A Data-Driven Approach to Support Clinical Renal Replacement Therapy

Critically ill patients with acute kidney injury (AKI) on continuous renal replacement therapy (CRRT) face high mortality, yet current risk assessment relies primarily on clinical parameters from electronic health records (EHR) and ignores minute-level circuit pressure waveforms generated by CRRT machines that track the extracorporeal circuit's interaction with the patient. Clinicians therefore cannot see deterioration as it develops. Risk is reassessed only when labs are drawn, while this continuous record is discarded because it is contaminated by shared-device records, non-physiological minutes, and sensor artifacts. To make the stream usable, we aligned machine records to charted therapy intervals to prevent cross-patient leakage, removed priming and downtime minutes, tuned denoising on a synthetic spike-injection benchmark, and masked unobserved intervals rather than imputing them. On this cleaned stream, we define a rolling day-wise task and a transformer-based stacked ensemble that late-fuses a window-reduced sequence transformer with classical models using circuit-instability features and clinical EHR variables. In a leak-safe benchmark on the multi-center CRRTnet cohort (976 patients, 4,585 treatment days), the machine-only model had the lowest standalone prognostic value (AUROC 0.625), followed by the EHR-only model (0.717). Integrating EHR and machine streams reached a one-day mortality AUROC of 0.766. SHAP attribution showed that circuit-instability descriptors raised the machine share of the top 15 combined-model features from 3 to 7 (20.0% to 46.7%), highlighting filter pressure, transmembrane pressure (TMP), and access-to-return difference (ARD). To our knowledge, this is the first patient-level mortality prediction incorporating CRRT machine data, turning a discarded bedside stream into a continuous risk signal.

Predicting future organ dysfunction in Intensive Care Unit (ICU) patients is critical for early clinical intervention, yet existing machine learning approaches have largely treated the Sequential Organ Failure Assessment (SOFA) score as an input to binary mortality prediction rather than as a continuous clinical outcome in its own right. We investigate the extent to which a Temporal Convolutional Net work (TCN) can predict next-day SOFA scores from multivariate ICU time-series data extracted from MIMIC-IV, characterise the relative contribution of each organ system to total SOFA variance and deterioration, and identify distinct trajectory patterns across ICU stays. A residual TCN trained on three-day sliding windows achieved a five-fold cross-validation R2 of 0.740 +- 0.013 and MAE of 1.431 +- 0.022, outperforming a naive persistence baseline on RMSE and R2. SHAP interpretability analysis revealed that the model functions primarily as a severity-anchoring mechanism rather than a true sequence model, with predictions dominated almost entirely by the most recent observation day. Cardiovascular dysfunction emerged as the strongest discriminator of both cross-sectional severity and acute deterioration, and unsupervised trajectory clustering identified two clinically meaningful phenotypes, an improving group (58.9%) and a persistently severe group (41.1%), differentiated by cardiovascular, hepatic, coagulation, and renal involvement. We conclude that TCNs can extract meaningful predictive signal from ICU physiological data, but that short input windows and complete-case selection bias currently limit their clinical utility, motivating future work on longer input horizons, alternative missing-data strategies, and external validation.

Accurate early prediction of Acute Kidney Injury (AKI) is critical for timely clinical intervention. However, existing deep learning models struggle with irregularly sampled data and suffer from the opaque "black-box" nature of sequential architectures, strictly limiting clinical trust. To address these challenges, we propose CT-Former, integrating continuous-time modeling with a Causal-Transformer. To handle data irregularity without biased artificial imputation, our framework utilizes a continuous-time state evolution mechanism to naturally track patient temporal trajectories. To resolve the black-box problem, our Causal-Attention module abandons uninterpretable hidden state aggregation. Instead, it generates a directed structural causal matrix to identify and trace the exact historical onset of severe physiological shocks. By establishing clear causal pathways between historical anomalies and current risk predictions, CT-Former provides native clinical interpretability. Training follows a decoupled two-stage protocol to optimize the causal-fusion process independently. Extensive experiments on the MIMIC-IV cohort (N=18,419) demonstrate that CT-Former significantly outperforms state-of-the-art baselines. The results confirm that our explicitly transparent architecture offers an accurate and trustworthy tool for clinical decision-making.