Background: Access to oral healthcare is not uniform globally, particularly in rural areas with limited resources, which limits the potential of automated diagnostics and advanced tele-dentistry applications. The use of digital caries detection and progression monitoring through photographic communication, is influenced by multiple variables that are difficult to standardize in such settings. The objective of this study was to develop a novel and cost-effective virtual computer vision AI system to predict dental cavitations from non-standardised photographs with reasonable clinical accuracy. Methods: A set of 1703 augmented images was obtained from 233 de-identified teeth specimens. Images were acquired using a consumer smartphone, without any standardised apparatus applied. The study utilised state-of-the-art ensemble modeling, test-time augmentation, and transfer learning processes. The “you only look once” algorithm (YOLO) derivatives, v5s, v5m, v5l, and v5x, were independently evaluated, and an ensemble of the best results was augmented, and transfer learned with ResNet50, ResNet101, VGG16, AlexNet, and DenseNet. The outcomes were evaluated using precision, recall, and mean average precision (mAP). Results: The YOLO model ensemble achieved a mean average precision (mAP) of 0.732, an accuracy of 0.789, and a recall of 0.701. When transferred to VGG16, the final model demonstrated a diagnostic accuracy of 86.96%, precision of 0.89, and recall of 0.88. This surpassed all other base methods of object detection from free-hand non-standardised smartphone photographs. Conclusion: A virtual computer vision AI system, blending a model ensemble, test-time augmentation, and transferred deep learning processes, was developed to predict dental cavitations from non-standardised photographs with reasonable clinical accuracy. This model can improve access to oral healthcare in rural areas with limited resources, and has the potential to aid in automated diagnostics and advanced tele-dentistry applications.

Post-surgical adverse outcomes, including mortality, intensive care readmission, and complications, remain major challenges for clinical decision-making. Existing machine learning approaches focus on outcome prediction while operating as opaque systems, limiting clinical trust and the translation of predictions into treatment decisions, and many clinical studies rely on synthetic data in which shared intermediate variables create circular dependencies between inputs and targets that compromise reported performance. We aimed to develop an explainable multimodal architecture and a rigorous evaluation methodology that address these gaps. We designed a two-stage architecture integrating supervised deep learning for risk prediction with conservative Q-learning for action recommendation. The first stage uses five modality-specific encoders for structured records, physiological time-series, chest radiographs, clinical notes, and surgical metadata, unified through cross-modal attention into a shared patient-state representation. The second stage applies offline reinforcement learning to recommend clinical actions while preventing value overestimation. We formally characterized a target-leakage flaw in synthetic pipelines and propose a real-data methodology using a verified clinical database, with event-censored temporal separation and uncertainty-weighted per-task training. Component-level behavior was validated on a controlled synthetic benchmark, demonstrating that the architecture functions as designed without claiming clinical validity. The cross-modal attention and risk-prediction components behaved as expected, whereas the offline reinforcement learning stage did not converge on the benchmark, indicating that value estimation requires further investigation on real clinical data. The architecture provides dual-level explainability through attention visualization and value decomposition, contributing a deployable design, a formal methodological critique of synthetic-data practices, and a complete framework for clinically valid evaluation.