Machine learning-based forecast of Helmet-CPAP therapy failure in Acute Respiratory Distress Syndrome patients.

BACKGROUND AND

OBJECTIVE

Helmet-Continuous Positive Airway Pressure (H-CPAP) is a non-invasive respiratory support that is used for the treatment of Acute Respiratory Distress Syndrome (ARDS), a severe medical condition diagnosed when symptoms like profound hypoxemia, pulmonary opacities on radiography, or unexplained respiratory failure are present. It can be classified as mild, moderate or severe. H-CPAP therapy is recommended as the initial treatment approach for mild ARDS. Even though the efficacy of H-CPAP in managing patients with moderate-to-severe hypoxemia remains unclear, its use has increased for these cases in response to the emergence of the COVID-19 Pandemic. Using the electronic medical records (EMR) from the Pulmonology Department of Vimercate Hospital, in this study we develop and evaluate a Machine Learning (ML) system able to predict the failure of H-CPAP therapy on ARDS patients.

METHODS

The Vimercate Hospital EMR provides demographic information, blood tests, and vital parameters of all hospitalizations of patients who are treated with H-CPAP and diagnosed with ARDS. This data is used to create a dataset of 622 records and 38 features, with 70%-30% split between training and test sets. Different ML models such as SVM, XGBoost, Neural Network, Random Forest, and Logistic Regression are iteratively trained in a cross-validation fashion. We also apply a feature selection algorithm to improve predictions quality and reduce the number of features.

RESULTS AND

CONCLUSIONS

The SVM and Neural Network models proved to be the most effective, achieving final accuracies of 95.19% and 94.65%, respectively. In terms of F1-score, the models scored 88.61% and 87.18%, respectively. Additionally, the SVM and XGBoost models performed well with a reduced number of features (23 and 13, respectively). The PaO2/FiO2 Ratio, C-Reactive Protein, and O2 Saturation resulted as the most important features, followed by Heartbeats, White Blood Cells, and D-Dimer, in accordance with the clinical scientific literature.