Azadeh Tabari1,2, Min Lang1,2, Daniel Polak3,4, Daniel Nicolas Splitthoff4, Bryan Clifford5, Wei-Ching Lo5, Lawrence L. Wald2,3,6, Stephen Cauley2,3, Otto Rapalino1,2, Pamela Schaefer1,2, John Conklin1,2,3, and Susie Y. Huang1,2,3,6
1Department of Radiology, Massachusetts General Hospital, Boston, MA, United States, 2Harvard Medical School, Boston, MA, United States, 3A. A. Martinos Center for Biomedical Imaging, Charlestown, MA, United States, 4Siemens Healthcare GmbH, Erlangen, Germany, 5Siemens Medical Solutions, Malvern, PA, United States, 6Harvard-MIT Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA, United States
Synopsis
Patient motion can degrade diagnostic
image quality to the point that scans must be re-acquired, or patients called
back. In this work, we performed a systematic clinical evaluation of SAMER, a
highly efficient retrospective motion mitigation approach. 62 patients from
emergency and inpatient care settings were scanned at 3T, and 14 cases were
identified with a range of patient motion. Two neuro-radiologists performed
blinded review of the images before and after motion correction, rating the
images for motion severity. In 13 of the 14 cases, reduced motion severity and
improved visualization of anatomy/pathology was obtained after SAMER motion
mitigation.
Introduction
Patient motion
during the 2 to 5 minutes typically used to acquire an MR image volume causes
the familiar “motion artifacts” that degrade diagnostic utility, often to the
point that scans must be re-acquired, or the patient called back for a repeat
scan [1]. A recent study at a US hospital found that 20% of MR scans were
repeated due to patient motion, including 29% of inpatient and/or emergency department
scans [2]. In the worst case, the radiologist simply lives with or “reads through”
the artifacts, possibly missing diagnostic information [3].
Many methods to detect and correct for motion in MRI have been explored [4], but few have gained traction in the clinical
setting. Alternatives are few and may be to the detriment of the patient,
including performing MRI under anesthesia, a procedure that increases risk,
examination duration and cost [5]. In this work, we performed an evaluation of SAMER
[6], a recently proposed retrospective motion-correction
approach that facilitates multi-scale motion estimation by leveraging optimized
data acquisition orderings and an ultra-fast scout prior. The motion mitigation
performance of SAMER was evaluated by neuroradiologists on 3D T1-weighted brain
MR images acquired on inpatients and emergency patients upon clinical deployment
at Massachusetts General Hospital.Methods
This single-center prospective study was approved by the IRB and conducted in accordance with HIPAA guidelines
for research. From August-October 2021, clinical
evaluation data were acquired from 62 patients in emergency and inpatient care
settings on 3T systems (MAGNETOM
Skyra and MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany) using a
20-channel head-neck coil. The imaging protocol included an R=4-fold accelerated T1-weighted MPRAGE sequence (Fig. 1A), which was acquired using
a custom linear+checkered sequence reordering [6]. This sequence was
incorporated into routine brain MRI protocols without contrast and with/without
contrast in order to assess the performance of motion correction on noncontrast
and contrast-enhanced exams. Retrospective
reconstructions of the MPRAGE data were performed with and without SAMER motion
correction. The 62 reconstructions without motion correction were screened for the
presence of motion by an independent rater, and 14 relevant cases were
identified. Details on the patient population are summarized in Fig. 1B.
All motion affected cases were visually reviewed by two
neuroradiologists (10 and 3 years of experience) in a blinded manner. A graded
5-tier scale (Fig. 1C, [2]) was used to measure the impact of motion artifacts
on diagnostic image quality. Discrepancies in the two neuroradiologists’ scores
were adjudicated by a third neuroradiologist (9 years of experience).Results
Figure 2 shows representative cases of the motion severity scale with
none (1), minimal (2), mild (3), moderate (4) and severe (5) motion. The SAMER
motion mitigated images are shown alongside the predicted motion time course (6
degree of freedom estimate of the rigid body motion parameters).
Figure 3 shows the adjudicated motion scores before and after correction.
In 13 of 14 cases with patient motion, SAMER produced improved scores. In the
outlier case (non-contrast T1-weighted MRI, patient 5), the SAMER
reconstruction led to a slightly worse image quality (increased from minimal to
mild motion). In 6 of 7 cases with moderate or severe motion, only mild motion
artifacts were present after the correction.
Figure 4 shows representative cases demonstrating improved visualization
of pathology after motion correction in both pre- and post-contrast MPRAGE
scans.Discussion
We have deployed and evaluated SAMER motion correction in an inpatient
clinical setting, where motion artifacts are a frequent clinical problem. Using
a predefined radiologist scoring system, SAMER reduced the impact of patient
motion in 93% (13 of 14) of the examined cases. In all but one case of moderate/severe
motion, only mild motion artifacts were present after the correction. Our pilot
study indicates that SAMER improves diagnostic image quality across a broad
range of pathology, including cases in which motion artifacts likely obscured the
visualization of key findings.
In one
case, model errors led to slightly reduced image quality after the correction. However,
retrospective techniques such as SAMER allow for the standard image reconstruction to be performed and
quantitatively compared alongside the motion-modeled solution. In future
workflows, the cleaner image could be automatically determined and provided for
clinical interpretation, thereby offering alternatives to radiologists and
radiologic technologists seeking to optimize image quality against the
competing demands of scan time and patient comfort.Acknowledgements
This work was supported by research grants from the National Institutes of Health (grant no. P41-EB030006) and Siemens Healthineers.References
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