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Application and performance of deep learning models for the automated diagnosis of cervical central spinal stenosis
Vasileios Mougios1, Robin Peretzke2,3, Alexandra Ertl2,3
1Department of Neurosurgery, Heidelberg University Hospital, Heidelberg, Germany.
Introduction:
Cervical central spinal stenosis (CCSS) is a leading cause of adult spinal cord dysfunction. Magnetic resonance imaging (MRI) is the reference standard, but reporting is time-consuming and subject to inter-observer variability. Artificial intelligence (AI)-especially deep-learning-may enable automated, consistent assessment.
Research Question:
Evaluation of performance metrics of AI models for diagnosing CCSS.
Material And Methods:
Following PRISMA 2020, we searched PubMed, Cochrane, Embase, IEEE Xplore, and Web of Science (2015-July 2025) for studies training and evaluating AI models using MRI to diagnose or grade CCSS. We excluded studies limited to foraminal stenosis, non-MRI modalities, thoracic/lumbar levels, segmentation-only or image-enhancement tools without diagnostic output, and studies focused solely on non-stenotic cervical pathologies. Data were extracted on MRI protocol, model type, data splits and external validation, stenosis classification, and diagnostic performance.
Results:
Ten studies (2019-2025) met inclusion criteria, predominantly single-centre and retrospective. Most models used T2-weighted axial and/or sagittal MRI; CNNs (e.g., ResNet-50, EfficientNet) and Transformer-based architectures were common. Sensitivities ranged roughly 0.67-1.00 and specificities 0.42-0.97 across models, with many reporting AUCs ≥0.90 and accuracies ≥0.85. Only one study reported true external test performance. Reporting of confidence intervals, processing time, and explainability (e.g., Grad-CAM) was inconsistent.
Discussion And Conclusion:
Deep-learning shows promising diagnostic performance for automated CCSS assessment on MRI and could reduce variability and reporting time. However, generalisability remains uncertain due to small, retrospective, largely single-centre cohorts and scarce external validation. Standardized reporting (e.g., CLAIM) and prospective, multi-centre validation is needed before routine clinical deployment.
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