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Central serous chorioretinopathy: An evidence-based treatment guideline.

Authors :
Feenstra HMA
van Dijk EHC
Cheung CMG
Ohno-Matsui K
Lai TYY
Koizumi H
Larsen M
Querques G
Downes SM
Yzer S
Breazzano MP
Subhi Y
Tadayoni R
Priglinger SG
Pauleikhoff LJB
Lange CAK
Loewenstein A
Diederen RMH
Schlingemann RO
Hoyng CB
Chhablani JK
Holz FG
Sivaprasad S
Lotery AJ
Yannuzzi LA
Freund KB
Boon CJF
Source :
Progress in retinal and eye research [Prog Retin Eye Res] 2024 Jul; Vol. 101, pp. 101236. Date of Electronic Publication: 2024 Feb 01.
Publication Year :
2024

Abstract

Central serous chorioretinopathy (CSC) is a relatively common disease that causes vision loss due to macular subretinal fluid leakage and it is often associated with reduced vision-related quality of life. In CSC, the leakage of subretinal fluid through defects in the retinal pigment epithelial layer's outer blood-retina barrier appears to occur secondary to choroidal abnormalities and dysfunction. The treatment of CSC is currently the subject of controversy, although recent data obtained from several large randomized controlled trials provide a wealth of new information that can be used to establish a treatment algorithm. Here, we provide a comprehensive overview of our current understanding regarding the pathogenesis of CSC, current therapeutic strategies, and an evidence-based treatment guideline for CSC. In acute CSC, treatment can often be deferred for up to 3-4 months after diagnosis; however, early treatment with either half-dose or half-fluence photodynamic therapy (PDT) with the photosensitive dye verteporfin may be beneficial in selected cases. In chronic CSC, half-dose or half-fluence PDT, which targets the abnormal choroid, should be considered the preferred treatment. If PDT is unavailable, chronic CSC with focal, non-central leakage on angiography may be treated using conventional laser photocoagulation. CSC with concurrent macular neovascularization should be treated with half-dose/half-fluence PDT and/or intravitreal injections of an anti-vascular endothelial growth factor compound. Given the current shortage of verteporfin and the paucity of evidence supporting the efficacy of other treatment options, future studies-ideally, well-designed randomized controlled trials-are needed in order to evaluate new treatment options for CSC.<br />Competing Interests: Declaration of competing interest Bailey Freund is an consultant for Bayer, Genentech, Heidelberg Engineering, Nidek, Novartis, Regeneron, and Zeiss. The author authors declare not to have conflicts of interest.<br /> (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
1873-1635
Volume :
101
Database :
MEDLINE
Journal :
Progress in retinal and eye research
Publication Type :
Academic Journal
Accession number :
38301969
Full Text :
https://doi.org/10.1016/j.preteyeres.2024.101236