CISepsis: a causal inference framework for early sepsis detection.

INTRODUCTION

The early prediction of sepsis based on machine learning or deep learning has achieved good results.Most of the methods use structured data stored in electronic medical records, but the pathological characteristics of sepsis involve complex interactions between multiple physiological systems and signaling pathways, resulting in mixed structured data. Some researchers will introduce unstructured data when also introduce confounders. These confounders mask the direct causality of sepsis, leading the model to learn misleading correlations. Finally, it affects the generalization ability, robustness, and interpretability of the model.

METHODS

To address this challenge, we propose an early sepsis prediction approach based on causal inference which can remove confounding effects and capture causal relationships. First, we analyze the relationship between each type of observation, confounder, and label to create a causal structure diagram. To eliminate the effects of different confounders separately, the methods of back-door adjustment and instrumental variable are used. Specifically, we learn the confounder and an instrumental variable based on mutual information from various observed data and eliminate the influence of the confounder by optimizing mutual information. We use back-door adjustment to eliminate the influence of confounders in clinical notes and static indicators on the true causal effect.

RESULTS

Our method, named CISepsis, was validated on the MIMIC-IV dataset. Compared to existing state-of-the-art early sepsis prediction models such as XGBoost, LSTM, and MGP-AttTCN, our method demonstrated a significant improvement in AUC. Specifically, our model achieved AUC values of 0.921, 0.920, 0.919, 0.923, 0.924, 0.926, and 0.926 at the 6, 5, 4, 3, 2, 1, and 0 time points, respectively. Furthermore, the effectiveness of our method was confirmed through ablation experiments.

DISCUSSION

Our method, based on causal inference, effectively removes the influence of confounding factors, significantly improving the predictive accuracy of the model. Compared to traditional methods, this adjustment allows for a more accurate capture of the true causal effects of sepsis, thereby enhancing the model's generalizability, robustness, and interpretability. Future research will explore the impact of specific indicators or treatment interventions on sepsis using counterfactual adjustments in causal inference, as well as investigate the potential clinical application of our method.