Authors
Arthur James, David Hajage, Noémie Simon-Tillaux, Sophie Tezenas du Montcel, Pierre Rufat, Bruno Riou, Mathieu Raux
Published in
PloS one. Volume 21. Issue 8. Pages e0354700. Epub Aug 17, 2026.
Abstract
Reliable mortality prediction is central to trauma research, quality assessment, and resource allocation. While the French national hospital discharge database (PMSI) provides comprehensive nationwide data, it does not capture clinical parameters required for established severity scores such as TRISS, which is used for predicting in-hospital survival after trauma and necessary for implementing national-level evaluations of health system performance. This study tested whether TRISS could nonetheless be accurately derived from PMSI data.
We conducted a retrospective study of adult patients admitted for severe trauma to an academic trauma center between 2012 and 2023. Clinical data from medical records were linked with corresponding PMSI records. Surrogate predictors of TRISS were derived from PMSI codes. An extreme gradient boosting (XGBoost) model was used, model performance was assessed using bootstrap validation and interpretability was explored through SHapley Additive exPlanations analyses.
A total of 2,523 trauma patients were successfully matched between PMSI and medical records. Median age was 35 years, 79% were male, and in-hospital mortality was 15%. Correlation between Simplified Acute Physiology Score II (SAPS II) in PMSI and medical records was strong (ρ = 0.88), while concordance for shock and coma was weak (κ ≈ 0.25). The XGBoost model using individual PMSI codes achieved the best performance (optimism-adjusted R2 = 0.72). SAPS II was the main contributor, with additional contributions from shock, coma, and anatomical injury codes.
TRISS can be reliably approximated from PMSI data using an XGBoost model. This approach enables patient-specific assessment of trauma severity and mortality risk from PMSI, opening perspectives for nationwide surveillance and quality evaluation of trauma care in France.
PMID:
42607050
Bibliographic data and abstract were imported from PubMed on 18 Aug 2026.
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