Topical Pharmacologic Interventions Versus Active Control, Placebo, or No Treatment for Epidemic Keratoconjunctivitis: Findings From a Cochrane Systematic Review.

Su-Hsun Liu, Barbara S Hawkins, Mark Ren, Sueko M Ng, Louis Leslie, Genie Han, Irene C Kuo

Journal: American journal of ophthalmology 2022;240():265-275

PMID: 35331686

Abstract

PURPOSE

To summarize key findings from a Cochrane systematic review of the effectiveness and safety of topical pharmacologic interventions compared with active control or placebo for epidemic keratoconjunctivitis (EKC).

DESIGN

Systematic review.

METHODS

We included randomized controlled trials that compared antiseptic agents, virustatic agents, or immune-modulating topical therapies with placebo or an active control. We adhered to Cochrane methods for trial selection, data extraction, risk of bias evaluation, and data synthesis.

RESULTS

Ten randomized controlled trials with 892 participants with acute or chronic EKC were included. Eight trials compared interventions with artificial tears or saline (n = 4) or with steroids (n = 4); two 3-arm trials contributed data to both comparisons. Estimates suggested that compared with tears, after povidone-iodine (PVP-I) alone (2 studies, 409 participants) more participants with acute EKC had resolution of symptoms (risk ratio [RR] 1.15 [95% confidence interval {CI} 1.07-1.24]) and signs (RR 3.19 [95% CI 2.29-4.45]) within 10 days. In 2 trials comparing treatments with steroid alone or steroid with levofloxacin, fewer eyes treated with PVP-I or polyvinyl alcohol iodine (PVA-I) plus steroid developed subepithelial infiltrates within 21 days (RR 0.08 [95% CI 0.01-0.55]; 69 eyes). No treatment was shown to improve resolution of infiltrates.

CONCLUSIONS

Low- to very low-level certainty of evidence suggested that PVP-I or PVA-I with steroid may confer some benefit in acute EKC, but imprecision from small sample sizes, the potential risk of bias from inadequate reporting or trial design, and variability in participant selection, outcome measurement, and reporting limit the amount and quality of evidence.

Copyright © 2022 Elsevier Inc. All rights reserved.

Address: From the Department of Ophthalmology (S-H.L., S.M.N., L.L.), School of Medicine, University of Colorado, Aurora, Colorado.; Wilmer Eye Institute (B.S.H., M.R., I.C.K.), Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore.; Department of Epidemiology (G.H.), Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.; Wilmer Eye Institute (B.S.H., M.R., I.C.K.), Department of Ophthalmology, Johns Hopkins University School of Medicine, Baltimore. Electronic address: [email protected].
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