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Related Experiment Video

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Development and Validation of an Interpretable Machine Learning Model for Predicting Thrombocythemia Risk During

Kailei Du1, Maofeng Wang2, Ping Yu3

  • 1Intensive Care Medicine, Affiliated Dongyang Hospital, Wenzhou Medical University, Dongyang, Zhejiang, 322100, People's Republic of China.

Journal of Blood Medicine
|February 19, 2026
PubMed
Summary

This study developed an interpretable machine learning model to predict thrombocythemia risk during third-generation cephalosporin therapy. The model accurately identifies patients at risk, improving treatment decisions for severe infections.

Keywords:
XGBoostmachine learningrisk predictionthird-generation cephalosporinthrombocythemia

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Area of Science:

  • Pharmacology
  • Medical Informatics
  • Machine Learning

Background:

  • Third-generation cephalosporins are crucial for severe infections but can cause thrombocythemia, complicating treatment.
  • Existing tools for predicting this risk lack accuracy and clinical interpretability.
  • There is a need for reliable methods to stratify thrombocythemia risk in patients receiving cephalosporins.

Purpose of the Study:

  • To develop and validate an interpretable machine learning (ML) model for predicting thrombocythemia risk in patients treated with third-generation cephalosporins.
  • To enhance clinical decision-making by providing accurate and understandable risk stratification.
  • To identify key predictors of thrombocythemia in this patient population.

Main Methods:

  • A retrospective cohort of 25,707 adult patients receiving third-generation cephalosporins was analyzed.
  • Machine learning algorithms (XGBoost, Random Forest, LightGBM) were trained and tested, with performance evaluated using ROC-AUC and Brier score.
  • SHAP analysis was employed for model interpretability, identifying key predictive factors.

Main Results:

  • The XGBoost model achieved superior performance with an AUC of 0.858 and a Brier score of 0.0088.
  • Key predictors included baseline platelet count, red blood cell count, creatinine, daily usage frequency, and sex.
  • Malignancies increased risk, while female sex showed a protective effect.

Conclusions:

  • An interpretable ML framework was successfully developed for precise thrombocythemia risk prediction during cephalosporin therapy.
  • This model balances high algorithmic performance with clinical actionability, aiding therapeutic decisions.
  • The findings offer a valuable tool for managing potential adverse events associated with cephalosporin treatment.