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Related Experiment Video

Updated: Jun 26, 2026

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data
14:27

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data

Published on: June 26, 2013

Longitudinal Biomarker Trajectories for EVD-Associated Infection Prediction: A Trajectory-Based Machine Learning

Hraq Sarkis1, Abed Alrazzak Kerhani1, Inka K Berglar1

  • 1Department of Neurosurgery, Technical University of Munich, School of Medicine and Health, Klinikum Rechts der Isar, Munich, Bavaria, Germany.

World Neurosurgery
|June 24, 2026
PubMed
Summary
This summary is machine-generated.

Machine learning predicts external ventricular drain (EVD)-associated infections by analyzing biomarker trends, identifying infection two days before clinical signs. This aids early intervention in neurocritical care.

Keywords:
SHAPbiomarker trajectoryexternal ventricular draingradient boostingmachine learningventriculitis

Related Experiment Videos

Last Updated: Jun 26, 2026

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data
14:27

Identification of Disease-related Spatial Covariance Patterns using Neuroimaging Data

Published on: June 26, 2013

Area of Science:

  • Neurocritical care
  • Infectious disease prediction
  • Machine learning in medicine

Background:

  • External ventricular drain (EVD)-associated infections occur in 1-40% of patients.
  • Assessing cerebrospinal fluid (CSF) parameters is challenging, particularly in hemorrhagic neurological disease.
  • This study addresses the need for real-time EVD-associated infection prediction.

Purpose of the Study:

  • To develop and validate a machine learning framework for real-time prediction of EVD-associated infection.
  • To identify key biomarkers and their temporal dynamics predictive of infection.
  • To determine the lead time between biomarker deterioration and clinical diagnosis.

Main Methods:

  • Retrospective analysis of 367 neurocritical patients with EVDs (8,419 patient-days).
  • Utilized seven serially monitored biomarkers: WBC, CRP, procalcitonin, CSF cell count, lactate, glucose, and protein.
  • Developed a machine learning ensemble and a composite scoring algorithm for biological onset analysis.

Main Results:

  • 88 out of 367 patients (24%) developed EVD-associated infection.
  • The machine learning ensemble achieved an AUC-ROC of 0.833 at 24 hours and 0.822 at 48 hours.
  • Biomarker deterioration preceded clinical diagnosis by a median of 2 days, with dynamic WBC and CSF lactate being key predictors.

Conclusions:

  • Longitudinal biomarker monitoring combined with machine learning enables timely prediction of EVD-associated infection.
  • Biomarker changes offer a lead time of approximately two days over clinical recognition.
  • Supports prospective evaluation of daily risk monitoring for EVD-associated infections in neurocritical care.