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Comparative study on the safety and efficacy of different cycloplegic agents in children with darkly pigmented irides

Dorothy S P Fan1, Srinivas K Rao, Joan S K Ng

  • 1Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong Eye Hospital, Hong Kong. dorothyfan@cuhk.edu.hk

Insights

For hyperopic children, a combination of tropicamide 0.5% and phenylephrine 0.5% (regimen I) proved as effective as tropicamide 1.0% and cyclopentolate 1.0% (regimen II) in older children, avoiding potential cyclopentolate toxicity.

Area of Science:

  • Ophthalmology
  • Pediatric Optometry
  • Pharmacology

Background:

  • The absence of an ideal cycloplegic drug for children necessitates research into safe and effective alternatives.
  • Hyperopic children with pigmented irides pose unique challenges for cycloplegic drug efficacy.

Purpose of the Study:

  • To assess the safety and efficacy of three distinct cycloplegic regimens in pediatric patients with hyperopia.
  • To compare cycloplegia responses across different age groups and in the presence of strabismus.

Main Methods:

  • A crossover study design evaluated tropicamide 0.5%/phenylephrine 0.5% (regimen I), tropicamide 1.0%/cyclopentolate 1.0% (regimen II), and atropine 1.0% (regimen III) in 25 children.
  • Cycloplegic refractions were measured to determine refractive error under cycloplegia.

Main Results:

  • All three regimens produced statistically significant cycloplegic refractions compared to manifest refractions (P < 0.001).
  • Regimen I and II showed no significant difference in efficacy for children older than 5 years or those without strabismus (P > 0.050).
  • Mean spherical equivalent refractions were +5.11 D (regimen I), +5.29 D (regimen II), and +5.71 D (regimen III).

Conclusions:

  • Tropicamide 0.5% and phenylephrine 0.5% is a viable alternative to tropicamide 1.0% and cyclopentolate 1.0% in older children.
  • This regimen offers a way to achieve effective cycloplegia while potentially avoiding cyclopentolate-associated adverse effects.
Abstract