Evidence map›Paper›PMID 42094155›Full record

ArticlemedRxiv : the preprint server for health sciences2026

One Size Fits All? Comparing Foundation and Task-specific Models for Retinal Fluid Segmentation.

Xiaoyu Sun, Saiyu You, Siqi Sun, Cindy X Cai, Joanna Abraham, Po-Yin Yen, Linying Zhang

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Xiaoyu SunInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.
Saiyu YouInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.
Siqi SunInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.
Cindy X CaiWilmer Eye Institute, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Joanna AbrahamInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.
Po-Yin YenInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.
Linying ZhangInstitute for Informatics, Data Science and Biostatistics, Washington University in St. Louis, St. Louis, MO, USA.ORCID 0000-0002-4356-4645

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal fluids, detectable through optical coherence tomography (OCT), are key biomarkers for retinal diseases such as diabetic macular edema and age-related macular degeneration, guiding treatment decisions and monitoring response to therapy. Automated segmentation of retinal fluids could support large-scale clinical research and the development of clinical decision support tools. Recent ophthalmic foundation models trained on massive retinal imaging datasets show promise across many downstream tasks, including disease risk prediction and biomarker segmentation, but their performance relative to task-specific models for specialized clinical tasks remains unclear. We compared a task-specific segmentation model (RetiFluidNet) and an ophthalmic foundation model (VisionFM) using a standard benchmarking dataset containing 4,248 OCT images from 48 patients with three retinal diseases. Models were evaluated using three-fold cross-validation and assessed for pixel-level segmentation accuracy and patient-level fluid burden estimation. The task-specific model achieved higher segmentation performance and more consistent fluid quantification across devices. These findings suggest that, for retinal fluid segmentation, specialized task-specific models currently remain more reliable than general-purpose foundation models, highlighting the need for targeted adaptation before clinical deployment.

Identifiers

PMID42094155
PMCPMC13142578

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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.