Using Population Data to Reduce Disparities in Colorectal Cancer Screening, Arkansas, 2006

dc.contributor.authorGreene, Paul
dc.contributor.authorMehta, Paulette
dc.contributor.authorYeary, Karen Hye-cheon Kim
dc.contributor.authorBursac, Zoran
dc.contributor.authorZhang, Jianjun
dc.contributor.authorGoldsmith, Geoff
dc.contributor.authorHenry-Tillman, Ronda
dc.contributor.departmentSurgery, School of Medicine
dc.date.accessioned2025-06-25T11:54:39Z
dc.date.available2025-06-25T11:54:39Z
dc.date.issued2012
dc.description.abstractIntroduction: Colorectal cancer is a common disease, and incidence and death rates are higher in medically underserved populations. The colorectal cancer death rate in Arkansas exceeds the national rate. The objective of this study was to examine population characteristics relevant to the design and implementation of a state-sponsored colorectal cancer screening program that is responsive to medically underserved populations. Methods: Trained interviewers in 2006 conducted a random-digit-dialed telephone survey comprising items selected from the Health Information National Trends Survey to characterize demographic factors, health care variables, and colorectal screening history in a sample (n = 2,021) representative of the Arkansas population. Univariate and multivariate analyses identified associations among population characteristics and screening status. Results: Participants who were aged 50 to 64, who did not have health insurance, or who had an annual household income of $15,000 or less were significantly less likely than their counterparts to be in compliance with screening guidelines. Those who reported having a health care provider, having 5 or more health care visits during the past year, and receiving physician advice for colorectal screening were more likely to be in compliance with screening guidelines. Although a larger percentage of white participants were in compliance with screening guidelines, blacks had higher screening rates than whites when we controlled for screening advice. Conclusion: Survey results informed efforts to decrease disparities in colorectal cancer screening in Arkansas. Efforts should focus on reimbursing providers and patients for screening costs, encouraging the use of physicians as a point of entry to screening programs, and promoting a balanced approach (ie, multiple options) to screening recommendations. Our methods established a model for developing screening programs for medically underserved populations.
dc.eprint.versionFinal published version
dc.identifier.citationGreene P, Mehta P, Yeary KH, et al. Using population data to reduce disparities in colorectal cancer screening, Arkansas, 2006. Prev Chronic Dis. 2012;9:E138. doi:10.5888/pcd9.110256
dc.identifier.urihttps://hdl.handle.net/1805/48977
dc.language.isoen_US
dc.publisherCDC
dc.relation.isversionof10.5888/pcd9.110256
dc.relation.journalPreventing Chronic Disease
dc.rightsCC0 1.0 Universalen
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/
dc.sourcePMC
dc.subjectColorectal neoplasms
dc.subjectSigmoidoscopy
dc.subjectColonoscopy
dc.subjectEarly detection of cancer
dc.titleUsing Population Data to Reduce Disparities in Colorectal Cancer Screening, Arkansas, 2006
dc.typeArticle
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