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Published on: January 16, 2019
Early Prediction of Multiple Organ Dysfunction in the Pediatric Intensive Care Unit
Sanjukta N Bose1,2, Joseph L Greenstein1, James C Fackler3
1Institute for Computational Medicine, The Johns Hopkins University, Baltimore, MD, United States.
Insights
Machine learning models can predict multiple organ dysfunction (MOD) in pediatric intensive care unit (PICU) patients over 22 hours in advance. This early warning system identifies high-risk patients with high accuracy, improving patient outcomes.
Area of Science:
- Pediatric critical care medicine
- Machine learning in healthcare
- Predictive analytics
Background:
- Multiple organ dysfunction (MOD) is a significant cause of mortality in pediatric intensive care units (PICUs).
- Early identification of patients at risk for MOD is crucial for timely intervention and improved outcomes.
Purpose of the Study:
- To develop and evaluate machine learning models for the early prediction of MOD risk in PICU patients.
- To assess the lead time and accuracy of these predictive models.
Main Methods:
- Retrospective observational cohort study of pediatric patients (<18 years) admitted to a single academic PICU.
- Organ dysfunction was labeled using International Pediatric Sepsis Consensus Conference (IPSCC) and Proulx et al. criteria.
- Four machine learning models (random forest, XGBoost, GLMBoost, Lasso-GLM) were trained to predict MOD using 24-hour rolling time windows.
Main Results:
- All models achieved an area under the receiver operating characteristics curve (AUC) ≥0.91.
- XGBoost model showed the highest performance (F1-score: 0.81) for predicting MOD based on Proulx criteria, with a median early warning time of 37 hours.
- Random forest model achieved a sensitivity of 0.72 and positive predictive value of 0.70 for IPSCC criteria, with a median warning time of 22.7 hours.
- Spectral clustering identified a high-risk group with a positive predictive value (PPV) of ≥0.93 for MOD onset.
Conclusions:
- Risk-based patient monitoring using machine learning can provide early warnings for MOD in PICU patients.
- The developed models offer a significant lead time (over 22 hours) for MOD onset.
- High-risk patient identification with high PPV (≥0.93) enables proactive clinical management.
Abstract:
Objective: The objective of the study is to build models for early prediction of risk for developing multiple organ dysfunction (MOD) in pediatric intensive care unit (PICU) patients. Design: The design of the study is a retrospective observational cohort study. Setting: The setting of the study is at a single academic PICU at the Johns Hopkins Hospital, Baltimore, MD. Patients: The patients included in the study were <18 years of age admitted to the PICU between July 2014 and October 2015. Measurements and main results: Organ dysfunction labels were generated every minute from preceding 24-h time windows using the International Pediatric Sepsis Consensus Conference (IPSCC) and Proulx et al. MOD criteria. Early MOD prediction models were built using four machine learning methods: random forest, XGBoost, GLMBoost, and Lasso-GLM. An optimal threshold learned from training data was used to detect high-risk alert events (HRAs). The early prediction models from all methods achieved an area under the receiver operating characteristics curve ≥0.91 for both IPSCC and Proulx criteria. The best performance in terms of maximum F1-score was achieved with random forest (sensitivity: 0.72, positive predictive value: 0.70, F1-score: 0.71) and XGBoost (sensitivity: 0.8, positive predictive value: 0.81, F1-score: 0.81) for IPSCC and Proulx criteria, respectively. The median early warning time was 22.7 h for random forest and 37 h for XGBoost models for IPSCC and Proulx criteria, respectively. Applying spectral clustering on risk-score trajectories over 24 h following early warning provided a high-risk group with ≥0.93 positive predictive value. Conclusions: Early predictions from risk-based patient monitoring could provide more than 22 h of lead time for MOD onset, with ≥0.93 positive predictive value for a high-risk group identified pre-MOD.
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