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重复低水平红光疗法对高度近视儿童青少年近视控制的随机临床试验。

Repeated Low-Level Red Light Therapy for Myopia Control in High Myopia Children and Adolescents: A Randomized Clinical Trial.

机构信息

Shanghai Eye Diseases Prevention &Treatment Center/ Shanghai Eye Hospital, School of Medicine, Tongji University, Shanghai, China.

Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; Shanghai Key Laboratory of Ocular Fundus Disease, Shanghai, China.

出版信息

Ophthalmology. 2024 Nov;131(11):1314-1323. doi: 10.1016/j.ophtha.2024.05.023. Epub 2024 Jun 6.

Abstract

PURPOSE

To assess the effectiveness and safety of repeated low-level red light (RLRL), which is a newly available treatment for myopia control in children and adolescents with high myopia.

DESIGN

Multicenter, randomized, parallel-group, single-blind clinical trial (randomized controlled trial; NCT05184621).

PARTICIPANTS

Between February 2021 and April 2022, 192 children aged 6 to 16 years were enrolled. Each child had at least 1 eye with myopia of cycloplegic spherical equivalent refraction (SER) at least -4.0 diopters (D), astigmatism of ≤2.0 D, anisometropia of ≤3.0 D, and best-corrected visual acuity (BCVA) of 0.2 logarithm of the minimum angle of resolution or better. Follow-up was completed by April 2023.

METHODS

Participants were randomly assigned at a 1:1 ratio to intervention (RLRL treatment plus single-vision spectacles) or control (single-vision spectacles) groups. The RLRL treatment was administered for 3 minutes per session, twice daily with a minimum interval of 4 hours, 7 days per week.

MEAN OUTCOME MEASURES

The primary outcome and key secondary outcome were changes in axial length (AL) and cycloplegic SER measured at baseline and the 12-month follow-up visit. Participants who had at least 1 postrandomization follow-up visit were analyzed for treatment efficacy.

RESULTS

Among 192 randomized participants, 188 (97.91%) were included in the analyses (96 in the RLRL group and 92 in the control group). After 12 months, the adjusted mean change in AL was -0.06 mm (95% confidence interval [CI], -0.10 to -0.02 mm) and 0.34 mm (95% CI, 0.30 to 0.39 mm) in the intervention and control groups, respectively. A total of 48 participants (53.3%) in the intervention group were still experiencing axial shortening >0.05 mm at the 12-month follow-up. The mean SER change after 12 months was 0.11 D (95% CI, 0.02to 0.19 D) and -0.75 D (95% CI, -0.88 to -0.62 D) in the intervention and control groups, respectively.

CONCLUSIONS

Repeated low-level red light demonstrates stronger treatment efficacy among those with high myopia, with 53.3% experiencing substantial axial shortening. Repeated low-level red light provides an excellent solution for the management of high myopia progression, a significant challenge in ophthalmology practice.

FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.

摘要

目的

评估重复低水平红光(RLRL)在儿童和青少年高度近视患者中的近视控制效果和安全性。

设计

多中心、随机、平行分组、单盲临床试验(随机对照试验;NCT05184621)。

参与者

2021 年 2 月至 2022 年 4 月期间,共纳入 192 名 6 至 16 岁的儿童。每个孩子至少有 1 只眼患有至少 -4.0 屈光度(D)的近视性睫状肌麻痹球镜等效折射(SER)、≤2.0 D 的散光、≤3.0 D 的屈光参差和最佳矫正视力(BCVA)为 0.2 对数最小分辨角或更好。随访于 2023 年 4 月完成。

方法

参与者以 1:1 的比例随机分配至干预(RLRL 治疗加单视眼镜)或对照(单视眼镜)组。RLRL 治疗每次 3 分钟,每天 2 次,两次治疗之间至少间隔 4 小时,每周 7 天。

主要观察指标

主要结局和关键次要结局为基线和 12 个月随访时轴向长度(AL)和睫状肌麻痹 SER 的变化。至少有 1 次随机后随访的参与者被纳入治疗效果分析。

结果

在 192 名随机参与者中,有 188 名(97.91%)纳入分析(RLRL 组 96 名,对照组 92 名)。12 个月后,干预组的平均 AL 变化为 -0.06 mm(95%置信区间[CI],-0.10 至 -0.02 mm),对照组为 0.34 mm(95% CI,0.30 至 0.39 mm)。在 12 个月的随访中,干预组共有 48 名(53.3%)参与者仍经历轴性缩短>0.05 mm。12 个月后 SER 的平均变化为 0.11 D(95% CI,0.02 至 0.19 D)和 -0.75 D(95% CI,-0.88 至 -0.62 D),分别在干预组和对照组。

结论

重复低水平红光在高度近视患者中表现出更强的治疗效果,53.3%的患者出现明显的轴向缩短。重复低水平红光为高度近视进展的管理提供了一个极好的解决方案,这是眼科实践中的一个重大挑战。

利益披露

作者在本文讨论的任何材料中均无专有或商业利益。

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