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.

Highlights

  • Pediatric multiple organ dysfunction syndrome (MODS) occurs in more than 25% of children admitted to the pediatric intensive care unit (PICU) [1,2,3] and is one of the leading pathways to mortality in critically ill children [4]

  • Since several criteria to choose thresholds from receiver operating characteristic (ROC) curves have been described, we compared our model performances based on two different methods: point nearest from (0, 1) on ROC curve and point corresponding to maximum F1-score

  • Most Multiple organ dysfunction (MOD) was present on PICU day 1, rendering a final data set of 293 and 687 MOD transitions using the International Pediatric Sepsis Consensus Conference (IPSCC) and Proulx criteria, respectively, that had >15 min of data prior to the time of transition

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Summary

Introduction

Pediatric multiple organ dysfunction syndrome (MODS) occurs in more than 25% of children admitted to the pediatric intensive care unit (PICU) [1,2,3] and is one of the leading pathways to mortality in critically ill children [4]. In a prospective study of 831 patients in a single PICU, more than 90% of deaths were associated with MODS [5, 6]. New and progressive MOD (NPMOD) is defined as concomitant dysfunction of two or more organ systems occurring after PICU admission with no or single organ dysfunction, or additional dysfunctional organs following admission with MOD [19]. There continues to be insufficient knowledge of the physiologic trajectory of patients who develop new, progressive, or persistent multiple organ dysfunction. We hypothesized that a complex set of physiologic patterns likely preceded adverse events such as simultaneous failure of more than one organ system

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