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The Prevalence of Diagnosis of Major Eye Diseases and their Associated Payments in the Medicare Fee-for-Service Program.医疗保险按服务项目付费计划中主要眼病的诊断患病率及其相关费用支付情况。
Ophthalmic Epidemiol. 2021 Sep 16:1-13. doi: 10.1080/09286586.2021.1968006.
2
Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the Right to Sight: an analysis for the Global Burden of Disease Study.2020 年失明和视力障碍的原因及 30 多年来的趋势,以及与 VISION 2020:看见的权利相关的可避免盲的患病率:全球疾病负担研究的分析。
Lancet Glob Health. 2021 Feb;9(2):e144-e160. doi: 10.1016/S2214-109X(20)30489-7. Epub 2020 Dec 1.
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Age-Related Macular Degeneration Preferred Practice Pattern®.年龄相关性黄斑变性首选实践模式®
Ophthalmology. 2020 Jan;127(1):P1-P65. doi: 10.1016/j.ophtha.2019.09.024. Epub 2019 Sep 25.
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Prevalence and Causes of Visual Impairment and Blindness in Chinese American Adults: The Chinese American Eye Study.美籍华裔成年人视力障碍和失明的患病率及病因:美籍华裔眼研究。
JAMA Ophthalmol. 2016 Jul 1;134(7):785-93. doi: 10.1001/jamaophthalmol.2016.1261.
5
Identification of Diabetic Retinopathy and Ungradable Image Rate with Ultrawide Field Imaging in a National Teleophthalmology Program.在全国远程眼科计划中使用超广角成像技术识别糖尿病视网膜病变和无法分级图像率。
Ophthalmology. 2016 Jun;123(6):1360-7. doi: 10.1016/j.ophtha.2016.01.043. Epub 2016 Mar 2.
6
Visual Impairment in White, Chinese, Black, and Hispanic Participants from the Multi-Ethnic Study of Atherosclerosis Cohort.来自动脉粥样硬化多民族队列研究的白人、华裔、黑人及西班牙裔参与者的视力损害情况
Ophthalmic Epidemiol. 2015;22(5):321-32. doi: 10.3109/09286586.2015.1066395.
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Clinical classification of age-related macular degeneration.年龄相关性黄斑变性的临床分类。
Ophthalmology. 2013 Apr;120(4):844-51. doi: 10.1016/j.ophtha.2012.10.036. Epub 2013 Jan 16.
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Age and gender variations in age-related macular degeneration prevalence in populations of European ancestry: a meta-analysis.年龄相关性黄斑变性在欧洲裔人群中的患病率的年龄和性别差异:一项荟萃分析。
Ophthalmology. 2012 Mar;119(3):571-80. doi: 10.1016/j.ophtha.2011.09.027. Epub 2011 Dec 15.
9
Prevalence of age-related macular degeneration in the US population.美国人群中年龄相关性黄斑变性的患病率。
Arch Ophthalmol. 2011 Jan;129(1):75-80. doi: 10.1001/archophthalmol.2010.318.
10
Forecasting age-related macular degeneration through 2050.预测到2050年与年龄相关的黄斑变性情况。
JAMA. 2009 May 27;301(20):2152-3. doi: 10.1001/jama.2009.729.

2019 年美国年龄相关性黄斑变性的患病率。

Prevalence of Age-Related Macular Degeneration in the US in 2019.

机构信息

NORC, University of Chicago, Chicago, Illinois.

Institute for Health Metrics and Evaluation, University of Washington, Seattle.

出版信息

JAMA Ophthalmol. 2022 Dec 1;140(12):1202-1208. doi: 10.1001/jamaophthalmol.2022.4401.

DOI:10.1001/jamaophthalmol.2022.4401
PMID:36326752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9634594/
Abstract

IMPORTANCE

Age-related macular degeneration (AMD) is a leading cause of vision loss and blindness. AMD prevalence has not been estimated for the US in over a decade and early-stage AMD prevalence estimates are scarce and inconsistently measured.

OBJECTIVE

To produce estimates of early- and late-stage AMD prevalence overall and by age, gender, race and ethnicity, county, and state.

DESIGN, SETTING, AND PARTICIPANTS: The study team conducted a bayesian meta-regression analysis of relevant data sources containing information on the prevalence of AMD among different population groups in the US.

DATA SOURCES

We included data from the American Community Survey (2019), the National Health and Nutrition Examination Survey (2005-2008), US Centers for Medicare & Medicaid Services claims for fee-for-service beneficiaries (2018), and population-based studies (2004-2016).

STUDY SELECTION

We included all relevant data from the US Centers for Disease Control and Prevention's Vision and Eye Health Surveillance System.

DATA EXTRACTION AND SYNTHESIS

The prevalence of early- and late-stage AMD was estimated and stratified when possible by factors including county, age group, gender, and race and ethnicity. Data analysis occurred from June 2021 to April 2022.

MAIN OUTCOMES OR MEASURES

The prevalence of early- (defined as retinal pigment epithelium abnormalities or the presence of drusen 125 or more microns in diameter in either eye) and late-stage (defined as choroidal neovascularization and/or geographic atrophy in either eye) manifestations of AMD.

RESULTS

This study used data from nationally representative and local population-based studies that represent the populations in which they were conducted. For 2019, we estimated that there were 18.34 million people 40 years and older (95% uncertainty interval [UI], 15.30-22.03) living with early-stage AMD, corresponding to a crude prevalence rate of 11.64% (95% UI, 9.71-13.98). We estimated there were 1.49 million people 40 years and older (95% UI, 0.97-2.15) living with late-stage AMD, corresponding to a crude prevalence rate of 0.94% (95% UI, 0.62-1.36). Prevalence rates of early- and late-stage AMD varied by demographic characteristics and geography.

CONCLUSIONS AND RELEVANCE

We estimated a higher prevalence of early-stage AMD and a similar prevalence of late-stage AMD as compared with earlier studies. State-level and county-level AMD estimates may help guide public health practice.

摘要

重要性

年龄相关性黄斑变性(AMD)是导致视力丧失和失明的主要原因。美国已经有十多年没有估计过 AMD 的患病率,而且早期 AMD 的患病率估计数据稀缺且测量方法不一致。

目的

总体以及按年龄、性别、种族和民族、县和州来估计早期和晚期 AMD 的患病率。

设计、设置和参与者:研究团队对包含美国不同人群 AMD 患病率信息的相关数据源进行了贝叶斯元回归分析。

数据来源

我们纳入了来自美国社区调查(2019 年)、国家健康和营养调查(2005-2008 年)、美国医疗保险和医疗补助服务中心(CMS)按服务收费受益人的索赔数据(2018 年)以及基于人群的研究(2004-2016 年)的数据。

研究选择

我们纳入了美国疾病控制与预防中心(CDC)视觉和眼健康监测系统的所有相关数据。

数据提取和综合

按县、年龄组、性别以及种族和民族等因素对早期和晚期 AMD 的患病率进行了估计和分层。数据分析于 2021 年 6 月至 2022 年 4 月进行。

主要结果或措施

早期(定义为视网膜色素上皮异常或双眼直径 125 微米或更大的沉积物存在)和晚期(定义为双眼脉络膜新生血管和/或地图样萎缩)AMD 表现的患病率。

结果

本研究使用了来自全国代表性和基于人群的本地研究的数据,这些研究代表了其所在人群。对于 2019 年,我们估计有 1834 万 40 岁及以上人群(95%不确定区间[UI],15.30-22.03)患有早期 AMD,粗患病率为 11.64%(95% UI,9.71-13.98)。我们估计有 149 万 40 岁及以上人群(95% UI,0.97-2.15)患有晚期 AMD,粗患病率为 0.94%(95% UI,0.62-1.36)。早期和晚期 AMD 的患病率因人口统计学特征和地理位置而异。

结论和相关性

与早期研究相比,我们估计早期 AMD 的患病率更高,晚期 AMD 的患病率相似。州和县级 AMD 估计值可能有助于指导公共卫生实践。