Evidence map›Paper›PMID 40973777›Full record

ArticleEye (London, England)2025

Dual site external validation of artificial intelligence-enabled treatment monitoring for neovascular age-related macular degeneration in England.

Henry David Jeffry Hogg, S James Talks, Justin Engelmann, Marion Dawn Teare, Michael Pogose, Praveen J Patel, K Balaskas, G Maniatopoulos, P A Keane

Abstract readValidation StudyMulticenter Study
In one paragraph

Article in Eye (London, England), 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

9 authors.

Henry David Jeffry HoggUniversity Hospitals Birmingham NHS Foundation Trust, Birmingham, UK. J.Hogg.1@bham.ac.uk.ORCID http://orcid.org/0000-0001-8044-7790
S James TalksNewcastle Eye Centre, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Justin EngelmannInstitute of Ophthalmology, University College London, London, UK.
Marion Dawn TearePopulation Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Michael PogoseHardian Health, Haywards Heath, UK.
Praveen J PatelNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.ORCID http://orcid.org/0000-0001-8682-4067
K BalaskasNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK.
G ManiatopoulosSchool of Business, University of Leicester, Leicester, UK.
P A KeaneMoorfields Eye Hospital NHS Foundation Trust, London, UK.

Funding

DH | National Institute for Health Research (NIHR) NIHR301467
6 · The paper itself

Abstract

backgroundMonitoring neovascular age-related macular degeneration (nAMD) is a significant contributor to ophthalmology demands in the NHS, with clinical capacity struggling to meet the demand. This task depends upon interpreting retinal optical coherence tomography (OCT) imaging, where artificial intelligence (AI) could rebalance clinical demand and capacity. However, evidence of safety and effectiveness in nAMD monitoring is lacking.

methodsUsing a published non-inferiority design protocol, 521 pairs of ipsilateral retinal OCTs from consecutive visits for nAMD treatment were collected from two NHS ophthalmology services. Real-world binary assessments of nAMD disease activity or stability were compared to an independent ophthalmic reading centre reference standard. An AI system capable of retinal OCT segmentation analysed the OCTs, applying thresholds for intraretinal and subretinal fluid to generate binary assessments. The relative negative predictive value (rNPV) of AI versus real-world assessments was calculated.

resultsReal-world assessments of nAMD activity showed a NPV of 81.6% (57.3-81.6%) and a positive predictive value (PPV) of 41.5% (17.8-62.3%). Optimised thresholds for intraretinal fluid increase (>1,000,000 µm³) and subretinal fluid increase (>2,000,000 µm³) for the AI system assessments produced an NPV of 95.3% (85.5-97.9%) and PPV of 57.8% (29.4-76.0%). The rNPV of 1.17 (1.11-1.23) met predefined criteria for clinical and statistical superiority and accompanied an rPPV of 1.39 (1.10-1.76).

conclusionsThis study suggests that the same thresholds for interpreting OCT-based AI analysis could reduce undertreatment and overtreatment in nAMD monitoring at different centres. Interventional research is needed to test the potential of supportive or autonomous AI assessments of nAMD disease activity to improve the quality and efficiency of services.

Indexed as

Angiogenesis InhibitorsArtificial IntelligenceWet Macular DegenerationAgedAged, 80 and overEnglandFemaleHumansIntravitreal InjectionsMaleRanibizumabSubretinal FluidTomography, Optical CoherenceVascular Endothelial Growth Factor AVisual AcuityAngiogenesis InhibitorsRanibizumabVascular Endothelial Growth Factor A

Identifiers

PMID40973777
PMCPMC12583501

What OpenQuestion holds

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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.