Examining Racial Disparities in Colorectal Cancer Screening and the Role of Online Medical Record Use: Findings From a Cross-Sectional Study of a National Survey.
Aldenise P Ewing, Fode Tounkara, Daniel Marshall, Abhishek V Henry, Mahmoud Abdel-Rasoul, Skylar McElwain, Justice Clark, Jennifer L Hefner, Portia J Zaire, Timiya S Nolan, Willi L Tarver, Chyke A Doubeni
{"title":"Examining Racial Disparities in Colorectal Cancer Screening and the Role of Online Medical Record Use: Findings From a Cross-Sectional Study of a National Survey.","authors":"Aldenise P Ewing, Fode Tounkara, Daniel Marshall, Abhishek V Henry, Mahmoud Abdel-Rasoul, Skylar McElwain, Justice Clark, Jennifer L Hefner, Portia J Zaire, Timiya S Nolan, Willi L Tarver, Chyke A Doubeni","doi":"10.2196/53229","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Colorectal cancer (CRC) is the second leading cause of cancer-related deaths in the United States. Early detection via routine CRC screening can significantly lower risks for CRC-specific morbidity and mortality. Public health initiatives between 2000 and 2015 nearly doubled CRC screening rates for some US adults. However, screening rates remain lowest for adults aged 45-49 years (20%), patients of safety net health care facilities (42%), adults without insurance (44%), and other subgroups compared with national averages (72%). Given the evolving landscape of digital health care and trends in web-based health information-seeking behaviors, leveraging online medical record (OMR) systems may be an underutilized resource to promote CRC screening utilization. Recognizing trends in OMR usage and patient demographics may enhance digital inclusion-a key social determinant of health-and support equitable web-based interventions aimed at boosting CRC screening across diverse populations.</p><p><strong>Objective: </strong>This study examined the association of accessing an OMR with CRC screening utilization and corresponding sociodemographic characteristics of US adults.</p><p><strong>Methods: </strong>In 2023, we conducted a secondary data analysis using a pooled, weighted sample from Health Information National Trends Survey (HINTS) 5 cycles, 2, 3, and 4 (2018-2020), a nationally representative survey assessing how US adults access and use health-related information. We analyzed the association between sociodemographic characteristics, medical conditions, OMR access, and CRC screening behaviors via logistic regression.</p><p><strong>Results: </strong>The sample included adults aged 45-75 years (N=5143). The mean age was 59 (SD 8) years for those who reported CRC screening and 52 (SD 6) years for those never screened. Nearly 70% (4029/5143) of participants reported CRC screening and 52% (2707/5143) reported OMR access in the past year. Adjusted odds of CRC screening were higher among non-Hispanic African American or Black adults than among non-Hispanic White adults (odds ratio [OR] 1.76, 95% CI 1.22-2.53), adults who accessed an OMR (OR 1.89, 95% CI 1.45-2.46), older individuals (OR 1.18, 95% CI 1.16-1.21), the insured (OR 3.69, 95% CI 2.34-5.82), and those with a professional or graduate degree versus those with a high school diploma or less (OR 2.65, 95% CI 1.28-5.47). Individuals aged 65-75 years were significantly more likely (P<.001) to be screened (1687/1831, 91%) than those aged 45-49 years (190/610, 29%).</p><p><strong>Conclusions: </strong>Promoting OMR access, especially among the most disadvantaged Americans, may assist in reaching national screening goals. Emphasis should be placed on the mutability of OMR use compared with most other statistically significant associations with CRC screening behaviors. OMR access provides an intervenable means of promoting CRC education and screening, especially among those facing structural barriers to cancer diagnoses and care. Future research should focus on tailored and accessible interventions that expand OMR access, particularly for younger populations.</p>","PeriodicalId":45538,"journal":{"name":"JMIR Cancer","volume":"10 ","pages":"e53229"},"PeriodicalIF":3.3000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11634048/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JMIR Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2196/53229","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Colorectal cancer (CRC) is the second leading cause of cancer-related deaths in the United States. Early detection via routine CRC screening can significantly lower risks for CRC-specific morbidity and mortality. Public health initiatives between 2000 and 2015 nearly doubled CRC screening rates for some US adults. However, screening rates remain lowest for adults aged 45-49 years (20%), patients of safety net health care facilities (42%), adults without insurance (44%), and other subgroups compared with national averages (72%). Given the evolving landscape of digital health care and trends in web-based health information-seeking behaviors, leveraging online medical record (OMR) systems may be an underutilized resource to promote CRC screening utilization. Recognizing trends in OMR usage and patient demographics may enhance digital inclusion-a key social determinant of health-and support equitable web-based interventions aimed at boosting CRC screening across diverse populations.
Objective: This study examined the association of accessing an OMR with CRC screening utilization and corresponding sociodemographic characteristics of US adults.
Methods: In 2023, we conducted a secondary data analysis using a pooled, weighted sample from Health Information National Trends Survey (HINTS) 5 cycles, 2, 3, and 4 (2018-2020), a nationally representative survey assessing how US adults access and use health-related information. We analyzed the association between sociodemographic characteristics, medical conditions, OMR access, and CRC screening behaviors via logistic regression.
Results: The sample included adults aged 45-75 years (N=5143). The mean age was 59 (SD 8) years for those who reported CRC screening and 52 (SD 6) years for those never screened. Nearly 70% (4029/5143) of participants reported CRC screening and 52% (2707/5143) reported OMR access in the past year. Adjusted odds of CRC screening were higher among non-Hispanic African American or Black adults than among non-Hispanic White adults (odds ratio [OR] 1.76, 95% CI 1.22-2.53), adults who accessed an OMR (OR 1.89, 95% CI 1.45-2.46), older individuals (OR 1.18, 95% CI 1.16-1.21), the insured (OR 3.69, 95% CI 2.34-5.82), and those with a professional or graduate degree versus those with a high school diploma or less (OR 2.65, 95% CI 1.28-5.47). Individuals aged 65-75 years were significantly more likely (P<.001) to be screened (1687/1831, 91%) than those aged 45-49 years (190/610, 29%).
Conclusions: Promoting OMR access, especially among the most disadvantaged Americans, may assist in reaching national screening goals. Emphasis should be placed on the mutability of OMR use compared with most other statistically significant associations with CRC screening behaviors. OMR access provides an intervenable means of promoting CRC education and screening, especially among those facing structural barriers to cancer diagnoses and care. Future research should focus on tailored and accessible interventions that expand OMR access, particularly for younger populations.
背景:结直肠癌(CRC)是美国癌症相关死亡的第二大原因。通过常规CRC筛查早期发现可显著降低CRC特异性发病率和死亡率的风险。2000年至2015年间的公共卫生倡议使一些美国成年人的CRC筛查率几乎翻了一番。然而,与全国平均水平(72%)相比,45-49岁的成年人(20%)、安全网卫生保健设施的患者(42%)、没有保险的成年人(44%)和其他亚组的筛查率仍然最低。鉴于数字医疗保健的不断发展和基于网络的健康信息寻求行为的趋势,利用在线医疗记录(OMR)系统可能是一种未充分利用的资源,以促进结直肠癌筛查的利用。认识到OMR使用趋势和患者人口统计数据可以增强数字包容(健康的关键社会决定因素),并支持公平的基于网络的干预措施,旨在促进不同人群的结直肠癌筛查。目的:本研究考察了美国成年人获得OMR与CRC筛查利用和相应的社会人口学特征的关系。方法:在2023年,我们使用来自健康信息国家趋势调查(HINTS) 5个周期、2、3和4个周期(2018-2020)的合并加权样本进行了二次数据分析,这是一项具有全国代表性的调查,评估了美国成年人如何获取和使用健康相关信息。我们通过逻辑回归分析了社会人口学特征、医疗条件、OMR获取和CRC筛查行为之间的关系。结果:样本包括45-75岁的成年人(N=5143)。报告CRC筛查者的平均年龄为59岁(SD 8),未筛查者的平均年龄为52岁(SD 6)。在过去一年中,近70%(4029/5143)的参与者报告了CRC筛查,52%(2707/5143)的参与者报告了OMR获取。非西班牙裔非裔美国人或黑人成年人CRC筛查的调整后几率高于非西班牙裔白人成年人(比值比[or] 1.76, 95% CI 1.22-2.53)、获得OMR的成年人(比值比[or] 1.89, 95% CI 1.45-2.46)、老年人(比值比[or] 1.18, 95% CI 1.16-1.21)、被保险人(比值比[or] 3.69, 95% CI 2.34-5.82)、具有专业或研究生学位的人高于具有高中或以下文凭的人(比值比]2.65,95% CI 1.28-5.47)。结论:促进OMR的获取,特别是在最弱势的美国人中,可能有助于实现国家筛查目标。与大多数其他与结直肠癌筛查行为有统计学意义的关联相比,重点应放在使用OMR的易变性上。获得OMR提供了一种可干预的手段,促进结直肠癌的教育和筛查,特别是在那些面临癌症诊断和护理结构性障碍的人群中。未来的研究应侧重于量身定制和可获得的干预措施,以扩大OMR的可及性,特别是针对年轻人群。