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Concurrent external validation of bloodstream infection probability models.

Stefan Rodic1, Brett N Hryciw1, Shehab Selim1

  • 1Department of Medicine, University of Ottawa, Canada.

Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
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Summary

Many models predicting bloodstream infection (BSI) probability show limited real-world performance. This study found restricted applicability, poor discrimination, and calibration issues, hindering clinical decision-making.

Keywords:
BactaeremiaBloodstream infectionExternal validationPredictive modelsSystematic review

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Area of Science:

  • Clinical Medicine
  • Infectious Diseases
  • Biostatistics

Background:

  • Accurate prediction of bloodstream infection (BSI) is crucial for timely clinical decisions.
  • Numerous multivariate models exist to estimate BSI probability.
  • External validation is essential to assess model generalizability.

Purpose of the Study:

  • To evaluate the real-world performance of existing BSI probability models.
  • To compare the applicability, discrimination, and accuracy of these models in a single patient cohort.
  • To identify common limitations affecting model utility.

Main Methods:

  • Retrieved validated BSI probability models from a systematic review.
  • Assessed model performance in a random sample of 4485 adult patients requiring blood cultures.
  • Measured model applicability, discrimination (c-statistic), and calibration (integrated calibration index).

Main Results:

  • Ten models (1991-2015) were evaluated; common issues included overfitting and variable categorization.
  • Seven models had restricted applicability (<15% of patients).
  • Observed discrimination was lower than reported (median c-statistic 60%), and calibration was frequently poor (median ICI 4.0%), with significant inter-model disagreement.

Conclusions:

  • Published BSI probability models often exhibit limited applicability, discrimination, and calibration in external validation.
  • Significant disagreement exists between models, complicating direct performance comparisons.
  • Model-specific validation group dissimilarities hinder robust external validation assessments.