Predictors of persistent central serous chorioretinopathy: a multicenter retrospective study - MICRoN report number four
- PMID: 41074999
- DOI: 10.1007/s00417-025-06969-5
Predictors of persistent central serous chorioretinopathy: a multicenter retrospective study - MICRoN report number four
Abstract
Purpose: While central serous chorioretinopathy (CSCR) frequently resolves after the first episode, in 30-50% of cases, subretinal fluid (SRF) persists and can substantially impair vision. To identify persistence predictors, this study compared demographic, clinical, and imaging data between patients with resolution and SRF persistence.
Methods: Retrospective data were collected at baseline and follow-up from 308 eyes of 295 patients with CSCR in collaboration with the Macula Society CSCR Study Group. Patients were divided into a resolved (RG) and a persistent CSCR group (PG). Patients with known recurrence after resolution were excluded. Optical coherence tomography (OCT) biomarkers including central macular thickness (CMT), subfoveal choroidal thickness (SFCT), neurosensory detachment height (NSD), Haller layer thickness, inner choroidal thickness (ICT), and choroidal vascularity index (CVI) were analysed.
Results: PG had 148 eyes and RG had 160 eyes. Mean age in PG vs RG was 47.62 ± 11.63 vs. 44.89 ± 10.12 years (p = 0.029). Mean presenting symptom duration was significantly greater in PG than RG (8.67 ± 23.33 vs. 4.33 ± 31.18 months) (p = 0.005). There was a higher frequency of complex cases (21.6%) in PG (p < 0.001). Baseline mean CMT (358.11 ± 157.02 microns) and NSD height (175.78 ± 134.34 microns) were significantly lower in PG (p = 0.007). Multivariate logistic regression analysis showed that each additional year of age was associated with a 22.3% increase in the odds of having persistent SRF.
Conclusion: Age at presentation, symptom duration, baseline CMT and NSD height may serve as practical risk stratifiers to identify eyes at high risk for chronicity in CSCR.
Key messages: What is known Delayed presentation and absence of early therapy predispose eyes to chronic CSCR. SFCT plays a predictive role in persistent CSCR. What is new Age at presentation is a significant predictor of persistent SRF. Baseline CMT and NSD height may serve as practical risk stratifiers to identify eyes at high risk for chronicity.
Keywords: CMT; NSD; OCT; Persistent CSCR.
© 2025. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Conflict of interest statement
Declarations. Ethical approval: The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of each centre: University of Pittsburgh, Hebrew University of Jerusalem, Yonsei University College of Medicine, L V Prasad Eye Institute, Casey Eye Institute at Oregon Health and Science University, Rungsit University, Northwestern University Feinberg School of Medicine, Federal University of São Paulo and Asociados de Macula Vitreo y Retina de Costa Rica. Research involving human participants and/or animals: This is a retrospective study involving patient data. Informed consent: A “waiver of informed consent” was obtained considering the retrospective nature of the study. Disclosure of potential conflicts of interest: The authors have no conflict of interest.
References
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- Semeraro F, Morescalchi F, Russo A, Gambicorti E, Pilotto A, Parmeggiani F, Bartollino S, Costagliola C (2019) Central serous chorioretinopathy: pathogenesis and management. Clin Ophthalmol 13:2341–2352. https://doi.org/10.2147/OPTH.S220845
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