TGRA-P: Task-driven model predicts 90-day mortality from ICU clinical notes on mechanical ventilation

With the outbreak and spread of COVID-19 worldwide, limited ventilators fail to meet the surging demand for mechanical ventilation in the ICU. Clinical models based on structured data that have been proposed to rationalize ventilator allocation often suffer from poor ductility due to fixed fields and laborious normalization processes. The advent of pre-trained models and downstream fine-tuning methods allows for learning large amounts of unstructured clinical text for different tasks. But the hardware requirements of large-scale pre-trained models and purposeless networks downstream have led to a lack of promotion in the clinical domain.

In this study, an innovative architecture of a task-driven predictive model is proposed and a Task-driven Gated Recurrent Attention Pool model (TGRA-P) is developed based on the architecture. TGRA-P predicts early mortality risk from patients' clinical notes on mechanical ventilation in the ICU, which is used to assist clinicians in diagnosis and decision-making.

Specifically, a Task-Specific Embedding Module is proposed to fine-tune the embedding with task labels and save it as static files for downstream calls. It serves the task better and prevents GPU overload. The Gated Recurrent Attention Unit (GRA) is proposed to further enhance the dependency of the information preceding and following the text sequence with fewer parameters. In addition, we propose a Residual Max Pool (RMP) to avoid ignoring words in common text classification tasks by incorporating all word-level features of the notes for prediction. Finally, we use a fully connected decoding network as a classifier to predict the mortality risk.

The proposed model shows very promising results with an AUROC of 0.8245±0.0096, an AUPRC of 0.7532±0.0115, an accuracy of 0.7422±0.0028 and F1-score of 0.6612±0.0059 for 90-day mortality prediction using clinical notes of ICU mechanically ventilated patients on the MIMIC-III dataset, all of which are better than previous studies. Moreover, the superiority of the proposed model in comparison with other baseline models is also statistically validated through the calculated Cohen's d effect sizes.

The experimental results show that TGRA-P based on the innovative task-driven prognostic architecture obtains state-of-the-art performance. In future work, we will build upon the provided code and investigate its applicability to different datasets. The model balances performance and efficiency, not only reducing the cost of early mortality risk prediction but also assisting physicians in making timely clinical interventions and decisions. By incorporating textual records that are challenging for clinicians to utilize, the model serves as a valuable complement to physicians' judgment, enhancing their decision-making process.