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Machine Learning Predicts Prolonged Acute Hypoxemic Respiratory Failure in Pediatric Severe Influenza
Michaël S Sauthier, Philippe A Jouvet1, Margaret M Newhams2
1Departments of Pediatrics, Sainte-Justine Hospital, Montreal, QC, Canada.
Insights
Early identification of prolonged acute hypoxemic respiratory failure in children with influenza is possible using machine learning on clinical data. This helps predict severe outcomes and guides resource allocation during pandemics.
Area of Science:
- Pediatric Critical Care Medicine
- Infectious Diseases
- Machine Learning in Healthcare
Background:
- Influenza virus is a significant cause of acute hypoxemic respiratory failure in children.
- Early identification of severe complications is crucial for patient stratification and pandemic preparedness.
Purpose of the Study:
- To identify clinical variables that best predict prolonged acute hypoxemic respiratory failure in critically ill, influenza-infected children.
- To develop a predictive model using machine learning algorithms.
Main Methods:
- Prospective, multicenter study involving 34 PICUs from 2009-2018.
- Included children (<18 years) without comorbid risk factors.
- Utilized Monte Carlo cross-validation with random forests and logistic regression on admission and day 2 clinical data.
Main Results:
- 258 children included; 4.2% mortality.
- By day 2, 65% had acute hypoxemic respiratory failure; 26% had prolonged (day 7) failure.
- A random forest model using day 2 variables (respiratory rate, FiO2, pH) achieved an AUC of 0.93, predicting prolonged failure.
Conclusions:
- Machine learning applied to routine clinical data can identify children with influenza likely to develop prolonged acute hypoxemic respiratory failure early.
- This predictive capability aids in clinical trial stratification and resource planning.
- Further validation is required before bedside implementation.
Abstract:
Influenza virus is a major cause of acute hypoxemic respiratory failure. Early identification of patients who will suffer severe complications can help stratify patients for clinical trials and plan for resource use in case of pandemic.
Objective:
We aimed to identify which clinical variables best predict prolonged acute hypoxemic respiratory failure in influenza-infected critically ill children. Acute hypoxemic respiratory failure was defined using hypoxemia cutoffs from international consensus definitions of acute respiratory distress syndrome in patients with ventilatory support. Prolonged acute hypoxemic respiratory failure was defined by acute hypoxemic respiratory failure criteria still present at PICU day 7.
Derivation Cohort:
In this prospective multicenter study across 34 PICUs from November 2009 to April 2018, we included children (< 18 yr) without comorbid risk factors for severe disease.
Validation Cohort:
We used a Monte Carlo cross validation method with N 2 random train-test splits at a 70-30% proportion per model.
Prediction Model:
Using clinical data at admission (day 1) and closest to 8 am on PICU day 2, we calculated the area under the receiver operating characteristic curve using random forests machine learning algorithms and logistic regression.
Results:
We included 258 children (median age = 6.5 yr) and 11 (4.2%) died. By day 2, 65% (n = 165) had acute hypoxemic respiratory failure dropping to 26% (n = 67) with prolonged acute hypoxemic respiratory failure by day 7. Those with prolonged acute hypoxemic respiratory failure had a longer ICU stay (16.5 vs 4.0 d; p < 0.001) and higher mortality (13.4% vs 1.0%). A multivariable model using random forests with 10 admission and eight day 2 variables performed best (0.93 area under the receiver operating characteristic curve; 95 CI%: 0.90-0.95) where respiratory rate, Fio2, and pH on day 2 were the most important factors.
Conclusions:
In this prospective multicentric study, most children with influenza virus-related respiratory failure with prolonged acute hypoxemic respiratory failure can be identified early in their hospital course applying machine learning onto routine clinical data. Further validation is needed prior to bedside implementation.
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