Treatment of central serous chorioretinopathy with topical NSAIDs

Sepehr Bahadorani,1 Kyle Maclean,1 Kendall Wannamaker,1 Edward Rickie Chu,1 Nathan Gresores,2 Jeong-Hyeon Sohn,1 Roberto Diaz-Rohena,1 Michael A Singer21Department of Ophthalmology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA; 2Medical Center Ophthalmology Associat...

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Autores principales: Bahadorani S, Maclean K, Wannamaker K, Chu ER, Gresores N, Sohn JH, Diaz­-Rohena R, Singer MA
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2019
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CSC
CSR
Acceso en línea:https://doaj.org/article/3d09e27f5f2a41e68a9509b25d8f3f63
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spelling oai:doaj.org-article:3d09e27f5f2a41e68a9509b25d8f3f632021-12-02T04:29:28ZTreatment of central serous chorioretinopathy with topical NSAIDs1177-5483https://doaj.org/article/3d09e27f5f2a41e68a9509b25d8f3f632019-08-01T00:00:00Zhttps://www.dovepress.com/treatment-of-central-serous-chorioretinopathy-with-topical-nsaids-peer-reviewed-article-OPTHhttps://doaj.org/toc/1177-5483Sepehr Bahadorani,1 Kyle Maclean,1 Kendall Wannamaker,1 Edward Rickie Chu,1 Nathan Gresores,2 Jeong-Hyeon Sohn,1 Roberto Diaz-Rohena,1 Michael A Singer21Department of Ophthalmology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA; 2Medical Center Ophthalmology Associates, San Antonio, TX, USAPurpose: Central serous chorioretinopathy (CSCR) is a common retinopathy that is often observed until resolution. The purpose of this study is to evaluate the effects of topical nonsteroidal anti-inflammatory drugs (NSAIDs) on timing of CSCR recovery.Methods: An IRB-approved retrospective review was conducted on patients that had been diagnosed with a new-onset, symptomatic case of CSCR. Patients were either observed only (13 untreated eyes) or treated with topical bromfenac or nepafenac (14 eyes) over an average of about a 4–5 week follow-up period.Results: There was no statistical significance between central macular thickness (CMT) and visual acuity of treatment and control groups at the initial presentation. However, at the follow-up visit, CMT reductions in the treatment group were significantly higher than in the control group (p<0.006).Conclusion: Use of topical NSAIDs in the treatment of acute CSCR leads to a faster rate of reduction in the subretinal fluid volume over a follow-up period of a few weeks.Keywords: central serous chorioretinopathy, CSCR, CSC, NSAIDs, bromfenac, nepafenac, subretinal fluid, SRFBahadorani SMaclean KWannamaker KChu ERGresores NSohn JHDiaz­-Rohena RSinger MADove Medical PressarticleCentral serous chorioretinopathyCSCRCSCCSRNSAIDsbromfenacnepafenacsubretinal fluidSRF.OphthalmologyRE1-994ENClinical Ophthalmology, Vol Volume 13, Pp 1543-1548 (2019)
institution DOAJ
collection DOAJ
language EN
topic Central serous chorioretinopathy
CSCR
CSC
CSR
NSAIDs
bromfenac
nepafenac
subretinal fluid
SRF.
Ophthalmology
RE1-994
spellingShingle Central serous chorioretinopathy
CSCR
CSC
CSR
NSAIDs
bromfenac
nepafenac
subretinal fluid
SRF.
Ophthalmology
RE1-994
Bahadorani S
Maclean K
Wannamaker K
Chu ER
Gresores N
Sohn JH
Diaz­-Rohena R
Singer MA
Treatment of central serous chorioretinopathy with topical NSAIDs
description Sepehr Bahadorani,1 Kyle Maclean,1 Kendall Wannamaker,1 Edward Rickie Chu,1 Nathan Gresores,2 Jeong-Hyeon Sohn,1 Roberto Diaz-Rohena,1 Michael A Singer21Department of Ophthalmology, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA; 2Medical Center Ophthalmology Associates, San Antonio, TX, USAPurpose: Central serous chorioretinopathy (CSCR) is a common retinopathy that is often observed until resolution. The purpose of this study is to evaluate the effects of topical nonsteroidal anti-inflammatory drugs (NSAIDs) on timing of CSCR recovery.Methods: An IRB-approved retrospective review was conducted on patients that had been diagnosed with a new-onset, symptomatic case of CSCR. Patients were either observed only (13 untreated eyes) or treated with topical bromfenac or nepafenac (14 eyes) over an average of about a 4–5 week follow-up period.Results: There was no statistical significance between central macular thickness (CMT) and visual acuity of treatment and control groups at the initial presentation. However, at the follow-up visit, CMT reductions in the treatment group were significantly higher than in the control group (p<0.006).Conclusion: Use of topical NSAIDs in the treatment of acute CSCR leads to a faster rate of reduction in the subretinal fluid volume over a follow-up period of a few weeks.Keywords: central serous chorioretinopathy, CSCR, CSC, NSAIDs, bromfenac, nepafenac, subretinal fluid, SRF
format article
author Bahadorani S
Maclean K
Wannamaker K
Chu ER
Gresores N
Sohn JH
Diaz­-Rohena R
Singer MA
author_facet Bahadorani S
Maclean K
Wannamaker K
Chu ER
Gresores N
Sohn JH
Diaz­-Rohena R
Singer MA
author_sort Bahadorani S
title Treatment of central serous chorioretinopathy with topical NSAIDs
title_short Treatment of central serous chorioretinopathy with topical NSAIDs
title_full Treatment of central serous chorioretinopathy with topical NSAIDs
title_fullStr Treatment of central serous chorioretinopathy with topical NSAIDs
title_full_unstemmed Treatment of central serous chorioretinopathy with topical NSAIDs
title_sort treatment of central serous chorioretinopathy with topical nsaids
publisher Dove Medical Press
publishDate 2019
url https://doaj.org/article/3d09e27f5f2a41e68a9509b25d8f3f63
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