Zhu Xingxue, Wang Yuliang, Liu Yujia, Ye Chaoying, Zhou Xingtao, Qu Xiaomei
Department of Ophthalmology and Vision Science, Eye & ENT Hospital, Fudan University, Shanghai, China.
NHC Key Laboratory of Myopia, Fudan University, Shanghai, China.
Heliyon. 2023 Jul 27;9(8):e18743. doi: 10.1016/j.heliyon.2023.e18743. eCollection 2023 Aug.
Little is known about changes in astigmatism during atropine treatment. We aimed to explore the effects of atropine 0.01% eye drops on both spherical and cylindrical refractive errors in myopic children.
Children aged 6-14 years with myopia ≥ -6.00 D and < -0.50 D, and total astigmatism > -2.00 D in at least one eye were enrolled. Subjects were randomised either to receive atropine 0.01% once nightly with single-vision lenses or simply to wear single-vision lenses and were followed up at 3-month intervals. Cycloplegic refraction and axial length were measured. The magnitude and direction of total astigmatism (TA), corneal astigmatism (CA), and residual astigmatism (RA) were evaluated.
Overall, 119 eyes (69 eyes in the atropine group and 50 eyes in the control group) were included in the final analyses after 9 months. Atropine-treated eyes showed significantly less progression of myopia than did control eyes (spherical equivalent: -0.35 ± 0.33 vs. -0.56 ± 0.49 D, p = 0.001; axial length: 0.20 ± 0.19 vs. 0.33 ± 0.19 mm, p < 0.001). Compared with control eyes (-0.04 ± 0.23 D), a significant increase in TA was observed in the atropine-treated eyes (-0.14 ± 0.29 D); this was mainly attributed to the increase in CA (-0.17 ± 0.26 D) rather than the minor decrease in RA (0.02 ± 0.32 D).
Atropine 0.01% was effective in preventing myopia progression, whereas 9 months of atropine treatment resulted in a clinically small, but statistically significant increase in TA in myopic Chinese children.
关于阿托品治疗期间散光的变化,人们了解甚少。我们旨在探讨0.01%阿托品滴眼液对近视儿童球镜和柱镜屈光不正的影响。
纳入年龄在6至14岁、近视度数≥-6.00 D且<-0.50 D、至少一只眼睛的总散光>-2.00 D的儿童。受试者被随机分为两组,一组每晚使用一次0.01%阿托品并佩戴单焦点镜片,另一组仅佩戴单焦点镜片,每3个月随访一次。测量睫状肌麻痹验光结果和眼轴长度。评估总散光(TA)、角膜散光(CA)和残余散光(RA)的大小和方向。
总体而言,9个月后,最终分析纳入了119只眼(阿托品组69只眼,对照组50只眼)。阿托品治疗的眼睛近视进展明显低于对照组(等效球镜:-0.35±0.33 D比-0.56±0.49 D,p = 0.001;眼轴长度:0.20±0.19 mm比0.33±0.19 mm,p<0.001)。与对照组眼睛(-0.04±0.23 D)相比,阿托品治疗的眼睛TA显著增加(-0.14±0.29 D);这主要归因于CA的增加(-0.17±0.26 D),而非RA的轻微下降(0.02±0.32 D)。
0.01%阿托品可有效预防近视进展,而9个月的阿托品治疗使中国近视儿童的TA有临床意义上的小幅增加,但具有统计学显著性。