Effect of race and HIV co-infection upon treatment prescription for hepatitis C virus

Summary Background Treatment rates for hepatitis C virus (HCV) have not been compared directly between HCV mono-infected and HCV–HIV co-infected patients in academic center settings. Methods We prospectively enrolled consecutive mono-infected and co-infected subjects at three academic centers in the...

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Published inInternational journal of infectious diseases Vol. 13; no. 4; pp. 449 - 455
Main Authors Butt, Adeel A, Tsevat, Joel, Leonard, Anthony C, Shaikh, Obaid S, McMahon, Deborah, Khan, Uzma A, Dorey-Stein, Zachariah, Re, Vincent Lo
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ltd 01.07.2009
Elsevier
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Summary:Summary Background Treatment rates for hepatitis C virus (HCV) have not been compared directly between HCV mono-infected and HCV–HIV co-infected patients in academic center settings. Methods We prospectively enrolled consecutive mono-infected and co-infected subjects at three academic centers in the USA. Clinical and laboratory data were gathered through interviews and medical records. Logistic regression analysis was used to determine the factors associated with treatment prescription for HCV. Results The 241 HCV mono-infected and 158 HCV–HIV co-infected subjects were similar in age, but there were more blacks (58.9% vs. 30.7%, p < 0.001) and males (81.6% vs. 58.5%, p < 0.001) in the latter group. The co-infected subjects were less likely to have a liver biopsy (43.7% vs. 71.4%, p < 0.001) or ever receive treatment for HCV (32.3% vs. 62.2%, p < 0.001). In bivariate analysis, subjects not prescribed treatment for HCV were more likely to be black, have HIV co-infection, and have ongoing alcohol abuse. In multivariate analysis, black race (odds ratio (OR) 0.44, 95% confidence interval (CI) 0.28–0.70) and HIV co-infection (OR 0.33, 95% CI 0.21–0.53) were independently associated with non-prescription of treatment. Conclusions Black race and HIV co-infection are associated with a lower likelihood of treatment for HCV. Addressing comorbidities in these populations may help to reduce such treatment disparities.
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ISSN:1201-9712
1878-3511
1878-3511
DOI:10.1016/j.ijid.2008.06.041