Evidence map›Paper›PMID 42015106›Full record

ArticleBMC ophthalmology2026

Pars planitis: a study of clinical features and treatment results.

Mehtap Caglayan, Dilbade Yildiz Ekinci

Abstract read
In one paragraph

Article in BMC 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.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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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

2 authors.

Mehtap CaglayanDepartment of Ophthalmology, University of Health Sciences/Gazi Yasargil Training and Research Hospital, Diyarbakır, Türkiye. drmehtap85@hotmail.com.ORCID http://orcid.org/0000-0003-4878-824X
Dilbade Yildiz EkinciDepartment of Ophthalmology, University of Health Sciences/Eskişehir City Hospital, Eskişehir, Türkiye.ORCID http://orcid.org/0000-0002-5535-264X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe aimed to report the clinical findings, treatment modalities, and success rates of pediatric cases with pars planitis followed up in our clinic. MATERIALS AND

methodsThis retrospective and cohort study included 46 eyes of 23 patients followed up with a diagnosis of pars planitis. Patients’ age, gender, age at symptom onset, follow-up period, initial and final visual acuity (VA) according to Snellen chart, angiographic findings and scores, initial immunosuppressive treatment, developing anterior and posterior segment complications, need for surgery, reason for and age at initiation of biological agents, side effects due to medications were recorded.

results15 of the patients were male and 8 were female, and the average age was 13.26 ± 3.18 (8–17) years. The average follow-up period was 38.09 ± 19.52 (6–72) months. According to the Snellen chart, initial and final best-corrected VA values ​​were 0.6 ± 0.3 and 0.8 ± 0.2, respectively, and they increased statistically significantly (p < 0.001). Fundus fluorescein angiography (FA) performed at the time of diagnosis revealed optic disc staining in all eyes and vascular leakage in 42 eyes. The FA score at the time of the initial visit was 17.09 ± 7.21, while the FA score at the last visit was 8.52 ± 6.9 (p < 0.001). Macular edema was detected in 10 eyes, retinoschisis was detected in 6 eyes, and papillitis was detected in 15 eyes. The preferred initial treatment was methotrexate in 17 patients, azathioprine in 4 patients, and methotrexate and adalimumab in 2 patients. During follow-up, biological agents were started in 20 of 23 patients.

conclusionPars planitis is a resistant and severe uveitis entity in children. With early diagnosis and early initiation of non-corticosteroid treatment, ocular complications that may develop can be prevented.

Indexed as

Immunosuppressive AgentsPars PlanitisAdolescentChildFemaleFluorescein AngiographyFollow-Up StudiesGlucocorticoidsHumansMaleRetrospective StudiesTreatment OutcomeVisual AcuityGlucocorticoidsImmunosuppressive AgentsClinical featuresImmunosuppressive therapyPars planitis

Identifiers

PMID42015106
PMCPMC13231666

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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.