Appl Clin Inform
DOI: 10.1055/a-2605-1847
Research Article

Special Issue on CDS Failures: Performance Degradation between Development and Deployment of a Predictive Model for Central-Line Associated Blood Stream Infections in Hospitalized Children

Jonathan M Beus
1   Pediatrics, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
2   Pediatrics, Emory University, Atlanta, United States (Ringgold ID: RIN1371)
,
Mark Mai
3   Critical Care, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
Nikolay P Braykov
1   Pediatrics, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
Swaminathan Kandaswamy
4   Emory University, Atlanta, United States (Ringgold ID: RIN1371)
,
Edwin Ray
1   Pediatrics, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
D Brad Cundiff
1   Pediatrics, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
Paulette Djachechi
1   Pediatrics, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
Sarah A Thompson
5   IS&T, Children's Healthcare of Atlanta Inc, Atlanta, United States (Ringgold ID: RIN1367)
,
Azade Tabaie
6   MedStar Health Research Institute, Hyattsville, United States (Ringgold ID: RIN121577)
,
Ryan Birmingham
7   Biomedical Informatics, Emory University, Atlanta, United States (Ringgold ID: RIN1371)
,
Rishi Kamaleswaran
8   Surgery, Duke University School of Medicine, Durham, United States (Ringgold ID: RIN12277)
,
Evan Orenstein
9   Pediatrics, Children's Healthcare of Atlanta Egleston Hospital, Atlanta, United States (Ringgold ID: RIN138610)
› Author Affiliations

Background: Central line-associated bloodstream infections (CLABSIs) are associated with substantial pediatric morbidity and mortality. The capacity to predict which children with central lines are at greatest risk of CLABSI could inform surveillance and prevention efforts. Our team previously published in silico predictive models for CLABSI. Objective: To prospectively implement a pediatric CLABSI predictive model and achieve adequate performance in offline validation for implementation in clinical practice. Methods: The most performant predictive models were deep learning models requiring substantial pre-processing of many features into 8-hour windows including the current day and up to 56 days prior for the current admission. To replicate this pre-processing, we created novel infrastructure to (1) organize current-day data for all the relevant features and (2) create a staged historical data store for those same features with application programming interfaces to connect the two. We compared predictive performance of these scores for CLABSI in the next 48 hours with two labels, one based on manual review of positive blood cultures in children with central lines and another based on positive blood culture and receipt of at least 4 days of new IV antibiotics. Results: The area under the receiver-operating characteristic (AUROC) fell from 0.97 from retrospective data to <0.60 despite multiple iterations of troubleshooting. Primary root causes included train/serve skew, feature leakage, and overfitting. Hypothesized secondary drivers were complex model specification, poor data governance and inadequate testing, challenging feature translation between real-time and historical data models, limited monitoring and logging infrastructure for troubleshooting, and suboptimal handoff between the model development and deployment teams. Conclusion: To bridge the gap from predictive model development to clinical deployment requires early and close coordination between data governance, data science, clinical informatics, and implementation engineers. Balancing predictive performance with implementation feasibility can accelerate the adoption of predictive clinical decision support systems.



Publication History

Received: 12 January 2025

Accepted after revision: 09 May 2025

Accepted Manuscript online:
12 May 2025

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