Background: The disproportionate mortality burden racial and ethnic groups endure compared to their non-Hispanic white (NHW) counterparts is a widely known public health issue in the United States.
Methods: We examined disparities in premature mortality through a measure of years of potential life lost (YPLL) among racial and ethnic groups after accounting for individual and place-based risk factors. Data were nearly 400,000 geocoded death records from Washington state mortality records from 2011 to 2018.
This study examines the association between educational attainment, relative to that of an intimate partner, and all-cause mortality for men and women in different-sex relationships. Research suggests some health benefits for partnered adults that arise from economic benefits and improved access to health-promoting tools. One way these benefits could be gained is through the pairing of the highly educated.
View Article and Find Full Text PDFObjectives: To characterize the leading causes of death for the urban American Indian/Alaska Native (AI/AN) population and compare with urban White and rural AI/AN populations.
Methods: We linked Indian Health Service patient registration records with the National Death Index to reduce racial misclassification in death certificate data. We calculated age-adjusted urban AI/AN death rates for the period 1999-2009 and compared those with corresponding urban White and rural AI/AN death rates.
Previous studies have shown an association between cervical cancer screening and racial/ethnic minority status, no usual source of care, and lower socioeconomic status. This study describes the demographics and health beliefs of women who report never being screened for cervical cancer by area of residence. Data from the 2010 Behavioral Risk Factor Surveillance System were used to study women aged 21-65 years who reported never being screened for cervical cancer.
View Article and Find Full Text PDFJ Public Health Manag Pract
May 2014
Context: Avon Foundation for Women grantees provide breast cancer services through patient navigation (PN) in an effort to alleviate barriers to care among underserved women.
Objective: To gain a better understanding of how PN programs function, this study explores variations in the use of navigators, types of services offered, description of clients they serve, tracking of treatment completion, and evaluation mechanisms.
Participants: Fifty-six Avon PN programs funded since 2008 throughout the United States were contacted.
J Community Health
February 2013
Colorectal cancer (CRC) screening is underused in the United States, and non-adherence with screening recommendations is high in some populations. This study describes the characteristics of people who have never been screened for CRC. In addition, we use the health belief model to examine the constructs associated with screening behavior.
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