TY - JOUR
T1 - Central serous chorioretinopathy
T2 - An evidence-based treatment guideline
AU - Feenstra, Helena M.A.
AU - van Dijk, Elon H.C.
AU - Cheung, Chui Ming Gemmy
AU - Ohno-Matsui, Kyoko
AU - Lai, Timothy Y.Y.
AU - Koizumi, Hideki
AU - Larsen, Michael
AU - Querques, Giuseppe
AU - Downes, Susan M.
AU - Yzer, Suzanne
AU - Breazzano, Mark P.
AU - Subhi, Yousif
AU - Tadayoni, Ramin
AU - Priglinger, Siegfried G.
AU - Pauleikhoff, Laurenz J.B.
AU - Lange, Clemens A.K.
AU - Loewenstein, Anat
AU - Diederen, Roselie M.H.
AU - Schlingemann, Reinier O.
AU - Hoyng, Carel B.
AU - Chhablani, Jay K.
AU - Holz, Frank G.
AU - Sivaprasad, Sobha
AU - Lotery, Andrew J.
AU - Yannuzzi, Lawrence A.
AU - Freund, K. Bailey
AU - Boon, Camiel J.F.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/7
Y1 - 2024/7
N2 - 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.
AB - 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.
KW - Central serous chorioretinopathy
KW - Micropulse laser
KW - Mineralocorticoid receptor antagonist
KW - Photodynamic therapy
KW - Treatment guideline
UR - http://www.scopus.com/inward/record.url?scp=85193589558&partnerID=8YFLogxK
U2 - 10.1016/j.preteyeres.2024.101236
DO - 10.1016/j.preteyeres.2024.101236
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C2 - 38301969
AN - SCOPUS:85193589558
SN - 1350-9462
VL - 101
JO - Progress in Retinal and Eye Research
JF - Progress in Retinal and Eye Research
M1 - 101236
ER -