Evidence map›Paper›PMID 40594126›Full record

ArticleScientific reports2025

A ubiquitous and interoperable deep learning model for automatic detection of pleomorphic gastroesophageal lesions.

Miguel Martins, Miguel José Mascarenhas, Maria João Almeida, João Afonso, Tiago Ribeiro, Pedro Cardoso, Francisco Mendes, Joana Mota, Patrícia Andrade, Hélder Cardoso and 3 more

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Miguel Martins *Department of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Miguel José Mascarenhas *Department of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal. miguelmascarenhassaraiva@gmail.com.
Maria João AlmeidaDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
João AfonsoDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Tiago RibeiroDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Pedro CardosoDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Francisco MendesDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Joana MotaDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Patrícia AndradeDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Hélder CardosoDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.
Miguel Mascarenhas-SaraivaGastroenterology Department, ManopH, Instituto CUF, Porto, Portugal.
João FerreiraDepartment of Mechanical Engineering, Faculty of Engineering of the University of Porto, Rua Dr. Roberto Frias, 4200-465, Porto, Portugal.
Guilherme MacedoDepartment of Gastroenterology, São João University Hospital, Alameda Professor Hernâni Monteiro, 4200-427, Porto, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, artificial intelligence (AI) has been widely explored to enhance capsule endoscopy (CE), with the goal of improving the efficiency of the reading process. While most AI models have been developed for small bowel and colon analysis, the development of esophagogastric (E-G) models has been limited due to the scarcity of frames captured during the procedure, making it challenging to develop a robust model. This study aims to develop an interoperable ubiquitous model capable detecting pleomorphic lesions in the E-G tract. We included 59,482 E-G frames, from 774 CE procedures of 5 centers, to develop a Convolutional Neural Network (CNN). The dataset was divided following an exam-based split, with 90% allocated for training - including a 5-fold cross validation - while the remaining was used for testing. The primary outcomes were: sensitivity, specificity, accuracy and area under the curve (AUC). During training, the CNN achieved mean sensitivity of 85.0% (IC95% 76.5-93.5), specificity of 96.3% (IC95% 93.9-98.7), accuracy of 93.6% (IC95% 91.7-95.4), and AUC-ROC of 0.98 (IC95% 0.97-0.98). During testing, the sensitivity, specificity and accuracy of CNN were 92.2%, 95.1% and 94.6%, respectively. CE-AI models capable of assessing E-G are crucial step toward developing a truly robust panendoscopic model. This ubiquitous and interoperable model capable of lesion detection in both esophagus and stomach, achieved good overall accuracy. However, prospective real-world studies comparing its performance with standard upper endoscopy are still needed to validate its clinical applicability.

Indexed as

Capsule EndoscopyDeep LearningEsophageal NeoplasmsAgedFemaleHumansMaleMiddle AgedNeural Networks, ComputerSensitivity and SpecificityArtificial intelligenceCapsule endoscopyEsophageal lesionsGastric lesionsPanendoscopy

Identifiers

PMID40594126
PMCPMC12218920

What Socratic holds

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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 Socratic graph.