Li Tao, Zhou Xiaodong
Department of Ophthalmology, Jinshan Hospital of Fudan University, Shanghai, China.
Department of Ophthalmology, Eye & ENT Hospital of Fudan University, Shanghai, China.
J Ophthalmol. 2021 Jul 28;2021:8873283. doi: 10.1155/2021/8873283. eCollection 2021.
To describe the age distribution and main causes of new registered irreversible visual impairment (VI) and to compare the five-year proportion of VI in Jinshan district, Shanghai, from 2009 to 2018.
The new irreversible VI data were collected in the registry system from the Disabled Persons' Federation in Jinshan district from January 1, 2009, to December 31, 2018. Age, gender, and causes of VI were included, and the 5-year proportion of VI was calculated.
The peak occurrence of blindness occurred in the 50-59 yrs group in 2009-2013 and in the ≥70 yrs group in 2014-2018. The peak occurrence of low vision occurred in the 40-49 yrs group in 2009-2013 and in the 50-59 yrs group in 2014-2018. Myopic macular degeneration (MMD, 15.5%), diabetic retinopathy (DR, 14.3%), and other optic nerve atrophy (ONA, 14.3%) were the three leading causes of blindness in 2009-2013, whereas MMD (21.3%), age-related macular degeneration (AMD, 19.6%), ONA (14.9%) were the three leading causes of blindness in 2014-2018. MMD (39.2%), DR (9.6%), ONA (8.8%) were the three leading causes of low vision in 2009-2013, whereas MMD (38.7%), AMD (23.3%), ONA (7.4%) were the three leading causes of low vision in 2014-2018. The proportions of blindness and low vision caused by AMD were higher in 2014-2018 than those in 2009-2013 (=0.034 and < 0.001, respectively).
The present study demonstrated an increasing trend in the number of irreversibly visually impaired individuals from 2009 to 2018. More attention should be paid to people with high myopia and old age.
描述新登记的不可逆视力损害(VI)的年龄分布及主要原因,并比较2009年至2018年上海金山区VI的五年占比情况。
收集2009年1月1日至2018年12月31日金山区残疾人联合会登记系统中的新不可逆VI数据。纳入年龄、性别及VI病因,并计算VI的五年占比。
2009 - 2013年失明的高发年龄段为50 - 59岁组,2014 - 2018年为≥70岁组。2009 - 2013年低视力的高发年龄段为40 - 49岁组,2014 - 2018年为50 - 59岁组。2009 - 2013年,近视性黄斑变性(MMD,15.5%)、糖尿病视网膜病变(DR,14.3%)和其他视神经萎缩(ONA,14.3%)是失明的三大主要原因;而2014 - 2018年,MMD(21.3%)、年龄相关性黄斑变性(AMD,19.6%)、ONA(14.9%)是失明的三大主要原因。2009 - 2013年,MMD(39.2%)、DR(9.6%)、ONA(8.8%)是低视力的三大主要原因;而2014 - 2018年,MMD(38.7%)、AMD(23.3%)、ONA(7.4%)是低视力的三大主要原因。2014 - 2018年由AMD导致的失明和低视力占比高于2009 - 2013年(分别为=0.034和<0.001)。
本研究表明2009年至2018年不可逆视力损害个体数量呈上升趋势。应更加关注高度近视人群和老年人。