Evidence map›Paper›PMID 40893421›Full record

ArticleOpen forum infectious diseases2025

Direct-Acting Antiviral Initiation Among People With Hepatitis C Virus (HCV) and HIV on Antiretroviral Therapy in the United States and Canada: Factors Driving the HCV Treatment Gap.

Raynell Lang, Elizabeth Humes, Asya Lyass, Leila H Borowsky, Brenna Hogan, Arthur Kim, Michael LaValley, Michael J Silverberg, H Nina Kim, Sonia Napravnik and 15 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Raynell LangDepartment of Medicine, University of Calgary, Alberta, Calgary, Canada.
Elizabeth HumesDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.
Asya LyassDepartment of Mathematics and Statistics, Boston University, Boston, Massachusetts, USA.
Leila H BorowskyDivisions of General Internal Medicine and Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Brenna HoganDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.
Arthur KimDivisions of General Internal Medicine and Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Michael LaValleyDepartment of Biostatistics, Boston University, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-8488-5170
Michael J SilverbergDivision of Research, Kaiser Permanente Northern California, Pleasanton, California, USA.ORCID https://orcid.org/0000-0001-9322-1395
H Nina KimDepartment of Medicine, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0001-6710-9666
Sonia NapravnikDepartments of Medicine and Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.ORCID https://orcid.org/0000-0002-9032-3713
Richard D MooreDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-8250-5069
Michael A HorbergKaiser Permanente Mid-Atlantic Permanente Research Institute, Kaiser Permanente Mid-Atlantic States, Washington, DC, USA.ORCID https://orcid.org/0000-0002-6971-7646
Frank J PalellaDivision of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0002-2277-6841
Greg D KirkDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.
Edward CachayDepartment of Medicine, University of California, San Diego, California, USA.ORCID https://orcid.org/0000-0002-2452-7558
George A YendewaDepartment of Medicine, Case Western Reserve University, Cleveland, Ohio, USA.ORCID https://orcid.org/0000-0002-8474-1812
Seble KassayeDepartment of Medicine, Georgetown University, Washington, DC, USA.
Kathleen McGinnisVeterans Affairs Connecticut Healthcare System, US Department of Veteran Affairs, West Haven, Connecticut, USA.
Sally B CoburnDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-6423-1137
Timothy R SterlingDepartment of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.ORCID https://orcid.org/0000-0002-4822-6979
Marina B KleinDepartment of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-3063-8430
Mari M KitahataDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Catherine LeskoDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-1717-2592
Virginia A TriantDivisions of General Internal Medicine and Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
Keri N AlthoffDepartment of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.

Funding

Enhancing cardiovascular risk estimation in individuals aging with HIV/HCV co-infectionR01AG062393 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI TRIANT, VIRGINIA ATHENA · 2019 to 2023
$4.5M
NIA NIH HHS R01 AG062393
6 · The paper itself

Abstract

Background: People with human immunodeficiency virus (HIV; PWH) are at increased risk of hepatitis C virus (HCV) coinfection and experiencing negative clinical outcomes. We evaluated direct-acting antiviral (DAA) initiation among PWH with HCV to identify factors associated with initiation. Methods: US and Canadian PWH ≥18 years with a detectable HCV RNA in the North American AIDS Cohort Collaboration on Research and Design were followed up from the latest of first detectable HCV viremia, antiretroviral therapy initiation, enrollment date, or 1 January 2014 until the first of DAA prescription, clearance of HCV viremia, loss to follow-up, death, or 31 December 2021. We estimated the cumulative incidence of DAA initiation accounting for the competing risks of death and HCV viral clearance. Cox proportional hazard models estimated crude and adjusted hazard ratios and 95% confidence intervals to identify factors associated with DAA initiation. Results: Among 6300 PWH with a detectable HCV RNA, 3672 (58%) initiated DAA. Accounting for the competing risks of death and HCV clearance, by 8 years after study entry 6% of eligible PWH had not initiated DAA. A lower rate of DAA initiation was identified among non-Hispanic black and Hispanic PWH compared with non-Hispanic white PWH. DAA initiation was lower among PWH reporting injection drug use as their HIV acquisition risk, at-risk alcohol use, smoking, detectable HIV viremia, or a history of AIDS. A higher Fibrosis-4 score was associated with increased DAA initiation. Conclusions: The DAA initiation gap among PWH engaged in care and eligible for treatment has greatly narrowed over time. Targeted approaches to increase equity in DAA initiation are needed to eliminate HCV among PWH.

Indexed as

direct-acting antiviralsdisparitiesHCV coinfectionpeople with HIVtreatment gap

Identifiers

PMID40893421
PMCPMC12391754

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.