- Define the requirements of an MR simulator including considerations for equipment selection, facility design and siting, and personnel and their roles;
- Describe general, patient-specific, and device MR safety considerations;
- Provide recommendations on RT-specific MR clinical workflows and acquisition protocols, including approaches for distortion and motion management;
- Outline recommended acceptance, commissioning and periodic QA for MR simulators (with emphasis on RT-specific QA tasks) following TG-100 principles, including defining the personnel effort required.
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This article by originally appeared on Aapm on June 20, 2016 at 07:00AM