Evidence map›Paper›PMID 37902331›Full record

ArticleJournal of clinical microbiology2023

Multi-center clinical evaluation of the Panther Fusion SARS-CoV-2/Flu A/B/RSV assay in nasopharyngeal swab specimens from symptomatic individuals.

Anjana Sasidharan, Rangaraj Selvarangan, Kennah Konrad, Matthew L Faron, Salika M Shakir, David Hillyard, Robert K McCall, Ian H McHardy, David C Goldberg, James J Dunn and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.1field-weighted citation impact, top 11% of its field
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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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 at 7 institutions in 1 country.

Anjana SasidharanChildren's Mercy Hospital , Kansas City, Missouri, USA.
Rangaraj SelvaranganChildren's Mercy Hospital , Kansas City, Missouri, USA.ORCID 0000-0003-3275-6657
Kennah KonradThe Medical College of Wisconsin , Milwaukee, Wisconsin, USA.
Matthew L FaronThe Medical College of Wisconsin , Milwaukee, Wisconsin, USA.
Salika M ShakirARUP Laboratories , Salt Lake City, Utah, USA.ORCID 0000-0003-4642-8574
David HillyardARUP Laboratories , Salt Lake City, Utah, USA.
Robert K McCallGeneuity Clinical Research Services , Maryville, Tennessee, USA.
Ian H McHardyScripps Health , San Diego, California, USA.ORCID 0000-0002-2121-5460
David C GoldbergAcutis Diagnostics , Hicksville, New York, USA.
James J DunnTexas Children's Hospital , Houston, Texas, USA.ORCID 0000-0002-7964-281X
Alexander L GreningerUniversity of Washington , Seattle, Washington, USA.ORCID 0000-0002-7443-0527
Christine LansangHologic, Inc. , San Diego, California, USA.
Rachel BoghHologic, Inc. , San Diego, California, USA.
Carmelle V RemillardHologic, Inc. , San Diego, California, USA.ORCID 0000-0002-8937-7781
Hologic (United States) · USARUP Laboratories (United States) · USChildren's Mercy Hospital · USMedical College of Wisconsin · USScripps Health · USTexas Children's Hospital · USUniversity of Washington · US

Funding

HHS | Biomedical Advanced Research and Development Authority (BARDA) 75A50120P00100HHS | Biomedical Advanced Research and Development Authority (BARDA) 75A50121P00022
6 · The paper itself

Abstract

The symptomology is overlapping for respiratory infections due to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), influenza A/B viruses, and respiratory syncytial virus (RSV). Accurate detection is essential for proper medical management decisions. This study evaluated the clinical performance of the Panther Fusion SARS-CoV-2/Flu A/B/RSV assay in nasopharyngeal swab (NPS) specimens from individuals of all ages with signs and symptoms of respiratory infection consistent with COVID-19, influenza, or RSV. Retrospective known-positive and prospectively obtained residual NPS specimens were collected during two respiratory seasons in the USA. Clinical performance was established by comparing Panther Fusion SARS-CoV-2/Flu assay results to a three-molecular assay composite comparator interpretation for SARS-CoV-2 and to the FDA-cleared Panther Fusion Flu A/B/RSV assay results for all non-SARS-CoV-2 targets. A total of 1,900 prospective and 95 retrospective NPS specimens were included in the analyses. The overall prevalence in prospectively obtained specimens was 20.7% for SARS-CoV-2, 6.7% for influenza A, and 0.7% for RSV; all influenza B-positive specimens were retrospective specimens. The positive percent agreement of the Panther Fusion assay was 96.9% (378/390) for SARS-CoV-2, 98.0% (121/123) for influenza A virus, 95.2% (20/21) for influenza B virus, and 96.6% (57/59) for RSV. The negative percent agreement was ≥98.5% for all target viruses. Specimens with discordant Panther Fusion SARS/Flu/RSV assay results all had cycle threshold values of ≥32.4 (by comparator or by Panther Fusion SARS/Flu/RSV assay). Only five co-infections were detected in the study specimens. The Panther Fusion SARS-CoV-2/Flu/RSV assay provides highly sensitive and specific detection of SARS-CoV-2, influenza A virus, influenza B virus, and RSV in NPS specimens.

Indexed as

COVID-19Influenza A virusInfluenza, HumanRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsRespiratory Tract InfectionsHumansInfluenza B virusNasopharynxProspective StudiesRetrospective StudiesSARS-CoV-2Sensitivity and Specificityclinical agreementinfluenzamolecular respiratory assaymultiplex assayPanther Fusionrespiratory syncytial virusSARS-CoV-2

Identifiers

PMID37902331
PMCPMC10662375
OpenAlexW4388014589

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.