Establishment and Validation of a Machine-Learning Prediction Nomogram Based on Lymphocyte Subtyping for Intra-Abdominal Candidiasis in Septic Patients.
Summary
In 633 septic patients with intra-abdominal infection, the authors built and validated a prediction nomogram for intra-abdominal candidiasis using lymphocyte subtyping plus clinical variables. Machine-learning (random forest) guided variable selection; multivariable logistic regression underpinned the nomogram. High-dose corticosteroid exposure and CD4+ T-cell parameters emerged as important predictors; the model demonstrated good discrimination, calibration, and clinical utility.
Key Findings
- Prospective cohort of 633 septic patients with intra-abdominal infection enabled model development and validation.
- Random forest identified key immune and clinical predictors; multivariable logistic regression constructed the nomogram.
- High-dose corticosteroid exposure and CD4+ T-cell metrics were important predictors; the model showed good discrimination, calibration, and clinical usefulness.
Clinical Implications
Integration of lymphocyte subtyping into bedside risk models may refine antifungal stewardship, reduce delays in therapy, and prioritize diagnostics (cultures, imaging) for suspected IAC.
Why It Matters
Provides a pragmatic, immune-informed tool to identify high-risk IAC early in sepsis, potentially enabling timely antifungal therapy and source control.
Limitations
- Abstract does not report external validation or specific performance metrics (e.g., AUC), limiting assessment of generalizability.
- Single-region cohort; performance in other settings and pathogen spectra remains to be tested.
Future Directions
External, multicenter validation; incorporation into EHR for real-time decision support; impact studies on antifungal timing, diagnostic yield, and outcomes.
Study Information
- Study Type
- Cohort
- Research Domain
- Diagnosis
- Evidence Level
- II - Prospective cohort study with model development and internal validation
- Study Design
- OTHER