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Discontinuation Approach and Follow-Up of Low-Concentration Atropine for Myopia Progression

医学 中止 阿托品 临床意义 麻醉 不利影响 儿科 眼科 梅德林 内科学 显著性差异 入射(几何) 临床试验 随机对照试验 眼病 回顾性队列研究
作者
Yuzhou Zhang,Xiu Juan Zhang,Ebenezer Zaabaar,Charlene C. Yim,Benjamin H. K. Yip,Ka Wai Kam,Mandy P. H. Ng,Alvin L. Young,Clement C. Tham,L J Chen,Chi Pui Pang,Jason C. Yam
出处
期刊:JAMA Ophthalmology [American Medical Association]
卷期号:144 (5): 396-396 被引量:4
标识
DOI:10.1001/jamaophthalmol.2026.0436
摘要

Importance: Some but not all clinical trials have found 0.05% atropine effective for myopia control; however, discontinuation management remains unclear. Objective: To evaluate a taper vs stop treatment discontinuation approach. Design, Setting, and Participants: This randomized clinical trial involved children aged 4 to 12 years originally from the Low-Concentration Atropine for Myopia Progression (LAMP) study who were followed up for 8 years. All children who completed year 5 follow-up and were receiving atropine treatment were randomized into taper and stop groups at a 1:1 ratio. Interventions: During the prediscontinuation period (year 6), participants in the taper group received 0.05% atropine for 6 months and then 0.025% atropine for another 6 months, while the stop group received 0.05% atropine eye drops for a full year. During the discontinuation period (years 7 and 8), all participants stopped the treatment and were monitored for 2 years. Main Outcomes and Measures: Myopia progression in the taper and stop groups over 3 years; proportion of good response to treatment discontinuation, defined as spherical equivalent (SEP) progression -0.5 diopter (D) or more in both eyes during the discontinuation period; and associated factors with myopia progression over 3 years. Results: Among 246 children who completed the year 5 follow-up, 180 children (73.2%) went on to complete 8 years of follow-up. The mean (SD) age was 13.47 (1.63) years; there were 139 male children (56.5%) and 107 female (43.5%). Over 3 years, SEP and axial length (AL) elongation were faster in the stop group than in the taper group: -0.78 D vs -0.54 D, respectively (difference, -0.24 D; 95% CI, -0.46 to -0.03 D; P = .02) and 0.44 mm vs 0.33 mm, respectively (difference, 0.11; 95% CI, 0.03 to 0.19 D; P = .01). The proportion of good response to treatment discontinuation in the taper group was greater than in the stop group (65.1% vs 42.6%, respectively; P = .003). Younger age and more myopic spherical equivalent/longer AL at prediscontinuation were associated with faster SEP and AL elongation over 3 years. Notably, the younger the age and the more myopic the spherical equivalent, the greater the estimated mean differences of SEP/AL elongation between the taper and stop groups. Conclusions and Relevance: This study found that over 3 years, the participants in the taper group had less myopia progression than the stop group, particularly in children who were younger and had more myopia. However, to our knowledge, the clinical relevance of this approximately 0.25-D difference between treatment groups is not well understood from the current medical literature.
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