arXiv:2607. 19864v1 Announce Type: cross Abstract: Diabetic retinopathy is a leading cause of preventable blindness; its early lesions are small, low contrast, and easily missed in manual screening.
By Z\"ubeyr \"Ozeren, Tansel Uyar
The study evaluates fundus-specific foundation models (FM) for detecting diabetic macular edema (DME) in retinal images. It compares two popular FM—RETFound and FLAIR—against a lightweight EfficientNet-B0 backbone across multiple datasets (IDRiD, MESSIDOR-2, and OCT-and-Eye-FundusImages). Results indicate that FM do not consistently outperform fine‑tuned CNNs; EfficientNet-B0 often matches or exceeds FM performance, with FLAIR being the most competitive FM.
By Franco Javier Arellano, Jos\'e Ignacio Orlando
CF‑NODE is a counterfactual test‑time adaptation framework designed for diabetic retinopathy grading across different cameras, clinics, and patient populations. It ranks internal spatial nodes by attention, feature magnitude, and similarity, then progressively attenuates the highest‑ranked nodes and calibrates predictions based on the stability of the expected grade response. Evaluated on five external datasets, CF‑NODE outperforms four existing methods, achieving higher AUC and macro‑F1 scores and providing more balanced recognition across severity levels.
By Sabarish G, Deepak Parashar
arXiv:2607. 03959v1 Announce Type: cross Abstract: Diabetic retinopathy (DR) is a leading cause of vision impairment worldwide, highlighting the need for accurate and accessible screening tools.
By Rashadul Hasan Badhon, Atalie Carina Thompson, Jennifer I. Lim, Theodore Leng, Minhaj Nur Alam
arXiv:2607. 02569v1 Announce Type: cross Abstract: This paper presents a safety-centered empirical evaluation of uncertainty-aware last-layer adaptation for referable diabetic retinopathy screening using RETFound, a self-supervised vision-transformer retinal foundation model used here as a frozen feature encoder, and the public APTOS 2019 and DDR diabetic retinopathy fundus image datasets.
By Karim Mardhani
The paper introduces Gated Knowledge‑Guided Prototype Transfer (GProtoT), a training‑free module that enhances zero‑support medical vision‑language models by transferring visual residuals from supported classes to missing ones using VLM similarity and clinical ontology distances. GProtoT employs an evidence gate to scale transfer based on semantic relevance, reducing negative transfer while modestly improving recall and accuracy in realistic one‑shot trials on MESSIDOR. The method requires no gradients, validation data, or extra inference, offering a low‑compute, accountable adaptation path for incomplete clinical supervision.
By Sumaiya Fazal, Rizwan Qureshi, Laleh Behjat, Samira Ebrahimi Kahou