Postoperative acute kidney injury (AKI) after major non-cardiac surgery carries substantial morbidity, yet early intraoperative risk stratification remains difficult. In this retrospective cohort study, we propose SynerT, a waveform-only hybrid temporal backbone that combines a causal dilated TCN with a hierarchy of dilated recurrent layers to encode early intraoperative physiologic trajectories for AKI risk prediction. Building on SynerT, we further design two model variants that extend the backbone with structured clinical context: SynerT-MM, a late-fusion multimodal extension that integrates hemodynamic burden summaries and preoperative covariates, and SynerTStack, a leakage-safe stacked ensemble that combines cross-validated predictions from SynerT-MM with strong tabular baselines at the meta-learning stage. All models are evaluated under a strict leakage-aware framework on VitalDB, a high-fidelity perioperative database, with prediction restricted to information available within the first 60 intraoperative minutes. Among 2,413 waveform-usable cases (180 AKI-positive; 7.46% prevalence), SynerT fell well below strong structured-data baselines, demonstrating that waveform-only temporal modeling is insufficient under strict early constraints. SynerTMM recovered discrimination by incorporating hemodynamic burden summaries and preoperative covariates, and SynerT-Stack achieved the best overall performance across AUROC, AUPRC, and F1-max. Cross-fitted Platt recalibration substantially corrected calibration defects in both multimodal variants, and decision-curve analysis confirmed the recalibrated stacked model delivered the strongest net clinical benefit across low-to-intermediate thresholds.
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.
An Intraoperative Hypotension (IOH) event is a frequent complication during administration of general anaesthesia with serious downstream consequences, yet clinical management remains reactive and not predictive. Existing predictive models, however, ignore drug infusion history as a valuable signal for prediction despite its direct pharmacological relevance. Our model achieves an Area Under the Receiver Operating Characteristic curve (AUROC) of 0.7360 and an Area Under the Precision-Recall Curve (AUPRC) of 0.1794, representing a 2.73-fold lift over the random guessing AUPRC baseline (0.0657), with the removal of propofol and remifentanil effect-site concentrations resulting in a 13.9% AUPRC drop compared to the full model. This is consistent with the hypothesis that pharmacokinetic trajectories encode impending haemodynamic changes before they manifest in the Mean Arterial Pressure (MAP). Additionally, this paper shows that training without lead-gap filtering degraded AUROC by 16.7%, empirically confirming that unfiltered models learn to detect ongoing hypotension rather than predict future events. Finally, a Mamba-based architecture achieves the aforementioned high prediction performance while maintaining a constant memory footprint across a range of sequence lengths, unlike the quadratic VRAM overhead typical of vanilla Transformers, making it the more practical choice for continuous intraoperative deployment.
Rithin Nagaraj, Sudiksha Chindula, Bhaskarjyoti Das
Progression to dialysis or end-stage renal disease is a rare but clinically important outcome. Clinicians need evidence on how medication exposures influence downstream risk. We constructed a fixed-window EHR cohort (90-day observation, 730-day prediction; N=81401; dialysis/ESRD prevalence: 1.1%) and modeled sequences of diagnoses, procedures, and medications with kidney laboratory trends (creatinine, BUN, eGFR). A transformer-based causal multi-head model was trained to estimate drug- and ingredient-level average treatment effects (ATEs) using counterfactual exposure removal and insertion under a full medication history setup. On test set, predictive performance reached an AUC of 0.694 and PR-AUC of 0.094. At the selected decision threshold (0.883), the model achieved an F1 score of 0.201 with a Brier score of 0.018. Post-hoc causal analyses of lab changes (eGFR, creatinine, BUN) using IPTW, AIPW, naive, and covariate-adjusted OLS methods assessed clinical directionality. Results showed partial protective-direction support for ACE/ARB exposures and worsening-direction signals for loop diuretics.