Clinical Decision Support System to Detect the Occurrence of Ventilator-Associated Pneumonia in Pediatric Intensive Care

Jerome Rambaud; Masoumeh Sajedi; Sally Al Omar; Maryline Chomtom; Michael Sauthier; Simon De Montigny; Philippe Jouvet

doi:10.3390/diagnostics13182983

Clinical Decision Support System to Detect the Occurrence of Ventilator-Associated Pneumonia in Pediatric Intensive Care

Diagnostics (Basel). 2023 Sep 18;13(18):2983. doi: 10.3390/diagnostics13182983.

Authors

Jerome Rambaud^{1

2}, Masoumeh Sajedi³, Sally Al Omar³, Maryline Chomtom⁴, Michael Sauthier¹, Simon De Montigny^{3

5}, Philippe Jouvet¹

Affiliations

¹ Pediatric Intensive Care Unit, Sainte-Justine Hospital, Montreal, QC H3T 1C5, Canada.
² Pediatric and Neonatal Intensive Care Unit, Armand-Trousseau Hospital, Sorbonne University, 75012 Paris, France.
³ Research Center, Sainte-Justine Hospital, Montreal, QC H3T 1C5, Canada.
⁴ Pediatric Intensive Care Unit, Caen University Hospital, 14000 Caen, France.
⁵ School of Public Health, Montréal University, Montreal, QC H2X 3E4, Canada.

Abstract

Objectives: Ventilator-associated pneumonia (VAP) is a severe care-related disease. The Centers for Disease Control defined the diagnosis criteria; however, the pediatric criteria are mainly subjective and retrospective. Clinical decision support systems have recently been developed in healthcare to help the physician to be more accurate for the early detection of severe pathology. We aimed at developing a predictive model to provide early diagnosis of VAP at the bedside in a pediatric intensive care unit (PICU).

Methods: We performed a retrospective single-center study at a tertiary-care pediatric teaching hospital. All patients treated by invasive mechanical ventilation between September 2013 and October 2019 were included. Data were collected in the PICU electronic medical record and high-resolution research database. Development of the clinical decision support was then performed using open-access R software (Version 3.6.1^®).

Measurements and main results: In total, 2077 children were mechanically ventilated. We identified 827 episodes with almost 48 h of mechanical invasive ventilation and 77 patients who suffered from at least one VAP event. We split our database at the patient level in a training set of 461 patients free of VAP and 45 patients with VAP and in a testing set of 199 patients free of VAP and 20 patients with VAP. The Imbalanced Random Forest model was considered as the best fit with an area under the ROC curve from fitting the Imbalanced Random Forest model on the testing set being 0.82 (95% CI: (0.71, 0.93)). An optimal threshold of 0.41 gave a sensitivity of 79.7% and a specificity of 72.7%, with a positive predictive value (PPV) of 9% and a negative predictive value of 99%, and with an accuracy of 79.5% (95% CI: (0.77, 0.82)).

Conclusions: Using machine learning, we developed a clinical predictive algorithm based on clinical data stored prospectively in a database. The next step will be to implement the algorithm in PICUs to provide early, automatic detection of ventilator-associated pneumonia.

Keywords: PICU; clinical decision system; pneumonia; ventilator associated.

Grants and funding

J.R. received a studentship from the scholarship supplement program from the Quebec Respiratory Health Research Network. This work was supported in part by the Quebec Respiratory Health Research Network. J.P.’s scientific research funds from the Canadian Foundation for Innovation, Fonds de Recherche Québec, Quebec Ministry of Health and Sainte-Justine Hospital.