Topical non‐steroidal anti‐inflammatory drugs for central serous chorioretinopathy: A systematic review and meta‐analysis

Author:

Larsson Janni M. E.1,Boberg‐Ans Lars C.1,Vangsted Andreas1,van Dijk Elon H. C.2,Grauslund Jakob345ORCID,Hajari Javad N.1,Klefter Oliver N.16,Schneider Miklos17ORCID,Subhi Yousif13ORCID

Affiliation:

1. Department of Ophthalmology Rigshospitalet Glostrup Denmark

2. Department of Ophthalmology Leiden University Medical Center Leiden the Netherlands

3. Department of Clinical Research University of Southern Denmark Odense Denmark

4. Department of Ophthalmology Odense University Hospital Odense Denmark

5. Department of Ophthalmology Vestfold Hospital Trust Tønsberg Norway

6. Department of Clinical Medicine University of Copenhagen Copenhagen Denmark

7. Department of Ophthalmology Semmelweis University Budapest Hungary

Abstract

AbstractCentral serous chorioretinopathy (CSC) is a prevalent exudative maculopathy and the ongoing verteporfin shortage restricts current treatment possibilities. Topical non‐steroidal anti‐inflammatory drugs (NSAID) have previously been proposed as a treatment for CSC, although its exact efficacy remains unclear. In this systematic review and meta‐analysis, we outlined the efficacy of topical NSAIDs for the treatment of CSC. We searched 11 literature databases on 13 December 2022, for any study describing topical NSAID treatment for CSC. Thirteen eligible studies were included with a total of 1001 eyes of 994 patients with CSC. Six studies were case reports, two were cohort studies and five were non‐randomized comparative studies. Where specified, topical NSAIDs used were bromfenac 0.09%, diclofenac 0.1%, ketorolac 0.4% and 0.5%, pranoprofen 0.1%, and nepafenac 0.1% and 0.3%. Studies were predominantly of cases with acute CSC and several case studies reported treatment outcomes simultaneously with discontinuation of corticosteroid use, which complicated treatment evaluation. Meta‐analyses of comparative studies revealed a statistically significant but clinically irrelevant best‐corrected visual acuity improvement of −0.04 logMAR (95% CI: −0.07 to −0.01 logMAR; p = 0.01) at 1‐month follow‐up, which became statistically insignificant at 3‐month follow‐up (−0.03 logMAR; 95% CI: −0.06 to 0.003 logMAR; p = 0.08). Further, we found no benefit in complete subretinal fluid resolution at 1‐month follow‐up (OR: 1.20; 95% CI: 0.81–1.76; p = 0.37) or 3‐month follow‐up (OR: 1.17; 95% CI: 0.86 to 1.59; p = 0.33). Taken together, available evidence does not support the use of topical NSAIDs for the treatment of CSC.

Publisher

Wiley

Subject

Ophthalmology,General Medicine

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