Janti Siddharam S, Mali Kalpana, Sahithi Eereti, Tejaswini Antarvedi, Kamble Bhushan, Kalluri Srividya
Ophthalmology, All India Institute of Medical Sciences, Bibinagar, Bibinagar, IND.
Pharmacology, Neelima Institute of Medical Sciences, Ghatkesar, IND.
Cureus. 2025 May 13;17(5):e84010. doi: 10.7759/cureus.84010. eCollection 2025 May.
Aim This study was conducted to evaluate the effectiveness and safety of 0.01% and 0.05% atropine eye drops in managing myopia progression in children compared to a placebo. Methods This randomized, interventional study was conducted from March 2022 to May 2023 at the All India Institute of Medical Sciences, Bibinagar, Telangana. A total of 272 children aged five to 16 years, with myopia ranging from -1.0 D to -6.0 D and an annual progression greater than 0.5 D, were enrolled. Participants were randomly assigned to three groups: Group A (n=88, atropine 0.01%), Group B (n=90, atropine 0.05%), and Group C (n=94, placebo). Comprehensive ophthalmic examinations, including cycloplegic refraction, axial length measurement, and fundus evaluation, were performed at baseline, six weeks, 12 weeks, and at the end of one year. Changes in refractive error, axial length, accommodation, and pupil size were analyzed. Results Both atropine treatments were effective in slowing myopia progression compared to the placebo. Atropine 0.05% significantly reduced refractive progression (0.263 ± 0.03 D) and axial elongation (0.138 ± 0.22 mm) compared to the placebo group (0.759 ± 0.8 D and 0.367 ± 0.33 mm, respectively). The 0.01% atropine group also demonstrated a reduction, although less pronounced (0.319 ± 0.05 D and 0.241 ± 0.22 mm, respectively). Both atropine groups exhibited an increase in the near point of accommodation and pupil size, with the 0.05% group showing more significant changes. Mild adverse effects, including near vision difficulties and photophobia, were reported but did not significantly impact patient compliance. Conclusion Atropine 0.05% is more effective than 0.01% atropine and placebo in slowing myopia progression in children. Although both concentrations led to increased near point of accommodation and pupil size, side effects were mild and well-tolerated.
本研究旨在评估0.01%和0.05%阿托品滴眼液与安慰剂相比,在控制儿童近视进展方面的有效性和安全性。方法:本随机干预性研究于2022年3月至2023年5月在印度特伦甘纳邦比宾纳加尔的全印度医学科学研究所进行。共招募了272名5至16岁的儿童,近视度数在-1.0 D至-6.0 D之间,年进展大于0.5 D。参与者被随机分为三组:A组(n = 88,0.01%阿托品)、B组(n = 90,0.05%阿托品)和C组(n = 94,安慰剂)。在基线、六周、12周和一年结束时进行全面的眼科检查,包括散瞳验光、眼轴长度测量和眼底评估。分析屈光不正、眼轴长度、调节和瞳孔大小的变化。结果:与安慰剂相比,两种阿托品治疗在减缓近视进展方面均有效。与安慰剂组(分别为0.759 ± 0.8 D和0.367 ± 0.33 mm)相比,0.05%阿托品显著降低了屈光进展(0.263 ± 0.03 D)和眼轴伸长(0.138 ± 0.22 mm)。0.01%阿托品组也有降低,尽管不太明显(分别为0.319 ± 0.05 D和0.241 ± 0.22 mm)。两个阿托品组的调节近点和瞳孔大小均增加,0.05%组的变化更显著。报告了包括近视力困难和畏光在内的轻度不良反应,但对患者依从性没有显著影响。结论:在减缓儿童近视进展方面,0.05%阿托品比0.01%阿托品和安慰剂更有效。虽然两种浓度都导致调节近点和瞳孔大小增加,但副作用轻微且耐受性良好。