ArticleResearch square2025
PRICE: A Personalized Recursive Intelligent Cost Estimation Framework for Rare Disease Diagnosis.
Article in Research square, 2025. 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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4 authors.
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Abstract
Background: Rare disease diagnosis often involves complex procedures that can be both costly and time-consuming. Traditional cost-effectiveness analyses typically employ static models, applying uniform diagnostic strategies across diverse patient populations. With advancements in artificial intelligence (AI) and a growing emphasis on personalized medicine, there is a pressing need for dynamic frameworks that assess diagnostic cost-effectiveness at the individual patient level. Methods: We introduce the PRICE framework-a novel, tree-based analytical model designed to evaluate the cost-effectiveness of diagnostic strategies, accommodating both expert-alone and AI-delegation decision-making modes. The model computes the expected cost of a diagnostic process via a back-propagation algorithm and quantifies effectiveness through a utility-based approach. Parameters such as disease prevalence, test costs, test performance metrics, and turnaround time are incorporated, allowing for individualized assessments. Results: We conducted a case study applying the framework to four diagnostic strategies for developmental delay (DD) and multiple congenital anomalies (MCA). The results demonstrate how PRICE can support patient decision-making by modeling outcomes under varying parameters such as test cost and accuracy. Additionally, we show that changes in AI performance influence the selection of optimal cost-efficient strategies under AI delegation. To facilitate interpretation and engagement, we developed an interactive web-based tool that visualizes and simulates diagnostic pathways in real time, enhancing decision-making support for both clinicians and patients. Conclusion: PRICE is a flexible cost-effective analysis framework that captures the sequential and recursive nature of real-world diagnostic workflows, with the ability to be extended to future AI-integrated clinical practice. It enables personalized evaluations of diagnostic strategies from both economic and clinical perspectives, promoting more informed and individualized decision-making, especially in rare disease diagnosis.
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