Evidence map›Paper›PMID 41762269›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2026

OCT findings as a biomarker of disease activity in retinopathy of prematurity.

Merve Oral, Hüseyin Baran Özdemi̇r, Şengül Özdek

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Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Merve OralDepartment of Ophthalmology, School of Medicine, Gazi University, Ankara, 06500, Turkey.
Hüseyin Baran Özdemi̇rDepartment of Ophthalmology, School of Medicine, Gazi University, Ankara, 06500, Turkey. huseyinbaranozdemir@gazi.edu.tr.
Şengül ÖzdekDepartment of Ophthalmology, School of Medicine, Gazi University, Ankara, 06500, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo determine the value of handheld spectral-domain OCT (SD-OCT) in detecting macular changes in retinopathy of prematurity (ROP) and their association with disease activity.

methodsThis cross-sectional study included 95 eyes of 59 infants diagnosed with treatment-requiring ROP. All eyes underwent indirect ophthalmoscopic examination and handheld SD-OCT imaging prior to treatment. Clinical staging, presence of plus disease, and prior therapies were recorded. OCT images were analyzed for cystoid macular edema (CME), retinoschisis, preretinal tissue, and subclinical retinal detachment. Associations between OCT findings and clinical parameters were evaluated.

resultsBased on indirect ophthalmoscopy, 34.7% of eyes were at stage 3, 34% stage 4 A, 12% stage 4B, 3% aggressive ROP, and 14% presented with persistent avascular retina. CME was detected in 6 eyes (6.3%), significantly associated with plus disease (67%, p = 0.04), but not with gestational age, birth weight, or ROP stage. Retinoschisis was identified in 7 eyes (7.3%), predominantly in stage 4 A cases (71.4%). Preretinal tissue (3.1%) was observed mainly in aggressive ROP eyes. OCT refined staging in one case, reclassifying stage 4 A as stage 4B due to macular involvement.

conclusionHandheld SD-OCT uncovers macular abnormalities invisible to ophthalmoscopy and can alter disease staging. The significant association of CME with plus disease highlights its potential as biomarkers of disease activity. Routine OCT integration could transform ROP evaluation by refining staging and guiding timely intervention.

Indexed as

Macula LuteaRetinaRetinopathy of PrematurityTomography, Optical CoherenceBiomarkersCross-Sectional StudiesFemaleFollow-Up StudiesFundus OculiGestational AgeHumansInfant, NewbornMaleOphthalmoscopyBiomarkersCystoid macular edemaOCT, handheld OCTOptical coherence tomographyPlus diseasePreretinal tissueRetinoschisisROP, retinopathy of prematuritySubclinical retinal detachment

Identifiers

PMID41762269
PMCPMC13197318

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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.