4.5 Article

Individualized SAR calculations using computer vision-based MR segmentation and a fast electromagnetic solver

期刊

MAGNETIC RESONANCE IN MEDICINE
卷 85, 期 1, 页码 429-443

出版社

WILEY
DOI: 10.1002/mrm.28398

关键词

electromagnetic; patient-specific; SAR; segmentation

资金

  1. NIH [R00EB019482, R01EB006847]
  2. Skolkovo Institute of Science and Technology Next Generation Program
  3. Real Colegio Complutense at Harvard University Research Fellowships

向作者/读者索取更多资源

The study introduces a fast patient-specific workflow for online SAR supervision, aiming to improve the correspondence between patient and model by creating an individualized electromagnetic model while the patient is on the table. This approach reduces reliance on general anatomical body models and may improve electromagnetic safety in MRI.
Purpose We propose a fast, patient-specific workflow for on-line specific absorption rate (SAR) supervision. An individualized electromagnetic model is created while the subject is on the table, followed by rapid SAR estimates for that individual. Our goal is an improved correspondence between the patient and model, reducing reliance on general anatomical body models. Methods A 3D fat-water 3T acquisition (similar to 2 minutes) is automatically segmented using a computer vision algorithm (similar to 1 minute) into what we found to be the most important electromagnetic tissue classes: air, bone, fat, and soft tissues. We then compute the individual's EM field exposure and global and local SAR matrices using a fast electromagnetic integral equation solver. We assess the approach in 10 volunteers and compare to the SAR seen in a standard generic body model (Duke). Results The on-the-table workflow averaged 7 ' 44 ''. Simulation of the simplified Duke models confirmed that only air, bone, fat, and soft tissue classes are needed to estimate global and local SAR with an error of 6.7% and 2.7%, respectively, compared to the full model. In contrast, our volunteers showed a 16.0% and 20.3% population variability in global and local SAR, respectively, which was mostly underestimated by the Duke model. Conclusion Timely construction and deployment of a patient-specific model is computationally feasible. The benefit of resolving the population heterogeneity compared favorably to the modest modeling error incurred. This suggests that individualized SAR estimates can improve electromagnetic safety in MRI and possibly reduce conservative safety margins that account for patient-model mismatch, especially in non-standard patients.

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