Evidence map›Paper›PMID 42473441›Full record

ArticleOphthalmology science2026

Rapid Access Macular Screening and Evaluation: A Datasheet for a Dataset to Diagnose and Triage Macular Diseases.

Ariel Yuhan Ong, Reena Chopra, Henry David Jeffry Hogg, Alastair K Denniston, Pearse A Keane

Abstract read
In one paragraph

Article in Ophthalmology science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

5 authors.

Ariel Yuhan OngMoorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.
Reena ChopraMoorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.
Henry David Jeffry HoggCollege of Medicine and Health, University of Birmingham, Birmingham, United Kingdom.
Alastair K DennistonNIHR Moorfields Biomedical Research Centre, London, United Kingdom.
Pearse A KeaneMoorfields Eye Hospital NHS Foundation Trust, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Macular disease can cause significant visual morbidity. Timely and accurate diagnosis and management is paramount. However, there is a lack of high-quality multimodal datasets reflective of real-world clinical practice to support research in this area. We present a large longitudinal real-world dataset that aims to address this gap. Design: Datasheet describing a multimodal dataset of routinely collected ophthalmic data focusing on possible macular disease. Participants: Adult patients (aged Methods: Data were curated from the INSIGHT Health Data Research Hub, one of the world's largest ophthalmic imaging bioresources, which aims to provide researchers with controlled access to anonymized routinely collected data. Clinical and imaging data derived from routine clinical care were exported, processed, and deidentified for secondary research use. Main Outcome Measures: This datasheet describes the demographic, clinical, and imaging metadata of the dataset, including a transparent overview of its strengths and weaknesses. Results: Rapid Access Macular Screening and Evaluation (RAMSEs) is a large and diverse real-world dataset. It was specifically designed to facilitate the diagnosis and triage of possible macular disease by providing access to multimodal imaging and clinical metadata. The current version of this dataset (time-locked as of July 2025) consists of retinal images and linked sociodemographic and clinical metadata from 85 444 patients with a median age of 63 (interquartile range 50-75) and a fairly even gender distribution (52.2% female). It comprises >4.9 million multimodal ophthalmic images (e.g. color fundus photographs, ultra-widefield imaging, fundus autofluorescence), including >1.4 million macula-centered OCT scans. Conclusions: We have developed a large multimodal real-world dataset, which was designed to address existing gaps in dataset size, disease distribution, and key clinical and sociodemographic metadata for possible macular disease. This valuable longitudinal resource can serve multiple purposes, including the development or robust clinical validation of artificial intelligence models, facilitating insights into real-world patient pathways and outcomes, or enabling research relating to epidemiology or big data analytics. This dataset may be made available through INSIGHT via a structured application process. Financial Disclosures: Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

Indexed as

DatasetMaculaOCTRetinal imaging

Identifiers

PMID42473441
PMCPMC13380802

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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.