国际眼科纵览 ›› 2014, Vol. 38 ›› Issue (4): 241-244.doi: 10.3706/ cma.j.issn.1673\|5803.2014.04.006

• 综述 • 上一篇    下一篇

低浓度阿托品治疗近视的临床研究进展

孙远 刘泉   

  1. 510060 广州, 中山大学中山眼科中心
  • 收稿日期:2014-03-20 出版日期:2014-08-22 发布日期:2014-09-02
  • 通讯作者: 刘泉,Email:drliuquan@163.com E-mail:drliuquan@163.com

Lowconcentration atropine treatment for myopia

SUN Yuan, LIU Quan   

  1. Zhongshan Ophthalmic Center, Sun Yatsen University, Guangzhou 510060, Guangdong Province, China
  • Received:2014-03-20 Online:2014-08-22 Published:2014-09-02
  • Contact: LIU Quan, Email: drliuquan@163.com E-mail:drliuquan@163.com

摘要: 阿托品是毒蕈碱受体抑制剂,1%浓度滴眼可以抑制近视的发展及眼轴的增长,但是畏光、视近模糊等常见的副作用限制了其临床应用。近期研究者逐渐将兴趣转向低浓度阿托品(小于1%浓度)的临床研究,发现低浓度阿托品滴眼可以有效延缓近视发展,比1%浓度的阿托品副作用更小,疗效也更持久稳定。

Abstract: Atropine is the antagonist of muscarinic receptor. 1% atropine was found to be able to inhibit myopia progression long ago. However, its usage was restricted due to the frequently happened side effects, such as photophobia and near vision blur. Recently, the focus of researchers shifted to the lowconcentration atropine, which was demonstrated to have effects of slowing the progression of myopia. Compared to 1% atropine, the effect of lowconcentration atropine is more sustained and durable, and the incidence of side effect is much more less.