Evidence map›Paper›PMID 37970568›Full record

ArticleWorld journal of virology2023

Performance evaluation of NeuMoDx 96 system for hepatitis B and C viral load.

Gagan Chooramani, Jasmine Samal, Nitiksha Rani, Gaurav Singh, Reshu Agarwal, Meenu Bajpai, Manoj Kumar, Manya Prasad, Ekta Gupta

Abstract read
In one paragraph

Article in World journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Gagan ChooramaniDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Jasmine SamalDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Nitiksha RaniDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Gaurav SinghDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Reshu AgarwalDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Meenu BajpaiDepartment of Transfusion Medicine, Institute of Liver & Biliary Sciences, New Delhi 110070, India.
Manoj KumarDepartment of Hepatology, Institute of Liver and Biliary Sciences, New Delhi 110070, India.
Manya PrasadDepartment of Epidemiology and Clinical Research, Institute of Liver and Biliary Sciences, New Delhi 110070, India.
Ekta GuptaDepartment of Clinical Virology, Institute of Liver & Biliary Sciences, New Delhi 110070, India. ektagaurisha@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatitis B virus (HBV) and hepatitis C virus (HCV) viral load (VL) estimation is essential for the management of both HBV and HCV infections. Due to a longer turnaround time for VL estimation, many patients drop out from the cascade of care. To achieve the global goals of reducing morbidity and mortality due to HBV/HCV and moving towards their elimination by 2030, molecular diagnostic platforms with faster and random (

aimTo evaluate the performance of the recently launched NeuMoDx 96 random access system with the conventional COBAS

methodsArchived once-thawed plasma samples were retrieved and tested on both platforms. Correlation between the assays was determined by linear regression and Bland-Altman analysis. The study included samples from 186 patients, 99 for HBV of which 49 were true infected HBV cases (hepatitis B surface antigen, anti-hepatitis B core antibody, and HBV DNA-positive) and 87 for HCV assay in which 39 were true positives for HCV infection (anti-HCV and HCV RNA-positive).

resultsThe median VL detected by NeuMoDx for HBV was 2.9 (interquartile range [IQR]: 2.0-4.3) log

conclusionThe overall concordance between both the systems was 100% for both HBV and HCV VL estimation. Moreover, no genotype-specific bias for HBV/HCV VL quantification was seen in both the systems. Our findings reveal that NeuMoDx HBV and HCV quantitative assays have shown overall good clinical performance and provide faster results with 100% sensitivity and specificity compared to the COBAS AmpliPrep/COBAS TaqMan system.

Indexed as

COBAS AmpliPrepHepatitis BHepatitis CNeuMoDxRandom accessViral load

Identifiers

PMID37970568
PMCPMC10642378

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