burn injuries remain insufficiently understood to prevent their occurrence.
Safety Standard
Specific absorption rate (SAR)
RF heating is quantitatively evaluated by the SAR, which is the amount of heat absorbed per unit mass of a human body. Analytically, this value is calculated for a simple homogenous sphere with radius R placed in a uniform RF magnetic field. The total heat generation P due to the RF eddy currents is31
where is the electrical conductivity of the substance in the sphere; D is the duty cycle of the RF pulse, which is the rate of the RF pulse duration; is the angular frequency of the RF magnetic field; and B1 is the RF magnetic pulse amplitude. By dividing Eq. 1 by the mass of the sphere, the average SAR (SARave) is expressed as
where is the density of the substance in the sphere. As indicated by Eq. 2, the SAR is proportional to the square of and hence to the square of the static magnetic field strength, and it tends to increase with the size of the sphere.
In MRI examinations, SARave is estimated using the transmission RF power (Ptrans) and the quality factor (Q value) of the RF transmit coil, with (Ql) and without (Qu) the subject load. Ptrans, Ql, and Qu are automatically known to the MRI system before the scan. The whole-body SARave of a patient is calculated using the following equation:32
where M is the mass of the patient. More precisely, taking into account the partial mass of a patient in an exposed area of B1, the partial-body SARave is calculated using the partial mass for M in Eq. 3. The partial mass is estimated according to the patient’s position in the MRI scanner. Moreover, using the patient’s height and weight, the patient’s body is usually modeled as a variety of homogeneous cylinders.
The upper allowable SAR values for safe MRI examinations are indicated in Standard 60601-2-33 of the International Electrotechnical Commission (IEC)33 (Table 2). In addition to the whole-body and partial-body SARave limits, the head SARave limit, which corresponds to the head transmit coil, is defined. The whole-body SARave limit value decided is based on environmental temperatures below 25°C; this limit value must be reduced when the environmental temperature rises. The local SAR limits in Table 2 are the values for MRI examinations using local transmit coils, which are coils other than the volume transmit coil (e.g., whole-body transmit coil and head transmit coil) and are commonly used in spectroscopic applications.33 According to the physiological effects of static, gradient, and RF magnetic fields, the operating mode classifies the necessity of medical supervision (first-level-controlled operating mode) and approval of the investigational review board (second-level-controlled operating mode), whereas the normal operating mode is applied in clinical practice. The FDA also regulates the upper limits of whole-body and head SARave for domestic clinical practice in the United States34 (Table 3), while regulations in the European Union and Japan are based on the IEC standard. Although the IEC determines the limit values for averaging through 6-min imaging, the FDA’s values are averaged over a longer scan time: 10 min for head SARave and 15 min for whole-body SARave. The IEC also restricts the short-term SAR (any 10 s during the scan) to twice the 6-min value.
Table 2.
Operating mode | Whole-body SAR (W/kg) | Partial-body SARa (W/kg) | Head SAR (W/kg) | Local SAR (W/kg)b | ||
---|---|---|---|---|---|---|
Headc | Trunk | Extremities | ||||
Normal | 2 | 2–10 | 3.2 | 10 | 10 | 20 |
First-level controlled | 4 | 4–10 | 3.2 | 20 | 20 | 40 |
Second-level controlled | > 4 | > (4–10) | > 3.2 | > 20 | > 20 | > 40 |
Averaged SARs over 6-min RF exposure. anormal operating mode: Partial-body SAR = 10 W/kg − (8 W/kg × exposed PATIENT mass/PATIENT mass) and first (second)-level-controlled operating mode: Partial-body SAR ≧ 10 W/kg − (6 W/kg × exposed PATIENT mass/PATIENT mass). bAveraged over mass of 10 g. cIn cases where the orbit is in the field of a small LOCAL RF TRANSMIT COIL, care should be taken to ensure that the temperature rise is limited to 1°C. SAR, specific absorption rate.
Table 3.
Site | SAR (W/kg) | Time (min) |
---|---|---|
Whole body | 4 | 15 |
Head | 3.2 | 10 |
SAR, specific absorption rate.
The SARave value is estimated using Eq. 3 and is displayed on the scanner console before running a scan; the scan proceeds when this value is lower than the upper limit value determined by the manufacturer. However, the displayed SARave is inaccurate because Ql and Qu are not measured in each scan; they are assigned conservative preset values in the factory to achieve a sufficient safety margin for SARave.32,35 The displayed SARave values are usually larger than the actual values;19,36,37 however, the SARave values are sometimes underestimated,32,35 and the risk of an excessive SAR remains.
The local SAR limits, i.e., the SAR values averaged for 10-g tissue, were determined by the IEC for local transmit coils (Table 2). These limit values also lead to safety concerns in clinical scans using volume coils. However, in commercial clinical MRI systems, the local SAR cannot be monitored. Although each scan is performed when the estimated whole-body SARave value is below the limit, the safety of the local SAR is not ensured due to the possibility of a local concentration of induced RF eddy currents that may cause burn injuries. Kainz pointed out this concern in preliminary and as-yet unpublished results of a phantom study: heating can result in a 48°C temperature rise in the normal operating mode of a 1.5T MRI system, with a maximum permissible whole-body SARave of 2 W/kg for an insulated straight wire (20 cm) with 1-cm-long bare ends.38 Therefore, a precise evaluation of the local SAR is crucial for preventing RF burn injuries.
Even with the same parameter settings in MR imaging, large variations in the displayed SARave values were reported among different MRI systems,39,40 suggesting that the displayed SARave does not always guarantee the safety of MR examination. Another preliminary study indicated that large errors in the displayed SARave values were observed in experiments based on the standard F2182 provided by ASTM International (see subsection “Assessment standards of RF heating due to implants”).38 To avoid these errors, the root mean square of B1+ (B1+rms) was introduced as a direct measurement of the RF electromagnetic field. B1+ refers to the rotating component of B1 for exciting spins, B1- refers to the anti-rotating component that does not function for spin excitation, and B1- for the receiver coil is used to represent the physical property of the MR signal, according to the mathematical formulation of a wave propagating in the opposite direction to that of the transmission wave.41,42 B1+rms is defined as
(4) |
where B1+(t) is the RF pulse waveform at the center of a volume RF transmit coil, and tx is the evaluation time, i.e., any 10-s period of the scan sequence used to average B1+(t)2 for all clinical scan sequences with various TRs.33 Since B1+(t) is designed for each pulse sequence, independent of the MR hardware, the B1+rms value is an RF exposure metric based on the scan sequences and is unaffected by variations in the MRI system. As the SAR is proportional to the square of B123 and because 95% of the B1 field in conventional quadrature excitation using volume transmit coils is homogeneous and is represented by B1+,14 the SARave in most clinical MR examinations using a volume transmit coil is proportional to the square of B1+rms. In addition to the displayed SARave value, since 2013, it has been a requirement for B1+rms to be displayed on the scanner console.43 This value is used to quantify the RF exposure heating due to implants, using the experimental relationship between B1+rms and the worst-case local SAR based on ASTM F2182 (see subsection “Assessment standards of RF heating due to implants”). The safety limit of B1+rms for an implant has been determined by implantable device manufacturers as an MR conditional value, for example, 2.0 µT at 1.5 T for a deep brain stimulation (DBS) system (Medtronic DBS system)44 and 2.8 µT at 3 T for pacing systems (Advisa DR MRI SureScan and Advisa SR MRI sureScan).45 Before the scan of a patient with such implants, the B1+rms of each scan displayed on the scanner console should be adjusted to lie within the safety limit by changing MRI parameters such as the TR or the echo train length. For MRI systems that cannot display B1+rms on their console, the SARave of each scan for such patients is further restricted by implantable device manufacturers, e.g., ≤ 0.1 W/kg for the DBS system.43 In addition to the MR conditional B1+rms values of some implants, the B1+rms limit (3.2 µT) for patients with implants under 1.5T MRI with circular volume transmission was determined in a safety imaging parameter set called the fixed parameter option: basic (FPO:B). This parameter set has other limit values for heating during MR examination: peak B1+ and dB/dt values of the gradient magnetic field. The FPO:B is a set of imaging parameters for safe MR examination of patients with implantable medical devices and is used as a simple MR conditional term for labeling device products.33
Temperature
The IEC determined the limits of the maximum temperatures of the human body during MRI examinations with regard to both core and local tissue temperatures33 (Table 4). When the human body is exposed to an RF field, the body temperature is regulated in response to RF heating by increasing skin blood flow and sweating for heat dissipation.46 This thermoregulation is inefficient at high heating levels, and fatal adverse effects, such as heat exhaustion and heat stroke, may occur. In one study, thermoregulation was modeled, and it was predicted that the core temperature of a lightly clothed healthy subject (37°C) could rise by 0.6°C at room temperature (24°C) during RF exposure under a whole-body SAR of 4 W/kg,47 which is the limiting value in the first-level-controlled operating mode (Table 3). Although the body temperature rose by 0.5°C after RF exposure with a whole-body SAR of 0.1–1.6 W/kg for patients, including those with impaired thermoregulation, no adverse effects were observed.48,49 According to these results, the international non-ionizing radiation committee of the International Radiation Protection Association (INIRC/IRPA) previously recommended limiting temperature rises due to RF exposure to 0.5°C for infants, pregnant women, and individuals with cardiocirculatory impairments, although no adverse effects were expected for temperature rises within 1°C for whole-body exposure or exposure of the head and trunk.50 A review of thermoregulation suggested that 39°C could be a conservative threshold for thermal protection of the human body, according to evidence that there no apparent adverse effects occur below 39°C.51 Therefore, it is reasonable that the temperature limits and the limit of core temperature rise were set as 39°C and 0.5°C, respectively, for the normal operation mode to ensure patient safety.
Table 4.
Operating mode | Maximum core temperature (°C) | Maximum local tissue temperature (°C) | Rise of core temperature (°C) |
---|---|---|---|
Normal | 39 | 39 | 0.5 |
First-level controlled | 40 | 40 | 1 |
For the second-level-controlled operating mode, determining the limits is the responsibility of the investigational review board. IEC, International Electrotechnical Commission.
As the tissue damage caused by heat depends on the temperature and its duration, the thermal dose, which is the cumulative equivalent minute at 43°C (CEM43°C), has been introduced to MRI examinations.52 CEM43°C is the duration in minute of tissue exposure at 43°C and reflects the equivalent tissue damage caused by this thermal exposure. The cell death rate depends on the temperature and is approximated using the following equation with the temperature dependence constant (R),52 which differs below and above the break point of the temperature (43°C)—1/4 for T < 43°C and 1/2 for T > 43°C—according to a hyperthermia study.53
(5) |
This equation is normalized to the cell death rate with heat exposure at 43°C, and k is a unital parameter (1/°C). The tissue temperature T(t) changes with time (t) during the MRI examination. CEM43°C is defined as
where te is the duration of the MRI examination. Using Eq. 6, various temperature–time histories can be translated into an equivalent number of minutes of heating at 43°C. The proposed guideline for CEM43°C is categorized into patient conditions of compromised/uncompromised thermoregulation and controlled/uncontrolled conditions of MRI examination (Table 5). Under controlled conditions, a medical doctor or a dedicated trained person should respond instantly to the heat-induced physiological stress of a patient. For patients with compromised thermoregulation under uncontrolled conditions, the limiting CEM43°C value is not defined; instead, a limiting temperature of 39°C for the normal operation mode in the IEC standard (Table 4) is adopted. To protect thermosensitive tissues, e.g., the central nervous system or eyes,54 the conservative thermal dose is limited to 2 min of CEM43°C, even for uncompromised thermoregulation patients in regular clinical practice (uncontrolled conditions) (Table 5). Under controlled conditions, the upper thermal dose limit for these patients is 9 min of CEM43°C.
Table 5.
Compromised thermoregulationa | Uncompromised thermoregulation | |
---|---|---|
Uncontrolled conditions | 39℃c | 2 min |
Controlled conditionsb | 2 min | 9 min |
aAll persons with impaired systemic thermoregulation (elderly, young children, or patients with fever) or reduced local thermoregulation due to scar, edematous tissue, and nerve diseases, including diabetic neuropathies and paraplegia. bA medical doctor or a dedicated specifically trained person is available to respond instantly and adequately to heat-induced physiological stress and patient complaints during MR. cThe safety limit temperature is defined for this condition. CEM, cumulative equivalent minute.
To comply with temperature (Table 4) or CEM43°C (Table 5) guidelines, information on the temperature in the core of the human body or in each piece of tissue is required. However, no techniques are available to monitor this information during an MRI examination; hence, simulation studies on temperature mapping of various patient cases have recently been performed according to these guidelines (see “Numerical Simulation of RF Heating”).
Assessment standards of RF heating due to implants
As RF exposure heats medical implants,55 the assessment standard for RF heating (ASTM-F2182)12 was established for passive implants, such as hip and knee prostheses. As per this standard, the local SAR is assessed by measuring the temperature rise on or near the implant, which is immersed in a gelled saline phantom with electrical and thermal properties similar to those of the human body (see subsection “Evaluation of SAR” in “Experimental Evaluation of RF Heating”). The temperature rise produced by approximately 15 min of RF exposure is monitored with fiber-optic or fluoroptic thermometry probes. Although ASTM F2182 necessitates measurement in the worst-case configuration and orientation of the passive implant, active implantable medical devices (AIMDs), such as pacemakers which have various configurations with leads, are beyond its scope. An assessment standard for AIMDs has also been established in ISO/TS 109474:2018.14 In this standard, the RF electric field is considered for both the experiment and the simulation. This is because the RF electric field is also produced in an MR scanner during the B1 exposure; this incident electric field is scattered by each segment of the implants (including leads), and all the scattered RF electric fields, which are mathematically formulated based on the incident electric field and the implant configuration, determine the SAR distribution.56 This standard provides four tiers of assessment methods for local RF power deposition around an AIMD, from the simplest temperature measurement method to the rigorous simulation method. Tiers 1 and 2 are for small AIMDs, whose lengths are far shorter than the RF wavelength in the human body, i.e., electrically short AIMDs such as cochlear implants. Tiers 3 and 4 are for AIMDs with large configurations that include leads, e.g., those of a pacemaker. This four-tier approach14 is currently applicable to 1.5T MRI systems with a cylindrical bore and body coil excitation.
Experimental Evaluation of RF Heating
Evaluation of SAR
The SARave of RF-exposed homogeneous phantoms can be measured using the calorimetric method provided by the National Electric Manufacturers Association.57 This method was developed to determine the SARave values of specific phantoms, which were designed to provide an RF coil loading equivalent to that of a human, by measuring the temperature rise of the phantom filler, such as an aqueous sodium chloride solution. The method requires the value of the phantom’s heat capacity, a temperature measurement system having accuracy within 0.1°C, and a long exposure time to produce a temperature rise at least 20 times larger than the error of the temperature measurement system. To assess the displayed SARave on the MRI console, Stralka and Bottomley developed an RF dosimeter that monitors the true SARave value of a small phantom. The loading of the dosimeter system is equivalent to that of an average human head or body. The accuracy of the monitored value was approximately 5% at 1.5 T.32 Further research improved its accuracy to 3% at 3 T by reducing the interference of the dosimetry circuitry in an MRI scanner.37 The pulse energy method can be used to determine the SARave either in a phantom or a human by measuring the forward and reflected RF powers at the transmit coil input and the coil power losses, that is, the Joule heat in the coil.57 Since this method requires a complex measurement setup and an expert engineer, its implementation in clinical practice is difficult.
Local SAR measurements in the phantom are stipulated in ASTM F2182.12 The local SAR is obtained from the initial slope of the graph of temperature changes measured with probes inserted in the ASTM phantom, using the following equation (neglecting the thermal diffusivity):
(7) |
where cs is the specific heat capacity of the gel used in the phantom, and is the temperature rise during time interval ( ). The SAR can also be determined using the electric-field strength (E), based on the following equation:
The E distribution in an ASTM phantom with a straight stainless steel rod was measured using a light-emitting diode array with a phototransistor, and good congruence with the temperature rise distribution was obtained.58
To investigate the in vivo local SAR, Katscher et al. introduced a noninvasive SAR mapping technique based on electrical properties tomography (EPT).59 The obtained SAR map of the phantom exhibited a good correlation with that calculated from the numerical simulation. This mapping method was applied on human volunteers, and the individual SARs were mapped.60 Although the SAR can be noninvasively mapped using this method, the obtained SAR values contain theoretical errors owing to the algorithmic limitation; i.e., the z and B1- components of the RF magnetic field are not accounted for. Thus, the SAR values obtained using this method tend to be lower than those obtained from numerical simulations (see “Numerical Simulation of RF Heating”); the average SAR (32%/35% for a phantom/human) and peak local SAR values of 10-g tissue (SAR10g) (26%/27%) were lower.60 To consider the effects of the z and B1- components of the RF magnetic field, a deep-learning method for predicting SAR on the basis of B1+ mapping was developed. The probability of underestimating the peak local SAR was reduced from 24% (the EPT-based method) to 13%, as validated through an experiment involving MRI of volunteers at 7 T.61
Evaluation of temperature
MRI parameters, such as the proton density,62 relaxation times,63 diffusion coefficient,64 and proton resonance frequency (PRF),65 change with respect to temperature. Using these properties, various MRI temperature measurement methods have been developed, and the temperatures of tissue samples66,67 and in vivo tissues68 have been successfully mapped. Among these methods, the PRF-based method is the most commonly used and has high precision.69,70 The nuclear magnetic resonance phenomenon associated with the temperature dependence of the PRF (0.01 ppm/°C) was first observed in 1966,71 and the temperatures of phantom and in vivo human tissues were measured using the PRF-based method in 199565,72 after the advent of MRI. This method was successfully used to measure the temperature rise of phantoms due to RF exposure in various MRI systems, e.g., a saline phantom at 1.5 T and 3 T,73,74 an aqueous cobalt phantom at 4T,73 and a gelatin phantom at 7 T.75
Temperature monitoring is crucial in high-intensity focused ultrasound (HIFU) ablation,76 and the PRF-based method has been applied in MRI scanners implemented with the HIFU system to determine the focused temperature rise for cancer treatment.77–80 To obtain a temperature map with high spatial and temporal resolution, a method that consecutively acquires the undersampled data of 3D imaging was developed. Using a retrospectively reconstructed temporal image set, temperature rise mapping of a rabbit thigh during HIFU heating was performed at 3 T with a temporal resolution of 2.0 s, and the temporal temperature changes were successfully mapped with a high spatial resolution.81 The temperature uncertainty of this mapping technique is approximately ± 1°C for the human brain. However, the reconstruction process requires several minutes to complete. Furthermore, by leveraging the power of computing, using graphics processing units for compressed-sensing-like imaging, a “real-time” MRI temperature mapping technique based on the PRF-based method was developed, and a 1.2-s scan time with an accuracy of ± 0.5°C for the 3D volume of a phantom was achieved.82
To map the temperature rise due to RF heating, the PRF method was first applied to the forearm for 2-min RF heating in a 3T MRI.83 Considering the clinical application of the PRF method, the scan time for which does not notably increase the total scan time, an asymmetric spin-echo technique84 or compressed sensing85 has been used to achieve fast temperature rise mapping in vivo. To monitor the whole-body temperature rise induced by RF exposure using the PRF, further development is needed for clinical practice, such as addressing the influence of motion, because the accuracy of the measured temperature is affected by human motion, e.g., that caused by respiration.86
Numerical Simulation of RF Heating
Principal methods
To simulate RF heating, Maxwell’s equations for the electromagnetic field need to be solved. The analytical solutions can only be derived for simplified cases, such as a sphere (Eq. 2).87 For complex cases, such as a human body, numerical simulation methods are used to approximate the solutions of Maxwell’s equations. For the numerical simulation of RF heating, the finite-difference time-domain (FDTD) method, finite integration technique (FIT), and finite element method (FEM) have mainly been used.
The FDTD method discretizes arbitrary 3D geometries using small orthogonal meshes known as Yee cells to approximate the differential forms of Maxwell’s equations.88 This method is a time-domain method that solves Maxwell’s equations using a time integral algorithm. The time-domain method has the advantage of a shorter computation time than that of the FEM frequency-domain method mentioned below. The FDTD method shapes curved surfaces of the modeling subjects using discrete meshes and causes errors in the inhomogeneous “partial volume” mesh, such as the subdivision of curved surfaces. These errors are reduced by increasing the number of meshes, i.e., reducing the mesh size or applying extended processing;89 however, the computation time increases, and high-performance hardware is needed. Although a mesh size of 1 mm3 is normally considered to be sufficiently small,90,91 the number of meshes should be optimized according to the complexity of the geometries, by considering the tradeoff between accuracy and computational ability.
The FIT discretizes 3D geometries into Maxwell’s grids, determining the electric field along the side of each mesh cell and the magnetic flux crossing each mesh cell surface.92 This method involves both time- and frequency-domain algorithms. It has been mathematically proven that the FIT in the time domain is equivalent to the FDTD method for Cartesian grids.93 The FIT can use any type of mesh that reduces the orthogonal “partial volume” mesh of the complex shape, such as a human model.93 In this method, the integral form of Maxwell’s equation is first applied to each discretized Maxwell’s grid, improving the calculation efficiency for nonorthogonal grids.
The FEM is a well-known simulation method for numerically solving partial differential equations in various fields. In electromagnetic analysis, the FEM is a frequency-domain method that is disadvantageous under high frequencies, as it solves Maxwell’s equation at each frequency. The FEM typically uses tetrahedral meshes,94 which can model complex shapes; however, it incurs higher computational costs (hardware or time) than the FDTD and FIT do.95
Models
To simulate RF heating, computational models require precise information on the frequency-dependent electromagnetic properties of conductivity, permittivity, and permeability. The widely used phantoms in RF heating examinations, such as the ASTM phantom,12 can be easily modeled for simulation because of their simple structure and materials. In contrast, the human body model requires detailed anatomical information and the electromagnetic properties of each tissue. The US National Library of Medicine undertook a virtual human project in 1986 and provided cross-sectional cryosection, CT, and MRI images of both males and females for scientific and medical uses.96 From these public images, whole- and partial-body models were created for SAR simulations.60,97–99 The electromagnetic properties of the relevant tissues are obtained from databases such as IT’IS100 or the literature.101,102 Instead of using public images, individual modeling has been performed using CT or MRI images of volunteers, e.g., a forearm model from MRI images83 and anatomical heart103 and bone models from CT images.104 In particular, for general usage, MRI data acquisition of a single subject was performed, and an adult human model referred to as Norman was created.105 Subsequently, a Japanese adult female model, called Naomi, was created by the same research group.106 In 2010, a series of human body models—referred to as the “virtual human family”—comprising a male model (Duke), a female model (Ella), and two children models (boy: Billie and girl: Thelonious) was developed using MRI scan data from volunteers selected based on the worldwide average height and body mass index for adult models and the German statistics for children models.107 This virtual family was expanded to a virtual population with the inclusion of models of both genders ranging from 3 to 84 years old, by recruiting volunteers according to the body standard of each gender and age; the 3-year-old child model was created by morphing the 5-year-old one. The spatial resolutions of all the models were improved to a minimum of 0.5 × 0.5 × 0.5 mm3 via re-segmentation.108 In addition, pregnant models were developed for different pregnancy periods on the basis of a 26-year-old female model.
RF coil modeling
Various RF transmit coils have been modeled for numerical simulation, such as the transverse electromagnetic (TEM) resonator,97,109–113 the array coil,114 the surface coil,83,97,115 the saddle coil,91 and birdcage coils,29,30, 59, 97,98,116–134, for field strengths ranging from 1.5 T to 9.4 T. The birdcage coil, which consists of end rings, rungs, and capacitors,135–137 is the most widely used coil for clinical MRI. There exist three types of birdcage coils: the low-pass type with capacitors on the rungs, the high-pass type with capacitors on the rings, and the bandpass type with capacitors on both the rungs and the rings.136,137 The number of rungs normally ranges from 8 to 32.121,135–137
SAR simulation
Numerical simulations have been widely used to estimate the SARs of phantoms59,60,125,138 and computational human models.60,139 Simulation results have been used as a gold standard to validate the results of experimental methods, such as EPT. In addition to validation studies, RF heating simulations have been conducted to investigate the dependence of the SAR on the RF frequency and transmit coil design, as well as on the human model (age and size), patient position, and posture in the MRI scanner.
A simulation study revealed the changes in the SAR distribution in a human head at various RF frequencies with a TEM resonator; a high SAR was observed in the fringe of the brain at 64 MHz and at the center of the brain at 340 MHz.111 In addition, the maximal local SAR was significantly larger than the SARave values in the normal operation mode (Table 2): 3–5 times the partial-body SARave limit for a head model (64–400 MHz) and 10–13 times the whole-body SARave limit value for a body model (64–128 MHz). Ibrahim et al. simulated the SAR of a head model for 8-, 16-, and 24-strut TEM resonators at 340 MHz;109 the peak SAR was almost equivalent among the three coils, but a conspicuous inhomogeneity in B1 was observed for the 8-strut resonators. Liu et al. compared birdcage coils with two ports (quadrature), four ports, and many sources (ideal), finding that the B1+ field patterns and SAR levels simulated with two different human models were similar.98 To achieve homogeneous RF excitation in high-tesla MRI systems, a multi-transmit mode (parallel transmit mode) that manipulates the RF currents of the body coil channels—RF shimming—has been introduced, which improved the B1 homogeneity.140 The SAR distribution is determined by the E field at each point of the imaged subject (Eq. 8), and this positional E field of the multi-transmit mode is the summation of fields that originate from each channel. The SAR distribution of this mode is calculated using the E field produced by each channel (Q-matrices) and the waveform of the RF current that flows in each channel.99 During RF shimming, the SAR distribution (and hence the maximum local SAR) changes because the waveform of each channel is modulated to optimize the RF homogeneity; in particular, the dynamic parallel transmission modulates both the amplitude and phase of the RF waveform of each channel.99 However, with regard to the SAR, this mode has a disadvantage: a simulation study with virtual family human models revealed that the whole-body SAR was increased by a factor of 1.6 and that the peak local SAR was increased by up to 13.4 in comparison with the standard circular polarization.120 To reduce the SAR and improve the B1 homogeneity in high-tesla MRI systems, a novel RF coil system concept was proposed, in which a single channel of a transmit/receive coil rapidly rotates around the subjects during the scan.141 A simulation of this rotating RF coil system with a head model at 7 T showed a lower SAR than that of the 8-channel parallel coil array, with an improvement in the B1 homogeneity.142
Model-dependent SAR characteristics exist as well. An SAR simulation at 1.5 T showed a lower (10–75%) peak SAR10g in children (age 5–14 years) and a fetus (36 weeks of gestation) than in adults.118 Another study indicated lower peak SAR10g values for neonate models (40 weeks of gestation) than for an adult model at 1.5 T and 3 T.143 The human model, which was referred to as Fat because it had the largest size in the virtual family, exhibited a higher peak local SAR than Duke and Ella did, indicating that SAR depends on the coil-body proximity: if the body is closer to the coil, more energy is delivered from the nearby coil rung, particularly in the multi-transmit mode.120 With regard to the patient position in a transmit coil, in a study involving 7T MRI, the head SAR in a head transmit coil was mapped by shifting the patient model translationally in each direction by 20 mm. The results indicated that the highest local SAR10g varied by up to 14%, 12%, and 22% in the x-, y-, and z-directions, respectively.127 In addition, a high local SAR10g was observed for the models when the arm was placed near the coil rung119 or the end ring of the transmit coil,129 due to the high electric field strength near the rungs and end rings. The typical arm loops in Duke and Billie significantly increased the maximal peak local SAR10g compared with that in the unlooped postures (Fig. 2).118 An experimental and simulation phantom study mimicking a human arm contacting the body trunk indicated that reducing the contact areas increases the temperature rise and the peak SAR of 1-g tissue.144 The same tendency was simulated using a human model with two different postures of arm–arm contacts forming closed loops. This dependence of the contact area on the SAR is understood as a concentration of the magnetically induced currents. Moreover, a correlation between the SAR and the magnetic flux in a formed loop is observed. However, electromagnetic induction remains unclear from a quantitative standpoint, and further analyses are needed.
Computational human models are sufficiently flexible to model not only healthy humans but also specific pathological models. An RF heating simulation of a brain tumor patient (the electrical properties of the tumor tissue were obtained from the results of an EPT study145) at 7 T indicated a 30% local SAR increase in the tumor; the conductivity increase for the tumor was twice that for the normal tissue, which suggests a substantial local SAR for the brain-tumor patient.146
Temperature simulation
The in vivo temperature has also been simulated, accounting for the thermoregulation function of humans,46 which is analytically modeled using the Pennes’ bioheat equation model147 or the discrete vessel model.148 The Pennes’ bioheat equation model describes the temperature (T) change with respect to SAR due to heat transfer to perfusing blood, as follows:147
(9) |
where , c, and k are the tissue density, the specific heat capacity of the tissue, and the tissue thermal conductivity, respectively. , , and are the blood mass density, the blood specific heat, and the arterial temperature, respectively. is the blood perfusion rate. is the heat generated by metabolism. The discrete vessel model considers convective heat transport due to discrete vessels by accounting for the geometrical structure of the vessels, the perfusion, and the tissue-vessel heat exchange.148 The simulated temperatures of a head obtained using the different thermoregulation function models were almost identical; the maximum temperature was only 0.16°C higher for the Pennes’ bioheat equation model than for the discrete vessel model under an exposure of an averaged head SAR as 2.6 W/kg for approximately 30 min.123 However, Pennes’ bioheat equations are usually used for RF heating simulations because of their simplicity, as they do not require precise anatomical information on the blood vessel network.123 Using Pennes’ bioheat equations, both SAR and temperature simulations were performed for a human head model with a birdcage transmit coil at 64 MHz, a TEM, and a surface transmit coil at 300 MHz under an RF exposure of 3.2 W/kg head SARave, which is the maximum allowable value in the normal operating mode.97 Although the safety limit of the temperature rise is 0.5°C for this case (Table 4), the temperature rise in the brain tissue exceeded 1°C for the surface coil transmission, indicating that caution should be exercised when a surface transmit coil is used.
The relationship between the local SAR and the local temperature is not straightforward because of spatial differences in physiological responses, such as the augmentation of perfusion and sweating. To investigate the effects of perspiration, radiation, and perfusion on the heat transfer, a temperature simulation of the human head model was performed with and without consideration of the heat transfer.97 The simulated temperatures in the two cases were almost identical, i.e., within 0.02°C for 30-min RF exposure of 3.0 W/kg (the maximum allowable SAR by the FDA at the time) with a head-sized TEM coil at various frequencies (64–400 MHz). This result indicates that the effect of temperature-induced physiological changes is negligible in the human head within a head-sized volume coil at various frequencies when the head SARave is within the safety limit.113 In contrast, for a body-sized volume coil, simulation of whole-body RF exposure for 1 h within the FDA-specified safety limit (4 W/kg) indicated peak tissue temperatures of 60°C for the nonregulated model and 42.8°C for the thermoregulated model, which accounted for the temperature-dependent perfusion augmentation.128 The results of the temperature simulation of a phantom using Pennes’ bioheat equations agreed with the experimental results obtained using the PRF-based method during the RF exposure of off-resonant frequency driving for heating from an adjacent circular surface coil; however, the simulation of a forearm with the same RF heating indicated a maximum temperature rise of 2°C, which is 25% higher than the experimental value.83 The primary reason for this disagreement may have been the differences in the tissue electromagnetic properties between the database values for the simulation and the volunteers’ (see subsection “Validity of simulation”).
Simulation of RF heating due to implants
The numerical simulation method is also convenient for ensuring the MRI compatibility of implantable medical devices with regard to RF heating.14 The conventional experimental method for evaluating RF heating due to implants was introduced in ASTM F2182 (see subsection “Assessment standards of RF heating due to implants” in “Safety Standard”). Modeling of this experimental condition has revealed that the maximum SAR depends on the lengths of the implants and the positions and combination of the implants in the ASTM phantom. Liu et al. investigated how the SAR of an orthopedic fixation device (a metallic plate with four screws) changes with respect to the plate length when the plate is placed parallel to the B0 direction in the ASTM phantom and observed the antenna effect; the SAR increased as the plate length approached the half-wavelength of the RF field in the phantom.126 Simulation results for external fixation devices—screws, bars, and clamps that combine the screws and bars—immersed in the ASTM phantom indicated that reducing the depth from the surface of the phantom and increasing the clamp spacing increased the peak local SAR, yielding a maximum temperature rise of 59°C under permissible whole-body SARave exposure (2 W/kg) in the normal operating mode for 15 min.29 Muranaka et al. reported that the maximal temperature was observed on the tip of a humerus nail placed in a gel phantom where the curvature was large and the surface area was small.149 Guo et al. evaluated the SAR and temperature by changing the combination of orthopedic implants (nails and plates) in the ASTM phantom; the average temperature rise in the dual-device case (two pieces of nail or plate) was 2.7 times larger than that due to a single device, suggesting that the combination of multiple implants changes RF heating significantly.150 The authors also reported that when the two nails were placed 10 mm apart from each other, where a strong electric field was observed (Fig. 3), the temperature rose by 33.5°C (thick nails) and 45°C (thin nails; not shown in Fig. 3). Hence, when two implants are placed close to each other, the electric field in the gap enhances the heating.
Simulations of implants, such as aneurysm clips,151 cardiac stents,152 and hip prostheses,122 have also been performed with human models under different magnetic field strengths. A slight enhancement in the SAR surrounding an aneurysm clip has been observed; the temperature rise was up to 0.8°C at 7 T, exceeding the limit (0.5°C) when the 51.5-mm aneurysm clip was located in the right middle cerebral artery.151 RF heating of coronary stents under 7T MRI has also been investigated.152 Longer stents led to a higher maximal local SAR, as did a smaller angle between the electric field of the dedicated transmit coil and the long axis of the stent. By modeling a coronary stent with a cylinder, heating due to a stent in a blood vessel under RF exposure at 4.7 T was estimated in a phantom model, and a strong dependence of temperature on the blood flow was observed, i.e., 37.8°C (0% flow reduction), 42.5°C (90%), and 54.6°C (100%), indicating potentially hazardous heating of coronary stents with restenosis in MRI.153 Even under the normal operating mode limit of whole-body SARave (2 W/kg) at both 1.5 T and 3 T, the simulated local SAR close to the edge of a hip prosthesis exceeded the maximum partial-body SAR limit value. Although no safety regulation pertaining to the local SAR exists for MRI examination using a volume RF transit coil, a reduction in the transmission power for patients with this implant has been recommended.122
The SAR, due to AIMDs, has also been simulated (see subsection “Assessment standards of RF heating due to implants” in “Safety Standard”). The local SAR values of DBS at 1.5 T were greater than or equal to those at 3 T, suggesting that 3T MRI should not be considered more dangerous than 1.5T MRI for patients with DBS leads.132 No clear rule-of-thumb for AIMD RF heating is available, and further simulation study is therefore needed.
Simulation of RF burn injuries
RF burn injury cases have been simulated to further understand the mechanism of such injuries from the standpoint of injury prevention. RF burn injuries occurring at the contact points (i.e., skin–skin contact between the thumb and skin of the thigh and skin–bore wall contact at the elbow) on the lateral side of the human body in an MRI scanner were modeled in silico and simulated.154 The positional dependence of the local SAR on the contact points in an MRI scanner was observed; this result revealed that the local SAR peaked when the contact points were close to the end ring of the transmit coil. This positional dependence is explained by the intrinsic distribution of the electric field arising from the RF transmit coil; the electric field was remarkably strong around the edge of the transmit coil. The simulation also indicated that the highest SAR values led to a high temperature, causing burn injuries under the maximum allowable whole-body SARave for the normal operating mode (Fig. 4). Simulation studies have drawn attention to the risk of RF heating in specific situations, e.g., patients with long implants122 or patient positions near the coil rungs and end rings.154 The simulated values of the local and global SARs quantify the risks of RF heating on the basis of the SAR safety limits, and simulation of RF heating facilitates an understanding of the mechanism of RF burn injuries.
Validity of simulation
For validation, the temperature simulation results were compared with experimental results obtained using thermometry. The temperature rise in orthopedic implants placed in the ASTM phantom was simulated, and the results exhibited a good correlation with the experimental values, i.e., the differences were within 0.5°C.126 In the simulation with Duke, small hotspots (maximum 39.8°C) were observed on the surfaces of both shoulders, and in an experiment involving a volunteer with anatomical dimensions similar to those of Duke, similar hotspots were observed within 1°C.128
The electromagnetic properties of computable models are crucial for simulation. For the phantom study, the electromagnetic properties of the phantom composition can be easily determined. However, the tissue electromagnetic properties of humans are difficult to measure individually. The simulation uncertainties due to individual variations in electromagnetic properties have been investigated by varying the tissue electromagnetic properties by ± 10% in a human model. The uncertainty for the whole-body SAR simulation was 9%, and that for the peak local SAR simulation was 12%.129 When the values of the tissue properties, such as the specific heat capacity or mass density, were increased by 10%, the calculated temperature changed by maximally 7%.83 In addition, upon changing the specific heat capacity of tissue and blood (±10%), the metabolic heat generation rate (±20%), and the thermal conductivity of tissue (±20%), the uncertainties in the temperature rise were calculated to be 3% and 13% for the constant perfusion and thermoregulated (in which the perfusion changes with respect to the temperature) models, respectively.128 Although the uncertainties of the constant perfusion model were less than those of the thermoregulated model, the perfusion rate properties used in the simulation were too simple to reflect actual thermoregulation, e.g., the constant perfusion rate only below the threshold temperature of 39°C.83 In the larger RF power exposure simulation, a higher temperature was obtained for the constant perfusion model (60°C) than for the thermoregulated model (42.8°C).128 Thus, the optimal thermoregulated model and tissue electromagnetic properties should be identified for accurate simulation.
Suggestions for Preventing RF Burn Injuries
Surveys in the United States, United Kingdom, and Japan have indicated that the key feature of RF burn injuries is “contact” (Table 1). The contact points where RF burns occur are classified into avoidable contacts, e.g., a calf-to-calf contact, and unavoidable ones with objects such as implants or tattoos (Table 6). An effective countermeasure to prevent RF burn injuries at avoidable contact points is avoiding contact with separation materials such as foam pads. A simulation study on skin-to-skin contacts of anatomic loop formation indicated that a 2-cm spacing significantly reduced the maximum local SAR at the contact points (Fig. 2).118 Although a further simulation study on the finger–thigh contact model indicated a significant reduction in the maximum local SAR with a 2-mm spacing,144 the MRI guidelines provided by the MHRA recommended the use of 1–2-cm-thick foam pads to insulate the patient from cables, from the bore, and between limbs.155 Therefore, the foam pads prevent RF burn injuries; however, the appropriate thicknesses and materials of the pads need to be determined. Since wetting the pad reduces the effectiveness,144 the hydroscopic properties of the pad materials should be considered as well.
Table 6.
Occurrence16 | Contacting object | Contact type | Countermeasure/Caution |
---|---|---|---|
Contact with an object | Tattoo, implant, etc. | Unavoidable contact | Caution to the resonant length and positioning/direction in the scanner with respect to the RF transmit coila |
MR coil, cable, etc. | Avoidable contact | Avoid contact (using foam padb) | |
Skin-to-skin contact | Calf, thigh-thumb, etc. | ||
Bore contact | Bore wall |
aThe exact countermeasures are still under investigation. bClothing or blankets as a form of insulation is not recommended.155
For unavoidable contact with implants or tattoos,27 attention should be paid to their lengths because the antenna effect increases the SAR when the length is equal to the half-wavelength. The RF wavelength is shorter inside the human body than in air because of the large permittivity of tissues. In addition to the RF wavelength, the RF electric field direction in the scanner should be considered because the electric field tangential to the implant dominantly determines the SAR.56 In a simulation study, the highest SAR was observed when a stent was set parallel to the electric field, and the SAR decreased with an increase in the angle of the stent in the electric field direction.152 The orientation of the implant with respect to the local electric field direction inside the patient significantly affects the local SAR. The electric field distribution inside the ASTM phantom has been measured; the results indicated that the electric field in the body stem part was largely z-directional, whereas that in the shoulder, neck, and bottom parts was x-directional.58 And significant implant heating was observed when a conductive rod was placed parallel to the measured local electric field in the ASTM phantom. When the long axes of implants or tattoos are orthogonal to the electric field, the SAR may be tolerable. However, further simulation with a computable human model is necessary.
In addition, the simulation results indicated an increase in the SAR when the body approached the part of the transmit coil where the electric field was strong,129,154 i.e., an edge or rung, depending on the coil type (e.g., high or low-pass). These results suggest a higher risk of RF burn injuries near the transmit coil. An ASTM phantom study with a straight wire (25 cm) set parallel to z-direction also revealed this tendency; when the wire in the phantom was placed close to the rung of the transmit coil, the maximum temperature rose.156 The SAR at each point is determined from the electric field using Eq. 8. Based on electromagnetic analysis, the electric field is decomposed into a magnetically induced component and a conservative electric field component.157 Although the former component has been considered as a major contributor to RF heating in MRI, the dominance of the latter component has been focused with increasing RF frequencies.158 A conservative electric field is generated by RF alternating charged particles that are moved to the boundary of conductive substances, such as the surface of the human body or the coil.158 The number of charged particles increases with the MR resonant frequency from the Maxwell’s equations, especially near the edge of the transmit coil where a strong electric field is generated (Fig. 5). Positioning that avoids such a strong electric field in the MRI scanner would reduce the risk of RF burn injuries.154
Conclusion
We summarized the RF burn injuries reported worldwide in recent decades and showed that “contact” on the human body is the primary cause of RF burn injuries. Even if compliance with the safety regulations pertaining to RF heating is ensured during MRI examinations, RF burn injuries occur, and the mechanism of these injuries requires further investigation. The development of numerical simulation techniques with computable human models is setting a precedent for precisely analyzing RF heating and is informing clinical practice. To prevent RF burn injuries, countermeasures and caution are recommended, focusing on avoidable or unavoidable “contact,” e.g., using foam pads to avoid “contact”; avoiding positioning the body near the RF transmit coil, where the electric field is strong; and paying attention to the antenna effect for large implants and tattoos.
Footnotes
Conflicts of Interest
The authors declare that they have no conflicts of interest.
References
- 1.ASTM International. F2052-06 Standard test method for measurement of magnetically induced displacement force. West Conshohocken:ASTM International, 2006. [Google Scholar]
- 2.ASTM International. F2213-06 Standard test method for measurement of magnetically induced torque on medical devices in the magnetic resonance environment. West Conshohocken:ASTM International, 2006. [Google Scholar]
- 3.Chaljub G, Kramer LA, Johnson RF 3rd, Johnson RF Jr, Singh H, Crow WN. Projectile cylinder accidents resulting from the presence of ferromagnetic nitrous oxide or oxygen tanks in the MR suite. AJR Am J Roentgenol 2001; 177:27–30. [DOI] [PubMed] [Google Scholar]
- 4.The new york times. Boy, 6, Dies of skull injury during M.R.I. https://www.nytimes.com/2001/07/31/nyregion/boy-6-dies-of-skull-injury-during-mri.html. (Accessed: Feb 8, 2022)
- 5.Le Bihan D, Mangin JF, Poupon C, et al. Diffusion tensor imaging: concepts and applications. J Magn Reson Imaging 2001; 13:534–546. [DOI] [PubMed] [Google Scholar]
- 6.Schaefer DJ, Bourland JD, Nyenhuis JA. Review of patient safety in time-varying gradient fields. J Magn Reson Imaging 2000; 12:20–29. [DOI] [PubMed] [Google Scholar]
- 7.Forbes LK, Crozier S. On a possible mechanism for peripheral nerve stimulation during magnetic resonance imaging scans. Phys Med Biol 2001; 46:591–608. [DOI] [PubMed] [Google Scholar]
- 8.So PP, Stuchly MA, Nyenhuis JA. Peripheral nerve stimulation by gradient switching fields in magnetic resonance imaging. IEEE Trans Biomed Eng 2004; 51:1907–1914. [DOI] [PubMed] [Google Scholar]
- 9.El Bannan K, Handler W, Chronik B, Salisbury SP. Heating of metallic rods induced by time-varying gradient fields in MRI. J Magn Reson Imaging 2013; 38:411–416. [DOI] [PubMed] [Google Scholar]
- 10.Shellock FG. Radiofrequency energy-induced heating during MR procedures: a review. J Magn Reson Imaging 2000; 12:30–36. [DOI] [PubMed] [Google Scholar]
- 11.ASTM International. F2503-13 Standard practice for marking medical devices and other items for safety in the magnetic resonance environment. West Conshohocken:ASTM International, 2008. [Google Scholar]
- 12.ASTM International. F2182-19 Standard test method for measurement of radio frequency induced heating on or near passive implants during magnetic resonance. West Conshohocken:ASTM International, 2020. [Google Scholar]
- 13.ASTM International. F2119-07 Standard test method for evaluation of MR image artifacts from passive implants. West Conshohocken:ASTM International, 2013. [Google Scholar]
- 14.International Organization for Standardization. ISO/TS 10974:2018: Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device. Geneva:International Organization for Standardization, 2018. [Google Scholar]
- 15.Grainger D. MHRA MRI safety guidance: Review of key changes and emerging issues. https://www.sor.org/getmedia/1356e6cb-8cac-4fc1-b183-8cd24f3a8285/io_2015_lr.pdf_1. (Accessed: Feb 8, 2022)
- 16.Delfino JG, Krainak DM, Flesher SA, Miller DL. MRI-related FDA adverse event reports: A 10-yr review. Med Phys 2019; 46:5562–5571. [DOI] [PubMed] [Google Scholar]
- 17.Doi T, Yamatani Y, Ueyama T, et al. [An investigative report concerning safety and management in the magnetic resonance environment: there are more accidents than expected]. Nihon Hoshasen Gijutsu Gakkai Zasshi 2011; 67:895–904. (in Japanese) [DOI] [PubMed] [Google Scholar]
- 18.Hardy PT, Weil KM. A review of thermal MR injuries. Radiol Technol 2010; 81:606–609. [PubMed] [Google Scholar]
- 19.Yamaguchi T, Abe Y, Ichino Y, et al. Heating sensation in patients with and without spinal fixation devices during MRI examination at different magnetic field strengths. J Magn Reson Imaging 2019; 49:525–533. [DOI] [PubMed] [Google Scholar]
- 20.Kim SJ, Kim KA. Safety issues and updates under MR environments. Eur J Radiol 2017; 89:7–13. [DOI] [PubMed] [Google Scholar]
- 21.Keevil S. Safety in magetic resonance imaging. Med Phys Int. 2016; 4:26–34. [Google Scholar]
- 22.Nakamura T, Fukuda K, Hayakawa K, et al. Mechanism of burn injury during magnetic resonance imaging (MRI)—simple loops can induce heat injury. Front Med Biol Eng 2001; 11:117–129. [DOI] [PubMed] [Google Scholar]
- 23.Panych LP, Madore B. The physics of MRI safety. J Magn Reson Imaging 2018; 47:28–43. [DOI] [PubMed] [Google Scholar]
- 24.Dempsey MF, Condon B. Thermal injuries associated with MRI. Clin Radiol 2001; 56:457–465. [DOI] [PubMed] [Google Scholar]
- 25.Dempsey MF, Condon B, Hadley DM. Investigation of the factors responsible for burns during MRI. J Magn Reson Imaging 2001; 13:627–631. [DOI] [PubMed] [Google Scholar]
- 26.Bennett MC, Wiant DB, Gersh JA, et al. Mechanisms and prevention of thermal injury from gamma radiosurgery headframes during 3T MR imaging. J Appl Clin Med Phys 2012; 13:3613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Wang JF, Hindman NM. Prevention of thermal burns from magnetic resonance imaging in patients with tattoos. J Am Acad Dermatol 2019; 80:e101–e102. [DOI] [PubMed] [Google Scholar]
- 28.Murbach MJ. EMF Risk Assessment: Exposure assessment and safety considerations in MRI and other environments. ETH Zürich Research Collection 2013. [Google Scholar]
- 29.Liu Y, Shen J, Kainz W, Qian S, Wu W, Chen J. Numerical investigations of MRI RF field induced heating for external fixation devices. Biomed Eng Online 2013; 12:12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Saniour I, Gaborit G, Duvillaret L, et al. Experimental and simulated distribution of the RF electrical field inside a birdcage coil. Proceedings of the 25th Annual Meeting & Exhibition of ISMRM, Honolulu, 2017; 2625. [Google Scholar]
- 31.Shellock FG. Magnetic resonance procedures: Health effects and safety. Boca Raton:CRC Press, 2000; 59. [Google Scholar]
- 32.Stralka JP, Bottomley PA. A prototype RF dosimeter for independent measurement of the average specific absorption rate (SAR) during MRI. J Magn Reson Imaging 2007; 26:1296–1302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.International Electrotechnical Commission. IEC 60601-2-33: Medical electrical equipment – Part 2-. Jeneva:International Electrotechnical Commission, 2010. [Google Scholar]
- 34.Food and Drug Administration. Guidance for industry and food and drug administration staff-criteria for significant riskinvestigations of Magnetic Resonance Diagnostic Devices. Silver Spring: Food and Drug Administration, 2014. [Google Scholar]
- 35.Seo Y, Wang ZJ. MRI scanner-independent specific absorption rate measurements using diffusion coefficients. J Appl Clin Med Phys 2017; 18:224–229. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.El-Sharkawy AM, Qian D, Bottomley PA, Edelstein WA. A multichannel, real-time MRI RF power monitor for independent SAR determination. Med Phys 2012; 39:2334–2341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Qian D, El-Sharkawy AM, Bottomley PA, Edelstein WA. An RF dosimeter for independent SAR measurement in MRI scanners. Med Phys. 2013; 40:122303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Kainz W. MR heating tests of MR critical implants. J Magn Reson Imaging 2007; 26:450–451. [DOI] [PubMed] [Google Scholar]
- 39.Ishikuro A, Ogura a, Hongou T, Inoue H, Yamazaki M. Comparison of specific absorption ratio monitoring values on various MRI systems. Jpn J Radiol Technol 2000; 56:731–736. (in Japanese) [Google Scholar]
- 40.Baker KB, Tkach JA, Nyenhuis JA, et al. Evaluation of specific absorption rate as a dosimeter of MRI-related implant heating. J Magn Reson Imaging 2004; 20:315–320. [DOI] [PubMed] [Google Scholar]
- 41.Hoult DI. The principle of reciprocity in signal strength calculations - A mathematical guide. Concepts Magn Reson 2000; 12:173–187. [Google Scholar]
- 42.Vaidya MV, Collins CM, Sodickson DK, Brown R, Wiggins GC, Lattanzi R. Dependence of B1+ and B1- Field patterns of surface coils on the electrical properties of the sample and the MR operating frequency. Concepts Magn Reson Part B Magn Reson Eng 2016; 46:25–40. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Medtronic. Indications, safety, and warnings Advisa MRI SureScan. https://www.medtronic.com/us-en/healthcare-professionals/products/cardiac-rhythm/pacemakers/advisa-mri/indications-safety-warnings.html. (Accessed: Feb 8, 2022)
- 44.Medtronic. Guidance for adjusting MRI scan sequence SAR and B1+rms values. http://www.mri-q.com/uploads/3/4/5/7/34572113/mri_guidance_-_sar___b1_rms_final_12.23.15.pdf. (Accessed: Feb 8, 2022)
- 45.Medtronic. MRI guidelines for Medtronic deepbrain stimulation systems. http://mriquestions.com/uploads/3/4/5/7/34572113/dbs_medtronics_contrib_228155.pdf. (Accessed: Feb 8, 2022)
- 46.Tansey EA, Johnson CD. Recent advances in thermoregulation. Adv Physiol Educ 2015; 39:139–148. [DOI] [PubMed] [Google Scholar]
- 47.Adair ER, Berglund LG. On the thermoregulatory consequences of NMR imaging. Magn Reson Imaging 1986; 4:321–333. [DOI] [PubMed] [Google Scholar]
- 48.Shellock FG, Crues JV. Temperature, heart rate, and blood pressure changes associated with clinical MR imaging at 1.5 T. Radiology 1987; 163:259–262. [DOI] [PubMed] [Google Scholar]
- 49.Schaefer DJ. Dosimetry and effects of MR exposure to RF and switched magnetic fields. Ann N Y Acad Sci 1992; 649:225–236. [DOI] [PubMed] [Google Scholar]
- 50.Protection of the patient undergoing a magnetic resonance examination. International Non-Ionizing Radiation Committee of the International Radiation Protection Association. Health Phys 1991; 61:923–928. [PubMed] [Google Scholar]
- 51.Miller MW, Ziskin MC. Biological consequences of hyperthermia. Ultrasound Med Biol 1989; 15:707–722. [DOI] [PubMed] [Google Scholar]
- 52.van Rhoon GC, Samaras T, Yarmolenko PS, Dewhirst MW, Neufeld E, Kuster N. CEM43°C thermal dose thresholds: a potential guide for magnetic resonance radiofrequency exposure levels? Eur Radiol 2013; 23:2215–2227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Sapareto SA, Dewey WC. Thermal dose determination in cancer therapy. Int J Radiat Oncol Biol Phys 1984; 10:787–800. [DOI] [PubMed] [Google Scholar]
- 54.Yarmolenko PS, Moon EJ, Landon C, et al. Thresholds for thermal damage to normal tissues: an update. Int J Hyperthermia 2011; 27:320–343. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Davis PL, Crooks L, Arakawa M, McRee R, Kaufman L, Margulis AR. Potential hazards in NMR imaging: heating effects of changing magnetic fields and RF fields on small metallic implants. AJR Am J Roentgenol 1981; 137:857–860. [DOI] [PubMed] [Google Scholar]
- 56.Park SM, Kamondetdacha R, Nyenhuis JA. Calculation of MRI-induced heating of an implanted medical lead wire with an electric field transfer function. J Magn Reson Imaging 2007; 26:1278–1285. [DOI] [PubMed] [Google Scholar]
- 57.National Electrical Manufacturers Association. MS 8-2016 Characterization of the specific absorption rate for magnetic resonance imaging systems. Rosslyn:National Electrical Manufacturers Association, 2016. [Google Scholar]
- 58.Nordbeck P, Fidler F, Weiss I, et al. Spatial distribution of RF-induced E-fields and implant heating in MRI. Magn Reson Med 2008; 60:312–319. [DOI] [PubMed] [Google Scholar]
- 59.Katscher U, Voigt T, Findeklee C, Vernickel P, Nehrke K, Dössel O. Determination of electric conductivity and local SAR via B1 mapping. IEEE Trans Med Imaging 2009; 28:1365–1374. [DOI] [PubMed] [Google Scholar]
- 60.Voigt T, Homann H, Katscher U, Doessel O. Patient-individual local SAR determination: in vivo measurements and numerical validation. Magn Reson Med 2012; 68:1117–1126. [DOI] [PubMed] [Google Scholar]
- 61.Meliadò EF, Raaijmakers AJE, Sbrizzi A, et al. A deep learning method for image-based subject-specific local SAR assessment. Magn Reson Med 2020; 83:695–711. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Kamimura Y, Amemiya Y. An NMR technique for non-invasive thermometry using M0 as the temperature-sensitive parameter. Automedica 1987; 8:295–313. [Google Scholar]
- 63.Gandhi S, Daniel B, Butts K. Temperature dependence of relaxation times in bovine adipose tissue. Proceedings of the 6th Scientific Meeting & Exhibition of ISMRM, Sydney, 1998; 701. [Google Scholar]
- 64.Le Bihan D, Delannoy J, Levin RL. Temperature mapping with MR imaging of molecular diffusion: application to hyperthermia. Radiology 1989; 171:853–857. [DOI] [PubMed] [Google Scholar]
- 65.De Poorter J. Noninvasive MRI thermometry with the proton resonance frequency method: study of susceptibility effects. Magn Reson Med 1995; 34:359–367. [DOI] [PubMed] [Google Scholar]
- 66.Chen J, Daniel BL, Pauly KB. Investigation of proton density for measuring tissue temperature. J Magn Reson Imaging 2006; 23:430–434. [DOI] [PubMed] [Google Scholar]
- 67.Bohris C, Schreiber WG, Jenne J, et al. Quantitative MR temperature monitoring of high-intensity focused ultrasound therapy. Magn Reson Imaging 1999; 17:603–610. [DOI] [PubMed] [Google Scholar]
- 68.Shibukawa S, Niwa T, Ohno N, et al. Optimal strategy for measuring intraventricular temperature using acceleration motion compensation diffusion-weighted imaging. Radiol Phys Technol 2020; 13:136–143. [DOI] [PubMed] [Google Scholar]
- 69.Wlodarczyk W, Hentschel M, Wust P, et al. Comparison of four magnetic resonance methods for mapping small temperature changes. Phys Med Biol 1999; 44:607–624. [DOI] [PubMed] [Google Scholar]
- 70.Quesson B, de Zwart JA, Moonen CT. Magnetic resonance temperature imaging for guidance of thermotherapy. J Magn Reson Imaging 2000; 12:525–533. [DOI] [PubMed] [Google Scholar]
- 71.Hindman JC. Proton resonance shift of water in the gas and liquid states. J Chem Phys 1966; 44:4582–4592. [Google Scholar]
- 72.Ishihara Y, Calderon A, Watanabe H, et al. A precise and fast temperature mapping using water proton chemical shift. Magn Reson Med 1995; 34:814–823. [DOI] [PubMed] [Google Scholar]
- 73.Shapiro EM, Borthakur A, Shapiro MJ, Reddy R, Leigh JS. Fast MRI of RF heating via phase difference mapping. Magn Reson Med 2002; 47:492–498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Cline H, Mallozzi R, Li Z, McKinnon G, Barber W. Radiofrequency power deposition utilizing thermal imaging. Magn Reson Med 2004; 51:1129–1137. [DOI] [PubMed] [Google Scholar]
- 75.Zhang X, Van de Moortele PF, Liu J, Schmitter S, He B. Quantitative prediction of radio frequency induced local heating derived from measured magnetic field maps in magnetic resonance imaging: A phantom validation at 7 T. Appl Phys Lett 2014; 105:244101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Rivens I, Shaw A, Civale J, Morris H. Treatment monitoring and thermometry for therapeutic focused ultrasound. Int J Hyperthermia 2007; 23:121–39. [DOI] [PubMed] [Google Scholar]
- 77.Wijlemans JW, Bartels LW, Deckers R, et al. Magnetic resonance-guided high-intensity focused ultrasound (MR-HIFU) ablation of liver tumours. Cancer Imaging 2012; 12:387–394. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Chu W, Staruch RM, Pichardo S, et al. Magnetic resonance-guided high-intensity focused ultrasound hyperthermia for recurrent rectal cancer: MR thermometry evaluation and preclinical validation. Int J Radiat Oncol Biol Phys 2016; 95:1259–1267. [DOI] [PubMed] [Google Scholar]
- 79.Merckel LG, Knuttel FM, Deckers R, et al. First clinical experience with a dedicated MRI-guided high-intensity focused ultrasound system for breast cancer ablation. Eur Radiol 2016; 26:4037–4046. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Anzidei M, Napoli A, Sandolo F, et al. Magnetic resonance-guided focused ultrasound ablation in abdominal moving organs: a feasibility study in selected cases of pancreatic and liver cancer. Cardiovasc Intervent Radiol 2014; 37:1611–1617. [DOI] [PubMed] [Google Scholar]
- 81.Todd N, Vyas U, de Bever J, Payne A, Parker DL. Reconstruction of fully three-dimensional high spatial and temporal resolution MR temperature maps for retrospective applications. Magn Reson Med 2012; 67:724–730. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Todd N, Prakash J, Odéen H, et al. Toward real-time availability of 3D temperature maps created with temporally constrained reconstruction. Magn Reson Med 2014; 71:1394–1404. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 83.Oh S, Ryu YC, Carluccio G, Sica CT, Collins CM. Measurement of SAR-induced temperature increase in a phantom and in vivo with comparison to numerical simulation. Magn Reson Med 2014; 71:1923–1931. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 84.Streicher MN, Schäfer A, Ivanov D, et al. Fast accurate MR thermometry using phase referenced asymmetric spin-echo EPI at high field. Magn Reson Med 2014; 71:524–533. [DOI] [PubMed] [Google Scholar]
- 85.Cao Z, Oh S, Otazo R, Sica CT, Griswold MA, Collins CM. Complex difference constrained compressed sensing reconstruction for accelerated PRF thermometry with application to MRI-induced RF heating. Magn Reson Med 2015; 73:1420–1431. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86.Rieke V, Butts Pauly K. MR thermometry. J Magn Reson Imaging 2008; 27:376–390. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.Lyshevski SE. Analytic solutions to Maxwell’s equations: sinusoidal steady-state and transient space-time problems in transverse magnetic and transverse electric field analysis. Proceedings of International Conference on Mathematical Methods in Electromagnetic Theory, Kharkov, 1998; 88–91. [Google Scholar]
- 88.Yee K. Numerical solution of initial boundary value problems involving maxwell’s equations in isotropic media. IEEE Trans Antennas Propag 1966; 14:302–307. [Google Scholar]
- 89.Holland R. Finite-difference solution of Maxwell’s equations in generalized nonorthogonal coordinates. IEEE Trans Nucl Sci 1983; 30:4589–4591. [Google Scholar]
- 90.Wang C, Shen GX, Yuan J, Qu P, Wu B. Theoretical and experimental investigation of the relationship among SAR, tissues and radio frequencies in MRI. Phys Med 2005; 21:61–64. [DOI] [PubMed] [Google Scholar]
- 91.Collins CM, Smith MB. Spatial resolution of numerical models of man and calculated specific absorption rate using the FDTD method: a study at 64 MHz in a magnetic resonance imaging coil. J Magn Reson Imaging 2003; 18:383–388. [DOI] [PubMed] [Google Scholar]
- 92.Weiland T. A discretization method for the solution of Maxwell’s equations for six-component fields. Arch Elektron Uebertrag 1977; 31:116–120. [Google Scholar]
- 93.Weiland T, Schuhmann R. Discrete electromagnetism by the finite integration technique. J Jpn Soc Appl Electromagn 2002; 10:159–169. [Google Scholar]
- 94.Coccioli R, Itoh T, Pelosi G, Silvester PP. Finite-element methods in microwaves: a selected bibliography. IEEE Antennas Propag Mag 1996; 38:34–48. [Google Scholar]
- 95.Fiedler TM, Ladd ME, Bitz AK. SAR simulations & safety. Neuroimage 2018; 168:33–58. [DOI] [PubMed] [Google Scholar]
- 96.National library of medicine. The Visible Human Project. https://www.nlm.nih.gov/research/visible/visible_human.html. (Accessed: Feb 8, 2022)
- 97.Collins CM, Liu W, Wang J, et al. Temperature and SAR calculations for a human head within volume and surface coils at 64 and 300 MHz. J Magn Reson Imaging 2004; 19:650–656. [DOI] [PubMed] [Google Scholar]
- 98.Liu W, Collins CM, Smith MB. Calculations of B1 distribution, specific energy absorption rate, and intrinsic signal-to-noise ratio for a body-size birdcage coil loaded with different human subjects at 64 and 128 MHz. Appl Magn Reson 2005; 29:5–18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 99.Graesslin I, Homann H, Biederer S, et al. A specific absorption rate prediction concept for parallel transmission MR. Magn Reson Med 2012; 68:1664–1674. [DOI] [PubMed] [Google Scholar]
- 100.Hasgall PA, Di Gennaro F, Baumgartner C, et al. IT’IS Database for thermal and electromagnetic parameters of biological tissues. 2018. [Google Scholar]
- 101.Joines WT, Zhang Y, Li C, Jirtle RL. The measured electrical properties of normal and malignant human tissues from 50 to 900 MHz. Med Phys 1994; 21:547–550. [DOI] [PubMed] [Google Scholar]
- 102.Gabriel C, Gabriel S, Corthout E. The dielectric properties of biological tissues: I. Literature survey. Phys Med Biol 1996; 41:2231–2249. [DOI] [PubMed] [Google Scholar]
- 103.Xiong G, Sun P, Zhou H, et al. Comprehensive modeling and visualization of cardiac anatomy and physiology from CT imaging and computer simulations. IEEE Trans Vis Comput Graph 2017; 23:1014–1028. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Neufeld E, Lloyd B, Schneider B, Kainz W, Kuster N. Functionalized anatomical models for computational life sciences. Front Physiol 2018; 9:1594. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 105.Dimbylow PJ. FDTD calculations of the whole-body averaged SAR in an anatomically realistic voxel model of the human body from 1 MHz to 1 GHz. Phys Med Biol 1997; 42:479–490. [DOI] [PubMed] [Google Scholar]
- 106.Dimbylow P. Development of the female voxel phantom, NAOMI, and its application to calculations of induced current densities and electric fields from applied low frequency magnetic and electric fields. Phys Med Biol 2005; 50:1047–1070. [DOI] [PubMed] [Google Scholar]
- 107.Christ A, Kainz W, Hahn EG, et al. The virtual family—development of surface-based anatomical models of two adults and two children for dosimetric simulations. Phys Med Biol 2010; 55:N23–38. [DOI] [PubMed] [Google Scholar]
- 108.Gosselin MC, Neufeld E, Moser H, et al. Development of a new generation of high-resolution anatomical models for medical device evaluation: the virtual population 3.0. Phys Med Biol 2014; 59:5287–5303. [DOI] [PubMed] [Google Scholar]
- 109.Ibrahim TS, Abduljalil AM, Baertlein BA, Lee R, Robitaill PM. Analysis of B1 field profiles and SAR values for multi-strut transverse electromagnetic RF coils in high field MRI applications. Phys Med Biol 2001; 46:2545–2555. [DOI] [PubMed] [Google Scholar]
- 110.Ibrahim TS, Kangarlu A, Chakeress DW. Design and performance issues of RF coils utilized in ultra high field MRI: experimental and numerical evaluations. IEEE Trans Biomed Eng 2005; 52:1278–1284. [DOI] [PubMed] [Google Scholar]
- 111.Wang Z, Lin JC, Mao W, Liu W, Smith MB, Collins CM. SAR and temperature: simulations and comparison to regulatory limits for MRI. J Magn Reson Imaging 2007; 26:437–441. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 112.Ibrahim TS, Tang L, Kangarlu A, Abraham R. Electromagnetic and modeling analyses of an implanted device at 3 and 7 tesla. J Magn Reson Imaging 2007; 26:1362–1367. [DOI] [PubMed] [Google Scholar]
- 113.Wang Z, Lin JC, Vaughan JT, Collins CM. Consideration of physiological response in numerical models of temperature during MRI of the human head. J Magn Reson Imaging 2008; 28:1303–1308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 114.Zhu Y, Alon L, Deniz CM, Brown R, Sodickson DK. System and SAR characterization in parallel RF transmission. Magn Reson Med 2012; 67:1367–1378. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Liorni I, Neufeld E, Kühn S, et al. Novel mechanistic model and computational approximation for electromagnetic safety evaluations of electrically short implants. Phys Med Biol 2018; 63:225015. [DOI] [PubMed] [Google Scholar]
- 116.Van den Berg CA, Bartels LW, van den Bergen B, et al. The use of MR B+1 imaging for validation of FDTD electromagnetic simulations of human anatomies. Phys Med Biol 2006; 51:4735–4746. [DOI] [PubMed] [Google Scholar]
- 117.Pawlenka M, Schaefers G. MR Safety of Implants: Numerical assessment of SAR distribution at design-simplified stents of different lengths placed inside a virtual phantom model investigated at an MR frequency of 63.9 MHz. Proceedings of the 17th Annual Meeting & Exhibition of ISMRM, Honolulu, 2009; 3103. [Google Scholar]
- 118.Murbach M, Cabot E, Neufeld E, et al. Local SAR enhancements in anatomically correct children and adult models as a function of position within 1.5 T MR body coil. Prog Biophys Mol Biol 2011; 107:428–433. [DOI] [PubMed] [Google Scholar]
- 119.Yeo DT, Wang Z, Loew W, Vogel MW, Hancu I. Local specific absorption rate in high-pass birdcage and transverse electromagnetic body coils for multiple human body models in clinical landmark positions at 3T. J Magn Reson Imaging 2011; 33:1209–1217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 120.Neufeld E, Gosselin MC, Murbach M, Christ A, Cabot E, Kuster N. Analysis of the local worst-case SAR exposure caused by an MRI multi-transmit body coil in anatomical models of the human body. Phys Med Biol 2011; 56:4649–4659. [DOI] [PubMed] [Google Scholar]
- 121.Gurler N, Ider YZ. FEM based design and simulation tool for MRI birdcage coils including eigenfrequency analysis. Proceedings of the 2012 COMSOL Conference in Milan, Milan, 2012. [Google Scholar]
- 122.Powell J, Papadaki A, Hand J, Hart A, McRobbie D. Numerical simulation of SAR induced around Co-Cr-Mo hip prostheses in situ exposed to RF fields associated with 1.5 and 3 T MRI body coils. Magn Reson Med 2012; 68:960–968. [DOI] [PubMed] [Google Scholar]
- 123.van Lier AL, Kotte AN, Raaymakers BW, Lagendijk JJ, van den Berg CA. Radiofrequency heating induced by 7T head MRI: thermal assessment using discrete vasculature or Pennes’ bioheat equation. J Magn Reson Imaging 2012; 35:795–803. [DOI] [PubMed] [Google Scholar]
- 124.Camps-Raga B, Goertz W, Schaefers G, Mezape Y, Shalev A. A comparative study of numerical and experimental evaluation of RF-induced heating for an endovascular stent-graft at 1.5T and 3T. Biomed Tech 2012; 57:27. [Google Scholar]
- 125.Buchenau S, Haas M, Splitthoff DN, Hennig J, Zaitsev M. Iterative separation of transmit and receive phase contributions and B1+ -based estimation of the specific absorption rate for transmit arrays. Magn Reson Mater Physics, Biol Med 2013; 26:463–476. [DOI] [PubMed] [Google Scholar]
- 126.Liu Y, Chen J, Shellock FG, Kainz W. Computational and experimental studies of an orthopedic implant: MRI-related heating at 1.5-T/64-MHz and 3-T/128-MHz. J Magn Reson Imaging 2013; 37:491–497. [DOI] [PubMed] [Google Scholar]
- 127.Wolf S, Diehl D, Gebhardt M, Mallow J, Speck O. SAR simulations for high-field MRI: how much detail, effort, and accuracy is needed? Magn Reson Med 2013; 69:1157–1168. [DOI] [PubMed] [Google Scholar]
- 128.Murbach M, Neufeld E, Capstick M, et al. Thermal tissue damage model analyzed for different whole-body SAR and scan durations for standard MR body coils. Magn Reson Med 2014; 71:421–431. [DOI] [PubMed] [Google Scholar]
- 129.Murbach M, Neufeld E, Kainz W, Pruessmann KP, Kuster N. Whole-body and local RF absorption in human models as a function of anatomy and position within 1.5T MR body coil. Magn Reson Med 2014; 71:839–845. [DOI] [PubMed] [Google Scholar]
- 130.Lucano E, Liberti M, Mendoza GG, et al. Assessing the electromagnetic fields generated by a radiofrequency MRI body coil at 64 MHz: defeaturing versus accuracy. IEEE Trans Biomed Eng 2016; 63:1591–1601. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 131.Hadert N, Liu Q, Zylka W. Numerical examinations of simplified spondylodesis models concerning energy absorption in magnetic resonance imaging. Curr Dir Biomed Eng 2016; 2:653–658. [Google Scholar]
- 132.Golestanirad L, Angelone LM, Iacono MI, Katnani H, Wald LL, Bonmassar G. Local SAR near deep brain stimulation (DBS) electrodes at 64 and 127 MHz: A simulation study of the effect of extracranial loops. Magn Reson Med 2017; 78:1558–1565. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 133.Guo R, Zheng J, Chen J. MRI RF-Induced heating in heterogeneous human body with implantable medical device, In: Halefoğlu AM, ed. High-resolution neuroimaging - basic physical principles and clinical applications, 1st ed. Rijeka:InTech, 2018; 64–79. [Google Scholar]
- 134.Guerin B, Iacono MI, Davids M, Dougherty D, Angelone LM, Wald LL. The ‘virtual DBS population’: five realistic computational models of deep brain stimulation patients for electromagnetic MR safety studies. Phys Med Biol 2019; 64:035021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 135.Hayes CE, Edelstein WA, Schenck JF, Mueller OM, Eash M. An efficient, highly hokogeneous radiofrequency coil for whole-body NMR imaging at 1.5 T. J Magn Reson 1985; 63:622–628. [Google Scholar]
- 136.Jin JM. Electromagnetics in magnetic resonance imaging. IEEE Antennas Propag Mag 1998; 40:7–22. [Google Scholar]
- 137.Kim YC, Kim HD, Yun BJ, Ahmad SF. A simple analytical solution for the designing of the birdcage RF coil used in NMR imaging applications. Appl Sci 2020; 10:2242. [Google Scholar]
- 138.Katscher U, Findeklee C, Voigt T. B1-based specific energy absorption rate determination for nonquadrature radiofrequency excitation. Magn Reson Med 2012; 68:1911–1918. [DOI] [PubMed] [Google Scholar]
- 139.Zhang X, Schmitter S, Van de Moortele PF, Liu J, He B. From complex B1 mapping to local SAR estimation for human brain MR imaging using multi-channel transceiver coil at 7T. IEEE Trans Med Imaging 2013; 32:1058–1067. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 140.Katscher U. Basic and tailored RF shimming in a multi-transmit whole body MR system. Prog Electromagn Res Symp 2008; 4:781–784. [Google Scholar]
- 141.Trakic A, Li BK, Weber E, Wang H, Wilson S, Crozier S. A rapidly rotating RF coil for MRI. Concepts Magn Reson Part B Magn Reson Eng 2009; 35B:59–66. [Google Scholar]
- 142.Trakic A, Jin J, Li MY, et al. A comparative numerical study of rotating and stationary RF coils in terms of flip angle and specific absorption rate for 7 T MRI. J Magn Reson 2013; 236:70–82. [DOI] [PubMed] [Google Scholar]
- 143.Malik SJ, Beqiri A, Price AN, Teixeira JN, Hand JW, Hajnal JV. Specific absorption rate in neonates undergoing magnetic resonance procedures at 1.5 T and 3 T. NMR Biomed 2015; 28:344–352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 144.Yang X, Zheng J, Wang Y, Long SA, Kainz W, Chen J. Body‐loop related MRI radiofrequency‐induced heating hazards: observations, characterizations, and recommendations. Magn Reson Med 2022; 87:337–348. [DOI] [PubMed] [Google Scholar]
- 145.van Lier ALHMW, Hoogduin JM, Polders DL, et al. Electrical conductivity imaging of brain tumours. Proceedings of the 19th Annual Meeting & Exhibition of ISMRM, Montréal, 2011; 4464. [Google Scholar]
- 146.Restivo MC, van den Berg CA, van Lier AL, et al. Local specific absorption rate in brain tumors at 7 tesla. Magn Reson Med 2016; 75:381–389. [DOI] [PubMed] [Google Scholar]
- 147.Pennes HH. Analysis of tissue and arterial blood temperatures in the resting human forearm. J Appl Physiol 1948; 1:93–122. [DOI] [PubMed] [Google Scholar]
- 148.Kotte A, van Leeuwen G, de Bree J, van der Koijk J, Crezee H, Lagendijk J. A description of discrete vessel segments in thermal modelling of tissues. Phys Med Biol 1996; 41:865–884. [DOI] [PubMed] [Google Scholar]
- 149.Muranaka H, Horiguchi T, Usui S, et al. Evaluation of RF heating on humerus implant in phantoms during 1.5T MR imaging and comparisons with electromagnetic simulation. Magn Reson Med Sci 2006; 5:79–88. [DOI] [PubMed] [Google Scholar]
- 150.Guo R, Zheng J, Wang Y, et al. Computational and experimental investigation of RF-induced heating for multiple orthopedic implants. Magn Reson Med 2019; 82:1848–1858. [DOI] [PubMed] [Google Scholar]
- 151.Noureddine Y, Kraff O, Ladd ME, et al. Radiofrequency induced heating around aneurysm clips using a generic birdcage head coil at 7 tesla under consideration of the minimum distance to decouple multiple aneurysm clips. Magn Reson Med 2019; 82:1859–1875. [DOI] [PubMed] [Google Scholar]
- 152.Winter L, Oberacker E, Özerdem C, et al. On the RF heating of coronary stents at 7.0 tesla MRI. Magn Reson Med 2015; 74:999–1010. [DOI] [PubMed] [Google Scholar]
- 153.Vrtnik S, Wencka M, Jelen A, Kim HJ, Dolinšek J. Coronary stent as a tubular flow heater in magnetic resonance imaging. J Anal Sci Technol 2015; 6. [Google Scholar]
- 154.Tang M, Okamoto K, Haruyama T, Yamamoto T. Electromagnetic simulation of RF burn injuries occurring at skin-skin and skin-bore wall contact points in an MRI scanner with a birdcage coil. Phys Medica 2021; 82:219–227. [DOI] [PubMed] [Google Scholar]
- 155.Grainger D. MHRA Safety guidelines for magnetic resonance imaging equipment in clinical use. https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/958486/MRI_guidance_2021-4-03c.pdf. (Accessed: Feb 8, 2022)
- 156.Valentinuzzi ME. Magnetotherapy, alternative medicines, hippocratic oath. Biomed Eng Online 2008; 7:1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 157.Park B, Webb AG, Collins CM. A method to separate conservative and magnetically-induced electric fields in calculations for MRI and MRS in electrically-small samples. J Magn Reson 2009; 199:233–237. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 158.Park BS, Rajan SS, Collins CM, Angelone LM. Analysis of conservative and magnetically induced electric fields in a low-frequency birdcage coil. J Electromagn Anal Appl 2013; 5:271–280. [Google Scholar]
- 159.Haik J, Daniel S, Tessone A, Orestein A, Winkler E. MRI induced fourth-degree burn in an extremity, leading to amputation. Burns 2009; 35:294–296. [DOI] [PubMed] [Google Scholar]
- 160.Eising EG, Hughes J, Nolte F, Jentzen W, Bockisch A. Burn injury by nuclear magnetic resonance imaging. Clin Imag 2010; 34:293–297. [DOI] [PubMed] [Google Scholar]
- 161.Yamazaki M, Yamada E, Kudou S, Higashida M. Study of a temperature rise in RF irradiation during MR imaging: measurements of local temperature using a loop phantom. Jpn J Radiol Technol 2005; 61:1125–1132. [DOI] [PubMed] [Google Scholar]