Evidence map›Paper›PMID 42656360›Full record

ArticleFrontiers in neuroscience2026

An interpretable multimodal model for early prediction of delayed hematoma progression in frontal lobe contusion: a machine learning approach.

Guoqing Jiang, Xianglong Liu, Qinghua Zhang, Tao Wang, Chenglei Zhang, Zhanfeng Niu, Shengyu Sun, Hua Sun, Yu Zhao, Liang Wu

Abstract read
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Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Guoqing Jiang *Department of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Xianglong Liu *School of Public Health, Ningxia Key Laboratory of Environmental Factors and Chronic Disease Control, Ningxia Medical University, Yinchuan, China.
Qinghua ZhangDepartment of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Tao WangDepartment of Neurosurgery, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, China.
Chenglei ZhangDepartment of Laboratory Medicine, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
Zhanfeng NiuDepartment of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Shengyu SunDepartment of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Hua SunDepartment of Perioperative Surgery and Anesthesiology, General Hospital of Ningxia Medical University, Yinchuan, China.
Yu ZhaoSchool of Public Health, Ningxia Key Laboratory of Environmental Factors and Chronic Disease Control, Ningxia Medical University, Yinchuan, China.
Liang WuDepartment of Neurosurgery, General Hospital of Ningxia Medical University, Yinchuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Early identification of delayed hematoma progression (DHP) in patients with frontal lobe contusion remains challenging in emergency settings. This study aimed to develop and externally validate an interpretable multimodal machine-learning model integrating routinely available clinical, laboratory, and CT imaging features to predict DHP. Methods: This retrospective multicenter study included a development cohort of 799 patients and an external validation cohort of 443 patients. The development cohort was divided into a training set and an internal test set using stratified sampling. Feature selection was performed exclusively within the training set using seven complementary methods. Ten machine-learning algorithms were trained and compared using five-fold cross-validation. Model performance was assessed using AUROC, accuracy, sensitivity, specificity, precision, F1-score, calibration analysis, and decision-curve analysis. SHapley Additive exPlanations (SHAP) was used to interpret the final model. Results: Ten predictors were selected, including baseline contusion volume, hematoma density-related features, hematoma surface area-to-volume ratio, lymphocyte-to-monocyte ratio, admission Glasgow Coma Scale score, glucose-to-potassium ratio, time to baseline CT, and eosinophil count. The support vector machine (SVM) model showed the highest AUROC point estimate in the internal test set, with an AUROC of 0.801, and achieved an external validation AUROC of 0.724, indicating moderate external discrimination. Conclusion: We developed an interpretable multimodal model for early prediction of DHP in patients with frontal lobe contusion. The model may assist early risk stratification and clinical monitoring, but further prospective, multicenter, and geographically diverse validation is required before broad clinical implementation.

Indexed as

delayed hematoma progressionfrontal lobe contusionmachine learningmultimodal modelsSHAP

Identifiers

PMID42656360
PMCPMC13506746

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.