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Central serous chorioretinopathy: an evidence-based treatment guideline

Central serous chorioretinopathy: an evidence-based treatment guideline
Central serous chorioretinopathy: an evidence-based treatment guideline
Central serous chorioretinopathy (CSC) is a relatively common disease that causes vision loss due to macular subretinal fluid leakage and 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) combined 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.
1350-9462
Feenstra, Helena
215a241a-169f-4931-a911-5294547f7bf4
Van Dijk, Elon H.C.
329df4dd-691a-4218-ba65-dcb884bb597a
Cheung, Chui Ming Gemmy
5ea55fb6-2341-44b2-ae58-be2393c9b097
Lotery, Andrew
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514
et al.
Feenstra, Helena
215a241a-169f-4931-a911-5294547f7bf4
Van Dijk, Elon H.C.
329df4dd-691a-4218-ba65-dcb884bb597a
Cheung, Chui Ming Gemmy
5ea55fb6-2341-44b2-ae58-be2393c9b097
Lotery, Andrew
5ecc2d2d-d0b4-468f-ad2c-df7156f8e514

Feenstra, Helena, Van Dijk, Elon H.C. and Cheung, Chui Ming Gemmy , et al. (2024) Central serous chorioretinopathy: an evidence-based treatment guideline. Progress in Retinal and Eye Research, [101236]. (doi:10.1016/j.preteyeres.2024.101236).

Record type: Article

Abstract

Central serous chorioretinopathy (CSC) is a relatively common disease that causes vision loss due to macular subretinal fluid leakage and 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) combined 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.

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Accepted/In Press date: 2 January 2024
e-pub ahead of print date: 1 February 2024
Published date: 1 February 2024

Identifiers

Local EPrints ID: 486883
URI: http://eprints.soton.ac.uk/id/eprint/486883
ISSN: 1350-9462
PURE UUID: 7c2fa1ce-e247-4e39-a296-195d39ab30b7
ORCID for Andrew Lotery: ORCID iD orcid.org/0000-0001-5541-4305

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Date deposited: 08 Feb 2024 17:32
Last modified: 16 Apr 2024 01:38

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Contributors

Author: Helena Feenstra
Author: Elon H.C. Van Dijk
Author: Chui Ming Gemmy Cheung
Author: Andrew Lotery ORCID iD
Corporate Author: et al.

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