ArticleScientific reports2025
Graduated atropine protocol effects on spherical equivalent and axial length in premyopic children.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed.
- Comments on Diversified segmental defocus optimization lenses with and without atropine for myopia prevention: a randomized clinical trial.Annals of translational medicine · 2026Article
- One year results of a pilot study on stepwise defocus incorporated multiple segment spectacle wear for myopia prevention in preschool children with premyopia.Scientific reports · 2026Article
- Myopia Management Consensus Statement in South Korean Children 2025 by the Korean Myopia Society for the Korean Association for Pediatric Ophthalmology and Strabismus.Korean journal of ophthalmology : KJO · 2026Review
- Identifying and Managing Pre-Myopia: A Narrative Review.Clinical ophthalmology (Auckland, N.Z.) · 2026Review
- Atropine Eye Drops in Childhood Myopia Control: A Review.International journal of medical sciences · 2026Review
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Authors and funding
3 authors.
Funding
Abstract
We evaluated the effects of a graduated-concentration atropine protocol on the progression of myopia in premyopic Korean children. This retrospective study included 64 premyopic children with an initial spherical equivalent (SE) between + 0.75 diopters (D) and - 0.50 D as determined by cycloplegic refraction. The graduated-concentration atropine protocol begins with an initial concentration of 0.025% or 0.05%. If the annual progression of myopic spherical equivalent (SE) exceeds 0.25 D, the concentration gradually increases to a maximum of 0.125%. SE and axial length (AL) measurements are recorded at baseline, 6 months, 1 year, and 2 years. At the 2-year follow-up, individuals were classified into the progression group, defined as an increase in myopic SE ≥ 0.5 D from baseline, and the stable group, characterized by an increase of < 0.5 D from baseline. Of the 64 patients, 41 were classified into the stable group and 23 into the progression group. At the 2-year follow-up, significant differences in SE progression were observed between the groups. Notably, the changes in SE and AL from baseline to the 1-year follow-up were also significantly smaller in the stable group than in the progression group. Changes in myopic SE ≥ 0.375 D or AL ≥ 0.220 mm within 1 year strongly predict myopic progression in the premyopic state. The graduated-concentration atropine protocol demonstrated satisfactory outcomes in 64% of premyopic children at the 2-year follow-up. These findings emphasize the efficacy of such a protocol for predicting myopia progression in premyopic children.
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Registered trials
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