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Official Description

MR safety determination by a physician or other qualified health care professional responsible for the safety of the MR procedure, including review of implant MR conditions for indicated MR examination, analysis of risk vs clinical benefit of performing MR examination, and determination of MR equipment, accessory equipment, and expertise required to perform examination, with written report

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 76016 pertains to the process of determining the safety of a magnetic resonance (MR) imaging procedure, specifically when a patient has an implanted medical device. This determination is conducted by a physician or another qualified healthcare professional who is responsible for ensuring the safety of the MR examination. The procedure involves a comprehensive review of the patient's implant MR conditions that are relevant to the indicated MR examination. The healthcare professional analyzes the potential risks versus the clinical benefits of performing the MR examination, taking into account the specific characteristics of the implanted device, such as pacemakers or neurostimulators, which may present contraindications or necessitate modifications to the examination protocol. Additionally, the safety determination includes an evaluation of incomplete or non-functioning devices that may not have clear safety condition labeling. The professional identifies the location and type of any foreign body present in the patient and reviews the details regarding the implant, including the manufacturer's labeling for any MRI restrictions or contraindications. The feasibility of the intended MRI exam is assessed based on these factors, along with the expected quality of the imaging that can be achieved while adhering to the implant's instructions and restrictions. Furthermore, the healthcare provider evaluates the potential risks to the patient, particularly by assessing the proximity of the implanted device to the target tissues and considering any risks of device malfunction, heat injury, or displacement during the MR examination. The report generated from this safety determination also outlines the requirements for any special accessory MR equipment needed and the expertise required to set up and conduct the examination safely. Recommendations for alternative diagnostic procedures may also be included, ensuring that all expectations, recommendations, and special precautions are communicated to the patient prior to finalizing the report.

© Copyright 2026 Coding Ahead. All rights reserved.

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