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Review Article

Artificial Intelligence for Predicting Secondary Complications and Clinical Outcomes in Traumatic Brain Injury: A Narrative Review

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DOI:

10.3791/70963

June 2nd, 2026

In This Article

Summary

Here, we present a narrative review evaluating artificial intelligence (AI)-based prediction tools for secondary complications and clinical outcomes in traumatic brain injury, appraising evidence maturity across five complication domains and identifying critical barriers to clinical implementation.

Abstract

Secondary complications following moderate-to-severe traumatic brain injury (TBI)—including elevated intracranial pressure (ICP), post-traumatic seizures, trauma-induced coagulopathy (TIC), and sepsis—substantially worsen patient prognosis. Current prognostic tools estimate overall mortality and disability at admission but do not predict specific, treatable complications during hospitalization. This narrative review evaluates whether AI-based prediction tools can address this unmet clinical need, appraises the maturity of evidence across five prediction domains, and identifies priorities for future research. A targeted literature search was conducted across PubMed, Embase, and Web of Science from January 2016–October 2025, supplemented by manual reference tracking. Studies were selected based on their relevance to AI or machine learning (ML) for predicting secondary complications or clinical outcomes in TBI patients. AI-based models achieve moderate predictive accuracy (area under the receiver operating characteristic curve [AUC] of 0.70–0.79) to good accuracy (AUC ≥ 0.80) for ICP crises, TIC, sepsis, and mortality. Seizure prediction has the least mature evidence, with no external validation studies. ICP prediction has the strongest evidence base, with external validation and independent replication. Mortality prediction has the largest evidence volume, with international multi-dataset validation. Critical methodological limitations persist: most models derive from retrospective, single-institution data; only approximately one-third have undergone external validation; and no randomized trials have demonstrated that AI-guided decisions improve patient outcomes. AI prediction tools show promise for forecasting secondary TBI complications, but current evidence does not support routine clinical implementation. Before adoption, these tools require rigorous external validation, prospective outcome trials, and systematic equity assessment across diverse populations.

Introduction

TBI constitutes a leading cause of death and long-term disability worldwide, with approximately 69 million incident cases occurring annually1,2. TBI is the principal cause of death and disability among individuals under 45 years of age, imposing profound healthcare, socioeconomic, and societal burdens1,2,3. A fundamental distinction in TBI pathophysiology separates primary injury—the immediate mechanical damage sustained at impact—from secondary injury, which evolves over subsequent hours to days through c....

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Review and Perspective

Search strategy and study selection

A targeted, non-systematic literature search was conducted across PubMed, Embase, and Web of Science from January 2016–October 2025. The 2016 start date was chosen to capture foundational ML publications predating the recent surge in deep learning research while maintaining a contemporary focus; its selection is specifically justified by the inclusion of Myers et al. (2016)10, a seminal study that established core methodological approaches for ML-based ICP prediction. The search was supplemented by manual screening of the reference lists of identified systemati....

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Conclusions

AI prediction tools demonstrate genuine potential for anticipating secondary TBI complications before their clinical emergence5,6,7. Representative studies across five complication domains report predictive accuracy ranging from moderate (AUC 0.70–0.79) to good (AUC ≥ 0.80), with the highest-performing models achieving AUC values up to 0.92 on internal validation (external validation AUC typically 0.76–0.80)5

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Disclosures

The authors declare no conflicts of interest. No commercial entity had any role in study design, interpretation, or the decision to submit for publication.

Acknowledgements

The authors received no specific funding for this work.

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Tags

Intracranial PressureSeizure PredictionTrauma Induced CoagulopathyMortality PredictionMachine Learning ModelsExternal Validation