Direct-Acting Antiviral Hepatitis C Treatment Cascade and Barriers to Treatment Initiation Among US Men and Women With and Without HIV

Author:

Haley Danielle F1ORCID,Edmonds Andrew2,Ramirez Catalina3,French Audrey L4,Tien Phyllis56,Thio Chloe L7,Witt Mallory D8,Seaberg Eric C9,Plankey Michael W10,Cohen Mardge H11,Adimora Adaora A23

Affiliation:

1. Department of Community Health Sciences, Boston University School of Public Health, Boston, Massachusetts, USA

2. Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA

3. Divison of Infectious Diseases, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA

4. Division of Infectious Diseases, Stroger (Cook County) Hospital, Chicago, Illinois, USA

5. Department of Medicine, University of California San Francisco, San Francisco, California, USA

6. Department of Veterans Affairs Medical Center, San Francisco, California, USA

7. Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA

8. Department of Medicine, Lundquist Institute, Harbor-University of California Los Angeles, Torrance, California, USA

9. Department of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA

10. Department of Medicine, Georgetown University Medical Center, Washington, District of Columbia, USA

11. Department of Medicine, Stroger (Cook County) Hospital, Chicago, Illinois, USA

Abstract

Abstract Background People with HIV are disproportionately coinfected with hepatitis C virus (HCV) and experience accelerated liver-related mortality. Direct-acting antivirals (DAAs) yield high sustained virologic response (SVR) rates, but uptake is suboptimal. This study characterizes the DAA-era HCV treatment cascade and barriers among US men and women with or at risk for HIV. Methods We constructed HCV treatment cascades using the Women’s Interagency HIV Study (women, 6 visits, 2015–2018, n = 2447) and Multicenter AIDS Cohort Study (men, 1 visit, 2015–2018, n = 2221). Cascades included treatment-eligible individuals (ie, HCV RNA-positive or reported DAAs). Surveys captured self-reported clinical (eg, CD4), patient (eg, missed visits), system (eg, appointment access), and financial/insurance barriers. Results Of 323/92 (women/men) treatment eligible, most had HIV (77%/70%); 69%/63% were black. HIV-positive women were more likely to attain cascade outcomes than HIV-negative women (39% vs 23% initiated, 21% vs 12% SVR); similar discrepancies were noted for men. Black men and substance users were treated less often. Women initiating treatment (vs not) reported fewer patient barriers (14%/33%). Among men not treated, clinical barriers were prevalent (53%). Conclusions HIV care may facilitate HCV treatment linkage and barrier navigation. HIV-negative individuals, black men, and substance users may need additional support. Clinical trials registration NCT00000797 (Women’s Interagency HIV Study); NCT00046280 (Multicenter AIDS Cohort Study).

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Human Genome Research Institute

National Institute on Aging

National Institute of Dental and Craniofacial Research

National Institute of Allergy and Infectious Diseases

National Institute of Neurological Disorders and Stroke

National Institute of Mental Health

National Institute on Drug Abuse

National Institute of Nursing Research

National Cancer Institute

National Institute on Alcohol Abuse and Alcoholism

National Institute on Deafness and Other Communication Disorders

National Institute of Diabetes and Digestive and Kidney Diseases

NIH

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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