2012
DOI: 10.1001/archophthalmol.2011.303
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The Steroids for Corneal Ulcers Trial

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Cited by 49 publications
(33 citation statements)
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“…The SCUT (the Steroids for Corneal Ulcers Trial) study found no significant difference in 3-month visual acuity and no major safety concerns between patients receiving topical steroid or placebo as adjunctive therapy in the treatment of bacterial corneal ulcers, 47 but a significant effect of corticosteroids was observed in subgroups with the worst visual acuity and central ulcer location at baseline compared with the placebo. These subgroups analyses suggest that patients with severe ulcers may benefit from the use of steroids as adjunctive therapy.…”
Section: Discussionmentioning
confidence: 99%
“…The SCUT (the Steroids for Corneal Ulcers Trial) study found no significant difference in 3-month visual acuity and no major safety concerns between patients receiving topical steroid or placebo as adjunctive therapy in the treatment of bacterial corneal ulcers, 47 but a significant effect of corticosteroids was observed in subgroups with the worst visual acuity and central ulcer location at baseline compared with the placebo. These subgroups analyses suggest that patients with severe ulcers may benefit from the use of steroids as adjunctive therapy.…”
Section: Discussionmentioning
confidence: 99%
“…6,7 A potential limitation to the SCUT may have been that corticosteroids or placebo were not administered early enough to show a difference across all degrees of ulcer severity. 1,10 Approximately one-third of SCUT patients received topical antibiotics for longer than 4 days before corticosteroid or placebo administration.…”
Section: Discussionmentioning
confidence: 99%
“…6,7 Of the 500 patients included in SCUT, 8 were excluded from the analysis because of missing data specifying the duration of antibiotic treatment before receiving the corticosteroid or placebo. On presentation, screened patients with corneal ulcers were immediately treated with moxifloxacin hydrochloride every hour while awake for the first 48 hours, then every 2 hours until enrolled in the study.…”
Section: Methodsmentioning
confidence: 99%
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“…The methods of the trial have been described previously. 1 Patients with culture-proven bacterial keratitis who had been treated with ≥48 hours of topical moxifloxacin were randomized to topical prednisolone phosphate or topical placebo. Certified refractionists assessed logarithm of the minimum angle of resolution (logMAR) best spectacle corrected visual acuity (BSCVA) with a Tumbling “E” chart at enrollment, 3 weeks (study window: 2.5–5 weeks), 3 months (window: 2.5–5 months), and 12 months (window: 10–14 months).…”
Section: Methodsmentioning
confidence: 99%