To Investigate the Effect of Combined Use of 0.01% Atropine and 2% Carteolol Hydrochloride Eye Drops on Early-Onset Myopic Control in Western Chinese Children.

IF 1.6 4区 医学 Q3 OPHTHALMOLOGY
Ophthalmic epidemiology Pub Date : 2026-12-01 Epub Date: 2026-07-21 DOI:10.1080/09286586.2026.2706249
Qiwen Chen, Xinyu Peng, Jing Fang, Qin Xiang, Ying Chen, Xinghan Wen
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引用次数: 0

Abstract

Purpose: To evaluate the inhibitory role of 0.01% atropine combined with 2% carteolol hydrochloride on myopia progression in children aged 3-8 years in western China.

Methods: A total of 78 myopic children (spherical equivalent refraction from -2.00D to -8.00D) were initially assigned based on parental willingness to a control group (artificial tears (Hialid®) once nightly) or a treatment group. The treatment group was then randomly divided into an atropine group (0.01% atropine + artificial tears) and a combination group (0.01% atropine +2% carteolol hydrochloride). Spherical equivalent (SE), axial length (AL), and intraocular pressure (IOP) were measured at baseline and 3, 6 months. Chi-square and Kruskal-Wallis tests, adjusted by multivariate regression and standardized mean differences (SMD), were applied. Analysis of Covariance (ANCOVA) addressed minor baseline variations. Repeated-measures analysis of variance evaluated ocular parameters across the three groups to assess the effect of IOP-lowering drugs on delaying myopia progression.

Results: Both treatment groups showed significantly reduced SE and AL progression at 3 and 6 months (all p < 0.001). At 6 months, the combination group exhibited significantly smaller AL increase (0.09 ± 0.10 mm) and SE progression (-0.09 ± 0.12 D) than the atropine group (AL: 0.47 ± 0.18 mm; SE: -0.51 ± 0.18 D) and control group (AL: 0.99 ± 0.16 mm; SE: -1.03 ± 0.15 D; all p < 0.001). IOP decreased in the combination group (-1.75 ± 4.24 mmHg) but increased in the other groups. Adverse reaction rates were comparable between groups (p > 0.05).

Conclusion: 0.01% atropine combined with 2% carteolol hydrochloride safely and effectively inhibits myopia progression in children with early-onset myopia.

探讨0.01%阿托品联合2%盐酸卡替洛尔滴眼液对中国西部儿童早发性近视的控制效果。
目的:评价0.01%阿托品联合2%盐酸卡替洛尔对西部地区3 ~ 8岁儿童近视进展的抑制作用。方法:根据家长意愿将78例近视儿童(球面等效屈光度-2.00D ~ -8.00D)初始分为对照组(每晚1次人工泪液(Hialid®))和治疗组。治疗组随机分为阿托品组(0.01%阿托品+人工泪液)和联合组(0.01%阿托品+2%盐酸卡替洛尔)。在基线和3,6个月时测量球面等效(SE)、轴长(AL)和眼内压(IOP)。采用多变量回归和标准化平均差(SMD)校正的卡方检验和Kruskal-Wallis检验。协方差分析(ANCOVA)处理了次要的基线变化。重复测量方差分析评估了三组的眼部参数,以评估降眼压药物延缓近视进展的效果。结果:两个治疗组在3个月和6个月时SE和AL进展均明显减少(p < 0.05)。结论:0.01%阿托品联合2%盐酸卡替洛尔安全有效地抑制儿童早发性近视的进展。
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 epidemiology
Ophthalmic epidemiology 医学-眼科学
CiteScore
3.70
自引率
5.60%
发文量
61
审稿时长
6-12 weeks
期刊介绍: Ophthalmic Epidemiology is dedicated to the publication of original research into eye and vision health in the fields of epidemiology, public health and the prevention of blindness. Ophthalmic Epidemiology publishes editorials, original research reports, systematic reviews and meta-analysis articles, brief communications and letters to the editor on all subjects related to ophthalmic epidemiology. A broad range of topics is suitable, such as: evaluating the risk of ocular diseases, general and specific study designs, screening program implementation and evaluation, eye health care access, delivery and outcomes, therapeutic efficacy or effectiveness, disease prognosis and quality of life, cost-benefit analysis, biostatistical theory and risk factor analysis. We are looking to expand our engagement with reports of international interest, including those regarding problems affecting developing countries, although reports from all over the world potentially are suitable. Clinical case reports, small case series (not enough for a cohort analysis) articles and animal research reports are not appropriate for this journal.
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