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      A Novel Strategy to Increase Identification of African-Born People With Chronic Hepatitis B Virus Infection in the Chicago Metropolitan Area, 2012–2014

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          Abstract

          Introduction

          Most research on hepatitis B virus (HBV) infection in the United States is limited to Asian populations, despite an equally high prevalence among African immigrants. The purpose of this study was to determine testing and detection rates of HBV infection among African-born people residing in the Chicago metropolitan area.

          Methods

          A hepatitis education and prevention program was developed in collaboration with academic, clinical, and community partners for immigrant and refugee populations at risk for HBV infection. Community health workers implemented chain referral sampling, a novel strategy for recruiting hard-to-reach participants, targeting African-born participants. Participants were tested in both clinical and nonclinical settings. To assess infection status, blood samples were obtained for hepatitis B surface antigen (HBsAg), core antibody, and surface antibody testing. Demographic information was collected on age, sex, health insurance status, country of origin, and years residing in the United States. Participants were notified of testing results, and HBsAg-positive participants were referred for follow-up medical care.

          Results

          Of 1,000 African-born people who received education, 445 (45%) agreed to participate in HBV screening. There were 386 (87%) participants tested in clinical and 59 (13%) tested in nonclinical sites. Compared with participants who were tested in clinical settings, participants tested in nonclinical settings were older, were less likely to have health insurance, and had lived in the United States longer ( P < .005 for each). Of these, most were from the Democratic Republic of the Congo (14%), Nigeria (13%), Ghana (11%), Somalia (11%), or Ethiopia (10%). There were 35 (8%) HBsAg-positive people, 37% had evidence of past infection, and 29% were immune.

          Conclusions

          Chain referral sampling identified many at-risk African-born people with chronic HBV infection. The large proportion of HBsAg-positive people in this sample reinforces the need for health promotion programs that are culturally appropriate and community-driven.

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          Most cited references13

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          The perpetual challenge of infectious diseases.

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            A discussion of chain referral as a method of sampling hard-to-reach populations.

            Nursing research often requires inquiry into sensitive topics that involve hidden or hard- to reach populations. However, identifying and sampling these populations for research purposes is often fraught with difficulties. Barriers include society's lack of tolerance of diverse groups, social stigma, concern for issues of confidentiality, and fear of exposure because of possible threats to security. Chain referral sampling techniques are proposed to minimize bias while maintaining privacy and confidentiality. Techniques of chain referral sampling are detailed for use in researching sensitive topics and hidden populations. When carefully planned and executed, this sampling design offers transcultural nurse researchers a reasonable method for accessing and studying special populations that are particularly hard-to-reach.
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              A culturally tailored navigator program for colorectal cancer screening in a community health center: a randomized, controlled trial.

              Minority racial/ethnic groups have low colorectal cancer (CRC) screening rates. To evaluate a culturally tailored intervention to increase CRC screening, primarily using colonoscopy, among low income and non-English speaking patients. Randomized controlled trial conducted from January to October of 2007. Single, urban community health center serving a low-income, ethnically diverse population. A total of 1,223 patients 52-79 years of age overdue for CRC screening, randomized to intervention (n = 409) vs. usual care control (n = 814) groups. Intervention patients received an introductory letter with educational material followed by phone or in-person contact by a language-concordant "navigator." Navigators (n = 5) were community health workers trained to identify and address patient-reported barriers to CRC screening. Individually tailored interventions included patient education, procedure scheduling, translation and explanation of bowel preparation, and help with transportation and insurance coverage. Rates of colorectal cancer screening were assessed for intervention and usual care control patients. Over a 9-month period, intervention patients were more likely to undergo CRC screening than control patients (27% vs. 12% for any CRC screening, p < 0.001; 21% vs. 10% for colonoscopy completion, p < 0.001). The higher screening rate resulted in the identification of 10.5 polyps per 100 patients in the intervention group vs. 6.8 in the control group (p = 0.04). Patients were from one health center. Some patients may have obtained CRC screening outside our system. A culturally tailored, language-concordant navigator program designed to identify and overcome barriers to colorectal cancer screening can significantly improve colonoscopy rates for low income, ethnically and linguistically diverse patients. ClinicalTrials.gov registration number: NCT00476970.
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                Author and article information

                Journal
                Prev Chronic Dis
                Prev Chronic Dis
                PCD
                Preventing Chronic Disease
                Centers for Disease Control and Prevention
                1545-1151
                2016
                01 September 2016
                : 13
                : E118
                Affiliations
                [1]Author Affiliations: Sharon Song, Matthew Johnson, Asian Health Coalition, Chicago, Illinois; Aaron M. Harris, Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia; Gary I. Kaufman, Sinai Health System, Mount Sinai Hospital Touhy Health Center, Chicago, Illinois; David Freedman, Heartland Health Centers, Chicago, Illinois; Michael T. Quinn, Karen E. Kim, University of Chicago, Division of the Biological Sciences and Office of Community Engagement and Cancer Disparities, Chicago, Illinois.
                Author notes
                Corresponding Author: Edwin Chandrasekar, MPPM, Asian Health Coalition, 180 West Washington St, Office 1000, Chicago, IL 60602. Telephone: 312-731-8634. Email: edwin@ 123456asianhealth.org .
                Article
                16_0162
                10.5888/pcd13.160162
                5008862
                27584874
                03f85c02-5ad2-4d91-99c3-2fa910826c2b
                History
                Categories
                Original Research
                Peer Reviewed

                Health & Social care
                Health & Social care

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