Low-Concentration Atropine for Myopia Progression (LAMP) Study A Randomized, Double-Blinded, Placebo-Controlled Trial of 0.05%, 0.025%, and 0.01% Atropine Eye Drops in Myopia Control

被引:452
作者
Yam, Jason C. [1 ]
Jiang, Yuning [1 ]
Tang, Shu Min [1 ]
Law, Antony K. P. [1 ]
Chan, Joyce J. [1 ]
Wong, Emily [1 ]
Ko, Simon T. [2 ]
Young, Alvin L. [1 ]
Tham, Clement C. [1 ]
Chen, Li Jia [1 ,3 ]
Pang, Chi Pui [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
[2] Tung Wah Eastern Hosp, Dept Ophthalmol, Hong Kong, Peoples R China
[3] Prince Wales Hosp, Dept Ophthalmol & Visual Sci, Hong Kong, Peoples R China
关键词
CHILDHOOD MYOPIA; REFRACTIVE ERRORS; TOPICAL ATROPINE; EYE DROPS; PREVALENCE; CHILDREN; CHINESE; 0.01-PERCENT; POPULATION; PREVENTION;
D O I
10.1016/j.ophtha.2018.05.029
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Low-concentration atropine is an emerging therapy for myopia progression, but its efficacy and optimal concentration remain uncertain. Our study aimed to evaluate the efficacy and safety of low-concentration atropine eye drops at 0.05%, 0.025%, and 0.01% compared with placebo over a 1-year period. Design: Randomized, placebo-controlled, double-masked trial. Participants: A total of 438 children aged 4 to 12 years with myopia of at least -1.0 diopter (D) and astigmatism of -2.5 D or less. Methods: Participants were randomly assigned in a 1: 1: 1: 1 ratio to receive 0.05%, 0.025%, and 0.01% atropine eye drops, or placebo eye drop, respectively, once nightly to both eyes for 1 year. Cycloplegic refraction, axial length (AL), accommodation amplitude, pupil diameter, and best-corrected visual acuity were measured at baseline, 2 weeks, 4 months, 8 months, and 12 months. Visual Function Questionnaire was administered at the 1-year visit. Main Outcome Measures: Changes in spherical equivalent (SE) and AL were measured, and their differences among groups were compared using generalized estimating equation. Results: After 1 year, the mean SE change was -0.27 +/- 0.61 D, -0.46 +/- 0.45 D, -0.59 +/- 0.61 D, and -0.81 +/- 0.53 D in the 0.05%, 0.025%, and 0.01% atropine groups, and placebo groups, respectively (P < 0.001), with a respective mean increase in AL of 0.20 +/- 0.25 mm, 0.29 +/- 0.20 mm, 0.36 +/- 0.29 mm, and 0.41 +/- 0.22 mm (P < 0.001). The accommodation amplitude was reduced by 1.98 +/- 2.82 D, 1.61 +/- 2.61 D, 0.26 +/- 3.04 D, and 0.32 +/- 2.91 D, respectively (P < 0.001). The pupil sizes under photopic and mesopic conditions were increased respectively by 1.03 +/- 1.02 mm and 0.58 +/- 0.63 mm in the 0.05% atropine group, 0.76 +/- 0.90 mm and 0.43 +/- 0.61 mm in the 0.025% atropine group, 0.49 +/- 0.80 mm and 0.23 +/- 0.46 mm in the 0.01% atropine group, and 0.13 +/- 1.07 mm and 0.02 +/- 0.55 mm in the placebo group (P < 0.001). Visual acuity and vision-related quality of life were not affected in each group. Conclusions: The 0.05%, 0.025%, and 0.01% atropine eye drops reduced myopia progression along a concentration-dependent response. All concentrations were well tolerated without an adverse effect on vision-related quality of life. Of the 3 concentrations used, 0.05% atropine was most effective in controlling SE progression and AL elongation over a period of 1 year. (C) 2018 by the American Academy of Ophthalmology.
引用
收藏
页码:113 / 124
页数:12
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