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We aim to evaluate the myopia control effect of defocus incorporated multiple segments' (DIMS) spectacle lens in combination with different concentrations of atropine (ATR). A retrospective cohort study was conducted and DIMS users were categorized according to ATR concentration: 55 DIMS alone, 55 DIMS-Low ATR (0.01%) and 50 DIMS-High ATR (0.125%) groups. All three myopia control methods were applied for one year. Primary outcomes measures were changes in spherical equivalent refraction (SER) and axial length (AXL). One-way ANOVA was utilized to compare the outcome differences among the three groups, and multiple linear regression was utilized to analyze the effects of age, sex, baseline SER and baseline AXL on myopia progression among the three groups. The cycloplegic SER progression was-0.30 ± 0.25 D, -0.17 ± 0.49 D and - 0.16 ± 0.14 D in DIMS, DIMS-Low ATR and DIMS-High ATR groups respectively. The DIMS group showed a significant higher cycloplegia SER progression (P = 0.003). The AXL elongation was 0.13 ± 0.08 mm, 0.06 ± 0.20 mm and 0.06 ± 0.14 mm in DIMS, DIMS-Low ATR and DIMS-High ATR groups respectively and AXL elongation was significantly higher in DIMS group (P = 0.011). The young age demonstrated positive correlation to the higher cycloplegia SER progression in all groups (all P < 0.05). The young age is also correlated to higher AXL elongation in the DIMS and DIMS-Low ATR groups (both P < 0.05). The myopia control effects of low- and high-concentration ATRs in DIMS users show no significant difference, while the addition of atropine in combination with DIMS spectacles had a greater effect on myopia control than DIMS spectacles alone.
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http://dx.doi.org/10.1038/s41598-025-91089-7 | DOI Listing |
Clin Ophthalmol
September 2025
Faculty of Biomedical Engineering, Czech Technical University in Prague, Kladno, Czech Republic.
Aim: The objective of this study was to evaluate the efficacy of DIMS (Defocus Incorporated Multiple Segments) in comparison to control group (CTRL) in a wide age group of European progressive myopes (6-26 years).
Methods: In this prospective, non-randomised observational study, 78 myopes with progression myopia to -0.25 to -8.
Vestn Oftalmol
September 2025
Azerbaijan Medical University, Baku, Azerbaijan.
Objective: This study evaluated changes in ocular parameters in patients with progressive myopia receiving 0.01% atropine.
Material And Methods: The study included 35 children (18 girls, 51.
J Inflamm Res
September 2025
Department of Optometry, School of Health and Welfare, Dongshin University, Naju, Korea.
Objective: To evaluate the therapeutic efficacy and inflammatory modulatory effects of combined 0.01% atropine eye drops and orthokeratology (OK) lenses in controlling myopia progression among adolescent patients.
Methods: This retrospective study analyzed clinical data from 90 adolescent patients (90 eyes) with myopia treated from April 2021 to June 2023.
Ophthalmic Physiol Opt
September 2025
Centre for Vision and Eye Research, Queensland University of Technology, Brisbane, Queensland, Australia.
Purpose: Few studies have comprehensively investigated the effect of low dose atropine on the binocular vision system beyond accommodative amplitude. This study examined the effect of 0.05% atropine eye drops on a range of accommodation and vergence parameters across a 10-day period.
View Article and Find Full Text PDFBr J Ophthalmol
September 2025
Department of Neurosciences, Reproductive and Odontostomatological Sciences, University of Naples Federico II, Naples, Italy.
Purpose: To determine the effects of advanced spectacle lens technologies on changes in spherical equivalent of refraction (SER) and axial length (AL) elongation in slowing down the progression of myopia in children and adolescents, by synthesising data from randomised controlled trials (RCTs).
Methods: A systematic review and meta-analysis was conducted to identify all RCTs up to 27 February 2025 that compared intervention groups with myopia control lenses and control groups with standard single vision lenses (SVLs). Data from eligible studies were extracted into specially-designed data collection forms without changing the original values.