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Ethical and Regulatory Perspectives on Generative Artificial Intelligence in Pathology
Brian R Jackson1, Hooman H Rashidi2, Jochen K Lennerz3
1From the Department of Pathology, University of Utah, Salt Lake City (Jackson).
Archives of Pathology & Laboratory Medicine
|September 19, 2024
Summary
Generative artificial intelligence (GenAI) offers significant potential in pathology and laboratory medicine but also presents new risks. Ethical frameworks are essential for responsible GenAI development and deployment in healthcare.
Area of Science:
- Medical Technology
- Artificial Intelligence in Healthcare
- Pathology and Laboratory Medicine
Background:
- Generative artificial intelligence (GenAI) is increasingly explored in pathology and laboratory medicine.
- While promising, GenAI introduces novel risks for patients, communities, professionals, and the scientific process.
Purpose of the Study:
- To summarize current frameworks for the ethical development and management of GenAI in healthcare settings.
Main Methods:
- Analysis of scientific journals.
- Review of organizational websites.
- Examination of recent guidelines on artificial intelligence ethics and regulation.
Main Results:
- Literature on AI ethics in medicine is extensive but nascent due to evolving technology.
- Effective GenAI integration requires robust processes and shared accountability.
- A multifaceted ecosystem of safety and ethical oversight is crucial.
Conclusions:
- Maximizing GenAI benefits and mitigating risks necessitates a collaborative approach.
- Shared accountability among vendors, healthcare organizations, regulators, and professionals is key.
- Ongoing development requires continuous adaptation of ethical oversight mechanisms.
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