Evidence map›Paper›PMID 39075249›Full record

ArticleJournal of imaging informatics in medicine2025

3D Features Fusion for Automated Segmentation of Fluid Regions in CSCR Patients: An OCT-based Photodynamic Therapy Response Analysis.

Elena Goyanes, Joaquim de Moura, José I Fernández-Vigo, Julián García-Feijóo, Jorge Novo, Marcos Ortega

Abstract read
In one paragraph

Article in Journal of imaging informatics in medicine, 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. Article
  2. Review
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

6 authors.

Elena GoyanesVARPA Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Universidade da Coruña, A Coruña, Spain.ORCID http://orcid.org/0009-0001-5328-2262
Joaquim de MouraVARPA Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Universidade da Coruña, A Coruña, Spain. joaquim.demoura@udc.es.ORCID http://orcid.org/0000-0002-2050-3786
José I Fernández-VigoRetina Unit, Ophthalmology Department, Hospital Clínico San Carlos, IdISSC, Madrid, Spain.ORCID http://orcid.org/0000-0001-8745-3464
Julián García-FeijóoRetina Unit, Ophthalmology Department, Hospital Clínico San Carlos, IdISSC, Madrid, Spain.ORCID http://orcid.org/0000-0002-7772-5718
Jorge NovoVARPA Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Universidade da Coruña, A Coruña, Spain.ORCID http://orcid.org/0000-0002-0125-3064
Marcos OrtegaVARPA Research Group, Instituto de Investigación Biomédica de A Coruña (INIBIC), Universidade da Coruña, A Coruña, Spain.ORCID http://orcid.org/0000-0002-2798-0788

Funding

Ministerio de Ciencia e Innovación FORT23/00010Ministerio de Ciencia e Innovación PDC2022-133132-I00Ministerio de Ciencia e Innovación PID2019-108435RB-I00Ministerio de Ciencia e Innovación TED2021-131201B-I00Xunta de Galicia ED431C 2020/24Xunta de Galicia ED481A-2023-152
6 · The paper itself

Abstract

Central Serous Chorioretinopathy (CSCR) is a significant cause of vision impairment worldwide, with Photodynamic Therapy (PDT) emerging as a promising treatment strategy. The capability to precisely segment fluid regions in Optical Coherence Tomography (OCT) scans and predict the response to PDT treatment can substantially augment patient outcomes. This paper introduces a novel deep learning (DL) methodology for automated 3D segmentation of fluid regions in OCT scans, followed by a subsequent PDT response analysis for CSCR patients. Our approach utilizes the rich 3D contextual information from OCT scans to train a model that accurately delineates fluid regions. This model not only substantially reduces the time and effort required for segmentation but also offers a standardized technique, fostering further large-scale research studies. Additionally, by incorporating pre- and post-treatment OCT scans, our model is capable of predicting PDT response, hence enabling the formulation of personalized treatment strategies and optimized patient management. To validate our approach, we employed a robust dataset comprising 2,769 OCT scans (124 3D volumes), and the results obtained were significantly satisfactory, outperforming the current state-of-the-art methods. This research signifies an important milestone in the integration of DL advancements with practical clinical applications, propelling us a step closer towards improved management of CSCR. Furthermore, the methodologies and systems developed can be adapted and extrapolated to tackle similar challenges in the diagnosis and treatment of other retinal pathologies, favoring more comprehensive and personalized patient care.

Indexed as

Central Serous ChorioretinopathyImaging, Three-DimensionalPhotochemotherapyTomography, Optical CoherenceDeep LearningHumansTreatment Outcome3D SegmentationCAD systemCentral serous chorioretinopathyDeep LearningOCTPhotodynamic Therapy

Identifiers

PMID39075249
PMCPMC11811378

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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.