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高度非球面小透镜目标眼镜对仅用阿托品单一疗法控制不佳的儿童的附加效应。

Additive Effect of Highly Aspherical Lenslet Target Spectacles to Children Inadequately Controlled by Atropine Monotherapy.

作者信息

Sim Bryan Xiangrong, Loh Kai Lyn, Htoon Hla Myint, Sri Yudah, Balakrishnan Maithily, Chan Poh Lin Pauline, Sim Ralene Zi Hui, Lam Crystal Shue Wen, Chia Audrey Wei Lin

机构信息

Singapore National Eye Centre (SNEC), Singapore.

Myopia Centre of Excellence, Singapore National Eye Centre (SNEC), Singapore.

出版信息

Ophthalmol Sci. 2025 Feb 26;5(4):100753. doi: 10.1016/j.xops.2025.100753. eCollection 2025 Jul-Aug.

Abstract

PURPOSE

Myopia progression in children, especially in East Asia, is a significant public health concern. This study evaluated the efficacy of combining myopia control spectacle lenses with Highly Aspherical Lenslet Target (HALT) technology and atropine in children who continued to progress on low-dose atropine (LDA).

DESIGN

Prospective cohort.

SUBJECTS

Children aged 6-11 years with ≥0.5 diopters (D) myopia progression over 6 months on LDA (0.01% or 0.025%) were recruited.

METHODS

All participants used HALT (Essilor Stellest) spectacle lenses while maintaining their LDA dose. The changes in spherical equivalent (SE) and axial length (AL) were tracked for 6 months before and 6-12 months after starting combination treatment.

MAIN OUTCOME MEASURES

Progression of SE and AL.

RESULTS

Fifty children (mean age 8.9 ± 1.1 years) were separated into group A (on 0.01% atropine daily, n20) and group B (on 0.01% atropine twice daily, n5 and 0.025% atropine nightly, n25). Most (86%) were ethnic Chinese. The baseline SE and AL showed no significant intergroup differences, with prior myopia progression (0.60D/0.24 mm) over 6 months. After adding HALT lenses, progression slowed to -0.06D/0.06 mm at 6 months and -0.15D/0.14 mm at 12 months. A hyperopic shift in AL was seen in 11 children (24%). However, the progression of >0.5D was noted in 20%, with 18% and 40% progressing by >0.3 mm and >0.15 mm, respectively. Univariate analysis suggested that children who progressed >0.10 mm over 6 months were more likely to be younger, whereas multivariate analysis suggested that change in AL was associated with smaller pupil size (possibly from poor compliance or absorption of atropine) at 6 months and younger age at 12 months, after controlling for sex, race, and baseline SE and AL. There were no complaints of glare, near, or peripheral blur in children after starting combination treatment.

CONCLUSIONS

The addition of HALT spectacle lenses significantly reduced myopia progression in children, aged 6-11 years, who were poorly controlled on LDA alone demonstrating a potential synergistic effect with LDA. These findings supported combination therapy for managing challenging myopia cases.

FINANCIAL DISCLOSURES

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

儿童近视进展,尤其是在东亚地区,是一个重大的公共卫生问题。本研究评估了将近视控制眼镜镜片与高非球面微透镜目标(HALT)技术和阿托品相结合,对在低剂量阿托品(LDA)治疗下仍持续进展的儿童的疗效。

设计

前瞻性队列研究。

研究对象

招募了年龄在6至11岁、在LDA(0.01%或0.025%)治疗下6个月内近视进展≥0.5屈光度(D)的儿童。

方法

所有参与者在维持LDA剂量的同时使用HALT(依视路Stellest)眼镜镜片。在开始联合治疗前6个月和治疗后6至12个月跟踪等效球镜度(SE)和眼轴长度(AL)的变化。

主要观察指标

SE和AL的进展情况。

结果

50名儿童(平均年龄8.9±1.1岁)被分为A组(每日使用0.01%阿托品,n = 20)和B组(每日使用0.01%阿托品两次,n = 5,每晚使用0.025%阿托品,n = 25)。大多数(86%)为华裔。基线SE和AL在组间无显著差异,之前6个月近视进展为(0.60D/0.24 mm)。添加HALT镜片后,6个月时进展减缓至-0.06D/0.06 mm,12个月时为-0.15D/0.14 mm。11名儿童(24%)出现眼轴长度远视性偏移。然而,20%的儿童进展>0.5D,分别有18%和40%的儿童进展>0.3 mm和>0.15 mm。单因素分析表明,6个月内进展>0.10 mm的儿童更可能年龄较小,而多因素分析表明,在控制性别、种族以及基线SE和AL后,6个月时眼轴长度的变化与瞳孔较小(可能由于阿托品依从性差或吸收不良)以及12个月时年龄较小有关。开始联合治疗后儿童未出现眩光、近视力或周边模糊的主诉。

结论

添加HALT眼镜镜片显著降低了6至11岁仅使用LDA控制不佳的儿童的近视进展,显示出与LDA的潜在协同效应。这些发现支持联合治疗用于管理具有挑战性的近视病例。

财务披露

专有或商业披露信息可在本文末尾的脚注和披露中找到。

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