Evidence map›Paper›PMID 39535186›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Clinical- and Cost-Effectiveness of Liver Disease Staging in Hepatitis C Virus Infection: A Microsimulation Study.

Rachel L Epstein, Sarah Munroe, Lynn E Taylor, Patrick R Duryea, Benjamin Buzzee, Tannishtha Pramanick, Jordan J Feld, Dimitri Baptiste, Matthew Carroll, Laurent Castera and 4 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

14 authors.

Rachel L EpsteinDepartment of Medicine, Section of Infectious Diseases, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0003-2831-8865
Sarah MunroeSection of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.ORCID 0009-0009-5591-1454
Lynn E TaylorDepartment of Pharmacy Practice and Clinical Research, University of Rhode Island, Kingston, Rhode Island, USA.
Patrick R DuryeaDepartment of Pharmacy Practice and Clinical Research, University of Rhode Island, Kingston, Rhode Island, USA.
Benjamin BuzzeeSection of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.
Tannishtha PramanickSection of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.
Jordan J FeldToronto Centre for Liver Disease, University Health Network, University of Toronto, Toronto, Ontario, Canada.
Dimitri BaptisteSection of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.
Matthew CarrollSection of Infectious Diseases, Boston Medical Center, Boston, Massachusetts, USA.
Laurent CasteraDepartment of Hepatology, Beaujon Hospital, Assistance Publique-Hopitaux de Paris, Université Paris Cité, Clichy, France.
Richard K SterlingDepartment of Internal Medicine, Division of Gastroenterology, Hepatology and Nutrition, Virginia Commonwealth University, Richmond, Virginia, USA.
Aurielle ThomasDepartment of Pharmacy Practice and Clinical Research, University of Rhode Island, Kingston, Rhode Island, USA.
Philip A ChanRhode Island Department of Health, Providence, Rhode Island, USA.
Benjamin P LinasDepartment of Medicine, Section of Infectious Diseases, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.

Funding

Translational ScienceP30AI042853 · NIAID · MIRIAM HOSPITAL · PI CURT G BECKWITH, DEBBIE M. CHENG · 1998 to 2026
$51.7M
Utilization of health services after engagement with opioid use disorder (OUD) treatment provider by individuals with and without post-traumatic stress disorderP30DA040500 · NIDA · WEILL MEDICAL COLL OF CORNELL UNIV · PI Yuhua Bao · 2015 to 2026
$20.7M
Perinatal care as a venue to reduce opioid overdoses and hepatitis C virus incidence (PreVenT OD HCV)K01DA052821 · NIDA · BOSTON MEDICAL CENTER · PI Rachel Lee Epstein · 2022 to 2026
$959k
Boston UniversityCatherine and Patrick Weldon Donaghue Foundation Greater Value Portfolio GrantCharles A. King Trust Postdoctoral Research FellowshipChobanian & Avedisian School of MedicineDepartment of Medicine Career InvestmentNIAID NIH HHS P30 AI042853NIDA NIH HHSNIDA NIH HHS K01 DA052821NIDA NIH HHS P30 DA040500NIH HHS K01DA052821Providence/Boston Center for AIDS Research P30AI042853
6 · The paper itself

Abstract

backgroundLiver disease assessment is a key aspect of chronic hepatitis C virus (HCV) infection pre-treatment evaluation but guidelines differ on the optimal testing modality given trade-offs in availability and accuracy. We compared clinical outcomes and cost-effectiveness of common fibrosis staging strategies.

methodsWe simulated adults with chronic HCV receiving care at US health centers through a lifetime microsimulation across five strategies: (1) no staging or treatment (comparator), (2) indirect serum biomarker testing (Fibrosis-4 index [FIB-4]) only, (3) transient elastography (TE) only, (4) staged approach: FIB-4 for all, TE only for intermediate FIB-4 scores (1.45-3.25), and (5) both tests for all. Outcomes included infections cured, cirrhosis cases, liver-related deaths, costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs). We used literature-informed loss to follow-up (LTFU) rates and 2021 Medicaid perspective and costs.

resultsFIB-4 alone generated the best clinical outcomes: 87.7% cured, 8.7% developed cirrhosis, and 4.6% had liver-related deaths. TE strategies cured 58.5%-76.6%, 16.8%-29.4% developed cirrhosis, and 11.6%-22.6% had liver-related deaths. All TE strategies yielded worse clinical outcomes at higher costs per QALY than FIB-4 only, which had an ICER of $12 869 per QALY gained compared with no staging or treatment. LTFU drove these findings: TE strategies were only cost-effective with no LTFU. In a point-of-care HCV test-and-treat scenario, treatment without any staging was most clinically and cost-effective.

conclusionsFIB-4 staging alone resulted in optimal clinical outcomes and was cost-effective. Treatment for chronic HCV should not be delayed while awaiting fibrosis staging with TE.

Indexed as

Cost-Benefit AnalysisHepatitis C, ChronicLiver CirrhosisAdultBiomarkersComputer SimulationElasticity Imaging TechniquesFemaleHepacivirusHumansMaleMiddle AgedQuality-Adjusted Life YearsSeverity of Illness IndexUnited StatesBiomarkersAPRIelastographyFIB-4guidelineshepatitis C

Identifiers

PMID39535186
PMCPMC11848265

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.