Evidence map›Paper›PMID 42166152›Full record

Trial reportJAMA ophthalmology2026

Diagnostic Accuracy of a Retinal Birefringence Scanning Device Compared With a Traditional Autorefraction Device.

Julius T Oatts, Patrick Takla, Ha-Neul Yu, Natan Hekmatjah, Maanasa Indaram, Jocelyn He, Gui-Shuang Ying, Jeremy D Keenan

Abstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in JAMA ophthalmology, 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
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Julius T OattsDivision of Pediatric Ophthalmology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Patrick TaklaDepartment of Ophthalmology, University of California, San Francisco.
Ha-Neul YuDepartment of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia.
Natan HekmatjahDepartment of Ophthalmology, Northwestern University, Chicago, Illinois.
Maanasa IndaramDepartment of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia.
Jocelyn HeDepartment of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia.
Gui-Shuang YingDepartment of Ophthalmology, University of Pennsylvania Perelman School of Medicine, Philadelphia.
Jeremy D KeenanDepartment of Ophthalmology, University of California, San Francisco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Photoscreening devices are commonly used to identify children at risk for eye disease, although they often demonstrate low specificity as a trade-off for high sensitivity. A newly introduced photoscreening device that uses a newer mechanism, retinal birefringence scanning, purports to detect amblyopia and strabismus directly, and may theoretically increase specificity. Objective: To compare the diagnostic performance of 2 photoscreening devices, the Spot Vision Screener (Welch Allyn), hereafter referred to as a traditional autorefraction device, and the Blinq vision scanner (Rebion), hereafter referred to as a retinal birefringence scanner, for detecting amblyopia, strabismus, or visually significant refractive error (VSRE). Design, Setting, and Participants: This was a prospective, randomized, masked, diagnostic accuracy cohort study. The study included consecutive children 18 years or younger referred as a new patient to the University of California, San Francisco, pediatric ophthalmology clinic between January 2024 and February 2025 for suspected vision problems. Exposures: Each participant underwent screening with the traditional autorefraction device and the retinal birefringence scanner in randomized testing order, followed by a comprehensive eye examination. Sensitivity, specificity, and area under the receiver operating characteristic curve (AUROC) were calculated for each device relative to the clinical reference standard. Main Outcomes and Measures: Sensitivity, specificity, and AUROC of both screening devices to detect amblyopia, strabismus, or VSRE. Results: Of 195 enrolled participants (median [IQR] age, 50 [25-66] months), 139 (mean [SD] age, 49.7 [35.6] months; 75 female [54.0%]) completed both photoscreening tests. The prevalence of amblyopia, strabismus, and VSRE was 15.1%, 32.4%, and 30.1%, respectively. The traditional autorefraction device demonstrated higher sensitivity than the retinal birefringence scanner for detecting amblyopia (29%; 95% CI, -2% to 50%; P = .03) and VSRE (41%; 95% CI, 17%-59%; P < .001), with no difference in sensitivity for detecting strabismus identified (-6%; 95% CI, -28% to 18%; P = .69). No differences in specificity were identified. Across all vision disorders, the AUROC for the retinal birefringence scanner was lower than that for the traditional autorefraction device, particularly for amblyopia (-0.13; 95% CI, -0.23 to -0.03; P = .01). Conclusions and Relevance: In this single-site diagnostic accuracy study, the traditional autorefraction device demonstrated greater overall diagnostic sensitivity than the retinal birefringence scanner for detecting amblyopia and refractive errors, with no difference in specificity for all conditions. These findings suggest that the traditional autorefraction device may be more reliable for comprehensive pediatric vision screening.

Indexed as

AmblyopiaRefraction, OcularRefractive ErrorsRetinaStrabismusVision ScreeningBirefringenceChildChild, PreschoolFemaleHumansMaleProspective StudiesReproducibility of ResultsROC CurveSensitivity and Specificity

Identifiers

PMID42166152
PMCPMC13195499

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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.