Evidence map›Paper›PMID 40152766›Full record

ArticleTranslational vision science & technology2025

Multimodal Artificial Intelligence Models Predicting Glaucoma Progression Using Electronic Health Records and Retinal Nerve Fiber Layer Scans.

Abigail Koornwinder, Youchen Zhang, Rohith Ravindranath, Robert T Chang, Isaac A Bernstein, Sophia Y Wang

Abstract read
In one paragraph

Article in Translational vision science & technology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

6 authors.

Abigail KoornwinderDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.
Youchen ZhangDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.
Rohith RavindranathDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.
Robert T ChangDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.
Isaac A BernsteinDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.
Sophia Y WangDepartment of Ophthalmology, Byers Eye Institute, Stanford University, Palo Alto, CA, USA.

Funding

Stanford Vision Research CoreP30EY026877 · NEI · STANFORD UNIVERSITY · PI Yang Hu · 2017 to 2026
$8.0M
Personalized Predictions for Glaucoma Progression Using Artificial Intelligence for Electronic Health RecordsK23EY032635 · NEI · STANFORD UNIVERSITY · PI WANG, SOPHIA YING · 2021 to 2025
$1.2M
NEI NIH HHS K23 EY032635NEI NIH HHS P30 EY026877
6 · The paper itself

Abstract

Purpose: The purpose of this study was to develop models that predict which patients with glaucoma will progress to require surgery, combining structured data from electronic health records (EHRs) and retinal fiber layer optical coherence tomography (RNFL OCT) scans. Methods: EHR data (demographics and clinical eye examinations) and RNFL OCT scans were identified for patients with glaucoma from an academic center (2008-2023). Comparing the novel TabNet deep learning architecture to a baseline XGBoost model, we trained and evaluated single modality models using either EHR or RNFL features, as well as fusion models combining both EHR and RNFL features as inputs, to predict glaucoma surgery within 12 months (binary). Results: We had 1472 patients with glaucoma who were included in this study, of which 29.9% (N = 367) progressed to glaucoma surgery. The TabNet fusion model achieved the highest performance on the test set with an area under the receiver operating characteristic curve (AUROC) of 0.832, compared to the XGBoost fusion model (AUROC = 0.747). EHR only models performed with an AUROC of 0.764 and 0.720 for the deep learning model and XGBoost models, respectively. RNFL only models performed with an AUROC of 0.624 and 0.633 for the deep learning and XGBoost models, respectively. Conclusions: Fusion models which integrate both RNFL with EHR data outperform models only utilizing one datatype or the other to predict glaucoma progression. The deep learning TabNet architecture demonstrated superior performance to traditional XGBoost models. Translational Relevance: Prediction models that utilize the wealth of structured clinical and imaging data to predict glaucoma progression could form the basis of future clinical decision support tools to personalize glaucoma care.

Indexed as

Artificial IntelligenceElectronic Health RecordsGlaucomaNerve FibersRetinal Ganglion CellsAgedDeep LearningDisease ProgressionFemaleHumansMaleMiddle AgedROC CurveTomography, Optical Coherence

Identifiers

PMID40152766
PMCPMC11954538

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.