Evidence map›Paper›PMID 41052060›Full record

ArticlePloS one2025

Effect of sustained virologic response on liver-related mortality among individuals living with hepatitis C by treatment era: A population-based retrospective cohort study.

Aysegul Erman, Karl Everett, William W L Wong, Farinaz Forouzannia, Christina Greenaway, Naveed Janjua, Jeffrey C Kwong, Beate Sander

Abstract read
In one paragraph

Article in PloS one, 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

8 authors.

Aysegul ErmanToronto Health Economics and Technology Assessment Collaborative (THETA), Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.ORCID https://orcid.org/0000-0002-7216-064X
Karl EverettICES, Toronto, ON, Canada.
William W L WongToronto Health Economics and Technology Assessment Collaborative (THETA), Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.
Farinaz ForouzanniaSchool of Pharmacy, University of Waterloo, Kitchener, ON, Canada.ORCID https://orcid.org/0000-0003-1833-823X
Christina GreenawayDivision of Infectious Diseases, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Naveed JanjuaBritish Columbia Centre for Disease Control (BCDC), Vancouver, BC, Canada.ORCID https://orcid.org/0000-0001-5681-719X
Jeffrey C KwongICES, Toronto, ON, Canada.
Beate SanderToronto Health Economics and Technology Assessment Collaborative (THETA), Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.ORCID https://orcid.org/0000-0003-2128-9133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSustained virologic response (SVR) is a validated surrogate marker for successful hepatitis C virus (HCV) treatment. Historically, interferon-based therapies, the standard of care for decades, offered only limited efficacy with respect to SVR. The recent introduction of highly effective direct-acting antivirals (DAAs) revolutionised treatment, expanding treatment eligibility among individuals with advanced liver disease (ALD) and drug/alcohol-related substance use disorder. Given these clinical policy shifts, we assessed the real-world impact of SVR on liver-related death for these key clinical groups for whom treatment had previously been less feasible.

methodsWe conducted a population-based, cohort study of Ontario residents with HCV viremia between January 1st, 1999, and December 31st, 2018, with follow-up to May 31st, 2021 (N = 73,411) and used cause-specific hazard models to explore the association between SVR and liver-related death.

resultsSVR was associated with a significant reduction in liver-related deaths (adjusted hazard ratio [aHR]: 0.22, 95%CI: 0.20-0.24). This benefit was consistent across all levels of liver disease severity, including individuals with (aHR: 0.11, 95%CI: 0.06-0.18) and without (aHR: 0.13, 95%CI: 0.10-0.17) cirrhosis, individuals with ALD (aHR: 0.24, 95%CI: 0.22-0.27) as well as among individuals with (aHR: 0.24, 95%CI: 0.21-0.27) and without (aHR: 0.21, 95%CI: 0.18-0.24) substance use disorder.

conclusionsThis study demonstrates the real-world impact of SVR on liver-related mortality and highlights the value of early treatment and continued support for populations who are marginalised.

Indexed as

Antiviral AgentsHepatitis CHepatitis C, ChronicSustained Virologic ResponseAdultAgedFemaleHepacivirusHumansLiverMaleMiddle AgedOntarioRetrospective StudiesAntiviral Agents

Identifiers

PMID41052060
PMCPMC12500089

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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.