Evidence map›Paper›PMID 40594951›Full record

ArticleScientific reports2025

Enhancing chronic wound assessment through agreement analysis and tissue segmentation.

Ana C Morgado, Rafaela Carvalho, Ana Filipa Sampaio, Maria J M Vasconcelos

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Research Progress on Artificial Intelligence in the Management of Diabetic Foot Ulcers.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ana C Morgado *Fraunhofer Portugal AICOS, Porto, Portugal.
Rafaela Carvalho *Fraunhofer Portugal AICOS, Porto, Portugal.
Ana Filipa Sampaio *Fraunhofer Portugal AICOS, Porto, Portugal.
Maria J M Vasconcelos *Fraunhofer Portugal AICOS, Porto, Portugal. maria.vasconcelos@fraunhofer.pt.

Funding

Agencia para a Competividade e Inovação, I.P. Aviso N.º 01/C05-i01/2021 ref 41
6 · The paper itself

Abstract

Accurate monitoring of chronic wound progression is crucial for assessing healing dynamics. However, the current manual process of tissue segmentation and quantification, which is an indicator of the healing progress, is time-consuming and subject to variability, so automated methods that can effectively monitor wound healing are required. In this work, inter-rater agreement analyses were conducted to evaluate the consistency of manual annotations performed by multiple experts and an automated methodology for tissue segmentation leveraging advanced deep learning techniques is proposed. For this, the convolutional neural network DeepLabV3-R50 and a transformer-based approach (SegFormer-B0) were explored. Furthermore, the potential of transferring knowledge from open wound segmentation models trained on different available datasets and fine-tuning them for this specific task was investigated. The tissue segmentation model is integrated into a framework that combines a wound and reference marker detection model with a wound segmentation model to refine the predicted tissue masks. The results show the benefits of employing previous knowledge gained from simpler tasks within the same domain, as well as the efficacy of post-processing operations. The top-performing tissue segmentation model, DeepLabV3-R50, achieved an overall mean Intersection over Union of 62.95% and a mean Dice score of 76.82% for the three analysed tissues on the Wounds dataset, when assessed independently. Considering the complete framework, the same model returns a mean Intersection over Union of 59.67% and a mean Dice of 74.38%, resulting in mean absolute errors of 14.33%, 14.31% and 8.84% for granulation, slough and eschar proportion estimation, respectively. Moreover, the obtained inter-rater agreement scores still emphasize the inherent complexity of the task, as even experienced healthcare professionals may differ in delineating tissue boundaries. Given the proven intricacy of tissue characterisation and the promising results that were achieved, the proposed pipeline contributes to streamline the tissue segmentation and quantification task, leading to the automation of the wound bed characterisation process and enhancing consistency and efficiency in wound healing.

Indexed as

Image Processing, Computer-AssistedWound HealingWounds and InjuriesAlgorithmsChronic DiseaseDeep LearningHumansNeural Networks, ComputerChronic woundsComputer visionImage segmentationInter-rater agreementTelemedicine

Identifiers

PMID40594951
PMCPMC12217643

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LicenceCC BY-NC-ND
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Registered trials

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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.