ArticleJournal of medical Internet research2026
Refined Exclusion in Medical AI: Data Justice and Patient Safety Governance.
Article in Journal of medical Internet research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
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Abstract
Medical AI is often evaluated using aggregate measures of discrimination, calibration, and accuracy. However, these measures can obscure clinically important variation across patient groups, institutions, devices, and workflows. This viewpoint defines refined exclusion as a governance condition in which an AI system appears successful in aggregate, while uncertainty, error, or reduced clinical reliability is concentrated in populations that are insufficiently represented, measured, validated, or monitored. The concept does not replace algorithmic fairness, hidden stratification, dataset shift, or subgroup performance analysis. It connects these mechanisms to a distinct consequence: an unequal distribution of safety that remains inadequately detected or corrected. Drawing on purposively selected, illustrative evidence from population health management, chest radiography, dermatology, computational pathology, medical foundation models, and clinical measurement, we distinguish model-level disparity, patient safety signals, and documented patient harm. We then frame data justice as a complementary governance approach with distributional, procedural, and substantive dimensions. The proposed lifecycle decision gates address intended use, subgroup learnability, data provenance, validation, procurement, local deployment, monitoring, updates, and patient feedback. Each gate links minimum evidence to decision authority and 1 of 4 actions: proceed, enrich or validate, restrict use, or pause or retire. Governance intensity should be proportionate to clinical risk and evidentiary uncertainty. By linking subgroup evidence gaps to institutional decisions and corrective action, the framework shifts attention from whether a model performs well on average to whether its safety is demonstrable for the populations and settings in which it will be used.
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Registered trials
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