Prospective Validation of a Rapid Host Gene Expression Test to Discriminate Bacterial From Viral Respiratory Infection.

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Ko, Emily R

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Henao, Ricardo

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Frankey, Katherine

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Petzold, Elizabeth A

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Isner, Pamela D

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Jaehne, Anja K

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Allen, Nakia

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Gardner-Gray, Jayna

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Hurst, Gina

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Pflaum-Carlson, Jacqueline

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Jayaprakash, Namita

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Rivers, Emanuel P

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Wang, Henry

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Ugalde, Irma

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Amanullah, Siraj

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Mercurio, Laura

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Chun, Thomas H

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May, Larissa

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Hickey, Robert W

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Lazarus, Jacob E

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Gunaratne, Shauna H

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Pallin, Daniel J

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Jambaulikar, Guruprasad

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Huckins, David S

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Ampofo, Krow

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Jhaveri, Ravi

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Jiang, Yunyun

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Komarow, Lauren

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Evans, Scott R

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Ginsburg, Geoffrey S

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Tillekeratne, L Gayani

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McClain, Micah T

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Burke, Thomas W

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Woods, Christopher W

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Tsalik, Ephraim L

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Antibacterial Resistance Leadership Group

dc.date.accessioned

2022-05-01T13:18:10Z

dc.date.available

2022-05-01T13:18:10Z

dc.date.issued

2022-04

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2022-05-01T13:18:09Z

dc.description.abstract

Importance

Bacterial and viral causes of acute respiratory illness (ARI) are difficult to clinically distinguish, resulting in the inappropriate use of antibacterial therapy. The use of a host gene expression-based test that is able to discriminate bacterial from viral infection in less than 1 hour may improve care and antimicrobial stewardship.

Objective

To validate the host response bacterial/viral (HR-B/V) test and assess its ability to accurately differentiate bacterial from viral infection among patients with ARI.

Design, setting, and participants

This prospective multicenter diagnostic study enrolled 755 children and adults with febrile ARI of 7 or fewer days' duration from 10 US emergency departments. Participants were enrolled from October 3, 2014, to September 1, 2019, followed by additional enrollment of patients with COVID-19 from March 20 to December 3, 2020. Clinical adjudication of enrolled participants identified 616 individuals as having bacterial or viral infection. The primary analysis cohort included 334 participants with high-confidence reference adjudications (based on adjudicator concordance and the presence of an identified pathogen confirmed by microbiological testing). A secondary analysis of the entire cohort of 616 participants included cases with low-confidence reference adjudications (based on adjudicator discordance or the absence of an identified pathogen in microbiological testing). Thirty-three participants with COVID-19 were included post hoc.

Interventions

The HR-B/V test quantified the expression of 45 host messenger RNAs in approximately 45 minutes to derive a probability of bacterial infection.

Main outcomes and measures

Performance characteristics for the HR-B/V test compared with clinical adjudication were reported as either bacterial or viral infection or categorized into 4 likelihood groups (viral very likely [probability score <0.19], viral likely [probability score of 0.19-0.40], bacterial likely [probability score of 0.41-0.73], and bacterial very likely [probability score >0.73]) and compared with procalcitonin measurement.

Results

Among 755 enrolled participants, the median age was 26 years (IQR, 16-52 years); 360 participants (47.7%) were female, and 395 (52.3%) were male. A total of 13 participants (1.7%) were American Indian, 13 (1.7%) were Asian, 368 (48.7%) were Black, 131 (17.4%) were Hispanic, 3 (0.4%) were Native Hawaiian or Pacific Islander, 297 (39.3%) were White, and 60 (7.9%) were of unspecified race and/or ethnicity. In the primary analysis involving 334 participants, the HR-B/V test had sensitivity of 89.8% (95% CI, 77.8%-96.2%), specificity of 82.1% (95% CI, 77.4%-86.6%), and a negative predictive value (NPV) of 97.9% (95% CI, 95.3%-99.1%) for bacterial infection. In comparison, the sensitivity of procalcitonin measurement was 28.6% (95% CI, 16.2%-40.9%; P < .001), the specificity was 87.0% (95% CI, 82.7%-90.7%; P = .006), and the NPV was 87.6% (95% CI, 85.5%-89.5%; P < .001). When stratified into likelihood groups, the HR-B/V test had an NPV of 98.9% (95% CI, 96.1%-100%) for bacterial infection in the viral very likely group and a positive predictive value of 63.4% (95% CI, 47.2%-77.9%) for bacterial infection in the bacterial very likely group. The HR-B/V test correctly identified 30 of 33 participants (90.9%) with acute COVID-19 as having a viral infection.

Conclusions and relevance

In this study, the HR-B/V test accurately discriminated bacterial from viral infection among patients with febrile ARI and was superior to procalcitonin measurement. The findings suggest that an accurate point-of-need host response test with high NPV may offer an opportunity to improve antibiotic stewardship and patient outcomes.
dc.identifier

2791032

dc.identifier.issn

2574-3805

dc.identifier.issn

2574-3805

dc.identifier.uri

https://hdl.handle.net/10161/24951

dc.language

eng

dc.publisher

American Medical Association (AMA)

dc.relation.ispartof

JAMA network open

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10.1001/jamanetworkopen.2022.7299

dc.subject

Antibacterial Resistance Leadership Group

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Humans

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Bacteria

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Bacterial Infections

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Virus Diseases

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Fever

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Gene Expression

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Adult

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Child

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Female

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Male

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Procalcitonin

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COVID-19

dc.title

Prospective Validation of a Rapid Host Gene Expression Test to Discriminate Bacterial From Viral Respiratory Infection.

dc.type

Journal article

duke.contributor.orcid

Ginsburg, Geoffrey S|0000-0003-4739-9808

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Tillekeratne, L Gayani|0000-0001-6012-7271

duke.contributor.orcid

Woods, Christopher W|0000-0001-7240-2453

duke.contributor.orcid

Tsalik, Ephraim L|0000-0002-6417-2042

pubs.begin-page

e227299

pubs.issue

4

pubs.organisational-group

Duke

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School of Medicine

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School of Nursing

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Nursing

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Basic Science Departments

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Clinical Science Departments

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Institutes and Centers

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Biostatistics & Bioinformatics

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Molecular Genetics and Microbiology

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Medicine

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Pathology

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Medicine, Cardiology

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Medicine, Infectious Diseases

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Duke Cancer Institute

pubs.publication-status

Published

pubs.volume

5

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