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Peer-reviewedCC BY 4.0PLOS One

Classification of recurrence status after surgical treatment of chronic subdural hemorrhage – A machine learning approach

  1. 1Department of Neurosurgery, RWTH Aachen University Hospital, Aachen, Germany
  2. 2Department of Neuroradiology, University Hospital Heidelberg, Heidelberg, Germany
  3. 3Department of Diagnostic and Interventional Neuroradiology, RWTH Aachen University, Aachen, Germany

Abstract

Background: Chronic subdural hematoma (cSDH) recurrence requiring reoperation occurs in 5–33% of cases. Predicting recurrence could enable risk-stratified surveillance, reducing imaging in low-risk patients while maintaining monitoring for high-risk individuals. We evaluated whether machine learning could achieve clinically actionable recurrence prediction using routinely available variables. Methods: This retrospective single-center study included 564 consecutive patients undergoing surgical cSDH evacuation (2015–2023), randomly divided into training (75%, n = 422) and test (25%, n = 142) sets. We developed and compared three models, regularized logistic regression, Random Forest, and XGBoost, using 31 predictor variables. Model development and tuning used 10-fold cross-validation on the training set; the best model was evaluated on the held-out test set. The primary outcome was postoperative recurrence requiring reoperation. Results: Postoperative recurrence occurred in 170 patients (30.1%). In the training set, XGBoost achieved the highest cross-validated ROC AUC (0.713, SE = 0.024), matching Random Forest and outperforming logistic regression (0.686). Hematoma volume, coagulation parameters, and disease severity markers (ICU admission, GCS) were the most influential predictors, though effect sizes remained modest. On the test set, the final XGBoost model achieved ROC AUC 0.688 (95% CI 0.590–0.772), with satisfactory average calibration but overconfident individual-level risk estimates (calibration slope 0.615). At the clinically relevant 90% sensitivity threshold, specificity was only 30.3%, allowing potential imaging reduction in roughly one-third of non-recurrence patients. Consistency between training and test performance indicated these limitations reflect predictor information content rather than overfitting. Conclusions: In this single-center cohort, machine learning models using routinely available clinical and radiographic variables did not achieve clinically actionable risk stratification for cSDH recurrence under internal validation, with discriminative capacity insufficient to identify a low-risk subgroup suitable for de-escalated surveillance. These findings suggest recurrence is driven by factors not captured in standard clinical assessment, supporting uniform or symptom-driven imaging strategies over risk-stratified approaches.

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BibTeX
@article{hamou2026classification,
  title = {{Classification of recurrence status after surgical treatment of chronic subdural hemorrhage – A machine learning approach}},
  author = {Hussam Hamou and Julius Kernbach and Hani Ridwan and Kimberley Fay-Rodrian and Hans Clusmann and Anke Hoellig and Michael Veldeman},
  journal = {PLOS One},
  year = {2026},
  month = sep,
  doi = {10.1371/journal.pone.0346756},
  url = {https://doi.org/10.1371/journal.pone.0346756},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Classification of recurrence status after surgical treatment of chronic subdural hemorrhage – A machine learning approach
AU  - Hussam Hamou
AU  - Julius Kernbach
AU  - Hani Ridwan
AU  - Kimberley Fay-Rodrian
AU  - Hans Clusmann
AU  - Anke Hoellig
AU  - Michael Veldeman
PY  - 2026
DA  - 2026/09/18
JO  - PLOS One
DO  - 10.1371/journal.pone.0346756
UR  - https://doi.org/10.1371/journal.pone.0346756
AB  - Background: Chronic subdural hematoma (cSDH) recurrence requiring reoperation occurs in 5–33% of cases. Predicting recurrence could enable risk-stratified surveillance, reducing imaging in low-risk patients while maintaining monitoring for high-risk individuals. We evaluated whether machine learning could achieve clinically actionable recurrence prediction using routinely available variables. Methods: This retrospective single-center study included 564 consecutive patients undergoing surgical cSDH evacuation (2015–2023), randomly divided into training (75%, n = 422) and test (25%, n = 142) sets. We developed and compared three models, regularized logistic regression, Random Forest, and XGBoost, using 31 predictor variables. Model development and tuning used 10-fold cross-validation on the training set; the best model was evaluated on the held-out test set. The primary outcome was postoperative recurrence requiring reoperation. Results: Postoperative recurrence occurred in 170 patients (30.1%). In the training set, XGBoost achieved the highest cross-validated ROC AUC (0.713, SE = 0.024), matching Random Forest and outperforming logistic regression (0.686). Hematoma volume, coagulation parameters, and disease severity markers (ICU admission, GCS) were the most influential predictors, though effect sizes remained modest. On the test set, the final XGBoost model achieved ROC AUC 0.688 (95% CI 0.590–0.772), with satisfactory average calibration but overconfident individual-level risk estimates (calibration slope 0.615). At the clinically relevant 90% sensitivity threshold, specificity was only 30.3%, allowing potential imaging reduction in roughly one-third of non-recurrence patients. Consistency between training and test performance indicated these limitations reflect predictor information content rather than overfitting. Conclusions: In this single-center cohort, machine learning models using routinely available clinical and radiographic variables did not achieve clinically actionable risk stratification for cSDH recurrence under internal validation, with discriminative capacity insufficient to identify a low-risk subgroup suitable for de-escalated surveillance. These findings suggest recurrence is driven by factors not captured in standard clinical assessment, supporting uniform or symptom-driven imaging strategies over risk-stratified approaches.
SN  - 1932-6203
ER  -