Evidence map›Paper›PMID 41965556›Full record

ArticleBMC ophthalmology2026

Long-term clinical outcomes and prognostic factors of central serous chorioretinopathy.

Dong Gyu Na, Chul Gu Kim, Jae Hui Kim

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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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2 · The registry

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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.

Dong Gyu NaDepartment of Ophthalmology, Kim's Eye Hospital, #156 Youngdeungpo-dong 4ga, Youngdeungpo-gu, Seoul, 150-034, South Korea.
Chul Gu KimDepartment of Ophthalmology, Kim's Eye Hospital, #156 Youngdeungpo-dong 4ga, Youngdeungpo-gu, Seoul, 150-034, South Korea.
Jae Hui KimDepartment of Ophthalmology, Kim's Eye Hospital, #156 Youngdeungpo-dong 4ga, Youngdeungpo-gu, Seoul, 150-034, South Korea. kimoph@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate long-term clinical outcomes and factors associated with recurrence and visual prognosis in patients with central serous chorioretinopathy(CSC).

methodsThis retrospective study included 140 eyes diagnosed with idiopathic CSC and followed-up for ≥ 5 years(mean, 98.9 months). Baseline demographics, clinical features, and visual outcomes were reviewed. Factors associated with recurrence and final best-corrected visual acuity(BCVA) were analyzed using multivariate regression.

resultsThe mean patient age was 49.2 ± 9.5 years. Resolution of the first episode occurred in all eyes, with 62.1% cases resolving within 6 months. CSC recurred in 55.7% cases at a mean of 25.7 months after resolution. The mean number of episodes was 2.1 ± 1.4. Mean logMAR(logarithm of minimum angle of resolution) BCVA was 0.18 ± 0.21 at baseline, 0.13 ± 0.19 at 1 year, 0.18 ± 0.28 at 3 years, and 0.25 ± 0.39 at the final visit. Compared to baseline values, BCVA significantly worsened at the final visit (P = 0.001). Visual deterioration of ≥ 0.3 logMAR occurred in 14.3% patients. Younger age was associated with a higher risk of recurrence(P = 0.042); on average, patients with recurrence were 3.4 years younger than those without recurrence. Longer total SRF duration(P = 0.018), development of CNV(P < 0.001), and worse baseline BCVA(P < 0.001) were all significantly associated with poorer final BCVA.

conclusionsDuring the long-term follow-up, more than half of the patients with CSC experienced recurrence; a subset developed significant visual deterioration. Longer SRF duration and CNV are major determinants of poor visual prognosis. Active interventions to promote SRF resolution may help preserve long-term visual outcomes in patients with persistent SRF.

Indexed as

Central Serous ChorioretinopathyVisual AcuityAdultFemaleFluorescein AngiographyFollow-Up StudiesHumansMaleMiddle AgedPrognosisRecurrenceRetrospective StudiesTime FactorsTomography, Optical CoherenceCentral serous chorioretinopathyLong-termOutcomesRecurrence

Identifiers

PMID41965556
PMCPMC13185301

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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.