# Interpretable machine learning for predicting 30-day mortality following intracranial hemorrhage surgery

**Authors:** Ziyang Wang, Wenbin Chen, Yan Shi

PMC · DOI: 10.3389/fneur.2026.1716346 · Frontiers in Neurology · 2026-02-13

## TL;DR

This study uses interpretable machine learning to predict 30-day mortality after brain hemorrhage surgery, identifying key factors that could help improve patient care.

## Contribution

The novel contribution is an interpretable XGBoost model with SHAP analysis to identify modifiable biomarkers for ICH mortality prediction.

## Key findings

- The XGBoost model achieved high accuracy (AUC 0.931-0.937) in predicting 30-day mortality after ICH surgery.
- SHAP analysis revealed postoperative pH, lactate, APTT, and CRP as key predictive factors.
- The model outperformed logistic regression and provided the greatest net benefit in decision curve analysis.

## Abstract

This study aims to utilize interpretable machine learning models based on perioperative data to forecast the 30-day mortality risk following intracranial hemorrhage (ICH) surgery. By employing SHapley Additive exPlanations (SHAP) to interpret the Extreme Gradient Boosting (XGBoost) model, we sought to identify modifiable prognostic factors to improve clinical decision-making.

A retrospective analysis was conducted on perioperative data from 1,271 ICH patients. After applying exclusion criteria, 992 patients were included. The dataset was randomly partitioned into training and validation cohorts (7:3 ratio). Multiple machine learning algorithms, including logistic regression, SVM, Random Forest, and XGBoost were developed. Model performance was rigorously assessed via ROC curves, calibration curves, and decision curve analysis (DCA), with hyperparameters optimized using 5-fold cross-validation.

The observed 30-day postoperative mortality rate was 13%. The XGBoost model achieved an AUC of 0.931 (95% CI 0.91–0.96) in the training cohort and 0.937 (95% CI 0.90–0.97) in the validation cohort, outperforming the logistic regression model (AUC 0.669). Decision curve analysis indicated that the XGBoost model provided the greatest net benefit within a threshold probability range of 5.79 to 33.52%. SHAP analysis identified postoperative pH, lactate, APTT, and CRP as the primary predictive factors.

This study establishes an interpretable XGBoost model that leverages perioperative data to accurately predict short-term mortality after ICH surgery. By highlighting the prognostic value of these modifiable biomarkers, the model serves as a practical tool for early risk stratification, assisting in the optimization of perioperative management in critical care settings.

## Linked entities

- **Diseases:** ICH (MONDO:0100533)

## Full-text entities

- **Genes:** SLC16A1 (solute carrier family 16 member 1) [NCBI Gene 6566] {aka HHF7, MCT, MCT1, MCT1D}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC16A3 (solute carrier family 16 member 3) [NCBI Gene 9123] {aka MCT 3, MCT 4, MCT-3, MCT-4, MCT3, MCT4}, PLA2G1B (phospholipase A2 group IB) [NCBI Gene 5319] {aka PLA2, PLA2A, PPLA2}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ITIH2 (inter-alpha-trypsin inhibitor heavy chain 2) [NCBI Gene 3698] {aka H2P, ITI-HC2, SHAP}
- **Diseases:** coronary artery disease (MESH:D003324), neuronal damage (MESH:D009410), sepsis (MESH:D018805), neurological deterioration (MESH:D009422), cognitive impairments (MESH:D003072), brain tissue damage (MESH:D017695), necrosis (MESH:D009336), Intracerebral hemorrhage (MESH:D002543), low cardiac output (MESH:D002303), CKD (MESH:D012080), coagulation disturbances (MESH:D001778), COPD (MESH:D029424), hypoxic (MESH:D002534), hemorrhage (MESH:D006470), ICH (MESH:D020300), cerebral edema (MESH:D001929), bradycardia (MESH:D001919), hypoxia (MESH:D000860), IOH (MESH:D007022), neurological dysfunctions (MESH:D009461), hematoma (MESH:D006406), critically ill (MESH:D016638), shock (MESH:D012769), lactate (MESH:D007775), inflammation (MESH:D007249), chronic kidney disease (MESH:D051436)
- **Chemicals:** calcium (MESH:D002118), hydrogen (MESH:D006859), diacetyl resveratrol (-), metformin (MESH:D008687), oxygen (MESH:D010100), Lactate (MESH:D019344)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945796/full.md

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Source: https://tomesphere.com/paper/PMC12945796