AC-Faster R-CNN: an improved detection architecture with high precision and sensitivity for abnormality in spine x-ray images.

In clinical medicine, localization and identification of disease on spinal radiographs are difficult and require a high level of expertise in the radiological discipline and extensive clinical experience. The model based on deep learning acquires certain disease recognition abilities through continuous training, thereby assisting clinical physicians in disease diagnosis. This study aims to develop an object detection network that accurately locates and classifies the abnormal parts in spinal x-ray photographs.This study proposes a deep learning-based automated multi-disease detection architecture called Abnormality Capture-Faster Region-based Convolutional Neural Network (AC-Faster R-CNN), which develops the feature fusion structure Deformable Convolution Feature Pyramid Network and the abnormality capture structure Abnormality Capture Head. Through the combination of dilated and deformable convolutions, the model better captures the multi-scale information of lesions. To further improve the detection performance, the contrast enhancement algorithm Contrast Limited Adaptive Histogram Equalization is used for image preprocessing.The proposed model is extensively evaluated on a testing set containing 1007 spine x-ray images and the experimental results show that the AC-Faster R-CNN architecture outperforms the baseline model and other advanced detection architectures. The mean Average Precision at Intersection over Union of 50% are 39.8%, the Precision and Sensitivity at the optimal cutoff point of Precision-Recall curve are 48.6% and 46.3%, respectively, reaching the current state-of-the-art detection level.AC-Faster R-CNN exhibits high precision and sensitivity in abnormality detection tasks of spinal x-ray images, and effectively locates and identifies abnormal areas. Additionally, this study would provide reference and comparison for the further development of medical automatic detection.