A Pilot Study on the Efficacy and Safety of 0.01% Atropine in German Schoolchildren with Progressive Myopia
Autor: | Lutz Joachimsen, Daniel Böhringer, Nikolai J. Gross, Michael Reich, Julia Stifter, Thomas Reinhard, Wolf A. Lagrèze |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: | |
Zdroj: | Ophthalmology and Therapy, Vol 8, Iss 3, Pp 427-433 (2019) |
Druh dokumentu: | article |
ISSN: | 2193-8245 2193-6528 |
DOI: | 10.1007/s40123-019-0194-6 |
Popis: | Abstract Introduction Although the interest is growing in topical low-dose atropine to control myopia in schoolchildren worldwide, its use in children of European ancestry remains controversial and solid evidence is sparse. The Oxford Centre for Evidence Based Medicine (OCEBM) classifies the evidence for this therapy as level I for East Asian populations, but only level IV in non-Asian populations. Methods Fifty-six children, aged a median of 11 years (range 6–17), were analysed after 12 months of topical treatment with 0.01% preservative-free atropine in both eyes at bedtime every day. Efficacy was assessed during treatment every 6 months. In a subset of 20 patients, treatment of the second eye was delayed by 1 day to enable a controlled safety assessment of side effects such as pupil dilation, hypoaccommodation, and near vision reduction. Results Prior to treatment, the mean myopic progression was estimated as 1.05 D/year; after 12 months of treatment with 0.01% atropine, it was 0.40 D/year (p |
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