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Atropine 0.5% eyedrops for the treatment of children with low myopia: A randomized controlled trial
Yan-Rong Wang1, Hong-Li Bian, Qi Wang
1Department of Ophthalmology, The People's Hospital of Yan'an Department of Ophthalmology, Affiliated Hospital of Yan'an University, Yan'an, China.
Insights
Atropine 0.5% eyedrops (ATE) effectively controlled low myopia (LM) in children by reducing spherical equivalent and axial length progression. The treatment demonstrated a good safety profile with no serious adverse events observed.
Area of Science:
- Ophthalmology
- Pediatric eye care
- Pharmacology
Background:
- Myopia is a growing concern in pediatric populations.
- Low myopia (LM) requires effective and safe management strategies.
- Atropine eyedrops are being investigated for myopia control.
Purpose of the Study:
- To evaluate the efficacy of atropine 0.5% eyedrops (ATE) in managing low myopia (LM) in children.
- To assess the safety profile of ATE for pediatric myopia control.
Main Methods:
- A randomized controlled trial involving 126 children with LM.
- Participants were divided into two groups: 0.5% ATE and placebo.
- Outcomes measured included changes in spherical equivalent (SE) and axial length (AL), and adverse events (AEs).
Main Results:
- 0.5% ATE significantly reduced myopia progression compared to placebo.
- ATE demonstrated a statistically significant reduction in both SE and AL increases (P < .01).
- No serious adverse events were reported in either the ATE or placebo groups.
Conclusions:
- Atropine 0.5% eyedrops are an efficacious treatment for controlling myopia in children with low myopia.
- The safety profile of ATE supports its use in pediatric myopia management.
- ATE offers a promising therapeutic option for slowing myopia progression in young patients.
Background:
This study aimed to assess the efficacy and safety of atropine 0.5% eyedrops (ATE) for the treatment of children with low myopia (LM).
Methods:
In this study, a total of 126 children with LM were randomly divided into an intervention group (administered 0.5% ATE) and a control group (administered a placebo), with 63 children in each group. The outcome measurements were changes in the spherical equivalent (SE), and axial length (AL), as well as adverse events (AEs).
Results:
Compared with placebo, administration of 0.5% ATE led to less progression in LM, as measured by SE, and less increase in AL (P < .01). In addition, no serious AEs occurred in both the groups.
Conclusion:
About 0.5% ATE was efficacious and safe for controlling myopia in children with LM.
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