COMPARING THE EFFICACY OF 0.01% ATROPINE EYE DROPS VERSUS PLACEBO EYE DROPS ON MYOPIA CONTROL IN SPECTACLES WEARERS

Background: Myopia is a common refractive error characterized by excessive axial elongation, causing light rays to focus anterior to the retina, resulting in blurred vision. It is particularly concerning in children, as early-onset myopia tends to progress rapidly and may lead to serious ocular complications. Atropine eye drops have been proposed as a pharmacological intervention to slow myopia progression. While high concentrations are well-studied, the long-term efficacy of 0.01% atropine remains under investigation. Objective: This study aimed to evaluate the effectiveness of low-dose atropine (0.01%) in slowing myopia progression among spectacle-wearing children. Methods: A randomized controlled trial was conducted at Jinnah Hospital, Lahore, including 68 children aged 5 to 15 years diagnosed with myopia. Participants were randomly assigned to receive either 0.01% atropine or a placebo for six months. Comprehensive ophthalmic assessments, including best-corrected visual acuity (BCVA), spherical equivalent refraction, and axial length measurements, were conducted at baseline and follow-up. Data analysis was performed using SPSS Version 27, applying paired t-tests and correlation analysis to assess treatment efficacy. Ethical approval was obtained, and informed consent was secured from all participants. Results: The mean age of participants was 9.25 ± 3.206 years, with 38 (55.9%) females and 27 (39.7%) males. The atropine group showed significant preservation of BCVA (right eye: r=0.966, p<0.001; left eye: r=0.934, p<0.001), whereas the placebo group had weaker correlations (right eye: r=0.310, p=0.074). Spherical equivalent in the right eye improved significantly with atropine (r=0.981, p<0.001), while the placebo group deteriorated (p<0.001). Axial length elongation was significantly lower in the atropine group (-0.14382 mm, p=0.000 right eye; -0.10382 mm, p=0.000 left eye) compared to the placebo group (-0.24647 mm, p=0.000 right eye; -0.23618 mm, p=0.000 left eye). Conclusion: The findings confirm that 0.01% atropine is a safe and effective intervention for slowing myopia progression in children, significantly reducing axial elongation and stabilizing refractive status without compromising visual acuity. Further long-term studies are recommended to assess its sustained efficacy.

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Journal
Insights-Journal of Health and Rehabilitation
Published
2025-03-15
DOI
https://doi.org/10.71000/fymm7c78
Primary Topic
Ophthalmology and Visual Impairment Studies
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article
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article

COMPARING THE EFFICACY OF 0.01% ATROPINE EYE DROPS VERSUS PLACEBO EYE DROPS ON MYOPIA CONTROL IN SPECTACLES WEARERS

Muhammad Asghar Ali, Umar Shafique, Tahira Jabeen, A. Mohsin et al.
Insights-Journal of Health and Rehabilitation
Ophthalmology and Visual Impairment Studies
article

COMPARING THE EFFICACY OF 0.01% ATROPINE EYE DROPS VERSUS PLACEBO EYE DROPS ON MYOPIA CONTROL IN SPECTACLES WEARERS

Muhammad Asghar Ali, Umar Shafique, Tahira Jabeen, A. Mohsin, Naveed Babar, Samina Zahoor, Sobia Yusif
article en

Abstract

Background: Myopia is a common refractive error characterized by excessive axial elongation, causing light rays to focus anterior to the retina, resulting in blurred vision. It is particularly concerning in children, as early-onset myopia tends to progress rapidly and may lead to serious ocular complications. Atropine eye drops have been proposed as a pharmacological intervention to slow myopia progression. While high concentrations are well-studied, the long-term efficacy of 0.01% atropine remains under investigation. Objective: This study aimed to evaluate the effectiveness of low-dose atropine (0.01%) in slowing myopia progression among spectacle-wearing children. Methods: A randomized controlled trial was conducted at Jinnah Hospital, Lahore, including 68 children aged 5 to 15 years diagnosed with myopia. Participants were randomly assigned to receive either 0.01% atropine or a placebo for six months. Comprehensive ophthalmic assessments, including best-corrected visual acuity (BCVA), spherical equivalent refraction, and axial length measurements, were conducted at baseline and follow-up. Data analysis was performed using SPSS Version 27, applying paired t-tests and correlation analysis to assess treatment efficacy. Ethical approval was obtained, and informed consent was secured from all participants. Results: The mean age of participants was 9.25 ± 3.206 years, with 38 (55.9%) females and 27 (39.7%) males. The atropine group showed significant preservation of BCVA (right eye: r=0.966, p<0.001; left eye: r=0.934, p<0.001), whereas the placebo group had weaker correlations (right eye: r=0.310, p=0.074). Spherical equivalent in the right eye improved significantly with atropine (r=0.981, p<0.001), while the placebo group deteriorated (p<0.001). Axial length elongation was significantly lower in the atropine group (-0.14382 mm, p=0.000 right eye; -0.10382 mm, p=0.000 left eye) compared to the placebo group (-0.24647 mm, p=0.000 right eye; -0.23618 mm, p=0.000 left eye). Conclusion: The findings confirm that 0.01% atropine is a safe and effective intervention for slowing myopia progression in children, significantly reducing axial elongation and stabilizing refractive status without compromising visual acuity. Further long-term studies are recommended to assess its sustained efficacy.

Insights-Journal of Health and RehabilitationVol. 3(2 (Health & Rehab))
Jinnah Postgraduate Medical Center (PK), College of Optometrists (GB), Superior University (PK)
Openalex Percentile: Top 91%
Ophthalmology and Visual Impairment Studies
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