cs.AIMay 16, 2026

From Static Risk to Dynamic Trajectories: Toward World-Model-Inspired Clinical Prediction

Authors: Pujun FengXiaoyu GuoSeyed Ehsan SaffariMin Hun LeeSiew-Kei LamErik CambriaXibin SunYangtao Zhou+5 more

Organizations: Faculty of Applied Sciences, Macao Polytechnic University, Macao SAR 999078, China. · Medin.ai, Beijing 100871, China. · School of Software & Microelectronics, Peking University, Beijing 100871, China. · Centre for Biomedical Data Science, Duke-NUS Medical School, National University of Singapore, Singapore 169857, Singapore. · Duke-NUS AI + Medical Sciences Initiative, Duke-NUS Medical School, Singapore 169857, Singapore. · School of Computing and Information Systems, Singapore Management University, Singapore 178902, Singapore. · College of Computing and Data Science, Nanyang Technological University, Singapore 639798, Singapore. · School of Public Health, Peking University, Beijing 100191, China. · School of Computer Science and Technology, Xidian University, Xi’an 710126, China. · School of Computer, Peking University, Beijing 100871, China. · School of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.

Abstract

Clinical decision-making is a feedback system where risk estimates influence treatment, which in turn changes disease trajectories, and both shape clinicians' measurement practices. Static prediction often fails clinically: models trained on observational care logs conflate disease biology with clinician behavior, particularly under treatment confounder feedback and irregular or informative observation. This Review focuses on intervention-aware disease trajectory modeling in clinical AI--methods estimating patient-specific longitudinal disease evolution and assessing trajectory changes under alternative treatments. We organize the field around six linked components: three decision tasks (factual forecasting, counterfactual estimation, policy evaluation) and three data-generating mechanisms (disease evolution, treatment assignment, observation process) that determine identifiability. We present the first unified framework bridging forecasting, counterfactual trajectories, and policy evaluation across discrete/continuous time, explicitly addressing treatment assignment, time-varying confounding, and observation bias. We synthesize key method families (multistate/joint models, temporal point-process, deep sequence architectures, longitudinal causal inference), map them to relevant components, and align evaluation with claim strength via overlap diagnostics, uncertainty quantification, off-policy robustness, and target-trial validation. This synthesis advances benchmark prediction to decision-grade clinical evidence, enabling treatment-sensitive individualized futures, pre-deployment policy stress-testing, and safer closed-loop learning health systems that adapt/abstain when evidence is insufficient.

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