Dependency-Aware Fusion for Vital-Sign Anomaly Detection in Intensive Care Monitoring
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Keywords

ICU monitoring
non-stationary time series
vital sign anomaly detection

Abstract

Intensive care units generate continuous multivariate physiological time series from heart rate, blood pressure, oxygen saturation, respiratory rate, body temperature, electrocardiographic signals, and medication-related records. These signals are highly non-stationary because patient conditions change with disease progression, treatment response, medication dosage, and clinical intervention. This study proposes a latent dependency fusion model for non-stationary vital sign anomaly detection in intensive care monitoring. The model first learns patient-specific temporal regimes through a gated sequence encoder. It then constructs latent dependency representations among physiological variables using cross-channel attention and dynamic correlation estimation. A residual-based anomaly scoring module is applied to detect abnormal physiological changes while reducing false alerts caused by normal post-treatment fluctuations. Experiments are conducted on an ICU monitoring dataset containing 18,400 patient stays, 64 physiological variables, and 1-minute observations collected over 21 months. The dataset includes 96 million timestamped records and 3,260 clinically annotated abnormal episodes, including sudden hypotension, oxygen desaturation, arrhythmia-related instability, abnormal respiratory deterioration, and post-operative shock signals. The proposed method reduces median warning delay from 27.5 minutes to 8.9 minutes compared with a single-channel temporal autoencoder. False alarms decrease to 3.4 alerts per patient-day. The Matthews correlation coefficient reaches 0.889 across mixed patient groups, and the average event-boundary deviation is reduced by 18.6 minutes. Online scoring processes 22,000 physiological points per second, with a median inference latency of 31 ms per patient window. These results indicate that latent dependency fusion can improve anomaly detection for non-stationary clinical time series in intensive care environments.

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Copyright (c) 2026 Sarah Mitchell, James Walker (Author)