Chidinma Onukwugha, Franz Castro, Bonnielin K Swenor, Varshini Varadaraj
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VD was self-reported blindness/serious difficulty seeing even when wearing glasses. Survey-weighted, multivariable logistic regression models were used to examine the relationship between VD and the outcomes of interest, adjusting for confounders.</p><p><strong>Results: </strong>Of the 1,258,919 participants surveyed from 2019 to 2021, 5.1% reported having VD. Adjusted models showed that adults with VD had greater odds of having no healthcare coverage (OR = 1.14, 95% CI = 1.04-1.24), no provider (OR = 1.12; 95% CI = 1.05-1.20), a health checkup > 1 year ago (OR = 1.12; 95% CI = 1.04-1.21), and of being unable to afford care (OR = 1.62, 95% CI = 1.52-1.73).</p><p><strong>Conclusion: </strong>Adults reporting VD faced more barriers accessing healthcare. These disparities could be explained by a differential distribution of social determinants of health, lack of accessibility of medical facilities and communication barriers. Policies aimed at strengthening provisions around accessibility of healthcare facilities might result in increased access to healthcare for this population.</p>","PeriodicalId":19607,"journal":{"name":"Ophthalmic epidemiology","volume":" ","pages":"1-6"},"PeriodicalIF":1.7000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Disparities in Healthcare Access for Adults with Self-Reported Vision Difficulty - Behavioral Risk Factor Surveillance System 2019-2021.\",\"authors\":\"Chidinma Onukwugha, Franz Castro, Bonnielin K Swenor, Varshini Varadaraj\",\"doi\":\"10.1080/09286586.2024.2407905\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Identifying barriers experienced by individuals with vision difficulty (VD) in accessing healthcare is crucial to inform public health policies to provide equitable healthcare. We examined the association between VD with healthcare access measures in the United States (U.S.).</p><p><strong>Methods: </strong>We used data on 1,258,919 participants surveyed from the 2019, 2020, and 2021 cycles of the Behavioral Risk Factor Surveillance System (BRFSS), a national telephone-based survey of U.S. adults ≥ 18 years. The following outcome of healthcare access were examined: no healthcare coverage, no healthcare provider, >1 year since last checkup, inability to afford healthcare. VD was self-reported blindness/serious difficulty seeing even when wearing glasses. Survey-weighted, multivariable logistic regression models were used to examine the relationship between VD and the outcomes of interest, adjusting for confounders.</p><p><strong>Results: </strong>Of the 1,258,919 participants surveyed from 2019 to 2021, 5.1% reported having VD. Adjusted models showed that adults with VD had greater odds of having no healthcare coverage (OR = 1.14, 95% CI = 1.04-1.24), no provider (OR = 1.12; 95% CI = 1.05-1.20), a health checkup > 1 year ago (OR = 1.12; 95% CI = 1.04-1.21), and of being unable to afford care (OR = 1.62, 95% CI = 1.52-1.73).</p><p><strong>Conclusion: </strong>Adults reporting VD faced more barriers accessing healthcare. These disparities could be explained by a differential distribution of social determinants of health, lack of accessibility of medical facilities and communication barriers. 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引用次数: 0
摘要
目的:确定有视力障碍(VD)的人在获得医疗保健服务时遇到的障碍对于制定公共卫生政策以提供公平的医疗保健服务至关重要。我们研究了美国(U.S.)视力障碍与医疗保健获取措施之间的关联:我们使用了行为风险因素监测系统(BRFSS)2019 年、2020 年和 2021 年周期调查的 1,258,919 名参与者的数据,BRFSS 是一项基于电话的全国性调查,调查对象为年龄≥ 18 岁的美国成年人。该系统通过电话对年龄≥18 岁的美国成年人进行全国性调查。调查结果包括:无医疗保险、无医疗服务提供者、距上次体检时间超过 1 年、无力负担医疗费用。视力障碍是指自我报告的失明/即使戴眼镜也看不清东西的严重困难。在对混杂因素进行调整后,我们使用了调查加权多变量逻辑回归模型来检验视力障碍与相关结果之间的关系:在2019年至2021年接受调查的1,258,919名参与者中,5.1%报告患有视力障碍。调整后的模型显示,患有 VD 的成年人无医疗保险(OR = 1.14,95% CI = 1.04-1.24)、无医疗服务提供者(OR = 1.12;95% CI = 1.05-1.20)、1 年前体检(OR = 1.12;95% CI = 1.04-1.21)和负担不起医疗费用(OR = 1.62,95% CI = 1.52-1.73)的几率更高:结论:报告患有职业病的成年人在获得医疗保健服务方面面临更多障碍。这些差异可能是由于健康的社会决定因素分布不同、缺乏医疗设施和沟通障碍造成的。旨在加强医疗设施可及性的政策可能会增加这一人群获得医疗服务的机会。
Disparities in Healthcare Access for Adults with Self-Reported Vision Difficulty - Behavioral Risk Factor Surveillance System 2019-2021.
Purpose: Identifying barriers experienced by individuals with vision difficulty (VD) in accessing healthcare is crucial to inform public health policies to provide equitable healthcare. We examined the association between VD with healthcare access measures in the United States (U.S.).
Methods: We used data on 1,258,919 participants surveyed from the 2019, 2020, and 2021 cycles of the Behavioral Risk Factor Surveillance System (BRFSS), a national telephone-based survey of U.S. adults ≥ 18 years. The following outcome of healthcare access were examined: no healthcare coverage, no healthcare provider, >1 year since last checkup, inability to afford healthcare. VD was self-reported blindness/serious difficulty seeing even when wearing glasses. Survey-weighted, multivariable logistic regression models were used to examine the relationship between VD and the outcomes of interest, adjusting for confounders.
Results: Of the 1,258,919 participants surveyed from 2019 to 2021, 5.1% reported having VD. Adjusted models showed that adults with VD had greater odds of having no healthcare coverage (OR = 1.14, 95% CI = 1.04-1.24), no provider (OR = 1.12; 95% CI = 1.05-1.20), a health checkup > 1 year ago (OR = 1.12; 95% CI = 1.04-1.21), and of being unable to afford care (OR = 1.62, 95% CI = 1.52-1.73).
Conclusion: Adults reporting VD faced more barriers accessing healthcare. These disparities could be explained by a differential distribution of social determinants of health, lack of accessibility of medical facilities and communication barriers. Policies aimed at strengthening provisions around accessibility of healthcare facilities might result in increased access to healthcare for this population.
期刊介绍:
Ophthalmic Epidemiology is dedicated to the publication of original research into eye and vision health in the fields of epidemiology, public health and the prevention of blindness. Ophthalmic Epidemiology publishes editorials, original research reports, systematic reviews and meta-analysis articles, brief communications and letters to the editor on all subjects related to ophthalmic epidemiology. A broad range of topics is suitable, such as: evaluating the risk of ocular diseases, general and specific study designs, screening program implementation and evaluation, eye health care access, delivery and outcomes, therapeutic efficacy or effectiveness, disease prognosis and quality of life, cost-benefit analysis, biostatistical theory and risk factor analysis. We are looking to expand our engagement with reports of international interest, including those regarding problems affecting developing countries, although reports from all over the world potentially are suitable. Clinical case reports, small case series (not enough for a cohort analysis) articles and animal research reports are not appropriate for this journal.