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Introduction of an Integrated Pathology Image Management, Artificial Intelligence, and Reporting System
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Supervised learning for infection risk inference using pathology data.

Bernard Hernandez1, Pau Herrero2, Timothy Miles Rawson3

  • 1Centre for Bio-Inspired Technology, Department of Electrical and Electronic Engineering, Imperial College London, B422 Bessemer Building, South Kensington Campus, London, SW7 2AZ, UK. b.hernandez-perez@imperial.ac.uk.

BMC Medical Informatics and Decision Making
|December 9, 2017
PubMed
Summary
This summary is machine-generated.

Biochemical markers can accurately predict infection risk, aiding clinical decisions on antimicrobial use. This helps combat antimicrobial resistance by preventing unnecessary prescriptions in hospitals.

Keywords:
Antimicrobial resistanceBehaviour changeBiochemical markersDecision supportInfectionMachine learningPredictive modellingSupervised learning

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Area of Science:

  • Biomedical Informatics
  • Clinical Pathology
  • Infectious Disease Epidemiology

Background:

  • Antimicrobial resistance (AMR) is a growing threat to public health, exacerbated by the overuse of antimicrobials in hospitals.
  • Clinical Decision Support Systems (CDSSs) can improve antimicrobial prescribing but may lead to unnecessary prescriptions without proper disease assessment.

Purpose of the Study:

  • To develop a reliable method for infection risk inference using routinely available laboratory data.
  • To support clinicians in making informed decisions regarding antimicrobial therapy initiation.

Main Methods:

  • Combined six biochemical markers with microbiology susceptibility test outcomes from over 1.5 million daily patient profiles.
  • Employed outlier detection, sampling techniques (SMOTE), and ten-fold cross-validation for robust model training and evaluation.
  • Assessed model performance under conditions of missing data and class imbalance.

Main Results:

  • Achieved high accuracy in infection risk inference with an area under the ROC curve of 0.80-0.83, sensitivity of 0.64-0.75, and specificity of 0.92-0.97.
  • Standardization proved more effective than normalization, and SMOTE improved sensitivity.
  • Models maintained performance with as few as four available biomarkers.

Conclusions:

  • Selected biochemical markers provide sufficient information for confident infection risk inference, even with incomplete or imbalanced data.
  • These findings can enhance CDSSs, enabling better antimicrobial stewardship and reducing unnecessary prescriptions.