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阿托品控制近视的研究综述。

A Review of Myopia Control with Atropine.

机构信息

1 Myopia Program, Brien Holden Vision Institute , Sydney, Australia .

2 Department of Clinical Research, Hai Yen Eye Care , Ho Chi Minh City, Vietnam .

出版信息

J Ocul Pharmacol Ther. 2018 Jun;34(5):374-379. doi: 10.1089/jop.2017.0144. Epub 2018 May 1.

Abstract

Myopia is a global public health issue with a worldwide prevalence of ∼30% and is estimated to rise to 50% by 2050. In addition to the burden associated with routine management of the condition, high myopia predisposes the eye to sight-threatening complications such as myopic maculopathy and glaucoma in adult life. Controlling onset and progression of myopia at a young age can reduce the risk of morbidity associated with high myopia. Progression of myopia can be slowed with various optical, environmental, and pharmaceutical strategies, of which atropine has proven to be the most effective. High-dose atropine (0.5%-1%) is the most effective, but it has significant trade-offs with respect to rebound of myopia on discontinuation and side effects such as photophobia and difficulty with near work (decreased accommodation). Low doses of atropine have been trialed and show a dose-dependent efficacy. However, its mode of action on the ocular tissues leading to slowing eye growth remains unclear and multiple mechanisms and sites in the eye have been postulated to play a role. This review summarizes the role of atropine in controlling myopia and the mechanisms studied to date.

摘要

近视是一个全球性的公共卫生问题,全球患病率约为 30%,预计到 2050 年将上升到 50%。除了与该疾病常规管理相关的负担外,高度近视还使眼睛易患近视性黄斑病变和青光眼等威胁视力的并发症。在年轻时控制近视的发病和进展可以降低与高度近视相关的发病率风险。各种光学、环境和药物策略都可以减缓近视的进展,其中阿托品已被证明是最有效的。高剂量阿托品(0.5%-1%)最有效,但它在停药后近视反弹和畏光、近视力困难(调节力下降)等副作用方面存在显著的权衡。已经尝试了低剂量的阿托品,并且显示出剂量依赖性的疗效。然而,其在眼组织上减缓眼轴增长的作用机制尚不清楚,并且已经推测出眼睛中的多个机制和部位发挥作用。这篇综述总结了阿托品在控制近视中的作用以及迄今为止研究的机制。

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