Systematic review and meta-analysis of atropine for myopia control in children
This systematic review and meta-analysis synthesized evidence from 34 randomized controlled trials involving children ≤16 years with myopia. The primary outcomes assessed were spherical equivalent refraction (SER) progression and axial length (AL) elongation, with a follow-up duration of ≥12 months.
The analysis found that atropine significantly reduced myopia progression across all concentrations. For SER, the weighted mean difference was 0.44 (95% CI 0.35 to 0.52) D/year for concentrations <0.1%, 0.81 (95% CI 0.50 to 1.13) D/year for 0.1% to <0.5%, and 1.06 (95% CI 0.88 to 1.24) D/year for ≥0.5%. Regarding AL elongation, reductions were -0.20 (95% CI -0.24 to -0.16) mm/year for <0.1% and -0.36 (95% CI -0.40 to -0.33) mm/year for ≥0.5%.
Ethnicity-specific pooled effects indicated greater reduction in East Asians (SER: 0.63 D/year; AL: -0.26 mm/year) compared to South Asians (SER: 0.40 D/year; AL: -0.13 mm/year) and white Europeans (SER: 0.18 D/year; AL: -0.11 mm/year). Adverse events, serious adverse events, discontinuations, and tolerability were not reported in the included studies.
The authors conclude that these findings support the role of atropine in myopia control and highlight the importance of ethnicity-specific considerations when prescribing and tailoring treatment strategies. Clinicians should interpret these efficacy results within the context of the available safety data limitations.