# A Novel Multi-branch ConvNeXt Architecture for Identifying Subtle Pathological Features in CT Scans

arXiv: https://arxiv.org/abs/2510.09107 · HTML: https://mlsanity.com/paper/2510.09107/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 6 of its 23 references that are in the map.
- First posted on arXiv 10 Oct 2025.

## Builds on (most cited first, 6 of 6)

- [Deep Residual Learning for Image Recognition](https://mlsanity.com/paper/1512.03385/) (2015)
- [Squeeze-and-Excitation Networks](https://mlsanity.com/paper/1709.01507/) (2017)
- [CBAM: Convolutional Block Attention Module](https://mlsanity.com/paper/1807.06521/) (2018)
- [COVID-CT-Dataset: A CT Scan Dataset about COVID-19](https://mlsanity.com/paper/2003.13865/) (2020)
- [RADNET: Radiologist Level Accuracy using Deep Learning for HEMORRHAGE detection in CT Scans](https://mlsanity.com/paper/1710.04934/) (2017)
- [Automatic Diagnosis of COVID-19 from CT Images using CycleGAN and Transfer Learning](https://mlsanity.com/paper/2104.11949/) (2021)

## Abstract (arXiv)

Intelligent analysis of medical imaging plays a crucial role in assisting clinical diagnosis, especially for identifying subtle pathological features. This paper introduces a novel multi-branch ConvNeXt architecture designed specifically for the nuanced challenges of medical image analysis. While applied here to the specific problem of COVID-19 diagnosis, the methodology offers a generalizable framework for classifying a wide range of pathologies from CT scans. The proposed model incorporates a rigorous end-to-end pipeline, from meticulous data preprocessing and augmentation to a disciplined two-phase training strategy that leverages transfer learning effectively. The architecture uniquely integrates features extracted from three parallel branches: Global Average Pooling, Global Max Pooling, and a new Attention-weighted Pooling mechanism. The model was trained and validated on a combined dataset of 2,609 CT slices derived from two distinct datasets. Experimental results demonstrate a superior performance on the validation set, achieving a final ROC-AUC of 0.9937, a validation accuracy of 0.9757, and an F1-score of 0.9825 for COVID-19 cases, outperforming all previously reported models on this dataset. These findings indicate that a modern, multi-branch architecture, coupled with careful data handling, can achieve performance comparable to or exceeding contemporary state-of-the-art models, thereby proving the efficacy of advanced deep learning techniques for robust medical diagnostics.
