Page 25 - Diagnostic Radiology - Interpreting the Risks Part Two_Neat
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SVMIC Diagnostic Radiology: Interpreting the Risks


                   humans can do things AI cannot. AI is designed to interpret

                   specific recognition tasks such as bleeding in the brain or
                   finding nodules on a pelvic x-ray. AI will not be able to consult

                   with other doctors regarding diagnosis and treatment, and it
                   will not be able to provide procedures such as local ablative

                   therapies or perform image-guided medical interventions which
                   are unique to the patient. Radiologists will continue to discuss

                   findings with patients, compare findings from past procedures,
                   and define the boundaries of technical parameters needed to

                   elicit the best diagnostic images for the patient.



                   The AI needed to replace even some of the daily tasks
                   radiologists perform is a long way from use in the daily practice

                   of radiology. The American College of Radiology found that
                   different imaging and algorithms of vendors focus on different

                   aspects of the patient’s case. For example, the FDA has
                   approved the use of some deep-learning nodule detectors,

                   but among the detectors, there were different goals each
                   detector had. Some detectors are programmed to determine

                   the probability of a tumor or lesion, the probability of cancer, or
                   a tumor or lesion’s location and unique qualities. The different

                   aims between the detectors would make the utilization of deep-
                   learning systems in a clinical practice very difficult. Accordingly,

                   the FDA is beginning to specify the inputs and outputs for
                   deep-learning software. Methodologies to determine the

                   efficacies and value of the algorithms are required by the FDA
                   and provided by the ACR. Currently the ACR is working towards

                   a compilation of use cases determined by factors such as body
                   part, disease type, etc., to provide continuity between findings of

                   the clinical process, requirements of images, and explanations
                   of outputs in order to aid current and future clinical practices.

                   Gathering these use cases will be a lengthy and complicated




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