Consent |
Develop informed consent for patients to sign detailing the actions and limitations of AI |
Develop consent forms to all literacy levels and test for understanding |
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Develop similar consent for providers |
Develop patient education materials that detail the purpose of AI and evaluate for understanding |
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Provide patients with “opt-out” of AI monitoring |
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Provide time limits or expiration to consent |
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Re-consent each year with evolving technology |
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Have consent documents approved by experts and medical review board |
Controls |
Adopt standards for suicide monitoring with AI, such as determining what percentage of at-risk individuals will be monitored |
Compare provider-informed vs. AI-only model to assess for increased accuracy with feedback |
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Form an AI oversight panel with multidisciplinary specialty |
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Request provider feedback routinely and update systems accordingly |
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Create a system for providers to defer or activate risk monitoring with explanation |
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Log model successes and failures, re-train models |
Communication |
Conduct focus groups with stakeholders to assess for appropriateness and utility of integrating AI into healthcare |
Develop provider materials and elicit feedback for appropriateness |
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Provide communication materials for provider use to discuss AI and the monitoring process |