Evidence map›Paper›PMID 39768004›Full record

ArticleBioengineering (Basel, Switzerland)2024

Detection of Disease Features on Retinal OCT Scans Using RETFound.

Katherine Du, Atharv Ramesh Nair, Stavan Shah, Adarsh Gadari, Sharat Chandra Vupparaboina, Sandeep Chandra Bollepalli, Shan Sutharahan, José-Alain Sahel, Soumya Jana, Jay Chhablani and 1 more

Abstract read
In one paragraph

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

11 authors.

Katherine DuDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.ORCID 0000-0002-1715-5426
Atharv Ramesh NairDepartment of Electrical Engineering, Indian Institute of Technology Hyderabad, Hyderabad 502284, India.
Stavan ShahDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.
Adarsh GadariDepartment of Computer Science, University of North Carolina at Greensboro, Greensboro, NC 27412, USA.
Sharat Chandra VupparaboinaDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.ORCID 0009-0003-5957-4316
Sandeep Chandra BollepalliDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.
Shan SutharahanDepartment of Computer Science, University of North Carolina at Greensboro, Greensboro, NC 27412, USA.
José-Alain SahelDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.
Soumya JanaDepartment of Electrical Engineering, Indian Institute of Technology Hyderabad, Hyderabad 502284, India.
Jay ChhablaniDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.ORCID 0000-0003-1772-3558
Kiran Kumar VupparaboinaDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, PA 15219, USA.

Funding

Virus Production and Manipulation of Protein/Gene Expression ModuleP30EY008098 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Yuanyuan Chen · 1989 to 2026
$17.8M
NEI NIH HHS P30 EY008098Research to Prevent Blindness 718740
6 · The paper itself

Abstract

Eye diseases such as age-related macular degeneration (AMD) are major causes of irreversible vision loss. Early and accurate detection of these diseases is essential for effective management. Optical coherence tomography (OCT) imaging provides clinicians with in vivo, cross-sectional views of the retina, enabling the identification of key pathological features. However, manual interpretation of OCT scans is labor-intensive and prone to variability, often leading to diagnostic inconsistencies. To address this, we leveraged the RETFound model, a foundation model pretrained on 1.6 million unlabeled retinal OCT images, to automate the classification of key disease signatures on OCT. We finetuned RETFound and compared its performance with the widely used ResNet-50 model, using single-task and multitask modes. The dataset included 1770 labeled B-scans with various disease features, including subretinal fluid (SRF), intraretinal fluid (IRF), drusen, and pigment epithelial detachment (PED). The performance was evaluated using accuracy and AUC-ROC values, which ranged across models from 0.75 to 0.77 and 0.75 to 0.80, respectively. RETFound models display comparable specificity and sensitivity to ResNet-50 models overall, making it also a promising tool for retinal disease diagnosis. These findings suggest that RETFound may offer improved diagnostic accuracy and interpretability for specific tasks, potentially aiding clinicians in more efficient and reliable OCT image analysis.

Indexed as

age-related macular degenerationautomated report generationfoundational modelmachine learningoptical coherence tomographyretinal imaging

Identifiers

PMID39768004
PMCPMC11672910

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.