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. Author manuscript; available in PMC: 2024 Feb 22.
Published in final edited form as: Annu Int Conf IEEE Eng Med Biol Soc. 2020 Jul;2020:6143–6146. doi: 10.1109/EMBC44109.2020.9175737

RF heating of deep brain stimulation implants during MRI in 1.2 T vertical scanners versus 1.5 T horizontal systems: A simulation study with realistic lead configurations

Ehsan Kazemivalipour 1,2,3, Jasmine Vu 1,4, Stella Lin 1, Bhumi Bhusal 1, Bach Thanh Nguyen 1, John Kirsch 5, Behzad Elahi 6, Joshua Rosenow 7, Ergin Atalar 2,3, Laleh Golestanirad 1,4
PMCID: PMC10882580  NIHMSID: NIHMS1967346  PMID: 33019373

Abstract

Patients with deep brain stimulation (DBS) implants are often denied access to magnetic resonance imaging (MRI) due to safety concerns associated with RF heating of implants. Although MR-conditional DBS devices are available, complying with manufacturer guidelines has proved to be difficult as pulse sequences that optimally visualize DBS target structures tend to have much higher specific absorption rate (SAR) of radiofrequency energy than current guidelines allow. The MR-labeling of DBS devices, as well as the majority of studies on RF heating of conductive implants have been limited to horizontal close-bore MRI scanners. Vertical MRI scanners, originally introduced as open low-field MRI systems, are now available at 1.2 T field strength, capable of high-resolution structural and functional imaging. No literature exists on DBS SAR in this class of scanners which have a 90° rotated transmit coil and thus, generate a fundamentally different electric and magnetic field distributions. Here we present a simulation study of RF heating in a cohort of forty patient-derived DBS lead models during MRI in a commercially available vertical open-bore MRI system (1.2 T OASIS, Hitachi) and a standard horizontal 1.5 T birdcage coil. Simulations were performed at two major imaging landmarks representing head and chest imaging. We calculated the maximum of 0.1g-averaged SAR (0.1g-SARMax) around DBS lead tips when a B1+ = 4 μT was generated on an axial plane passing through patients body. For head landmark, 0.1g-SARMax reached 220±188 W/kg in the 1.5 T birdcage coil, but only 14±11 W/kg in the OASIS coil. For chest landmark, 0.1g-SARMax was 24±17 W/kg in the 1.5 T birdcage coil and 3±2 W/kg in the OASIS coil. A paired two-tail t-test revealed a significant reduction in SAR with a large effect-size during head MRI (p < 1.5×10−8, Cohen’s d = 1.5) as well as chest MRI (p < 6.5×10−10, Cohen’s d = 1.7) in 1.2 T Hitachi OASIS coil compared to a standard 1.5 T birdcage transmitter. Our findings suggest that open-bore vertical scanners may offer an untapped opportunity for MRI of patients with DBS implants.

I. Introduction

Deep brain stimulation (DBS) is the neurosurgical procedure of choice for treating several major neurological and psychiatric disorders, which uses an implantable pulse generator (IPG) in patient’s chest to deliver electrical pulses to specific nuclei in the brain via subcutaneous leads and extensions. Patients with DBS implants can significantly benefit from magnetic resonance imaging (MRI), both for electrode localization and for monitoring of stimulation-induced changes in function of brain networks. Unfortunately, however, MRI is often inaccessible to these patients due to the interaction between RF fields of the MRI scanner and DBS leads causing safety concerns associated with RF heating of implants [1]. As a result, conditions under which MRI is indicated for DBS patients are restrictive: only 1.5 T horizontal scanners are allowed and only pulse sequences with highly reduced power (whole-head SAR of <0.1 W/kg - 30 times lower than the FDA limit, or rmsB1+ field < 2 μT) are recommended.

To date, the majority of MRI safety studies have been performed on horizontal closed-bore MRI systems. Vertical scanners, originally introduced as low-field open-bore systems, are now available at high field strength capable of high-resolution structural and functional studies. No literature (except our recent work [2]) exists on RF heating of DBS implants inside this class of scanners which have a 90° rotated transmit coil and thus generate a fundamentally different distribution of electric and magnetic fields inside patient’s body. As the orientation and phase of MRI incident electric field along the trajectory of an elongated implant has a substantial effect on the local SAR at the electrode tips [1, 38], we hypothesized that vertical scanners generate a statistically different RF heating compared to horizontal systems. Our hypothesis is based on a preliminary study of RF heating of DBS implants in three (3) realistic patient models which showed 4- to 14-fold reduction in the maximum local SAR around DBS electrodes in a vertical 1.2 T coil compared to a horizontal 1.5 T coil [2]. Here we extend our previous work to include a cohort of 20 patient models with bilateral DBS leads (40 lead models in total) with realistic trajectories. We also investigated the effect of imaging landmark on RF heating in both coils.

II. Methods

A. RF coil models

Numerical models of a 1.2 T high-pass radial planar birdcage coil made of 12 vertical rungs, and a 1.5 T high-pass birdcage coil consisting of 16 horizontal rungs were constructed and tuned to their respective Larmor frequencies (50.35 MHz for proton imaging at 1.2 T and 64 MHz for 1.5 T). The vertical coil was modeled to mimic Hitachi OASIS system. Fig. 1 shows the geometrical details of both coil models and their B1+ field maps on the central coronal and axial planes passing through a human body model with no implant. Horizontal birdcage coil dimensions were chosen similar to those reported in the literature [9]. The vertical coil was derived by four feeding ports arranged in the upper and lower segments, based on information provided by the manufacturer. Both coils were derived in the quadrature excitation mode by feeding their ports with the same amplitudes and different phases as shown in Fig. 1. The body model was placed in two different positions within the coils to mimic head and chest imaging landmarks (Fig. 2).

Fig. 1 -.

Fig. 1 -

Coil configuration of 1.2 T vertical and 1.5 T horizontal coils loaded with a human body model placed at two different positions corresponding to head and chest imaging.

Fig. 2 -.

Fig. 2 -

Geometry configuration of (A) 1.2 T high-pass radial planar birdcage coil and (B) 1.5 T high-pass birdcage coil. (C-D) B1+ field maps on the central coronal and axial planes passing through the human body model with no implants. The input power of coils is adjusted to generate a mean B1+ = 4 μT over a circular plane placed on an axial plane passing through coils’ iso-center.

B. Patient-derived DBS lead models and numerical simulations

We simulated 40 DBS lead models with realistic trajectories based on postoperative computed tomography (CT) images from 20 patients with bilateral DBS leads. Northwestern University’s ethics review board approved the prospective use of imaging data for modeling and simulation. The 3D implant models were constructed utilizing a similar process outlined in our previous works [5, 10, 11]. The implant details as used in numerical simulations are shown in Fig. 3. Each lead was modeled as a solid straight platinum-iridium (Pt:Ir) core (diameter = 0.5 mm, σ = 4 × 106 S/m) embedded into a urethane insulation (diameter = 1 mm, εr = 3.5) with a 2mm exposed tip. Lead models were registered to a standard homogeneous head and torso model (σ = 0.47 S/m, εr = 80).

Fig. 3 –

Fig. 3 –

(A) Examples of post-operative CT images of three patients (patient numbers ID1-ID3). (B) Reconstructed models of isolated DBS leads. Lead trajectories were extracted using CT images of 20 patients with bilateral DBS implantation (patient numbers ID1-ID20) and were registered in a homogenous body phantom for electromagnetic simulations.

All simulations were implemented in ANSYS Electronic Desktop 19.2 (ANSYS Inc., Canonsburg, PA). For each simulation, the input power of coils was adjusted to produce a mean B1+ = 4 μT over a circular plane with a diameter of 48 mm positioned inside the body model on an axial plane passing through coil’s iso-center. The maximum of 0.1g-averaged SAR (0.1g-SARmax) was calculated inside a cubic area of 20×20×20 mm3 surrounding the tip of the lead. Upon numerical convergence, the computing space had roughly 4.6 and 4 million tetrahedral meshes in vertical and horizontal cases, respectively. The computation time on a Dell PowerEdge R740xd system with 1.5 TB RAM and two Intel(R) Xenon(R) Gold 6140 CPUs (2.3 GHz, 36 cores) was ~12 hours and ~4 hours, for each case respectively.

III. Results

Fig. 4 shows the distribution of local SAR for the patient who showed the highest value of 0.1g-SARmax among all patients, for both vertical and horizontal coils and at both imaging landmarks (ID11). For the head (chest) landmark, the 0.1g-SARmax around the tips of left and right leads were reduced by 27-fold (9-fold) and 16-fold (10-fold), respectively, in the vertical coil compared to the horizontal coil. Fig. 5 depicts box plot of the 0.1g-SARmax over all 40 lead models. For the head landmark, the 0.1g-SARmax was 14±11 W/kg for the OASIS vertical coil and 220±188 W/kg for the horizontal birdcage coil. At the chest landmark, the 0.1g-SARmax was 3±2 W/kg for the OASIS coil and 24±17 W/kg for the horizontal birdcage. A paired two-tail t-test showed a significant reduction in SAR with a large effect-size during head MRI (p < 1.5×10−8, Cohen’s d = 1.5) as well as chest MRI (p < 6.5×10−10, Cohen’s d = 1.7) in 1.2 T Hitachi OASIS coil compared to a standard 1.5 T birdcage transmitter.

Fig. 4 -.

Fig. 4 -

Local SAR distributions in patient 11 (ID11) for the 1.2 T vertical and 1.5 T horizontal coils both with head and chest landmarks on an axial plane that passes through the tips of implants. The input power of coils is adjusted to generate a mean B1+ = 4μT over a circular plane placed on an axial plane passing through coils’ iso-center.

Fig. 5 -.

Fig. 5 -

Local 0.1g-SARmax over 40 leads shown for the 1.2 T vertical and 1.5 T horizontal coils for head and chest landmarks. The outliers were plotted individually using a red ‘+’ symbol.

IV. Discussion And Conclusions

Over the past decade, DBS has evolved to a remarkable treatment for a variety of mental and neurological disorders. MRI is extremely useful in patients with DBS implants both for electrode localization and ruling out complications, and for evaluating the stimulation’s therapeutic effects. The key impediment for these patients to benefit from MRI is the RF heating due to the interaction between RF fields of the MR scanner and DBS leads and extensions. Recent years have witnessed a spike in attempts to mitigate the problem of MRI-induced implant heating. Most of these efforts have focused to modify the geometry, structure or material of implants to suppress induced currents [1214] or to alter the MRI hardware to reduce its interaction with the implant [4, 11, 1528].

The existing literature on MRI RF safety as well as MR-labeling of DBS devices are limited to horizontal closed-bore MRI scanners. Vertical MRI systems which produce a substantially different distribution of magnetic and electric fields have not been studied in the context of RF heating of implants. Our work presents the first finite element simulation study of DBS device RF heating in a relatively large sample (N = 40) of patient-derived realistic lead models to compare RF heating in labeled 1.5 T systems and currently unlabeled vertical 1.2 T vertical scanners. On average, we found that 0.1g-averaged SAR was reduced by 16-fold for head imaging and by 8-fold for chest imaging in MRI with a 1.2 T vertical coil compared to a standard 1.5 T horizontal body coil. Interestingly, vertical scanners were originally developed to facilitate open-access to patient and thus, provide an ideal platform for image-guided DBS surgery. These results, if verified in experiments, can open the door to a plethora of MRI applications to guide and interpret DBS therapy.

Acknowledgments

This work was supported by the NIH grants R00EB021320 and R03EB025344.

References

  • [1].Rezai AR et al. , “Neurostimulation system used for deep brain stimulation (DBS): MR safety issues and implications of failing to follow safety recommendations,” Invest Radiol, vol. 39, no. 5, pp. 300–303, May 2004, doi: 10.1097/01.rli.0000124940.02340.ab. [DOI] [PubMed] [Google Scholar]
  • [2].Golestanirad L et al. , “RF heating of deep brain stimulation implants in open-bore vertical MRI systems: A simulation study with realistic device configurations,” Magn Reson Med, Nov 2 2019, doi: 10.1002/mrm.28049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [3].Yeung CJ, Susil RC, and Atalar E, “RF heating due to conductive wires during MRI depends on the phase distribution of the transmit field,” Magn Reson Med, vol. 48, no. 6, pp. 1096–1098, Dec 2002, doi: 10.1002/mrm.10310. [DOI] [PubMed] [Google Scholar]
  • [4].Eryaman Y, Akin B, and Atalar E, “Reduction of Implant RF Heating Through Modification of Transmit Coil Electric Field,” Magn Reson Med, vol. 65, no. 5, pp. 1305–1313, May 2011, doi: 10.1002/mrm.22724. [DOI] [PubMed] [Google Scholar]
  • [5].Golestanirad L et al. , “RF-induced heating in tissue near bilateral DBS implants during MRI at 1.5T and 3T: The role of surgical lead management,” Neuroimage, vol. 184, pp. 566–576, Jan 1 2019, doi: 10.1016/j.neuroimage.2018.09.034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [6].Golestanirad L et al. , “Changes in the specific absorption rate (SAR) of radiofrequency energy in patients with retained cardiac leads during MRI at 1.5T and 3T,” Magn Reson Med, vol. 81, no. 1, pp. 653–669, Jan 2019, doi: 10.1002/mrm.27350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [7].Golestanirad L et al. , “Local SAR near deep brain stimulation (DBS) electrodes at 64 MHz and 127 MHz: A simulation study of the effect of extracranial loops” Magn Reson Med, vol. 88, no. 4, pp. 1558–1565, 2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [8].Golestanirad L et al. , “Variation of RF heating around deep brain stimulation leads during 3.0 T MRI in fourteen patient-derived realistic lead models: The role of extracranial lead management,” Proc. Intl. Soc. Magn Reson Med 25 2017. [Google Scholar]
  • [9].Yeo DT, Wang Z, Loew W, Vogel MW, and H. I, “Local SAR in High Pass Birdcage and TEM Body Coils for Multiple Human Body Models in Clinical Landmark Positions at 3T,” J Magn Reson Imaging, vol. 33(5), pp. 1209–1217, 2011. May, doi: 10.1002/jmri.22544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [10].Golestanirad L et al. , “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, vol. 78, no. 4, pp. 1558–1565, Oct 2017, doi: 10.1002/mrm.26535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [11].McElcheran CE et al. , “Numerical Simulations of Realistic Lead Trajectories and an Experimental Verification Support the Efficacy of Parallel Radiofrequency Transmission to Reduce Heating of Deep Brain Stimulation Implants during MRI,” Sci Rep-Uk, vol. 9, Feb 14 2019, doi: ARTN 212410.1038/s41598-018-38099-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [12].McCabe S and Scott J, “A Novel Implant Electrode Design Safe in the RF Field of MRI Scanners,” IEEE T Microw Theory, vol. 65, no. 9, pp. 3541–3547, Sep 2017, doi: 10.1109/Tmtt.2017.2669977. [DOI] [Google Scholar]
  • [13].Golestanirad L et al. , “Reducing RF-Induced Heating Near Implanted Leads Through High-Dielectric Capacitive Bleeding of Current (CBLOC),” IEEE T Microw Theory, vol. 67, no. 3, pp. 1265–1273, Mar 2019, doi: 10.1109/Tmtt.2018.2885517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [14].Serano P, Angelone LM, Katnani H, Eskandar E, and Bonmassar G, “A Novel Brain Stimulation Technology Provides Compatibility with MRI,” Sci Rep-Uk, vol. 5, Apr 29 2015, doi: ARTN980510.1038/srep09805. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [15].McElcheran CE, Yang BS, Anderson KJT, Golenstani-Rad L, and Graham SJ, “Investigation of Parallel Radiofrequency Transmission for the Reduction of Heating in Long Conductive Leads in 3 Tesla Magnetic Resonance Imaging,” Plos One, vol. 10, no. 8, Aug 3 2015, doi: ARTN e013437910.1371/journal.pone.0134379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [16].McElcheran CE, Yang BS, Anderson KJ, Golestanirad L, and Graham SJ, “Parallel radiofrequency transmission at 3 tesla to improve safety in bilateral implanted wires in a heterogeneous model,” Magn Reson Med, vol. 78, no. 6, pp. 2406–2415, Dec 2017, doi: 10.1002/mrm.26622. [DOI] [PubMed] [Google Scholar]
  • [17].Eryaman Y et al. , “Parallel Transmit Pulse Design for Patients with Deep Brain Stimulation Implants,” Magn Reson Med, vol. 73, no. 5, pp. 1896–1903, May 2015, doi: 10.1002/mrm.25324. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [18].Guerin B, Angelone LM, Dougherty D, and Wald LL, “Parallel transmission to reduce absorbed power around deep brain stimulation devices in MRI: Impact of number and arrangement of transmit channels,” Magn Reson Med, Aug 7 2019, doi: 10.1002/mrm.27905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [19].Wei P-S, Yang B, McElcheran C, Golestanirad L, and Graham SJ, “Reducing Radiofrequency-induced Heating in Realistic Deep Brain Stimulation Lead Trajectories using Parallel Transmission,” Proc. Int. Soc. Magn. Reson. Med, vol. 26, 2018. [Google Scholar]
  • [20].McElcheran C, Golestanirad L, and Graham S, “Heating Reduction in Unilateral And Bilateral Implanted Leads At 3T Using Parallel Radiofrequency Transmission in a Heterogeneous Head Model,” Proc. Intl. Soc. Mag. Reson. Med, vol. 24, 2016. [DOI] [PubMed] [Google Scholar]
  • [21].McElcheran CE, Yang B, Anderson KJ, Golenstanirad L, and Graham SJ, “Investigation of Parallel Radiofrequency Transmission for the Reduction of Heating in Long Conductive Leads in 3 Tesla Magnetic Resonance Imaging,” PLoS One, vol. 10, no. 8, p. e0134379, 2015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [22].McElcheran Clare, Golestanirad L, and Graham S, “Reduced Heating of Implanted Electrical Conductors Using Parallel Radiofrequency Transmission,” Proc. Intl. Soc. Mag. Reson. Med 22 2014. [Google Scholar]
  • [23].Golestnirad L, Keil B, Bonmassar G, Mareyam A, and Wald LL, “A rotating transmit coil and 32ch receive array for high-resolution brain imaging of DBS patients,” Proc. Intl. Soc. Mag. Reson. Med 23, 2015. [Google Scholar]
  • [24].Kazemivalipour E et al. , “Reconfigurable MRI technology for low-SAR imaging of deep brain stimulation at 3T: Application in bilateral leads, fully-implanted systems, and surgically modified lead trajectories,” Neuroimage, vol. 199, pp. 18–29, Oct 1 2019, doi: 10.1016/j.neuroimage.2019.05.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [25].Eryaman Y, Turk EA, Oto C, Algin O, and Atalar E, “Reduction of the radiofrequency heating of metallic devices using a dual-drive birdcage coil,” Magn Reson Med, vol. 69, no. 3, pp. 845–852, Mar 2013, doi: 10.1002/mrm.24316. [DOI] [PubMed] [Google Scholar]
  • [26].Golestanirad L et al. , “Construction and modeling of a reconfigurable MRI coil for lowering SAR in patients with deep brain stimulation implants,” Neuroimage, vol. 147, pp. 577–588, Feb 15 2017, doi: 10.1016/j.neuroimage.2016.12.056. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [27].Golestanirad L et al. , “Feasibility of Using Linearly Polarized Rotating Birdcage Transmitters and Close-Fitting Receive Arrays in MRI to Reduce SAR in the Vicinity of Deep Brain Simulation Implants,” Magn Reson Med, vol. 77, no. 4, pp. 1701–1712, Apr 2017, doi: 10.1002/mrm.26220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [28].Golestanirad L et al. , “Reconfigurable MRI coil technology can substantially reduce RF heating of deep brain stimulation implants: First in-vitro study of RF heating reduction in bilateral DBS leads at 1.5 T,” Plos One, vol. 14, no. 8, Aug 7 2019, doi: ARTNe022004310.1371/journal.pone.0220043. [DOI] [PMC free article] [PubMed] [Google Scholar]

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