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Updated: Aug 5, 2026

Inducement and Evaluation of a Murine Model of Experimental Myopia
Published on: January 22, 2019
Low-Concentration Atropine (0.01%, 0.025%, 0.05%) for Myopia Progression in Children: A Systematic Review and
Qi Wan1, Qiong Wang1, Ran Wei1
1Department of Ophthalmology, West China Hospital of Sichuan University, Chengdu 610044, China.
Insights
Low-concentration atropine eye drops effectively control myopia progression in children, with higher concentrations showing greater efficacy. All tested doses (0.01%-0.05%) are safe, but 0.01% offers a good balance of effectiveness and tolerability.
Area of Science:
- Ophthalmology
- Clinical Trials
- Public Health
Background:
- Myopia is a global epidemic, projected to affect 50% of the world population by 2050.
- Low-concentration atropine eye drops (0.01%, 0.025%, 0.05%) are a primary intervention for myopia control.
- Existing meta-analyses lack recent trial data and separate analyses for premyopia prevention.
Purpose of the Study:
- To systematically review and meta-analyze the efficacy and safety of low-concentration atropine for myopia progression control.
- To evaluate the effectiveness of these concentrations for premyopia prevention.
- To analyze outcomes based on atropine concentration, follow-up duration, and population.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials (RCTs).
- Searched PubMed, Web of Science, Embase, and Cochrane CENTRAL up to April 2026.
- Included RCTs comparing low-concentration atropine (0.01%-0.05%) with placebo in children; meta-analysis used random-effects models.
Main Results:
- Eight RCTs (n=1756) were included. 0.01% atropine showed significant efficacy for myopia progression at 1 and 2 years.
- The 0.05% concentration demonstrated the largest effect on myopia progression.
- All concentrations exhibited an excellent safety profile with no serious adverse events; premyopia prevention data showed high heterogeneity.
Conclusions:
- Low-concentration atropine is effective for myopia progression control, with a dose-dependent effect (0.05% > 0.025% > 0.01%).
- The 0.01% concentration provides a favorable balance between efficacy and tolerability.
- Further research is needed to validate 0.05% efficacy and conduct well-designed RCTs for premyopia prevention.
Abstract:
Objective: Myopia has reached epidemic proportions globally, with approximately 50% of the world population projected to be affected by 2050. Low-concentration atropine eye drops (0.01%, 0.025%, 0.05%) have emerged as a primary intervention for myopia control. Several meta-analyses on this topic have been published; however, none have included the most recent trials nor separately analyzed premyopia prevention outcomes. This systematic review and meta-analysis evaluates the efficacy and safety of these concentrations for myopia progression control and premyopia prevention. Methods: We searched PubMed, Web of Science, Embase, and Cochrane CENTRAL from database inception through April 2026. Randomized controlled trials (RCTs) comparing 0.01%, 0.025%, or 0.05% atropine with placebo or no treatment in children were included. Studies were screened using PICOS criteria (Population, Intervention, Comparison, Outcomes, Study design). Meta-analysis was performed using DerSimonian-Laird random-effects models. Subgroup analyses were conducted by concentration, follow-up duration, and population (myopia progression vs. premyopia prevention). Results: Of 18 full-text articles assessed, 8 RCTs (n = 1756) met all PICOS criteria and were included in the quantitative synthesis. For myopia progression, 0.01% atropine demonstrated significant efficacy at 1 year (pooled MD = +0.291 D, 95% CI: 0.199 to 0.384; p < 0.0001; I2 = 29.1%) and at 2 years (pooled MD = +0.174 D, 95% CI: 0.056 to 0.291; p = 0.0038; I2 = 0%). The 0.05% concentration showed the largest effect (pooled MD = +0.520 D, 95% CI: 0.409 to 0.630; p < 0.0001; I2 = 0%). Clinically, a 0.25 D difference over 1-2 years may translate to approximately 0.50 D cumulative benefit over a typical 5-year treatment course, potentially reducing the risk of high myopia. For premyopia prevention, a narrative synthesis was performed due to extreme heterogeneity between studies (I2 = 99.2%). All concentrations showed an excellent safety profile with no serious adverse events. Conclusions: Low-concentration atropine is effective for myopia progression control at all three concentrations, with a concentration-dependent gradient (0.05% > 0.025% > 0.01%). The 0.01% concentration offers a reasonable balance of efficacy and tolerability. Further independent validation of the 0.05% concentration is warranted. The premyopia prevention indication requires additional well-designed RCTs.
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