Effect of Atropine 0.01% Eye Drops on the Difference in Refraction and Axial Length between Right and Left Eyes.

IF 2 4区 医学 Q2 OPHTHALMOLOGY Ophthalmic Research Pub Date : 2023-01-01 Epub Date: 2023-01-05 DOI:10.1159/000528878
Xintong Liang, Shifei Wei, Shi-Ming Li, Wenzai An, Jialing Du, Yunyun Sun, Jiahe Gan, Weiling Bai, Zhining Cai, Qianqian Song, Lei Yin, Ningli Wang
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Abstract

Introduction: This study sought to determine whether the application of 0.01% atropine eye drops could impact the disparity in refraction and axial length (AL) between the right and left eyes in Chinese children.

Methods: The study was designed as a double-blind, placebo-controlled randomized trial. A total of 220 children aged 6-12 years were recruited from the Beijing Tongren Hospital in Beijing, China. Participants were randomized in a 1:1 ratio and were prescribed 0.01% atropine or placebo eye drops to be administered once a night to both eyes for the duration of 1 year. The cycloplegic refraction and AL were recorded including baseline, 6 months, and again at the 12 months.

Results: After 1-year follow-up period, 76 (69%) and 83 (75%) subjects of the initial 220 participants were identified as the 0.01% atropine and placebo groups, respectively. The inter-ocular difference in spherical equivalent refraction (SER) and AL demonstrated stable values in the 0.01% atropine treatment group (SER: p = 0.590; AL: p = 0.322) analyzed after 1 year, but found a significant increase (SER: p < 0.001; AL: p = 0.001) in the placebo group. Furthermore, over 1 year, eyes with greater myopia in the atropine group exhibited slower myopia progression (0.45 ± 0.44 D) than the lesser myopic eye (0.56 ± 0.44 D) (p = 0.003).

Conclusion: This study demonstrated that 0.01% atropine could maintain the inter-ocular SER and AL difference. And 0.01% atropine appeared to be more effective in delaying the progression of myopia in eyes with more myopia than in the less myopic eyes.

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0.01%阿托品滴眼液对左右眼屈光度和眼轴长度差异的影响。
引言:本研究旨在确定0.01%阿托品滴眼液的应用是否会影响中国儿童左右眼屈光度和眼轴长度(AL)的差异。方法:本研究设计为双盲、安慰剂对照的随机试验。共有220名6-12岁的儿童从中国北京同仁医院招募。参与者按1:1的比例随机分组,并被开具0.01%阿托品或安慰剂滴眼液,每晚给双眼一次,持续1年。记录睫状肌麻痹性屈光和AL,包括基线、6个月和12个月时再次记录。结果:经过一年的随访,最初220名参与者中的76名(69%)和83名(75%)受试者分别被确定为0.01%阿托品组和安慰剂组。在1年后分析的0.01%阿托品治疗组中,球面等效折射率(SER)和AL的眼间差异显示出稳定值(SER:p=0.590;AL:p=0.322),但在安慰剂组中发现显著增加(SER:p<;0.001;AL:p=0.001)。此外,在1年多的时间里,阿托品组中高度近视眼的近视进展(0.45±0.44 D)比低度近视眼(0.56±0.44 D)慢(p=0.003)。结论:本研究表明0.01%阿托品可以维持眼间SER和AL的差异。0.01%阿托品在延缓近视程度高的眼睛近视进展方面比近视程度低的眼睛更有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ophthalmic Research
Ophthalmic Research 医学-眼科学
CiteScore
3.80
自引率
4.80%
发文量
75
审稿时长
6-12 weeks
期刊介绍: ''Ophthalmic Research'' features original papers and reviews reporting on translational and clinical studies. Authors from throughout the world cover research topics on every field in connection with physical, physiologic, pharmacological, biochemical and molecular biological aspects of ophthalmology. This journal also aims to provide a record of international clinical research for both researchers and clinicians in ophthalmology. Finally, the transfer of information from fundamental research to clinical research and clinical practice is particularly welcome.
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