Naveen Kumarasami

Bargava Subramanian, Naveen Kumarasami, Praveen Shastry et al.

Study Design: This study presents the development of an autonomous AI system for MRI spine pathology detection, trained on a dataset of 2 million MRI spine scans sourced from diverse healthcare facilities across India. The AI system integrates advanced architectures, including Vision Transformers, U-Net with cross-attention, MedSAM, and Cascade R-CNN, enabling comprehensive classification, segmentation, and detection of 43 distinct spinal pathologies. The dataset is balanced across age groups, genders, and scanner manufacturers to ensure robustness and adaptability. Subgroup analyses were conducted to validate the model's performance across different patient demographics, imaging conditions, and equipment types. Performance: The AI system achieved up to 97.9 percent multi-pathology detection, demonstrating consistent performance across age, gender, and manufacturer subgroups. The normal vs. abnormal classification achieved 98.0 percent accuracy, and the system was deployed across 13 major healthcare enterprises in India, encompassing diagnostic centers, large hospitals, and government facilities. During deployment, it processed approximately 100,000 plus MRI spine scans, leading to reduced reporting times and increased diagnostic efficiency by automating the identification of common spinal conditions. Conclusion: The AI system's high precision and recall validate its capability as a reliable tool for autonomous normal/abnormal classification, pathology segmentation, and detection. Its scalability and adaptability address critical diagnostic gaps, optimize radiology workflows, and improve patient care across varied healthcare environments in India.

Praveen Shastry, Sowmya Chowdary Muthulur, Naveen Kumarasami et al.

Background: This study proposes a Vision-Language Model (VLM) leveraging the SIGLIP encoder and Gemma-3b transformer decoder to enhance automated chronic tuberculosis (TB) screening. By integrating chest X-ray images with clinical data, the model addresses the challenges of manual interpretation, improving diagnostic consistency and accessibility, particularly in resource-constrained settings. Methods: The VLM architecture combines a Vision Transformer (ViT) for visual encoding and a transformer-based text encoder to process clinical context, such as patient histories and treatment records. Cross-modal attention mechanisms align radiographic features with textual information, while the Gemma-3b decoder generates comprehensive diagnostic reports. The model was pre-trained on 5 million paired medical images and texts and fine-tuned using 100,000 chronic TB-specific chest X-rays. Results: The model demonstrated high precision (94 percent) and recall (94 percent) for detecting key chronic TB pathologies, including fibrosis, calcified granulomas, and bronchiectasis. Area Under the Curve (AUC) scores exceeded 0.93, and Intersection over Union (IoU) values were above 0.91, validating its effectiveness in detecting and localizing TB-related abnormalities. Conclusion: The VLM offers a robust and scalable solution for automated chronic TB diagnosis, integrating radiographic and clinical data to deliver actionable and context-aware insights. Future work will address subtle pathologies and dataset biases to enhance the model's generalizability, ensuring equitable performance across diverse populations and healthcare settings.