Efficacy of weekly dose of 1% atropine for myopia control in Chinese children

IF 3.7 2区 医学 Q1 OPHTHALMOLOGY
Linlin Du, Li Ding, Jun Chen, Jingjing Wang, Jinliuxing Yang, Sichen Liu, Xun Xu, Xiangui He, Jiannan Huang, Mengjun Zhu
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引用次数: 0

Abstract

Purpose To assess the effect of weekly 1% atropine use on children’s myopia progression and whether the effect is sustainable. Methods Medical records of myopic children aged 3–15 years receiving weekly 1% atropine for more than 1 year were retrospectively reviewed. Axial length (AL) and spherical equivalent refraction (SER) at every visit were collected. The changes in AL or SER over time were analysed using generalised estimating equation. The related factors of myopic progression were performed by multiple linear regression. The performance of short-term AL change to predict atropine-poor responders (AL change >0.2 mm/year) was assessed using receiver operating characteristic analysis. Results A total of 694 participants with a mean age of 8.83 years were included. The participants with follow-up time reached 1, 2, 3 and 4 years were 256 (36.9%), 250 (36.0%), 143 (20.6%) and 45 (6.5%) separately. The cumulative change in AL was 0.05 mm, 0.24 mm, 0.47 mm, 0.56 mm separately for 1-year, 2-year, 3-year and 4- year treatment. Approximate 0.20 mm elongation per year was observed since the second-year of the treatment. Older age and lower initial myopic refraction were independently associated with less myopic progression. A decrease in AL of more than 0.04 mm during the initial 2 months could serve as an indicator for identifying fast progressors (AL change >0.2 mm/year) over a 2-year period, with sensitivity and specificity rates of 0.78 and 0.73, respectively. Conclusion Weekly 1% atropine may be a potentially effective treatment with longer lasting effects for children with myopia control especially in those with older age and lower myopia. Data are available on reasonable request. The data that support the findings of this study are available from the corresponding author, MZ, on reasonable request.
每周使用 1%阿托品控制中国儿童近视的疗效
目的 评估每周使用 1%阿托品对儿童近视发展的影响,以及这种影响是否具有持续性。方法 回顾性审查每周使用 1%阿托品超过 1 年的 3-15 岁近视儿童的病历。收集每次就诊时的轴长(AL)和球面等效屈光度(SER)。使用广义估计方程分析了 AL 或 SER 随时间的变化。通过多元线性回归分析近视发展的相关因素。使用接收器操作特征分析法评估了短期AL变化预测阿托品不良反应者(AL变化>0.2毫米/年)的性能。结果 共纳入 694 名参与者,平均年龄为 8.83 岁。随访时间达到 1、2、3 和 4 年的参与者分别为 256 人(36.9%)、250 人(36.0%)、143 人(20.6%)和 45 人(6.5%)。在 1 年、2 年、3 年和 4 年的治疗中,AL 的累积变化分别为 0.05 毫米、0.24 毫米、0.47 毫米和 0.56 毫米。从治疗的第二年开始,每年大约有 0.20 毫米的伸长。年龄越大、初始近视屈光度越低,近视进展越小。在最初的两个月中,AL 下降超过 0.04 毫米可作为识别两年内快速进展者(AL 变化大于 0.2 毫米/年)的指标,其敏感性和特异性分别为 0.78 和 0.73。结论 每周使用 1%阿托品可能是一种有效的治疗方法,对儿童近视控制有较持久的效果,尤其是对年龄较大和近视度数较低的儿童。如有合理要求,可提供相关数据。支持本研究结果的数据可向通讯作者 MZ 索取。
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
CiteScore
10.30
自引率
2.40%
发文量
213
审稿时长
3-6 weeks
期刊介绍: The British Journal of Ophthalmology (BJO) is an international peer-reviewed journal for ophthalmologists and visual science specialists. BJO publishes clinical investigations, clinical observations, and clinically relevant laboratory investigations related to ophthalmology. It also provides major reviews and also publishes manuscripts covering regional issues in a global context.
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