ArticleBioengineering (Basel, Switzerland)2024
A Dual-Branch Residual Network with Attention Mechanisms for Enhanced Classification of Vaginal Lesions in Colposcopic Images.
Article in Bioengineering (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- A nomogram-based prediction model for assessing the risk of vain and stump cancer recurrence following radical surgery for cervical cancer.Discover oncology · 2026Article
- Semi-supervised learning for colposcopic image classification using generative adversarial networks.Frontiers in medicine · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
Vaginal intraepithelial neoplasia (VAIN), linked to HPV infection, is a condition that is often overlooked during colposcopy, especially in the vaginal vault area, as clinicians tend to focus more on cervical lesions. This oversight can lead to missed or delayed diagnosis and treatment for patients with VAIN. Timely and accurate classification of VAIN plays a crucial role in the evaluation of vaginal lesions and the formulation of effective diagnostic approaches. The challenge is the high similarity between different classes and the low variability in the same class in colposcopic images, which can affect the accuracy, precision, and recall rates, depending on the image quality and the clinician's experience. In this study, a dual-branch lesion-aware residual network (DLRNet), designed for small medical sample sizes, is introduced, which classifies vaginal lesions by examining the relationship between cervical and vaginal lesions. The DLRNet model includes four main components: a lesion localization module, a dual-branch classification module, an attention-guidance module, and a pretrained network module. The dual-branch classification module combines the original images with segmentation maps obtained from the lesion localization module using a pretrained ResNet network to fine-tune parameters at different levels, explore lesion-specific features from both global and local perspectives, and facilitate layered interactions. The feature guidance module focuses the local branch network on vaginal-specific features by using spatial and channel attention mechanisms. The final integration involves a shared feature extraction module and independent fully connected layers, which represent and merge the dual-branch inputs. The weighted fusion method effectively integrates multiple inputs, enhancing the discriminative and generalization capabilities of the model. Classification experiments on 1142 collected colposcopic images demonstrate that this method raises the existing classification levels, achieving the classification of VAIN into three lesion grades, thus providing a valuable tool for the early screening of vaginal diseases.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.