Evidence map›Paper›PMID 42636668›Full record

ArticleJournal of clinical virology : the official publication of the Pan American Society for Clinical Virology2026

Evaluation of false positive enteric viruses results from the BIOFIRE® FILMARRAY® gastrointestinal PCR panel.

Preeti Chhabra, Jordan Cates, Eddie Bartlett, Shane A Embury, Amina Rizwan, Fiancee A Williams, Anita K Kambhampati, Vincent C Marconi, Lauren Epstein, Rijalda Jasarevic and 14 more

Abstract readEvaluation Study
In one paragraph

Article in Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Preeti ChhabraDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States. Electronic address: PChhabra@cdc.gov.
Jordan CatesDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Eddie BartlettCherokee Nation Operational Solutions, Tulsa, OK, United States.
Shane A EmburyCherokee Nation Operational Solutions, Tulsa, OK, United States.
Amina RizwanCherokee Nation Operational Solutions, Tulsa, OK, United States.
Fiancee A WilliamsCherokee Nation Operational Solutions, Tulsa, OK, United States.
Anita K KambhampatiDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Vincent C MarconiDepartment of Global Health, Emory University Rollins School of Public Health, Atlanta, GA, United States; Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States; Atlanta Veterans Affairs Medical Center, Atlanta, GA, United States.
Lauren EpsteinDepartment of Medicine, Emory University School of Medicine, Atlanta, GA, United States; Atlanta Veterans Affairs Medical Center, Atlanta, GA, United States.
Rijalda JasarevicAtlanta Veterans Affairs Medical Center, Atlanta, GA, United States.
Colleen S KraftDepartment of Global Health, Emory University Rollins School of Public Health, Atlanta, GA, United States; Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States.
Maria C Rodriguez-BarradasInfectious Diseases Section, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Rosalba Gomez MoronesInfectious Diseases Section, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
Miguel A CovarrubiasInfectious Diseases Section, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX, United States.
David O BeenhouwerVeterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, United States.
Evan GoldinVeterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, United States.
Sheldon T BrownJames J. Peters Veterans Affairs Medical Center, Bronx, NY, United States.
Ismael PenaJames J. Peters Veterans Affairs Medical Center, Bronx, NY, United States.
Cynthia A Lucero-ObusanVeterans Affairs Palo Alto Health Care System, Palo Alto, CA, United States; Veterans Health Administration, Office of Public Health, Washington, DC, United States.
Mark HolodniyVeterans Affairs Palo Alto Health Care System, Palo Alto, CA, United States; Division of Infectious Diseases & Geographic Medicine, Stanford University, Stanford, CA, United States.
Rashi GautamDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Sara A MirzaDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Jan VinjéDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Surveillance Platform for Enteric and Respiratory Infectious Organisms at the VA (SUPERNOVA) AGE Surveillance Group

Funding

Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
Intramural CDC HHS CC999999NIAID NIH HHS P30 AI050409
6 · The paper itself

Abstract

backgroundThe BioFire® FilmArray® Gastrointestinal (GI) Panel targets 22 pathogens associated with acute gastroenteritis (AGE). While the Veterans Affairs SUPERNOVA surveillance platform uses this assay to test stool specimens from hospitalized Veterans across five U.S. medical centers, increasing reports of false positives, particularly for norovirus, have raised concerns regarding the assay's accuracy.

objectiveTo verify BioFire®-positive viral results from the SUPERNOVA study using molecular reference methods at the Centers for Disease Control and Prevention (CDC). STUDY

designA total of 415 stool specimens (2018-2023) from both hospitalized and outpatient Veterans with AGE that tested positive by BioFire® GI panel for at least one of five viruses (norovirus, rotavirus, sapovirus, astrovirus, or adenovirus 40/41) were retested using CDC reference methods, including RT-qPCR and conventional RT-PCR with Sanger sequencing. Specimens were considered true positive when confirmed by two of the three testing methods.

resultsOf the 415 specimens, 327 (78.8%) were confirmed positive for at least one virus. Norovirus was the most frequent (n = 207; 63.3%), followed by sapovirus (39; 11.9%), rotavirus A (37; 11.3%), astrovirus (36; 11.0%), and adenovirus 40/41 (10; 3.1%). False-positive rates were highest for norovirus (26.5%), followed by rotavirus (21.3%) and sapovirus (18.8%). Norovirus false-positives were more frequent in hospitalized patients (35.5%) than in outpatients (19.2%), particularly among individuals aged 40-60 years. Norovirus false positives trended upward starting in 2021. DISCUSSION: These results confirm performance concerns with the BioFire® GI Panel, particularly for norovirus, the most frequently identified virus. Confirmatory testing of questionable positives should be considered.

Indexed as

GastroenteritisMolecular Diagnostic TechniquesVirusesAdenoviridaeFalse Positive ReactionsFecesFemaleHumansMaleMiddle AgedNorovirusRotavirusSapovirusSensitivity and SpecificityUnited StatesAdenovirusAstrovirusBioFire GI PanelNorovirusRotavirusSapovirus

Identifiers

PMID42636668
PMCPMC13531351

What OpenQuestion holds

Textmetadata
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.