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光学干预控制近视。

Optical interventions for myopia control.

机构信息

School of Optometry, Aston University, Birmingham, UK.

University of Houston, College of Optometry, Houston, TX, USA.

出版信息

Eye (Lond). 2024 Feb;38(3):455-463. doi: 10.1038/s41433-023-02723-5. Epub 2023 Sep 22.

DOI:10.1038/s41433-023-02723-5
PMID:37740053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10858277/
Abstract

A range of optical interventions have been developed to slow the progression of myopia. This review summarizes key studies and their outcomes. Peer-reviewed, randomized controlled clinical trials of at least 18 months duration were identified. Randomized clinical trials were identified and summarised: 13 for spectacles, 5 for overnight orthokeratology, 5 for soft contact lenses, and 3 for orthokeratology combined with low concentration atropine. Overnight orthokeratology trials were the most consistent with 2-year slowing of axial elongation between 0.24 and 0.32 mm. Other modalities were more variable due to the wide range of optical designs. Among spectacle interventions, progressive addition lenses were the least effective, slowing axial elongation and myopia progression by no more than 0.11 mm and 0.31 D, respectively. In contrast, novel designs with peripheral lenslets slow 2-year elongation and progression by up to 0.35 mm and 0.80 D. Among soft contact lens interventions, medium add concentric bifocals slow 3-year elongation and progression by only 0.07 mm and 0.16 D, while a dual-focus design slows 3-year elongation and progression by 0.28 mm and 0.67 D. In summary, all three optical interventions have the potential to significantly slow myopia progression. Quality of vision is largely unaffected, and safety is satisfactory. Areas of uncertainty include the potential for post-treatment acceleration of progression and the benefit of adding atropine to optical interventions.

摘要

已经开发出一系列光学干预措施来减缓近视的进展。本综述总结了关键研究及其结果。确定了至少持续 18 个月的同行评审、随机对照临床试验。确定并总结了随机临床试验:13 项用于眼镜,5 项用于过夜角膜塑形术,5 项用于软性隐形眼镜,3 项用于角膜塑形术联合低浓度阿托品。过夜角膜塑形术试验与 2 年期间眼轴伸长减缓 0.24 至 0.32 毫米最一致。其他方式因光学设计范围广泛而更加多变。在眼镜干预中,渐进多焦点镜片效果最差,眼轴伸长和近视进展分别减缓不超过 0.11 毫米和 0.31 屈光度。相比之下,具有周边透镜的新型设计可将 2 年的伸长和进展减缓高达 0.35 毫米和 0.80 屈光度。在软性隐形眼镜干预中,中加同心双焦点仅在 3 年内减缓伸长和进展 0.07 毫米和 0.16 屈光度,而双焦点设计可在 3 年内减缓伸长和进展 0.28 毫米和 0.67 屈光度。总之,所有三种光学干预措施都有可能显著减缓近视进展。视力质量基本不受影响,安全性令人满意。不确定的领域包括治疗后进展加速的可能性以及向光学干预添加阿托品的益处。

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Six years of wearer experience in children participating in a myopia control study of MiSight® 1 day.参与 MiSight® 1 天离焦控制近视研究的儿童 6 年的佩戴者经验。
Cont Lens Anterior Eye. 2023 Aug;46(4):101849. doi: 10.1016/j.clae.2023.101849. Epub 2023 May 6.
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Sci Rep. 2023 Apr 4;13(1):5475. doi: 10.1038/s41598-023-32700-7.
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A comparison of myopia control in European children and adolescents with defocus incorporated multiple segments (DIMS) spectacles, atropine, and combined DIMS/atropine.多焦点离焦眼镜(DIMS)、阿托品与 DIMS/阿托品联合治疗欧洲儿童青少年近视控制的比较。
PLoS One. 2023 Feb 16;18(2):e0281816. doi: 10.1371/journal.pone.0281816. eCollection 2023.
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Combined 0.01% atropine with orthokeratology in childhood myopia control (AOK) study: A 2-year randomized clinical trial.0.01%阿托品联合角膜塑形术用于儿童近视控制(AOK)研究:一项为期2年的随机临床试验。
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