Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Apr;36(4):1095-1102.
doi: 10.1111/jgh.15228. Epub 2020 Sep 8.

Barriers to hepatitis C direct-acting antiviral therapy among HIV/hepatitis C virus-coinfected persons

Affiliations

Barriers to hepatitis C direct-acting antiviral therapy among HIV/hepatitis C virus-coinfected persons

Lauren P Jatt et al. J Gastroenterol Hepatol. 2021 Apr.

Abstract

Background and aim: Direct-acting antivirals (DAAs) have increased hepatitis C virus (HCV) treatment opportunities for vulnerable HIV/HCV coinfected persons. The aim of this study was to identify the frequency of and potential barriers to DAA prescription in HIV/HCV patients during the first few years of DAA availability in the United States.

Methods: The AIDS Healthcare Foundation electronic medical record system was queried to identify all HCV viremic HIV-infected patients in care at AIDS Healthcare Foundation Healthcare centers in January 2015-August 2017 and compare characteristics by receipt of a DAA prescription. Multivariate logistic regression analyses were conducted to examine factors associated with DAA prescription.

Results: Of 826 eligible patients, 355 (43%) were prescribed a DAA; among those not prescribed a DAA, 301 (64%) had well-controlled HIV (HIV RNA ≤ 200 copies per mL). In multivariate logistic regression analysis, patients with a history of substance use (odds ratio [OR], 0.51 [95% confidence interval 0.35-0.73]) or on select HIV antiretroviral regimens were less likely to be prescribed a DAA. Those who had well-controlled HIV (OR, 5.03 [3.06-8.27]), CD4 + T cell count >200 cells per mm3 (OR, 1.85 [1.04-3.30]), estimated glomerular filtration rate >60 mL/min/1.73 m2 (OR, 3.32 [1.08-10.15]), or established care prior to January 2015 (OR, 1.57 [1.08-2.29] were more likely to be prescribed a DAA.

Conclusions: In addition to lack of HIV suppression, select antiretroviral regimens, substance use, and kidney disease appeared to limit DAA prescription in the early interferon-free DAA era. Many were not prescribed DAAs despite HIV suppression. Further research is needed to determine if the observed associations persist today.

Keywords: AIDS/HIV; Access to care; Antiretroviral therapy; Direct-acting antiviral (DAA) therapy; Disparities; HCV treatment; Substance use.

PubMed Disclaimer

Conflict of interest statement

Potential conflicts of interest. K.W.C. has received research funding to the institution from Gilead, Merck Sharp & Dohme and Amgen. D.B. has received research support to the NIH AIDS Clinical Trials Group (ACTG) from Abbvie and Regeneron for an ACTG-sponsored trial. L.P.J., M.M.G, R.G., A.S.C., and C.T. have no conflicts of interest to disclose.

Figures

Figure 1.
Figure 1.. Study Eligibility
ICD: International Classification of Diseases; HIV: human immunodeficiency virus; HCV: hepatitis C virus; EMR: Electronic Medical Record; AHF: AIDS Health Foundation; and DAA: Direct Acting Antiviral.
Figure 2.
Figure 2.. Total number and type of HCV DAA prescriptions at Aids Healthcare Foundation over time (by quarter, January 2015 – August 2017)
HCV: hepatitis C virus; DAA Direct Acting Antiviral; SOF: Sofosbuvir; LDV: Ledipasvir; RBV: Ribavirin; OBV: Ombitasvir; PTV/r: Paritaprevir/ritonavir; DSV: Dasabuvir; DCV: Daclatasvir; EBR: Elbasvir; GZR: Grazoprevir; and VEL: Velpatasvir.
Figure 3.
Figure 3.. Multiple logistic regression model for the odds of a patient being prescribed a DAA by patient characteristic (n=727)
ALT: alanine aminotransferase; AA: African-American; HIV: human immunodeficiency virus; eGFR: Estimated Glomerular filtration rate; AHF: AIDS Health Foundation; INSTI: integrase strand transfer inhibitor; TDF: tenofovir disoproxil fumarate; ABC: abacavir; COBI: cobicistat; TAF: tenofovir alafenamide; PI: protease inhibitor; NNRTI: non-nucleoside reverse transcriptase inhibitor; OR: odds ratio; LCL: lower confidence limit; UCL: upper confidence limit.

Similar articles

Cited by

References

    1. WHO | HIV and hepatitis coinfections [Internet]. [cited 2020 Feb 27]. Available from: https://www.who.int/hiv/topics/hepatitis/hepatitisinfo/en/
    1. Lo Re V, Kallan MJ, Tate JP, Localio AR, Lim JK, Goetz MB, et al. Hepatic decompensation in antiretroviral-treated patients co-infected with HIV and hepatitis C virus compared with hepatitis C virus-monoinfected patients: a cohort study. Ann Intern Med. 2014. March 18;160(6):369–79. - PMC - PubMed
    1. Chen T-Y, Ding EL, Seage Iii GR, Kim AY. Meta-analysis: increased mortality associated with hepatitis C in HIV-infected persons is unrelated to HIV disease progression. Clin Infect Dis Off Publ Infect Dis Soc Am. 2009. November 15;49(10):1605–15. - PMC - PubMed
    1. Thein H-H, Yi Q, Dore GJ, Krahn MD. Natural history of hepatitis C virus infection in HIV-infected individuals and the impact of HIV in the era of highly active antiretroviral therapy: a meta-analysis. AIDS Lond Engl. 2008. October 1;22(15):1979–91. - PubMed
    1. de Lédinghen V, Barreiro P, Foucher J, Labarga P, Castéra L, Vispo ME, et al. Liver fibrosis on account of chronic hepatitis C is more severe in HIV-positive than HIV-negative patients despite antiretroviral therapy. J Viral Hepat. 2008. June;15(6):427–33. - PubMed

Substances