Development and validation of data-driven, decision tree-based algorithms for identifying Behçet's disease in claims

Ken-Ei Sada1, Yoshia Miyawaki2, Ryo Yanai3

  • 1Department of Clinical Epidemiology, Kochi Medical School, Nankoku, Japan.

Insights

Developing data-driven algorithms for Behçet

Area of Science:

  • Rheumatology
  • Medical Informatics
  • Data Science

Background:

  • Behçet's disease diagnosis in Japan relies on clinical criteria.
  • Accurate identification of Behçet's disease patients using administrative data is challenging.
  • Existing diagnostic algorithms may lack precision and external validation.

Purpose of the Study:

  • To develop and externally validate novel, data-driven algorithms for identifying Behçet's disease patients in Japan.
  • To assess the utility of variable selection methods and decision tree models for this purpose.
  • To improve the accuracy of claims-based research for Behçet's disease.

Main Methods:

  • Retrospective cross-sectional study of 13,538 patients from six tertiary hospitals.
  • Claims data linked to chart-confirmed Behçet's disease diagnoses.
  • Utilized Least Absolute Shrinkage and Selection Operator, Boruta, and Recursive Feature Elimination for feature selection.
  • Developed rule-based algorithms from decision tree models and evaluated diagnostic performance.

Main Results:

  • Diagnosis codes alone showed high sensitivity (1.000) and specificity (0.992) but modest positive predictive value (PPV).
  • Incorporating prescriptions for sulphamethoxazole-trimethoprim and colchicine significantly improved PPV (0.793 in test set, 0.865 in external validation).
  • The developed algorithms maintained high sensitivity and specificity while enhancing PPV.

Conclusions:

  • Integrating prescription data with diagnosis codes enhances the accuracy of identifying Behçet's disease patients in claims data.
  • A data-driven framework combining variable selection and decision tree analysis offers a validated and scalable approach.
  • This methodology supports more reliable claims-based research for Behçet's disease.
Abstract

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