Literature DB >> 32118531

Comparison of the performance of the Panther Fusion respiratory virus panel to R-Gene and laboratory developed tests for diagnostic and hygiene screening specimens from the upper and lower respiratory tract.

Tina Ganzenmueller1,2, Rolf Kaiser3, Claas Baier4, Marlies Wehrhane2, Brigitta Hilfrich2, Jenny Witthuhn2, Sandra Flucht2, Albert Heim2.   

Abstract

Introduction. Diagnosis of acute respiratory infections (ARIs) can be facilitated by the Panther Fusion (PF) automatic, random access PCR system for the detection of influenzavirus A (Flu A) and B (Flu B), parainfluenzavirus (Paraflu), respiratory syncytial virus (RSV), human metapneumovirus (hMPV), rhinovirus (RV) and human adenovirus (AdV) in nasopharyngeal swabs.Aim. To evaluate the performance of PF in comparison with established methods, including subsets of (1) lower respiratory tract (LRT) specimens and (2) upper respiratory tract (URT) hygiene screening specimens of patients without ARI symptoms.Methodology. The performance characteristics of PF were compared with bioMérieux R-Gene and laboratory-developed PCR tests (LDTs). Overall, 1544 specimens with 6658 individual diagnostic requests were analysed.Results. The overall concordances of PF and LDTs for Flu A, Flu B and AdV were 98.4, 99.9 and 96.1%, respectively; by re-testing of discrepant specimens concordances increased to 99.4, 99.9 and 98.0%, respectively. Initial concordances of PF and R-Gene assays for RSV, Paraflu, hMPV and RV were 98.4, 96.3, 99.3 and 96.0%, respectively, and retest concordances were 99.7, 97.9, 99.9 and 98.9%, respectively. No differences to the overall performance were found for the subgroups of LRT and hygiene screening specimens. PCR cycle threshold (Ct) values correlated very well between methods, indicating that a semi-quantitative diagnostic approach using Ct values (e.g. highly vs. weakly positive) could augment the diagnostic information.Conclusion. PF performed similar to R-Gene and LDTs not only for its intended use but also for LRT and hygiene screening specimens with shorter hands-on and turnaround times.

Entities:  

Keywords:  Panther Fusion; R-Gene; hygiene screening; laboratory-developed PCR tests; respiratory viruses

Year:  2020        PMID: 32118531     DOI: 10.1099/jmm.0.001133

Source DB:  PubMed          Journal:  J Med Microbiol        ISSN: 0022-2615            Impact factor:   2.472


  3 in total

1.  Target capture sequencing reveals a monoclonal outbreak of respiratory syncytial virus B infections among adult hematologic patients.

Authors:  Claas Baier; Jiabin Huang; Kerstin Reumann; Daniela Indenbirken; Felicitas Thol; Christian Koenecke; Ella Ebadi; Albert Heim; Franz-Christoph Bange; Sibylle Haid; Thomas Pietschmann; Nicole Fischer
Journal:  Antimicrob Resist Infect Control       Date:  2022-06-21       Impact factor: 6.454

2.  Rapid random access detection of the novel SARS-coronavirus-2 (SARS-CoV-2, previously 2019-nCoV) using an open access protocol for the Panther Fusion.

Authors:  Anne K Cordes; Albert Heim
Journal:  J Clin Virol       Date:  2020-02-28       Impact factor: 3.168

3.  Performance evaluation of Panther Fusion SARS-CoV-2 assay for detection of SARS-CoV-2 from deep throat saliva, nasopharyngeal, and lower-respiratory-tract specimens.

Authors:  River Chun-Wai Wong; Ann Han Wong; Yolanda Iok-Ieng Ho; Eddie Chi-Man Leung; Raymond Wai-Man Lai
Journal:  J Med Virol       Date:  2020-10-08       Impact factor: 20.693

  3 in total

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