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2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status

BACKGROUND: The impact of alcohol use and HIV infection on receipt of direct-acting antiviral (DAA) therapy and subsequent cure of chronic hepatitis C virus (HCV) is unknown. METHODS: Using the Veterans Health Administration (VA) Birth Cohort (>4.5 million patients born 1945–1965), we performed a...

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Autores principales: Cartwright, Emily J, Rentsch, Christopher T, Esserman, Denise A, Tate, Janet P, Fiellin, David A, Lo Re, Vincent, Justice, Amy C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253010/
http://dx.doi.org/10.1093/ofid/ofy210.1877
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author Cartwright, Emily J
Rentsch, Christopher T
Esserman, Denise A
Tate, Janet P
Fiellin, David A
Lo Re, Vincent
Justice, Amy C
author_facet Cartwright, Emily J
Rentsch, Christopher T
Esserman, Denise A
Tate, Janet P
Fiellin, David A
Lo Re, Vincent
Justice, Amy C
author_sort Cartwright, Emily J
collection PubMed
description BACKGROUND: The impact of alcohol use and HIV infection on receipt of direct-acting antiviral (DAA) therapy and subsequent cure of chronic hepatitis C virus (HCV) is unknown. METHODS: Using the Veterans Health Administration (VA) Birth Cohort (>4.5 million patients born 1945–1965), we performed a cohort study among HCV RNA+ patients with at least one outpatient visit between 1 January 2014 and 31 May 2017; laboratory values were assessed through 30 November 2017. Alcohol use (abstinent, lower risk drinking, hazardous/binge drinking, diagnosis of alcohol use disorder [AUD]) was assessed in the year prior to the initial outpatient visit based on Alcohol Use Disorders Identification Test-Consumption questionnaire scores and validated ICD AUD codes. We defined DAA receipt based on filled prescriptions and achievement of HCV cure as sustained virologic response ≥12 weeks after treatment (SVR12). We calculated frequency of DAA receipt and SVR12 by alcohol use category and HIV status. We estimated associations between alcohol use and SVR12 by HIV status using logistic regression. RESULTS: Among 134,491 HCV RNA+ patients with known alcohol use status, 3,670 (3%) were HIV+. More HIV+ patients were dispensed DAA therapy than uninfected persons (53.6% vs. 49.5%; P < 0.0001). Abstinent and lower risk drinkers were more likely to receive DAAs than hazardous/binge drinkers or those with an AUD (52.9%, 51.5%, 47.1%, 44.6%, respectively; P < 0.0001, Figure 1). While high SVR12 rates were observed across all alcohol use categories (range, 88.8–92.4% HIV+; 90.1–93.2% uninfected), those with AUD experienced modestly lower rates of SVR12 compared with abstinent individuals (89.1% vs. 92.1% HIV+; 90.1% vs. 91.6% HIV−, Figure 2). After adjusting for age, FIB-4, BMI, and hepatic decompensation, HIV− patients with an AUD were significantly less likely to achieve SVR12 compared with abstinent patients (OR, 0.88; 95% CI 0.81–0.94, Figure 3). [Image: see text] [Image: see text] [Image: see text] CONCLUSION: HIV+ patients and abstinent or lower risk drinkers were more likely to receive DAAs compared with uninfected patients and hazardous/binge drinkers or those with an AUD. High SVR12 rates were observed across all alcohol categories. These findings indicate a potential role for alcohol interventions along with HCV care and treatment. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62530102018-11-28 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status Cartwright, Emily J Rentsch, Christopher T Esserman, Denise A Tate, Janet P Fiellin, David A Lo Re, Vincent Justice, Amy C Open Forum Infect Dis Abstracts BACKGROUND: The impact of alcohol use and HIV infection on receipt of direct-acting antiviral (DAA) therapy and subsequent cure of chronic hepatitis C virus (HCV) is unknown. METHODS: Using the Veterans Health Administration (VA) Birth Cohort (>4.5 million patients born 1945–1965), we performed a cohort study among HCV RNA+ patients with at least one outpatient visit between 1 January 2014 and 31 May 2017; laboratory values were assessed through 30 November 2017. Alcohol use (abstinent, lower risk drinking, hazardous/binge drinking, diagnosis of alcohol use disorder [AUD]) was assessed in the year prior to the initial outpatient visit based on Alcohol Use Disorders Identification Test-Consumption questionnaire scores and validated ICD AUD codes. We defined DAA receipt based on filled prescriptions and achievement of HCV cure as sustained virologic response ≥12 weeks after treatment (SVR12). We calculated frequency of DAA receipt and SVR12 by alcohol use category and HIV status. We estimated associations between alcohol use and SVR12 by HIV status using logistic regression. RESULTS: Among 134,491 HCV RNA+ patients with known alcohol use status, 3,670 (3%) were HIV+. More HIV+ patients were dispensed DAA therapy than uninfected persons (53.6% vs. 49.5%; P < 0.0001). Abstinent and lower risk drinkers were more likely to receive DAAs than hazardous/binge drinkers or those with an AUD (52.9%, 51.5%, 47.1%, 44.6%, respectively; P < 0.0001, Figure 1). While high SVR12 rates were observed across all alcohol use categories (range, 88.8–92.4% HIV+; 90.1–93.2% uninfected), those with AUD experienced modestly lower rates of SVR12 compared with abstinent individuals (89.1% vs. 92.1% HIV+; 90.1% vs. 91.6% HIV−, Figure 2). After adjusting for age, FIB-4, BMI, and hepatic decompensation, HIV− patients with an AUD were significantly less likely to achieve SVR12 compared with abstinent patients (OR, 0.88; 95% CI 0.81–0.94, Figure 3). [Image: see text] [Image: see text] [Image: see text] CONCLUSION: HIV+ patients and abstinent or lower risk drinkers were more likely to receive DAAs compared with uninfected patients and hazardous/binge drinkers or those with an AUD. High SVR12 rates were observed across all alcohol categories. These findings indicate a potential role for alcohol interventions along with HCV care and treatment. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253010/ http://dx.doi.org/10.1093/ofid/ofy210.1877 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Cartwright, Emily J
Rentsch, Christopher T
Esserman, Denise A
Tate, Janet P
Fiellin, David A
Lo Re, Vincent
Justice, Amy C
2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title_full 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title_fullStr 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title_full_unstemmed 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title_short 2224. Receipt and Virologic Outcomes of HCV Direct-Acting Antivirals by Alcohol Use and HIV Status
title_sort 2224. receipt and virologic outcomes of hcv direct-acting antivirals by alcohol use and hiv status
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253010/
http://dx.doi.org/10.1093/ofid/ofy210.1877
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