Evidence map›Paper›PMID 30797050›Full record

ArticleJournal of hepatology2019

Deriving the optimal limit of detection for an HCV point-of-care test for viraemic infection: Analysis of a global dataset.

J Morgan Freiman, Jianing Wang, Philippa J Easterbrook, C Robert Horsburgh, Francesco Marinucci, Laura F White, George Kamkamidze, Mel Krajden, Anne Loarec, Richard Njouom and 7 more

Abstract read
In one paragraph

Article in Journal of hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Five Years of HCV Dried Blood Spot Testing in At-Risk Populations and the Impact of Reduced Sensitivity on Missed Diagnoses.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  2. Article
  3. Article
  4. Performance Evaluation of the Xpert® HCV Test on Fingerstick Blood in a Prospective Observational Clinical Study at CLIA-Waived Sites in the United States.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Observational
  5. Article
  6. Performance of a novel DiaRD-HCV RNA RTqPCR kit for quantification of HCV RNA in clinical samples.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
  7. Article
  8. Article
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  11. Review
  12. Article
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  15. Article
  16. Optimizing diagnostic algorithms to advance Hepatitis C elimination in Italy: A cost effectiveness evaluation.Liver international : official journal of the International Association for the Study of the Liver · 2022
    Article
  17. Diagnostic Performance and Usability of the GenedriveDiagnostics (Basel, Switzerland) · 2021
    Article
  18. Article
  19. Article
  20. In-field evaluation of Xpert® HCV viral load Fingerstick assay in people who inject drugs in Tanzania.Liver international : official journal of the International Association for the Study of the Liver · 2020
    Article
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

17 authors.

J Morgan FreimanBoston Medical Center, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA. Electronic address: j.morgan.freiman@bmc.org.
Jianing WangBoston Medical Center, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA.
Philippa J EasterbrookGlobal Hepatitis Programme, World Health Organization, Geneva, Switzerland.
C Robert HorsburghDepartment of Biostatistics, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA; Department of Epidemiology, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA; Global Health, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA.
Francesco MarinucciFIND, Geneva, Switzerland.
Laura F WhiteDepartment of Biostatistics, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA.
George KamkamidzeGeorgia Hepatitis C Elimination Program, Tbilisi, Georgia.
Mel KrajdenBritish Columbia Centre for Disease Control, Vancouver, Canada.
Anne LoarecEpicentre, Medecins Sans Frontières, Paris, France.
Richard NjouomCentre Pasteur of Cameroon, Yaoundé, Cameroon.
Kihn V NguyenNational Hospital of Tropical Diseases, Hanoi, Viet Nam.
Gamal ShihaDepartment of Internal Medicine, University of Mansoura, Egypt; Egyptian Liver Research Institute and Hospital, Mansoura, Egypt.
Reham SolimanEgyptian Liver Research Institute and Hospital, Mansoura, Egypt.
Sunil S SolomonYR Gaitonde Centre for AIDS Research and Education, Chennai, India; Johns Hopkins University School of Medicine, Baltimore, USA.
Tengiz TsertsvadzeGeorgia Hepatitis C Elimination Program, Tbilisi, Georgia.
Claudia M DenkingerFIND, Geneva, Switzerland.
Benjamin LinasBoston Medical Center, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA; Department of Epidemiology, Section of Infectious Diseases, Boston University School of Public Health, Boston, USA. Electronic address: Benjamin.linas@bmc.org.

Funding

Translational ScienceP30AI042853 · NIAID · MIRIAM HOSPITAL · PI CURT G BECKWITH · 1998 to 2026
$51.7M
The Asia-Pacific HIV Research CollaborationU01AI069907 · NIAID · FOUNDATION FOR AIDS RESEARCH · PI ANNETTE H SOHN · 2006 to 2026
$44.8M
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 ZACHARY Franklin MEISEL · 2015 to 2026
$20.7M
Institutional Career DevelopmentKL2TR001411 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MORONE, NATALIA E. · 2015 to 2024
$5.9M
Simulation Modeling to Improve HIV/HCV Screening, Treatment and CareR01DA031059 · NIDA · BOSTON MEDICAL CENTER · PI LINAS, BENJAMIN P. · 2012 to 2015
$2.1M
NCATS NIH HHS KL2 TR001411NIAID NIH HHS P30 AI042853NIAID NIH HHS U01 AI069907NIDA NIH HHS P30 DA040500NIDA NIH HHS R01 DA031059World Health Organization 001
6 · The paper itself

Abstract

BACKGROUND &

aimsAffordable point-of-care tests for hepatitis C (HCV) viraemia are needed to improve access to treatment in low- and middle-income countries. Our aims were to determine the target limit of detection (LOD) necessary to diagnose the majority of people with HCV eligible for treatment, and identify characteristics associated with low-level viraemia (LLV) (defined as the lowest 3% of the distribution of HCV RNA) to understand those at risk of being misdiagnosed.

methodsWe established a multi-country cross-sectional dataset of first available quantitative HCV RNA measurements linked to demographic and clinical data. We excluded individuals on HCV treatment. We analysed the distribution of HCV RNA and determined critical thresholds for detection of HCV viraemia. We then performed logistic regression to evaluate factors associated with LLV, and derived relative sensitivities for significant covariates.

resultsThe dataset included 66,640 individuals with HCV viraemia from across the world. The LOD for the 95th and 99th percentiles were 3,311 IU/ml and 214 IU/ml. The LOD for the 97th percentile was 1,318 IU/ml (95% CI 1,298.4-1,322.3). Factors associated with LLV, defined as HCV RNA <1,318 IU/ml, were younger age 18-30 vs. 51-64 years (odds ratios [OR] 2.56; 95% CI 2.19-2.99), female vs. male sex (OR 1.32; 95% CI 1.18-1.49), and advanced fibrosis stage F4 vs. F0-1 (OR 1.44; 95% CI 1.21-1.69). Only the younger age group had a decreased relative sensitivity below 95%, at 93.3%.

conclusionsIn this global dataset, a test with an LOD of 1,318 IU/ml would identify 97% of viraemic HCV infections among almost all populations. This LOD will help guide manufacturers in the development of affordable point-of-care diagnostics to expand HCV testing and linkage to care in low- and middle-income countries. LAY SUMMARY: We created and analysed a dataset from 12 countries with 66,640 participants with chronic hepatitis C virus infection. We determined that about 97% of those with viraemic infection had 1,300 IU/ml or more of circulating virus at the time of diagnosis. While current diagnostic tests can detect as little as 12 IU/ml of virus, our findings suggest that increasing the level of detection closer to 1,300 IU/ml would maintain good test accuracy and will likely enable development of more affordable portable tests for use in low- and middle-income countries.

Indexed as

HepacivirusHepatitis C, ChronicLimit of DetectionRNA, ViralViremiaAdultFemaleGlobal HealthHumansMaleMiddle AgedPoint-of-Care TestingReproducibility of ResultsSerologic TestsVirologyRNA, ViralDiagnosisHepatitis C virusLimit of detectionPoint-of-careViraemia, Affordable

Identifiers

PMID30797050
PMCPMC7014921

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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.