Dies ist eine Übersichtsseite mit Metadaten zu dieser wissenschaftlichen Arbeit. Der vollständige Artikel ist beim Verlag verfügbar.
A Framework for Trustworthy Healthcare AI: A Model-Type-Aware Minimum Evaluation and Reporting Standard (Preprint)
0
Zitationen
1
Autoren
2026
Jahr
Abstract
<sec> <title>BACKGROUND</title> Artificial intelligence (AI) is rapidly reshaping healthcare by supporting earlier diagnosis, assisting clinical decision-making, and improving operational efficiency. However, most systems remain deployed within human-in-the-loop workflows, and hospitals lack a standardized framework to evaluate fairness, reliability, accuracy, and real-world safety. Prior failures illustrate how ambiguous objectives and unvalidated proxy targets can produce inequitable outcomes and erode clinical trust. </sec> <sec> <title>OBJECTIVE</title> This paper proposes a unified, model-type-aware minimum evaluation and reporting standard capable of assessing both traditional classification models and generative large language models (LLMs) via transparent reporting of performance markers, subgroup fairness analyses, and hallucination detection. </sec> <sec> <title>METHODS</title> We developed the framework by synthesizing recurring, documented failure modes of healthcare AI with widely used regulatory and risk-management concepts, iteratively mapping risks to concrete evidence artifacts that developers can produce, evaluators can audit, and purchasers can compare across vendors. </sec> <sec> <title>RESULTS</title> The resulting standard comprises three layers: universal disclosures applicable to all healthcare AI systems (U1–U5), minimum evaluation requirements for clinical ML models (C1–C6), and minimum evaluation requirements for LLM/RAG systems (G1–G6), supported by lifecycle governance expectations for post-deployment monitoring, versioning, and rollback. </sec> <sec> <title>CONCLUSIONS</title> Current FDA pathways provide a foundation but remain insufficient for governing continual-learning systems and generative models in clinical workflows. We propose that the FDA extend these mechanisms to require mandatory disclosure of training data provenance and standardized benchmarks for clinical safety and relevance. Establishing such a framework is crucial to ensure that AI advances deliver autonomously safe and trustworthy healthcare. </sec>
Ähnliche Arbeiten
Explainable Artificial Intelligence (XAI): Concepts, taxonomies, opportunities and challenges toward responsible AI
2019 · 8.707 Zit.
Stop explaining black box machine learning models for high stakes decisions and use interpretable models instead
2019 · 8.613 Zit.
High-performance medicine: the convergence of human and artificial intelligence
2018 · 8.159 Zit.
BioBERT: a pre-trained biomedical language representation model for biomedical text mining
2019 · 6.875 Zit.
Proceedings of the 19th International Joint Conference on Artificial Intelligence
2005 · 5.781 Zit.