A Hybrid Deep Learning Model Combining Tabular Transformers and Temporal Convolutional Network for Sepsis Prediction
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How to Cite

G., Sona, Anitha D., and Narmatha B. 2026. “A Hybrid Deep Learning Model Combining Tabular Transformers and Temporal Convolutional Network for Sepsis Prediction”. Journal of Innovative Image Processing 8 (2): 518-35. https://doi.org/10.36548/jiip.2026.2.005.

Keywords

Sepsis
Tabular Transformer
Temporal Convolutional Network
Clinical Time-Series Data
Early Detection

Abstract

Sepsis develops whenever our immune system's response to an infection becomes dysregulated, leading to extensive inflammation and organ damage. It is a severe immune system imbalance that, if ignored, can cause tissue damage, various organ failures, and death. Using multivariate clinical time-series data, a hybrid deep learning system combining a Temporal Convolutional Network (TCN) and a Tabular Transformer is developed for early prediction. The Sepsis Prediction Dataset is used in this work. The dataset consists of 40 clinical variables that have been gathered continuously in Intensive Care Unit (ICU) settings, which include vital signs, laboratory results, and demographic data. Two parallel branches are used for designing the proposed structure. The first branch, named the Tabular Transformer branch, learns the representations and interactions of variables through the handling of dynamic and categorical data. The Temporal Convolutional Network branch processes the sequential inputs by using dilated temporal convolution to detect long-range patterns within physiological signals. After concatenating both outputs and passing them into a fully connected layer, it makes predictions regarding the early phases of sepsis. With regard to its early predictions four to six hours before the clinical diagnoses, its sensitivity, specificity, accuracy, and F1-score were found to be 96.65%, 98.32%, 98.9%, and 96.3% respectively. These results indicate that the early detection of sepsis would improve as a result of integrating continuous patient data along with temporal patterns. Further validation of the developed model needs to be made on other clinical datasets.

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