Abstract

BackgroundObjectives were to build a machine learning algorithm to identify bloodstream infection (BSI) among pediatric patients with cancer and hematopoietic stem cell transplantation (HSCT) recipients, and to compare this approach with presence of neutropenia to identify BSI.MethodsWe included patients 0–18 years of age at cancer diagnosis or HSCT between January 2009 and November 2018. Eligible blood cultures were those with no previous blood culture (regardless of result) within 7 days. The primary outcome was BSI. Four machine learning algorithms were used: elastic net, support vector machine and two implementations of gradient boosting machine (GBM and XGBoost). Model training and evaluation were performed using temporally disjoint training (60%), validation (20%) and test (20%) sets. The best model was compared to neutropenia alone in the test set.ResultsOf 11,183 eligible blood cultures, 624 (5.6%) were positive. The best model in the validation set was GBM, which achieved an area-under-the-receiver-operator-curve (AUROC) of 0.74 in the test set. Among the 2236 in the test set, the number of false positives and specificity of GBM vs. neutropenia were 508 vs. 592 and 0.76 vs. 0.72 respectively. Among 139 test set BSIs, six (4.3%) non-neutropenic patients were identified by GBM. All received antibiotics prior to culture result availability.ConclusionsWe developed a machine learning algorithm to classify BSI. GBM achieved an AUROC of 0.74 and identified 4.3% additional true cases in the test set. The machine learning algorithm did not perform substantially better than using presence of neutropenia alone to predict BSI.

Highlights

  • Objectives were to build a machine learning algorithm to identify bloodstream infection (BSI) among pediatric patients with cancer and hematopoietic stem cell transplantation (HSCT) recipients, and to compare this approach with presence of neutropenia to identify BSI

  • One of the most important toxicities of cancer treatment is bloodstream infection (BSI), defined as a microbial pathogen isolated from a blood culture

  • Identifying the risk of BSI is important as those at lower risk may benefit from less intensive interventions such as outpatient management of fever, while those at higher risk may benefit from more intensive interventions such as broader empiric antibiotics or antibacterial prophylaxis [7, 8]

Read more

Summary

Introduction

Objectives were to build a machine learning algorithm to identify bloodstream infection (BSI) among pediatric patients with cancer and hematopoietic stem cell transplantation (HSCT) recipients, and to compare this approach with presence of neutropenia to identify BSI. One of the most important toxicities of cancer treatment is bloodstream infection (BSI), defined as a microbial pathogen isolated from a blood culture. BSIs are important because they are responsible for considerable morbidity, healthcare utilization and treatment-related mortality [2, 3]. BSIs may result in infection-related mortality in children who might otherwise be cured [4, 5]. Patients without cancer undergoing hematopoietic stem cell transplantation (HSCT) are at risk for life-threatening BSI [6]. Identifying the risk of BSI is important as those at lower risk may benefit from less intensive interventions such as outpatient management of fever, while those at higher risk may benefit from more intensive interventions such as broader empiric antibiotics or antibacterial prophylaxis [7, 8]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call