Outcomes in randomized controlled trials on slowing myopia: A systematic review.

IF 1.8 Q2 OPHTHALMOLOGY
Yiyang Xu, Nan Chen, Fei Zhang, Xuanling Zeng, Tianlin Wang, Wanying Xia, Xingyue Yang
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引用次数: 0

Abstract

Introduction: This review aims to analyse the application of the measure methods and measure contents of the outcomes reported in studies on slowing myopia, and the associations between outcomes and study characteristics.

Methods: Publications were identified by a search of seven electronic databases including China National Knowledge Infrastructure, China Biology Medicine, Wanfang database, CQVIP database, PubMed, Cochrane Library and Excerpta Medica Database, for relevant terms like myopia and randomized controlled trial from construction to Sept. 15th, 2023. The basic information of studies was extracted, including publishing time, region, intervention duration, sample size, intervention and outcome. Additionally, the measurements of outcomes were explored. The risk of bias of all studies included were assessed.

Results: Altogether, 599 randomized controlled trials were included, including vision (52.75 %), refraction (64.94 %), eye axial length (47.25 %) and response rate (38.23 %). Since 478 studies (79.80 %) were published in Chinese, the included studies were divided into subgroups according to the study language. The number of research published in Chinese was surged since 2005. The rate of refraction was gradually increased from 27.27 % before 2005 to 71.08 % in the past 2 years. 121 studies in English were included in this study. The usage frequency of refraction was ≥75 % in each period and that of eye axial length kept at more than half. In the studies lasting >6 months, the usage frequencies of refraction and axial length were >90 %. They accounted for 91.30 % and 82.61 % in the studies using contact lenses, and both 94.12 % in the studies using spectacles.

Conclusion: More and more attention is paid in slowing myopia, and the reported outcomes are diverse. Based on the analysis of the outcomes, there is a lack of an agreed-upon standardised set of outcomes in clinical trials for slowing myopia.

减缓近视的随机对照试验结果:一项系统综述。
本综述旨在分析缓变性近视研究中所报道的结果测量方法和测量内容的应用,以及结果与研究特点的关系。方法:检索中国国家知识基础设施、中国生物医学、万方数据库、CQVIP数据库、PubMed、Cochrane图书馆、摘录医学数据库等7个电子数据库,检索建设至2023年9月15日近视相关术语和随机对照试验等文献。提取研究的基本信息,包括发表时间、地区、干预持续时间、样本量、干预措施和结局。此外,还探讨了结果的测量方法。对纳入的所有研究的偏倚风险进行评估。结果:共纳入599项随机对照试验,包括视力(52.75%)、屈光(64.94%)、眼轴长(47.25%)和有效率(38.23%)。由于有478项研究(79.80%)以中文发表,因此根据研究语言将纳入的研究分为亚组。自2005年以来,用中文发表的研究论文数量激增。折射率由2005年以前的27.27%逐渐上升到近2年的71.08%。本研究共纳入121项英文研究。各周期屈光使用频率≥75%,眼轴长使用频率保持在一半以上。在持续6个月的研究中,屈光和眼轴长度的使用频率为90%。在使用隐形眼镜的研究中占91.30%和82.61%,在使用眼镜的研究中占94.12%。结论:缓变性近视越来越受到人们的重视,报道的治疗结果也多种多样。基于对结果的分析,在减缓近视的临床试验中缺乏一套一致认可的标准化结果。
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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来源期刊
Journal of Optometry
Journal of Optometry OPHTHALMOLOGY-
CiteScore
5.20
自引率
0.00%
发文量
60
审稿时长
66 days
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