Aaron Pruitt1, Yingmin Liu1, Ning Jin2, Peter Speier3, Chong Chen1, Orlando Simonetti1, and Rizwan Ahmad1
1The Ohio State University, Columbus, OH, United States, 2Siemens Medical Solutions USA, Inc., Columbus, OH, United States, 3Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
In this work, we incorporate Pilot Tone as part of our previously described highly accelerated and fully self-gated 4D flow framework to perform retrospective cardiac binning. We compare cardiac triggers derived from Pilot Tone directly with those derived from self-gating and ECG in and demonstrate agreement in aortic and pulmonary artery flow quantification between 4D flow images reconstructed us ECG-, SG-, and PT-based cardiac binning.
Introduction
Modern
innovations in highly accelerated, free-running 4D/5D cardiac acquisitions have
predominantly relied on techniques such as self-gating (SG) as alternative
means to quantify and compensate for physiological motion without requiring the
use of ECG or respiratory navigators.1 While SG has been used widely
for such applications, the need to repetitively reacquire identical k-space central
points or trajectories inherently limits its generalizability beyond
specialized pulse sequences and reduces the acquisition efficiency. Recently,
the novel Pilot Tone technology has been proposed,2 which leverages an
externally transmitted RF signal to obtain surrogates for respiratory3
and cardiac4 motions and does not require explicit pulse sequence
modification. In this work, we compare the precision cardiac trigger estimation
derived from PT and SG and evaluate the feasibility of incorporating PT into
our previously described highly accelerated, fully self-gated 4D flow framework5
for retrospective cardiac binning. Methods
Eight
healthy subjects were prospectively recruited for this study in accordance with
institutional guidelines. Imaging was carried out on a 1.5T clinical scanner
(MAGNETOM Sola, Siemens Healthcare, Erlangen, Germany) equipped with a
dedicated Pilot Tone RF transmitter embedded within the 12-channel chest
receive array. All subjects were scanned
using a prototype self-gated 4D flow sequence5 with sagittal
whole-heart coverage. Acquisition parameters for 4D flow were as follows: FOV =
240-288 mm x 240-288 mm x 140-168 mm, spatial resolution = 2.5-3.0 mm isotropic,
TR = 4.6-4.7 ms, TE = 2.6-2.7 ms, flip angle = 7⁰, and Venc = 150 cm/s. Scans were acquired for approximately
570 s. Throughout the 4D flow scan, synchronous raw ECG, SG, and PT signals were
obtained. As reference, breath-held phase-contrast (2D-PC) images were subsequently
acquired transecting the ascending aorta (Aao) and main pulmonary artery (MPA)
using routine clinical parameters and retrospective ECG gating.
To
obtain cardiac triggers, the interleaved SG readout lines (~42 ms) and PT
signals (~4.7 ms) were processed using a prototype algorithm developed in Matlab (Mathworks, Natick, WA). First, SG and PT signals were extracted from the raw data and band-pass filtered
(0.5 Hz to 3 Hz). Filtered data underwent principal component analysis followed
by independent component analysis; cardiac surrogate signals were automatically
chosen from among these components using spectral analysis. Peak-detection via
computation of interpolated zero-crossings yielded cardiac triggers for
subsequent binning. Cardiac triggers derived from SG and PT were additionally compared
with respect to ECG through the following metrics: false positive rate, false
negative rate, bias, and precision error. Briefly, false positives represent
erroneous SG/PT triggers without corresponding ECG trigger, false negatives
represent triggers capture by ECG but not SG/PT, bias is the systemic temporal
shift between SG/PT and ECG triggers, and precision error is the standard
deviation of the pairwise difference between corresponding SG/PT and ECG triggers.
Respiratory motion surrogates were derived from the raw SG signals using a
combination of temporal low pass filtering (0.5 Hz) followed by PCA and used to
derive respiratory weights incorporated into image reconstruction.6
Weights were fixed at 50% respiratory efficiency and centered at the end-expiratory
phase.
Before
reconstruction, all undersampled 4D flow scans were cropped to a 5-minute
segments and binned using ECG, SG, and PT into 20 cardiac phases. The binned
and weighted k-space were reconstructed at R = 22.0 – 23.1 using ReVEAL4D,7
which, in addition to enforcing wavelet sparsity, explicitly models the
magnitude and phase relationships across encodings. To assess the impact of
cardiac binning on flow quantification, net volumetric flow was computed across
the Aao and MPA for 2D-PC and ECG-, SG-, and PT-derived 4D flow reconstructions
and evaluated using Bland-Altman analysis. Results
Across
all subjects, cardiac triggers derived from PT yield a moderately greater false
positive rate with respect to ECG than SG, with PT and SG on average accounting
for 11.8 and 2.1 false positive triggers, respectively. Similarly, PT-derived
triggers exhibit increased false negatives compared with SG, with a mean of 10.3
and 4.0 false negatives, respectively. Triggers from both PT and SG show small negative
biases with respect to ECG, with means of -18.2 ms for PT and -3.4 ms for SG.
Trigger precision error was found to be slightly higher for PT, but still
acceptable, at 29.3 ms for PT compared with 19.0 ms for SG. Further analysis is
presented in Table 1. Signals and cardiac triggers for ECG, SG, and PT are
shown in Figure 1 for one representative subject.
Figure
2 depicts Bland-Altman plots comparing the aggregate Aao and MPA net volumetric
flow quantified from reconstructed 4D flow images binned using ECG (QECG),
self-gating (QSG), and Pilot Tone (QPT) with flow derived
from the 2D-PC reference (Q2D). Overall, flow quantification derived
from SG and PT yields good agreement with the 2D-PC reference as well as
similar agreement as ECG, suggesting comparable and accurate binning of the 4D
flow data from both methods. Conclusions
This
early data suggests that PT-derived cardiac triggers may provide sufficiently
precise estimation of the cardiac cycle and allow for comparable quantification
when paired with highly accelerated 4D flow as compared with ECG and SG.Acknowledgements
This
work was supported by NIH R01HL135489.References
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