# Preoperative deep vein thrombosis in tibial plateau fractures: development and internal validation of an interpretable multivariable machine-learning diagnostic model

**Authors:** Dejun Cun, Junru Li, Paian He, Lin Zhou, Hang Dong, Feng Huang, Ziwei Jiang

PMC · DOI: 10.3389/fmed.2026.1730477 · Frontiers in Medicine · 2026-02-13

## TL;DR

A machine learning model was developed to predict preoperative deep vein thrombosis in tibial plateau fracture patients using routine clinical data.

## Contribution

An interpretable XGBoost model was developed and validated for preoperative DVT risk prediction in TPF patients.

## Key findings

- The model achieved an AUROC of 0.840 with good calibration and clinical utility.
- D-dimer and age were identified as the most influential predictors of preoperative DVT.
- The model showed net clinical benefit but requires external validation for broader use.

## Abstract

Preoperative deep vein thrombosis (DVT) is common in tibial plateau fractures (TPF), yet few tools target this window with calibration and clinical utility reporting.

Single-center retrospective cohort (2019–2024) of adults undergoing surgery for isolated TPF. Outcome: duplex ultrasonography–confirmed DVT before initiation of therapeutic anticoagulation. Candidate predictors included demographics; injury features (Schatzker type/side, injury-to-surgery interval); and coagulation, inflammatory, and nutritional–immune indices. Features were selected by the intersection of LASSO and Boruta. Data were split 7:3 into training/validation; seven algorithms were tuned with 5-fold cross-validation. Validation assessed AUROC (95% confidence interval), Brier score, calibration, and decision-curve analysis (DCA). Model interpretability was assessed using SHAP (Shapley Additive Explanations).

Among 894 patients, 299 (33.4%) had preoperative DVT. Nine predictors were retained: D-dimer, age, erythrocyte sedimentation rate, prognostic nutritional index, C-reactive protein, lymphocyte count, Schatzker type, neutrophil count, and smoking. XGBoost performed best (AUROC 0.840, 95% confidence interval 0.790–0.884; accuracy 0.787; sensitivity 0.640; specificity 0.860; F1 score 0.667; Brier 0.149) and provided net clinical benefit on DCA. Tree-ensemble models showed training–validation performance gaps, indicating overfitting. SHAP ranked D-dimer and age as dominant with non-linear effects; higher C-reactive protein and erythrocyte sedimentation rate, lower prognostic nutritional index, advanced Schatzker types, and smoking increased risk.

An interpretable XGBoost model based on routine preoperative variables identifies TPF patients at high risk of preoperative DVT and may guide ultrasound triage and perioperative management. External (multicenter and temporal) validation with recalibration and prospective impact assessment are required.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SHROOM4 (shroom family member 4) [NCBI Gene 57477] {aka MRXSSDS, SHAP, shrm4}, NEURL1 (neuralized E3 ubiquitin protein ligase 1) [NCBI Gene 9148] {aka NEUR1, NEURL, RNF67, bA416N2.1, neu, neu-1}, SERPINE2 (serpin family E member 2) [NCBI Gene 5270] {aka GDN, GDNPF, PI-7, PI7, PN-1, PN1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** bone injury (MESH:D001847), TPF (MESH:D000092463), DVT (MESH:D020246), intra-articular fracture (MESH:D057072), subchondral (MESH:D001845), coagulation (MESH:D001778), hypertension (MESH:D006973), malnutrition (MESH:D044342), venous thromboembolism (MESH:D054556), hip fractures (MESH:D006620), peri-knee avulsions (MESH:D007718), thrombosis (MESH:D013927), comminution (MESH:D018460), tissue injury (MESH:D017695), ankle-fracture (MESH:D064386), coronary artery disease (MESH:D003324), orthopedic trauma (MESH:D009140), articular depression (MESH:D003866), fibular head avulsion (MESH:D006258), distal femur fractures (MESH:D000092524), diabetes (MESH:D003920), HD (MESH:D006816), endothelial dysfunction (MESH:D014652), polytrauma (MESH:D009104), open injury (MESH:D006259), Fracture (MESH:D050723), post-injury pain (MESH:D010146), patellar fractures (MESH:D031222), Trauma (MESH:D014947), Inflammatory (MESH:D007249), venous stasis (MESH:D054070), or pelvic/acetabular fractures (OMIM:142700), pulmonary embolism (MESH:D011655), hypoalbuminemia (MESH:D034141), hypercoagulability (MESH:D019851), hereditary/acquired thrombophilia (MESH:C540694), venous thrombogenesis (MESH:D014647), obesity (MESH:D009765)
- **Chemicals:** alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Flavobacterium sp. H (species) [taxon 253821]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945751/full.md

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Source: https://tomesphere.com/paper/PMC12945751