Skip to content

4 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Sep 2026

From Clinical Free Text to Auditable Concepts: An Agentic Framework for Interpretable Prediction

Across application domains, predictive signals often sit in unstructured free text rather than structured fields, yet turning that text into useful and interpretable features is difficult. Running large language models (LLMs) over an entire corpus is costly and hard to reproduce, while end-to-end text representations can rely on surface cues that are difficult to inspect. We present an agentic workflow that takes a prediction task and a raw text corpus as input and produces an auditable feature layer. The first two agents use an LLM to derive a task-specific predictor taxonomy and weakly label a bounded text sample; routed local extractors then process the corpus, and a deterministic builder aggregates the evidence into a dynamic, longitudinal concept bottleneck. We evaluate the framework on medication discontinuation in a longitudinal oncology cohort and 30-day readmission in MIMIC-IV. With gradient boosting, the longitudinal bottleneck increases area under the receiver operating characteristic curve (AUROC) over coarse concept buckets from 0.700 to 0.761 for medication discontinuation and from 0.576 to 0.609 for readmission. The proposed framework achieves predictive performance comparable to direct BioClinicalBERT prediction on both tasks while additionally providing explicit, interpretable, and traceable task-specific concepts. LLM use is confined to a bounded weak-labeling stage costing $24.00 and $23.39, respectively, compared with projected costs of $10,648 and $11,519 for exhaustive sentence-level LLM processing of the full corpora, demonstrating the substantial cost efficiency of the proposed agentic system.

C. Ni, W. Liu, Q. Song et al. · 0 citations
Preprint Jul 2026

DRIFT: Direct-Recursive Intervention-Conditioned Forecasting of ICU Physiological Trajectories

Many time-series forecasts depend not only on prior observations but also on actions specified during the forecast period. In intensive care units (ICUs), future vital signs and laboratory values are influenced by treatments such as vasopressors. However, models that predict the full future sequence all at once make little use of these treatments, whereas autoregressive models can accumulate errors. We introduce DRIFT, a hybrid framework in which a direct model produces the primary forecast and a recursive, action-conditioned model contributes constrained corrections. We evaluate DRIFT on 6,046 admissions from MIMIC-IV and 8,345 admissions from eICU-CRD. Averaged across the 8-, 24-, and 48-hour forecast endpoints, DRIFT reduces mean absolute error for mean arterial pressure (MAP) by 0.673% relative to an action-conditioned Temporal Fusion Transformer (TFT-action) on MIMIC-IV and achieves the lowest corresponding error among the compared models on eICU-CRD. Although the overall accuracy improvement is modest, a MIMIC-IV audit restricted to windows in which the supplied treatment sequence was altered showed that DRIFT achieved lower observed-target MAP error than TFT-action at 8 and 24 hours. Treatment-sequence alteration increased DRIFT's MAP error by 0.21-0.26 mmHg more than it increased TFT-action's error, with prediction changes occurring primarily after the supplied paths diverged. In a separate robustness experiment, the MAP advantage persisted under three shared checkpoint-selection rules emphasizing overall endpoint error, MAP error, or both equally.

Weixin Liu, Juming Xiong, C. Ni et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.