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Richard Koebe

Publications and source records attributed to Richard Koebe.

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A Multimodal Deep Learning Framework for Predicting ICU Deterioration: Integrating ECG Waveforms with Clinical Data and Clinician Benchmarking

Artificial intelligence holds strong potential to support clinical decision making in intensive care units where timely and accurate risk assessment is critical. However, many existing models focus on isolated outcomes or limited data types, while clinicians integrate longitudinal history, real time physiology, and heterogeneous clinical information. To address this gap, we developed MDS ICU, a unified multimodal machine learning framework that fuses routinely collected data including demographics, biometrics, vital signs, laboratory values, ECG waveforms, surgical procedures, and medical device usage to provide continuous predictive support during ICU stays. Using 63001 samples from 27062 patients in MIMIC IV, we trained a deep learning architecture that combines structured state space S4 encoders for ECG waveforms with multilayer perceptron RealMLP encoders for tabular data to jointly predict 33 clinically relevant outcomes spanning mortality, organ dysfunction, medication needs, and acute deterioration. The model achieved strong discrimination with AUROCs of 0.90 for 24 hour mortality, 0.92 for sedative administration, 0.97 for invasive mechanical ventilation, and 0.93 for coagulation dysfunction. Calibration analysis showed close agreement between predicted and observed risks, with consistent gains from ECG waveform integration. Comparisons with clinicians and large language models showed that model predictions alone outperformed both, and that providing model outputs as decision support further improved their performance. These results demonstrate that multimodal AI can deliver clinically meaningful risk stratification across diverse ICU outcomes while augmenting rather than replacing clinical expertise, establishing a scalable foundation for precision critical care decision support.

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Towards actionable hypotension prediction -- predicting catecholamine therapy initiation in the intensive care unit

Hypotension in critically ill ICU patients is common and life-threatening. Escalation to catecholamine therapy marks a key management step, with both undertreatment and overtreatment posing risks. Most machine learning (ML) models predict hypotension using fixed MAP thresholds or MAP forecasting, overlooking the clinical decision behind treatment escalation. Predicting catecholamine initiation, the start of vasoactive or inotropic agent administration offers a more clinically actionable target reflecting real decision-making. Using the MIMIC-III database, we modeled catecholamine initiation as a binary event within a 15-minute prediction window. Input features included statistical descriptors from a two-hour sliding MAP context window, along with demographics, biometrics, comorbidities, and ongoing treatments. An Extreme Gradient Boosting (XGBoost) model was trained and interpreted via SHapley Additive exPlanations (SHAP). The model achieved an AUROC of 0.822 (0.813-0.830), outperforming the hypotension baseline (MAP < 65, AUROC 0.686 [0.675-0.699]). SHAP analysis highlighted recent MAP values, MAP trends, and ongoing treatments (e.g., sedatives, electrolytes) as dominant predictors. Subgroup analysis showed higher performance in males, younger patients (<53 years), those with higher BMI (>32), and patients without comorbidities or concurrent medications. Predicting catecholamine initiation based on MAP dynamics, treatment context, and patient characteristics supports the critical decision of when to escalate therapy, shifting focus from threshold-based alarms to actionable decision support. This approach is feasible across a broad ICU cohort under natural event imbalance. Future work should enrich temporal and physiological context, extend label definitions to include therapy escalation, and benchmark against existing hypotension prediction systems.

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