Comparison of different concentrations atropine in controlling children and adolescent myopia: an umbrella review of systematic reviews and meta-analyses.

IF 0.9
Frontiers in ophthalmology Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fopht.2024.1447558
Baizhou Chen, Yao Ni, Jinghan Chen, Shuwen Xing, Zhaotian Zhang
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Abstract

Purpose: To evaluate the myopia control effect of different concentrations atropine in children and adolescent.

Methods: Meta-analyses and systematic reviews available in the Pubmed, Embase, and Cochrane Library databases from the databases' inception to August 2023 were searched to evaluate the efficacy and tolerability of different concentrations' atropine in controlling myopia progression. Overall effects were performed using random-effects model. AMSTAR 2 tool was used to assess the quality of included studies. Prespecified outcomes were weight mean difference (WMD) with 95% credible interval (95% CI) of annual spherical equivalent refraction (SER) changes and annual axial length (AL) changes.

Results: 19 systematic reviews/meta-analyses of different atropine concentrations were included in the analysis. 14 studies reported SER changes, and 17 reported AL changes. In terms of the studies' overall methodological quality level (measured using AMSTAR 2), 1 study was rated high, 7 moderate, 7 low, and 4 critically low. The 0.01% atropine was found to have statistically significance (annual SER change WMD 0.27 [95% CI 0.21 - 0.34] D/year; annual AL change WMD -0.09 [95% CI -0.1 to -0.07]) mm/year), 0.05% atropine was preferred considering efficacy and tolerability (annual SER change WMD 0.54 [95% CI 0.49 - 0.58] D/year; annual AL change WMD -0.21 [95% CI -0.12 to -0.02]) mm/year).

Conclusions: Different atropine concentrations alleviated children and adolescent myopia progression. However, higher-quality evidence and further investigation are needed to clarify the dose-response relationship, and practical guidelines must be developed to determine myopia control efficacy.

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比较不同浓度的阿托品对控制儿童和青少年近视的作用:系统综述和荟萃分析总览。
目的:评估不同浓度的阿托品对儿童和青少年近视的控制效果:方法:检索Pubmed、Embase和Cochrane图书馆数据库中自数据库建立至2023年8月的荟萃分析和系统综述,以评估不同浓度的阿托品在控制近视发展方面的疗效和耐受性。总体效应采用随机效应模型。AMSTAR 2 工具用于评估纳入研究的质量。预设结果为每年球面等效屈光度(SER)变化和每年轴长(AL)变化的加权平均差(WMD)及 95% 可信区间(95% CI):19项关于不同浓度阿托品的系统综述/计量分析被纳入分析。14 项研究报告了 SER 的变化,17 项研究报告了 AL 的变化。从研究的总体方法学质量水平(采用 AMSTAR 2 测量)来看,1 项研究被评为高,7 项为中,7 项为低,4 项为极低。研究发现,0.01% 的阿托品具有统计学意义(年度 SER 变化 WMD 为 0.27 [95% CI 0.21 - 0.34] D/年;年度 AL 变化 WMD 为 -0.09 [95% CI -0.1 to -0.07])毫米/年),0.01% 的阿托品具有统计学意义(年度 SER 变化 WMD 为 0.27 [95% CI 0.21 - 0.34] D/年;年度 AL 变化 WMD 为 -0.09 [95% CI -0.1 to -0.07])毫米/年。结论:考虑到疗效和耐受性(年SER变化WMD为0.54 [95% CI 0.49 - 0.58] D/年;年AL变化WMD为-0.21 [95% CI -0.12至-0.02])毫米/年),0.05%的阿托品更可取:不同浓度的阿托品可缓解儿童和青少年近视的发展。结论:不同浓度的阿托品可减轻儿童和青少年近视的发展,但还需要更高质量的证据和进一步的研究来阐明剂量-反应关系,并且必须制定实用的指南来确定近视控制的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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