Robert Xu1,2 and Graham Wright1,2
1Medical Biophysics, University of Toronto, Toronto, ON, Canada, 2Schulich Heart Research Program, Sunnybrook Research Institute, Toronto, ON, Canada
Synopsis
The
objective of this study is to explore the use of a rapidly updated dynamic
motion model to correct for respiratory motion induced errors during MRI-guided
cardiac interventions. The motivation for the proposed technique is to improve
the accuracy of MRI guidance by taking advantage of the anatomical context
provided by the high-resolution prior images and the respiratory motion
information present in a series of real-time MR images. To achieve this goal,
the proposed dynamic motion model is updated continuously, and is used to
predict the motion estimate for realigning the prior volume with the real-time
images during an intervention.Introduction
Traditionally, cardiovascular interventions have
been performed under X-ray fluoroscopy guidance. Recently, the use of MRI as an
alternative interventional guidance tool
1-3 has been
investigated due to its superior soft tissue imaging contrast. However, guidance
with real-time MRI is limited by spatial resolution, whereas
high-resolution prior roadmaps do not reflect patient respiratory motion during
the intervention. In this study, we propose a novel dynamic
motion-modeling technique to correct for this respiratory motion.
Methods
Cardiac images were acquired from 8 subjects with a 1.5T GE MRI
scanner. Two separate image acquisition protocols were used. For each subject,
a high-resolution scan was performed to acquire a 3D prior roadmap image,
followed by a low-resolution real-time scan. The prior roadmap consists of a
multi-slice stack of images covering the left ventricle (LV). The GE FIESTA
sequence was used with resolution=1.2×1.2×8 mm3, and FOV=30 cm. The
acquired prior images were gated to end expiration and mid-diastole. For
the real-time images, a fast spiral balanced SSFP scan was acquired with
in-plane resolution=1.8×1.8×8 mm3, and an effective temporal
resolution=67 ms. During the real-time scan, the subjects were able to breath
freely, and the cardiac and respiratory physiology signals were acquired
through the ECG leads and respiratory bellows respectively.
To correct for the respiratory motion induced misalignment between
the real-time and prior images, we adopted the general motion-modeling
framework illustrated in Fig. 1. Each prior volume was registered to the ECG-gated (mid-diastole) real-time free-breathing images using a GPU accelerated version of our
previously reported multiscale registration algorithm4. The
individual rigid-body motion parameters were extracted and fitted as a function
of the respiratory physiology data (Fig. 1). The derived motion model ϕ can then be
used to estimate the motion correction transform M=ϕ(s) based on the
given respiratory physiology data s during the intervention.
Unfortunately, the limitation of this approach is that the model is built based
on images acquired at the beginning of the procedure. This is problematic for
respiratory motion compensation during the procedure, as the subject’s
breathing pattern may change over time. Therefore, we propose an extension to
the above framework, which is to continuously update the model in
real-time. The proposed approach is illustrated in Fig. 2. Specifically, for
each heartbeat, we performed motion estimation and regenerated a motion model
based on the K=10 most recent real-time images and their
corresponding respiratory surrogate values by using the previously described
framework (Fig. 1). The updated motion model was then used to predict the
motion correction estimate for the subsequent input image.
Results
With the GPU accelerated image registration
algorithm, each individual motion estimation could be complete in 176.9 ms,
while regeneration of the updated dynamic motion model requires approximately
5.3 ms. The image registration alone is not fast enough for correction within
the diastolic window of the same cardiac cycle, but it is sufficiently fast for
updating the dynamic motion model once every heartbeat. The accuracy of the
model based motion correction was evaluated via the Dice similarity coefficient
(DSC), which computed the overlap between the manual segmentation contours of the
LV endocardium belonging to the corresponding prior and real-time images
respectively (Fig. 3). The average perpendicular distance (APD) between the LV
endocardial contours was also computed. In retrospective analysis, we generated
two subject-specific motion models to correct for the respiratory motion
induced misalignment. The first model was built based on the framework
illustrated in Fig. 1, where only the real-time images and the corresponding
respiratory surrogate values acquired in the initial
K heart
cycles were used to generate the static model
ϕ(s). The
second model was built based on the framework illustrated in Fig. 2. This
dynamic model
ϕt(s) was
continuously updated after each cardiac cycle. Both models were used for motion
correction, and compared to the reference image registration approach, which lags behind by 1 heart cycle. The highest mean DSC value (93.0 ± 3.3%) and the lowest
mean APD (1.78 ± 0.84 mm) were achieved using the dynamic model correction
method. These results were statistically significant compared to the reference
and static model correction approaches (Fig. 4). A comparison of the different
motion correction approaches is also demonstrated in a subject where large breathing
variations occurred during the real-time scan (Fig. 5).
Conclusions
We have presented a dynamic motion-modeling based
alignment method that can potentially improve the feasibility of MRI-guided
cardiac interventions. Specifically, the proposed correction framework can
reduce respiratory induced motion errors by aligning the prior roadmap to the
dynamically updated real-time images. This will facilitate improved
interventional guidance accuracy in corresponding cardiac procedures.
Acknowledgements
The authors would like to acknowledge the funding support from GE Healthcare, Canadian
Institutes of Health Research Operating Grant MOP-93531, and the Federal
Development Agency of Canada. References
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