Comparative performance of two commercial sample-to-result systems for hepatitis C virus quantitation and genotyping.


Journal

Expert review of molecular diagnostics
ISSN: 1744-8352
Titre abrégé: Expert Rev Mol Diagn
Pays: England
ID NLM: 101120777

Informations de publication

Date de publication:
12 2020
Historique:
pubmed: 8 9 2020
medline: 16 10 2021
entrez: 7 9 2020
Statut: ppublish

Résumé

Accurate assays for hepatitis C virus (HCV) quantitation and genotyping are important for the management of HCV infection. In this study, we evaluated the performance of cobas HCV and cobas HCV GT assays (Roche) for HCV quantitation and genotyping on the cobas 4800 System. We compared the performance of the cobas HCV assays with another commercial system (Abbott The limit-of-detection of the cobas HCV assay in our center was higher (15 IU/mL) than the manufacturer claim (9.2 IU/mL). The assay showed high analytical specificity, accuracy, precision, and linearity. Performance was congruent with the RealTi Our results confirm that the cobas 4800 System is a reliable platform for HCV quantitation and genotyping. The cobas HCV GT assay is a good choice for genotype 1b/6 endemic areas in east Asia, clearly outperforming the RealTi

Identifiants

pubmed: 32893699
doi: 10.1080/14737159.2020.1820327
doi:

Substances chimiques

RNA, Viral 0
Reagent Kits, Diagnostic 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1253-1258

Auteurs

Cyril C Y Yip (CCY)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.

Siddharth Sridhar (S)

Department of Microbiology, The University of Hong Kong , Hong Kong Special Administrative Region, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong , Hong Kong Special Administrative Region, China.
Research Centre of Infection and Immunology, The University of Hong Kong , Hong Kong Special Administrative Region, China.
Carol Yu Centre for Infection, The University of Hong Kong , Hong Kong Special Administrative Region, China.

John H N Lau (JHN)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.

Andrew K W Cheng (AKW)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.

Kit-Hang Leung (KH)

Department of Microbiology, The University of Hong Kong , Hong Kong Special Administrative Region, China.

Jonathan H K Chen (JHK)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.

Kwok-Hung Chan (KH)

Department of Microbiology, The University of Hong Kong , Hong Kong Special Administrative Region, China.

Vincent C C Cheng (VCC)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.

Kwok-Yung Yuen (KY)

Department of Microbiology, Queen Mary Hospital , Hong Kong Special Administrative Region, China.
Department of Microbiology, The University of Hong Kong , Hong Kong Special Administrative Region, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong , Hong Kong Special Administrative Region, China.
Research Centre of Infection and Immunology, The University of Hong Kong , Hong Kong Special Administrative Region, China.
Carol Yu Centre for Infection, The University of Hong Kong , Hong Kong Special Administrative Region, China.
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Li Ka Shing Faculty of Medicine, The University of Hong Kong , Hong Kong Special Administrative Region, China.

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