Development and external validation of a multimodal artificial intelligence mortality prediction model of critically ill patients using multicenter data
This work addresses mortality prediction in critical care to aid clinical decision-making, but it is incremental as it builds on existing multimodal approaches with external validation.
The researchers tackled the problem of predicting in-hospital mortality for critically ill patients by developing a multimodal deep learning model using structured and unstructured clinical data, achieving AUROC scores up to 0.92 and demonstrating improved performance with notes and imaging in external validation across multiple datasets.
Early prediction of in-hospital mortality in critically ill patients can aid clinicians in optimizing treatment. The objective was to develop a multimodal deep learning model, using structured and unstructured clinical data, to predict in-hospital mortality risk among critically ill patients after their initial 24 hour intensive care unit (ICU) admission. We used data from MIMIC-III, MIMIC-IV, eICU, and HiRID. A multimodal model was developed on the MIMIC datasets, featuring time series components occurring within the first 24 hours of ICU admission and predicting risk of subsequent inpatient mortality. Inputs included time-invariant variables, time-variant variables, clinical notes, and chest X-ray images. External validation occurred in a temporally separated MIMIC population, HiRID, and eICU datasets. A total of 203,434 ICU admissions from more than 200 hospitals between 2001 to 2022 were included, in which mortality rate ranged from 5.2% to 7.9% across the four datasets. The model integrating structured data points had AUROC, AUPRC, and Brier scores of 0.92, 0.53, and 0.19, respectively. We externally validated the model on eight different institutions within the eICU dataset, demonstrating AUROCs ranging from 0.84-0.92. When including only patients with available clinical notes and imaging data, inclusion of notes and imaging into the model, the AUROC, AUPRC, and Brier score improved from 0.87 to 0.89, 0.43 to 0.48, and 0.37 to 0.17, respectively. Our findings highlight the importance of incorporating multiple sources of patient information for mortality prediction and the importance of external validation.