Oluyemi Aboyewa1,2, KyungPyo Hong2, Fuchang Jiang1, Bhumi Bhusal2, Giorgio Bonmassar3, Andrada Popescu4, Gregory Webster5, Laleh Golestanirad1,2, and Daniel Kim1,2
1Department of Biomedical Engineering, McCormick School of Engineering, Northwestern University, Evanston, IL, United States, 2Department of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, United States, 3AA. Martinos Center Massachusetts General Hospital Harvard Medical School, Charlestown, MA, United States, 4Department of Medical Imaging, Ann & Robert H. Lurie Children's Hospital, Chicago, IL, United States, 5Division of Cardiology, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital, Chicago, IL, United States
Synopsis
This study investigated
whether wideband late-gadolinium enhancement (LGE) and T1 mapping pulse
sequences can suppress image artifacts induced by an ICD positioned 12cm
inferior to the heart in a pediatric anthropomorphic phantom. The ICD induced a
peak-to-peak center frequency shift of 970Hz across the heart. The normalized mean
signal intensity within the heart was 1.91±1.20 and 0.98±0.39, for standard and
wideband LGE with ICD, respectively. The mean myocardial T1 was 1486.1±607.7
and 1728.3±332.3msec for standard and wideband T1 mapping, respectively. Our
results demonstrate that wideband pulse sequences can suppress image artifacts induced
by an ICD in a pediatric anthropomorphic phantom.
Introduction
Infants and children with
heart disease often require cardiac implanted electronic devices (CIED) [1]. The optimal approach to affixing a CIED
to the heart of a young patient is to open the chest and sew the cardiac lead
directly to the myocardium (“epicardial leads”) as opposed to passing it
through veins and affix to the inside of the heart (“endocardial leads”). Unfortunately,
once an epicardial lead configuration has
been implanted, it is considered a relative contraindication to MRI due to the
unknown risk of radiofrequency (RF) heating caused by CIEDs with epicardial
leads [1]. The latest HRS/AHA/ACCF guideline
makes no formal recommendation for MRI in pediatric patients with CIED, other
than the case-by-case decision based on the risk/benefit ratio. As the field is
gathering data to evaluate MR safety, it is paramount to prepare cardiovascular
magnetic resonance methods such as late-gadolinium enhancement (LGE) and T1
mapping that produce diagnostically acceptable image quality, thereby
amplifying the benefit. In this study, we sought to evaluate whether wideband
LGE [2] and wideband T1 mapping [3] are capable of suppressing image artifacts
induced by an implantable cardioverter-defibrillator (ICD) in a pediatric
anthropomorphic phantom with a patient-specific epicardial lead configuration. Materials and Methods
Pediatric phantom:
A 3D-printed anthropomorphic phantom was designed and constructed based on a segmented
MRI of a 2.5-year-old patient [4]. The phantom consists of an artificial
heart and a human-shaped body filled with a tissue-equivalent gel [5]. The heart was made from agar gel and
impregnated with a vitamin E-capsule (fish oil) to simulate myocardial scarring
at the apex. An ICD (Medtronic, USA) was placed
at the abdomen 12 cm below the heart (see fig 1). MRI: All images were
acquired with and without ICD in a coronal plane on a 1.5 T MRI scanner (Aera,
Siemens). We performed multi-echo B0 mapping to measure the center frequency
offset induced by the ICD using the following imaging parameters: field-of-view
(FOV)=300x225 mm$$$^2$$$, reconstruction matrix=64x48, slice thickness=10
mm, first/second echo times (TE)=0.86/1.85 msec, repetition time (TR)= 3.1 msec,
flip angle (FA)=15°, receiver bandwidth=1955 Hz/pixel, spoiled gradient echo
(GRE) readout, asymmetric echo (0.73), and parallel imaging (GRAPPA) factor=2 [6]. We performed both standard and wideband LGE
and T1 mapping sequences using the following relevant imaging parameters: FOV=360x270
mm$$$^2$$$, reconstruction matrix=192x144, slice thickness=6 mm, TE/TR=1.01/2.15
msec for LGE and 0.89/2.01 msec for T1 mapping, receiver bandwidth=1860
Hz/pixel, FA=15°, GRE, and GRAPPA=2. For LGE, the inversion time (TI) was set
to 1200 msec, in order to null the signal of myocardium. For LGE, the frequency
bandwidth of inversion-recovery (IR) RF pulse was 1 and 4 kHz for standard and
wideband [7], respectively (see Figure 2), and
inversion time (TI) was 1200 msec. For T1 mapping, the frequency bandwidth of
saturation-recovery (SR) RF pulse was 2.5 and 8.9 kHz for standard and wideband
[3], respectively, and saturation recovery time
(TS) was 1000 msec. Image analysis: We calculated the B0 map from two
phase-unwrapped images with different TEs. To compare the standard and wideband
LGE sequences, we normalized the LGE images scanned with ICD by those obtained
without ICD (reference). We manually drew the region of interest (ROI) in the
heart and calculated 1) peak-to-peak center frequency shift in the B0 map and
2) mean and standard deviation (SD) of the signal intensities in the normalized
LGE images and mean and SD of T1 values in the T1 maps. Results
Figure 3 shows two
phase-wrapped images with different TEs and their corresponding B0 map. The
peak-to-peak center frequency variation across the heart was 970 Hz, which is 13.7-times
higher than center frequency variation of 71 Hz across the heart in non-device
patients at 1.5 T [8]. Figure 4 shows standard and wideband LGE images
without and with ICD. The normalized mean and SD of signal intensity were 1.91
± 1.20 and 0.98 ± 0.39 for standard and wideband, respectively. Figure 5 shows
standard and wideband T1 maps with ICD. The mean myocardial T1 values were
1486.1 ± 607.7 and 1728.3 ± 332.3 msec for standard and wideband, respectively.Conclusion
This study demonstrated
that wideband LGE and T1 mapping pulse sequences are capable of suppressing image
artifacts induced by an ICD in a pediatric anthropomorphic phantom. Future
studies are warranted to investigate both MR safety and image quality in pediatrics
with a CIED.Acknowledgements
This work was partially supported by the following grants: National Institutes of Health (R01HL116895, R01HL138578,
R21EB024315, R21AG055954, R01HL151079, R21EB030806) and American Heart
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