通过两种管理机制有效降低近视度数加深。

IF 1 4区 医学 Q4 OPHTHALMOLOGY
Nir Erdinest, Maya Atar-Vardi, Itay Lavy, Naomi London, David Landau, Eran Pras, Yair Morad
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引用次数: 0

摘要

目的:确定 0.01% 阿托品治疗 3 年对抑制近视发展的有效性,以及与周边散焦隐形眼镜可能产生的叠加效应和停止治疗 1 年后的反弹效应:这项前瞻性研究纳入了127名8至5岁的儿童,分为三个治疗组:0.01%阿托品和单焦眼镜组(At+SV,36人)、0.01%阿托品和周边散焦隐形眼镜组(At+PDCL,30人)以及0.01%阿托品和双焦隐形眼镜组(At+DF,25人)。对照组配戴单光眼镜(36 人)。在 3 年的治疗期间和停止治疗后 1 年,每 6 个月测量一次球面等效屈光度:阿托品组的近视度数在治疗的 3 年中有所下降,第二年和第三年的下降幅度大于第一年(P < 0.01):第一年、第二年和第三年分别为-0.42 ± 0.34、-0.42 ± 0.34、-0.42 ± 0.34、-0.42 ± 0.34、-0.42 ± 0.34、-0.42 ± 0.34、-0.42 ± 0.34。42±0.34、-0.19±0.18和-0.22±0.19屈光度(D);At+SV组为-0.26±0.21、-0.14±0.37和-0.15±0.31屈光度;At+DF组为-0.22±0.15、-0.15±0.22和-0.11±0.14屈光度。停止治疗1年后,近视度数加深:At+SV组为-0.29 ± 0.28 D,At+PDCL组为-0.13 ± 0.28 D,At+DF组为-0.09 ± 0.18 D。3年后,At+SV组与At+PDCL组或At+DF组之间的近视度数进展差异无统计学意义(P < .05):结论:小剂量阿托品已被证实是一种有效的治疗方法,可在 3 年内延缓近视的发展,在治疗的第二年和第三年更为有效。与单一疗法相比,联合疗法在该组人群中并没有表现出明显的统计学优势。从统计学角度看,At+DF 组的反弹效应低于 At+SV 组。[20XX;X(X):XXX-XXX.].
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effective Decrease in Myopia Progression With Two Mechanisms of Management.

Purpose: To ascertain the effectiveness of 0.01% atropine treatment to inhibit myopia progression and the possible additive potency with peripheral defocus contact lenses over 3 years and the rebound effect 1 year after cessation of treatment.

Methods: This prospective study included 127 children aged 8 to 5 years, divided into three treatment groups: 0.01% atropine and single-vision spectacles (At+SV, n = 36), 0.01% atropine and peripheral defocus contact lens (At+PDCL, n = 30), and 0.01% atropine and dual-focus contact lens (At+DF, n = 25). A control group was prescribed single-vision spectacles (n = 36). Cycloplegic spherical equivalence refraction was measured every 6 months during 3 years of treatment and 1 year after cessation.

Results: Myopia progression decreased over 3 years of treatment, more during the second and third years than the first year, to a statistically significant degree in the atropine groups (P < .01): in the first, second, and third years, respectively, -0.42 ± 0.34, -0.19 ± 0.18, -0.22 ± 0.19 diopters (D) in the At+SV group, -0.26 ± 0.21, -0.14 ± 0.37, and -0.15 ± 0.31 D in the At+PDCL group, and -0.22 ± 0.15, -0.15 ± 0.22, and -0.11 ± 0.14 D in the At+DF group. Myopia progressed 1 year after cessation of treatment: -0.29 ± 0.28 D in the At+SV group, -0.13 ± 0.28 D in the At+PDCL group, and -0.09 ± 0.18 D in the At+DF group. After 3 years, there was no statistically significant difference in myopia progression between the At+SV and At+PDCL or At+DF groups (P < .05).

Conclusions: Low-dose atropine has been substantiated in this cohort as an effective treatment to decelerate myopia progression over 3 years, more effective in the second and third years of treatment. The combination treatment did not exhibit a statistically significant advantage over monotherapy in this cohort. The At+DF group exhibited a statistically lower rebound effect than the At+SV group. [J Pediatr Ophthalmol Strabismus. 2024;61(3):204-210.].

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来源期刊
CiteScore
1.80
自引率
8.30%
发文量
115
审稿时长
>12 weeks
期刊介绍: The Journal of Pediatric Ophthalmology & Strabismus is a bimonthly peer-reviewed publication for pediatric ophthalmologists. The Journal has published original articles on the diagnosis, treatment, and prevention of eye disorders in the pediatric age group and the treatment of strabismus in all age groups for over 50 years.
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