Chung Yeon Woong, Park Shin Hae, Shin Sun Young
Department of Ophthalmology, College of Medicine, St. Vincent's Hospital, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Ophthalmology & Visual Science, College of Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Banpo-Daero 222, Seocho-Gu, Seoul, 06591, Republic of Korea.
Sci Rep. 2025 Apr 30;15(1):15210. doi: 10.1038/s41598-025-98660-2.
We evaluated the effects of a graduated-concentration atropine protocol on the progression of myopia in premyopic Korean children. This retrospective study included 64 premyopic children with an initial spherical equivalent (SE) between + 0.75 diopters (D) and - 0.50 D as determined by cycloplegic refraction. The graduated-concentration atropine protocol begins with an initial concentration of 0.025% or 0.05%. If the annual progression of myopic spherical equivalent (SE) exceeds 0.25 D, the concentration gradually increases to a maximum of 0.125%. SE and axial length (AL) measurements are recorded at baseline, 6 months, 1 year, and 2 years. At the 2-year follow-up, individuals were classified into the progression group, defined as an increase in myopic SE ≥ 0.5 D from baseline, and the stable group, characterized by an increase of < 0.5 D from baseline. Of the 64 patients, 41 were classified into the stable group and 23 into the progression group. At the 2-year follow-up, significant differences in SE progression were observed between the groups. Notably, the changes in SE and AL from baseline to the 1-year follow-up were also significantly smaller in the stable group than in the progression group. Changes in myopic SE ≥ 0.375 D or AL ≥ 0.220 mm within 1 year strongly predict myopic progression in the premyopic state. The graduated-concentration atropine protocol demonstrated satisfactory outcomes in 64% of premyopic children at the 2-year follow-up. These findings emphasize the efficacy of such a protocol for predicting myopia progression in premyopic children.
我们评估了梯度浓度阿托品方案对韩国近视前期儿童近视进展的影响。这项回顾性研究纳入了64名近视前期儿童,其初始等效球镜度(SE)通过睫状肌麻痹验光确定在+0.75屈光度(D)至-0.50 D之间。梯度浓度阿托品方案从初始浓度0.025%或0.05%开始。如果近视等效球镜度(SE)的年进展超过0.25 D,浓度逐渐增加至最大0.125%。在基线、6个月、1年和2年时记录SE和眼轴长度(AL)测量值。在2年随访时,个体被分为进展组(定义为近视SE较基线增加≥0.5 D)和稳定组(特征为较基线增加<0.5 D)。64例患者中,41例被分为稳定组,23例被分为进展组。在2年随访时,两组之间观察到SE进展的显著差异。值得注意的是,稳定组从基线到1年随访时SE和AL的变化也显著小于进展组。1年内近视SE变化≥0.375 D或AL变化≥0.220 mm强烈预测近视前期状态下的近视进展。在2年随访时,梯度浓度阿托品方案在64%的近视前期儿童中显示出满意的结果。这些发现强调了该方案在预测近视前期儿童近视进展方面的有效性。