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逐步降低浓度阿托品治疗近视的十年队列研究。

Stepwise low concentration atropine for myopic control: a 10-year cohort study.

机构信息

Department of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, 123, Da-Pi Road, Niao-Sung District, Kaohsiung, 88301, Taiwan, R.O.C.

Department of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, 123, Da-Pi Road, Niao-Sung District, Kaohsiung, 88301, Taiwan, R.O.C..

出版信息

Sci Rep. 2021 Aug 30;11(1):17344. doi: 10.1038/s41598-021-96698-6.

Abstract

The aim of this study was to analyze changes in refraction and evaluate the variables in school children who received atropine as myopic control for 10 years. Low-concentration atropine (0.05%) was prescribed initially, and the dose was increased in a stepwise manner if rapid myopic progression (≥ 0.5D per half year) was noted during the regular follow-up visit. 23 children with a mean age of 6.96 ± 1.07 years were included. The initial spherical equivalent was - 1.25 ± 0.84 D. The overall mean myopic progression was - 0.30 ± 0.27 D/year. Younger initial age, female, higher initial spherical equivalent and the need of higher concentration of atropine were found to be risk factors for myopic progression in multivariate mixed-effect analysis (p = 0.013, 0.017, 0.024 and 0.014). Children who kept using a lower concentration of atropine (≤ 0.1%) tended to have slower myopic progression throughout the 10-year course than those who shifted to higher concentrations (> 0.1%) (p ≤ 0.001). Stepwise low concentration of atropine might be effective for long-term myopic control in school students. Those who had poor response to lower concentration of atropine may have the risk of faster progression, even with high concentration of atropine. Additional or alternative treatment might be considered.

摘要

本研究旨在分析屈光度的变化,并评估接受阿托品进行近视控制 10 年的学龄儿童的各项变量。初始给予低浓度阿托品(0.05%),如果在定期随访中发现近视进展较快(每半年≥0.5D),则逐步增加剂量。共纳入 23 名平均年龄为 6.96±1.07 岁的儿童。初始球镜等效值为-1.25±0.84 D。总体平均近视进展为-0.30±0.27 D/年。多变量混合效应分析显示,初始年龄较小、女性、初始球镜等效值较高以及需要较高浓度阿托品,是近视进展的危险因素(p=0.013、0.017、0.024 和 0.014)。在整个 10 年期间,持续使用较低浓度阿托品(≤0.1%)的儿童,其近视进展速度较使用较高浓度阿托品(>0.1%)的儿童更慢(p≤0.001)。逐步使用低浓度阿托品可能对长期控制学龄儿童近视有效。那些对低浓度阿托品反应不佳的患者,即使使用高浓度阿托品,也可能有进展较快的风险。可能需要考虑额外或替代的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e71/8405709/5df648618689/41598_2021_96698_Fig1_HTML.jpg

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