Efficacy and Safety of Carbonic Anhydrase Inhibitors in the Management of Central Serous Chorioretinopathy

<b>Purpose:</b> To evaluate the efficacy and safety of carbonic anhydrase inhibitors for central serous chorioretinopathy (CSCR). <b>Methods:</b> The study protocol (PROSPERO registry no. CRD42024589621) involved a search of major databases (Cochrane CENTRAL, PubMed/MEDLINE, and Google Scholar) for studies comparing carbonic anhydrase inhibitors with placebo for the treatment of CSCR. Data were pooled using a random-effects model. Effect measures were risk ratios (RRs) for dichotomous outcomes, and mean differences with 95% CIs for continuous outcomes. <b>Results:</b> The analysis included 225 patients from 7 observational studies, with 133 in the carbonic anhydrase inhibitor group and 92 in the placebo group. No significant change in best-corrected visual acuity was observed in the carbonic anhydrase inhibitor group compared with placebo (mean difference, 0.01 logMAR, 95% CI, -0.08 to 0.11; <i>P</i> = .76). Carbonic anhydrase inhibitors significantly reduced subfoveal choroidal thickness (mean difference, -12.80 µm, 95% CI, -24.66 to -0.94; <i>P</i> = .03) and central macular thickness (mean difference, -52.18 µm, 95% CI, -98.20 to -6.15; <i>P</i> = .03), but no significant differences between groups were observed in incidence of complete resolution of subretinal fluid (RR, 1.45, 95% CI, 0.90-2.36; <i>P</i> = .13) or CSCR recurrence (RR, 0.67, 95% CI, 0.20-2.22; <i>P</i> = .51). Incidence of adverse events was significantly higher in the carbonic anhydrase inhibitor group compared with placebo (RR, 8.75, 95% CI, 1.24-61.79; <i>P</i> = .03). <b>Conclusions:</b> Carbonic anhydrase inhibitors reduce subfoveal choroidal thickness and central macular thickness in CSCR but do not improve visual acuity or achieve complete fluid resolution. In addition, carbonic anhydrase inhibitors pose a higher risk of adverse events, indicating the need for cautious use and further research on their long-term efficacy and safety.

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Journal
Journal of VitreoRetinal Diseases
Published
2026-03-23
DOI
https://doi.org/10.1177/24741264261428320
Primary Topic
Retinal Diseases and Treatments
Type
article
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article

Efficacy and Safety of Carbonic Anhydrase Inhibitors in the Management of Central Serous Chorioretinopathy

Ayesha Shaukat, Abdullah Ahmed, Hashem Abu Serhan, Muhammad Ansari et al.
Journal of VitreoRetinal Diseases
Retinal Diseases and Treatments
article

Efficacy and Safety of Carbonic Anhydrase Inhibitors in the Management of Central Serous Chorioretinopathy

Ayesha Shaukat, Abdullah Ahmed, Hashem Abu Serhan, Muhammad Ansari, Humza Saeed, Muhammad Safiullah, Muhammad Zain Ul Haq, Muhammad Shahmeer Ullah Shah, Saad Ashraf
article en

Abstract

<b>Purpose:</b> To evaluate the efficacy and safety of carbonic anhydrase inhibitors for central serous chorioretinopathy (CSCR). <b>Methods:</b> The study protocol (PROSPERO registry no. CRD42024589621) involved a search of major databases (Cochrane CENTRAL, PubMed/MEDLINE, and Google Scholar) for studies comparing carbonic anhydrase inhibitors with placebo for the treatment of CSCR. Data were pooled using a random-effects model. Effect measures were risk ratios (RRs) for dichotomous outcomes, and mean differences with 95% CIs for continuous outcomes. <b>Results:</b> The analysis included 225 patients from 7 observational studies, with 133 in the carbonic anhydrase inhibitor group and 92 in the placebo group. No significant change in best-corrected visual acuity was observed in the carbonic anhydrase inhibitor group compared with placebo (mean difference, 0.01 logMAR, 95% CI, -0.08 to 0.11; <i>P</i> = .76). Carbonic anhydrase inhibitors significantly reduced subfoveal choroidal thickness (mean difference, -12.80 µm, 95% CI, -24.66 to -0.94; <i>P</i> = .03) and central macular thickness (mean difference, -52.18 µm, 95% CI, -98.20 to -6.15; <i>P</i> = .03), but no significant differences between groups were observed in incidence of complete resolution of subretinal fluid (RR, 1.45, 95% CI, 0.90-2.36; <i>P</i> = .13) or CSCR recurrence (RR, 0.67, 95% CI, 0.20-2.22; <i>P</i> = .51). Incidence of adverse events was significantly higher in the carbonic anhydrase inhibitor group compared with placebo (RR, 8.75, 95% CI, 1.24-61.79; <i>P</i> = .03). <b>Conclusions:</b> Carbonic anhydrase inhibitors reduce subfoveal choroidal thickness and central macular thickness in CSCR but do not improve visual acuity or achieve complete fluid resolution. In addition, carbonic anhydrase inhibitors pose a higher risk of adverse events, indicating the need for cautious use and further research on their long-term efficacy and safety.

Journal of VitreoRetinal Diseases
King Edward Medical University (PK), Rawalpindi Medical University (PK), Allama Iqbal Medical College (PK), Dow University of Health Sciences (PK), Hamad Medical Corporation (QA)
Openalex Percentile: Top 12%
Retinal Diseases and Treatments
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