Wideband Cardiac MR Perfusion Pulse Sequence for Imaging Patients with implantable cardioverter defibrillator
KyungPyo Hong1,2 and Daniel Kim1

1Radiology, UCAIR, University of Utah, Salt Lake City, UT, United States, 2Bioengineering, University of Utah, Salt Lake City, UT, United States

Synopsis

Patients with end-stage heart failure (HF) often require advanced therapeutics, but current clinical profiles and biomarkers are not adequate for predicting outcomes. Myocardial perfusion reserve may be an important predictor, but it is technically challenging to perform perfusion MRI in patients with end-stage HF because they often have implantable cardioverter defibrillator (ICD), which generates significant image artifacts. We developed a novel cardiac perfusion pulse sequence using a wideband saturation pulse. Compared with standard perfusion MRI, wideband perfusion MRI suppresses image artifacts induced by ICD.

Introduction

Patients with end-stage heart failure (HF) may require advanced therapeutics to recover their failing heart. However, current clinical profiles and biomarkers do not adequately predict which therapeutic is appropriate. Myocardial perfusion reserve and fibrosis, which can be measured with MRI, may be important predictors for guiding advanced therapeutics. However, patients with end-stage HF often have implantable cardioverter defibrillators (ICD), which induces severe image artifacts that render standard perfusion MRI useless. We had developed a novel cardiac T1 mapping method [1] using BISTRO [2] as a wideband saturation pulse for measuring diffuse myocardial fibrosis in patients with ICD. In this study, we implemented BISTRO as a wideband saturation pulse to enable first-pass myocardial perfusion MRI in patients with end-stage HF.

Methods

Pulse Sequence: We implemented optimized BISTRO as a train of 4 adiabatic hyperbolic secant pulses (each pulse duration = 2.82 ms, net frequency bandwidth = 9.2 kHz) into a cardiac perfusion MRI pulse sequence using TurboFLASH readout. For convenience, we call this method wideband perfusion MRI. We then compared the performance between wideband and standard cardiac perfusion MRI in 4 human subjects (see below for more details). Conventional perfusion MRI sequence utilized a train of three 90˚ rectangular pulses as the saturation pulse (net frequency bandwidth = 2.9 kHz). Both pulse sequences used identical image parameters, including: FOV = 360 mm x 270 mm (PE), slice thickness = 8 mm, acquisition matrix = 192 x 144 (PE), TE = 1.3 ms, TR = 2.7 ms, readout duration = 194 ms, receiver bandwidth = 1000 Hz/pixel, flip angle = 12˚, acceleration factor (GRAPPA) = 2, linear k-space ordering, inversion time = 106 ms.

Subject: We recruited four healthy volunteers (two males; age = 32.7 ± 6.7 yrs). To mimic a realistic situation, we taped an ICD (VITALITY AVT, Boston Scientific) on the left breast, approximately 5-10 cm away from heart [1,3]. All subjects provided written informed consent.

MR Imaging: We imaged 4 subjects on a 3T MRI system (Prisma, Siemens). (Residual Mz after saturation pulse) Prior to Gd-BOPTA administration, we performed saturation-no-recovery experiment to calculate residual longitudinal magnetization (Mz) after wideband and standard saturation pulses, as previously described [4]. This experiment was conducted in a 2-chamber plane, as the image artifact is often seen in the anterior wall. (First-pass Perfusion MRI) Each subject underwent two perfusion MRIs with 30 min delay between the first and second perfusion MRI acquisitions, where each perfusion MRI was conducted with 0.075 mmol/kg of Gd-BOPTA. The pulse sequence order was randomized to minimize potential bias.

Image Analysis: We calculated residual Mz by dividing the T1-weighted image by the proton density image (i.e., equilibrium magnetization). We calculated mean residual Mz for seven myocardial segments in a 2-chamber view [5]. For perfusion MRI, to compare signal intensities between different segments, we normalized the T1-weighted images by a proton density weighted image. This process corrects for surface coil inhomogeneity.

Results

Figure 1 shows severe image artifacts using a standard perfusion MRI sequence. Note that the same artifacts disappear with a wideband perfusion MRI pulse sequence. Averaging the results over 4 subjects (Figure 2), for each segment, the mean residual Mz values were higher for standard than wideband pulse sequences. Figure 3 shows perfusion images pre-contrast, at peak blood enhancement, and at peak wall enhancement. Note that artifacts are visible in standard images, whereas they are suppressed in wideband images. Normalized signal-time curves of artifact-affected and remote zones illustrate this difference (see Figure 4). Figure 5 shows standard and wideband perfusion images at peak blood enhancement for subjects 2-4. In all four cases, standard perfusion MRI produced image artifacts, whereas wideband perfusion MRI suppressed image artifacts.

Discussions

This study demonstrated feasibility of wideband cardiac perfusion MRI for assessment of perfusion reserve in patients implanted with ICD. This new perfusion MRI sequence, in conjunction with wideband late gadolinium-enhanced (LGE) MRI [3] and wideband cardiac T1 mapping [1], may enable comprehensive assessment of cardiac health in patients with end-stage HF for guiding advanced therapeutics. .

Acknowledgements

This work was supported in part by the following grants:

NIH-5R01HL116895-02 and AHA-14GRNT18350028

References

[1] Hong K, et al., MRM 2015; 74:336-345.

[2] Luo Y, et al., MRM 2001; 45(6):1095-1102.

[3] Rashid S, et al., Radiology 2014; 270(1):269-274.

[4] Kim D, et al., MRM 2009; 62:1368-1378.

[5] Cerqueira MD, et al., Circulation 2002; 105:539-542.

Figures

Figure 1. Representative proton density, T1-weighted, and residual magnetization images of standard (row 1) and wideband (row 2) scans in a subject with attached ICD during no Gd-injection. Red contours represent the 2-chember view of heart, and bright spots within red contours show the artifacts induced by ICD.

Figure 2. Plot of mean and standard deviation of residual Mz for each of seven myocardial segments. Residual Mz was less than 5% for wideband perfusion MRI, whereas for standard perfusion MRI artifact-affected segments had high residual Mz. BI=basal inferior, MI=mid inferior, AI=apical inferior, AA=apical anterior, MA=mid anterior, BA=basal anterior.

Figure 3. Representative perfusion images in a subject with ICD obtained using standard (first row) and wideband (second row) acquisitions. Each imaging was at pre-contrast (left column), at peak blood enhancement (mid column), and at peak wall enhancement (right column). White arrows point to the artifacts induced by ICD.

Figure 4. Normalized signal-time curves over 40 heart beats of a subject with ICD using standard and wideband perfusion scans (corresponding to Figure 3). The same artifact-affected and remote zones were used.

Figure 5. Standard (left column) and wideband (right column) perfusion images at peak blood enhancement: subject 2 (row 1), subject 3 (row 2), and subject 4 (row 3). Arrows point to artifacts induced by ICD.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
3133