Low-dose atropine 0.01% for the treatment of childhood myopia: a pan-India multicentric retrospective study

Br J Ophthalmol. 2024 Mar 20;108(4):588-592. doi: 10.1136/bjo-2023-324450.

Abstract

Objective: The objective of this study was to assess the efficacy of low-dose atropine 0.01% in controlling myopia progression among Indian children over a 2-year period.

Methods: This retrospective study, conducted across 20 centres in India, monitored the progression of myopia over 2 years after initiating treatment with 0.01% atropine eye drops. This included children between 6 and 14 years with baseline myopia ranging from -0.5 D to -6 D, astigmatism≤-1.5 D, anisometropia ≤ -1 D and documented myopia progression of ≥0.5 D in the year prior to starting atropine. Subjects with any other ocular pathologies were excluded.

Results: A total of 732 children were included in the data analysis. The mean age of the subjects was 9.3±2.7 years. The mean myopia progression at baseline (1 year before starting atropine) was -0.75±0.31 D. The rate of myopia progression was higher in younger subjects and those with higher baseline myopic error. After initiating atropine, myopia progression significantly decreased to -0.27±0.14 D at the end of the first year and -0.24±0.15 D at the end of the second year (p<0.001). Younger children (p<0.001) and higher baseline myopia (p<0.001) was associated with greater myopia progression and poor treatment response (p<0.001 for both).

Conclusion: Low-dose atropine (0.01%) effectively reduces myopia progression over 2 years in Indian children.

Keywords: Treatment Medical.

MeSH terms

  • Atropine* / therapeutic use
  • Child
  • Disease Progression
  • Humans
  • Mydriatics / therapeutic use
  • Myopia* / diagnosis
  • Myopia* / drug therapy
  • Ophthalmic Solutions / therapeutic use
  • Refraction, Ocular
  • Retrospective Studies

Substances

  • Atropine
  • Ophthalmic Solutions
  • Mydriatics