Evidence map›Paper›PMID 41023658›Full record

ArticleBMC infectious diseases2025

Use of the BIOFIRE

Zachary A Weishampel, Ajith Nagahawatte, Gaya Wijayaratne, Subodha S Wickramasinghe, Bradly Nicholson, Jack Anderson, Sky Vanderburg, Chathuranga Lakmal Fonseka, Madureka Premamali, Robert J Rolfe and 9 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. 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

19 authors.

Zachary A Weishampel *Duke University, Durham, NC, United States of America. zachary.weishampel@duke.edu.
Ajith Nagahawatte *Duke Global Health Institute, Durham, NC, United States of America.
Gaya WijayaratneFaculty of Medicine, Department of Microbiology, University of Ruhuna, Galle, Sri Lanka.
Subodha S WickramasingheFaculty of Medicine, Department of Microbiology, University of Ruhuna, Galle, Sri Lanka.
Bradly NicholsonRuhuna-Duke Centre for Infectious Diseases, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Jack AndersonDuke University, Durham, NC, United States of America.
Sky VanderburgPulmonary and Critical Care, Montage Health, Monterey, CA, United States of America.
Chathuranga Lakmal FonsekaRuhuna-Duke Centre for Infectious Diseases, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Madureka PremamaliRuhuna-Duke Centre for Infectious Diseases, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Robert J RolfeDuke University, Durham, NC, United States of America.
U H B Y DilshanRuhuna-Duke Centre for Infectious Diseases, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
Ruvini KurukulasooriyaRuhuna-Duke Centre for Infectious Diseases, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
D L B PiyasiriNational Hospital Galle, Galle, Sri Lanka.
Truls ØstbyeDuke University, Durham, NC, United States of America.
Christopher W WoodsDuke University, Durham, NC, United States of America.
Lana AbusalemDuke University, Durham, NC, United States of America.
Armstrong ObaleDuke University, Durham, NC, United States of America.
L Gayani Tillekeratne *Duke University, Durham, NC, United States of America.
Champica K Bodinayake *Duke Global Health Institute, Durham, NC, United States of America. bodinayake@gmail.com.

Funding

Vanderbilt-Emory-Cornell-Duke Global Health Fellowship Consortium-Expanding Diversity for Global Equity (EDGE)D43TW009337 · FIC · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALIYU, MUKTAR HASSAN, HEIMBURGER, DOUGLAS CORBETT · 2017 to 2021
$6.3M
Novel Diagnostics to Improve Antimicrobial Stewardship for Acute Respiratory Tract Infections in Resource-Limited SettingsK23AI125677 · NIAID · DUKE UNIVERSITY · PI TILLEKERATNE, GAYANI · 2017 to 2021
$905k
FIC NIH HHS D43 TW009337National Institutes of Allergy and Infectious Diseases K23AI125677NIAID NIH HHS K23 AI125677
6 · The paper itself

Abstract

backgroundLower respiratory tract infections (LRTIs) account for a heavy burden of illness in low- and middle-income country settings, but the etiology of these infections is often unknown. In this study, we applied the BIOFIRE

methodsWe enrolled children and adults hospitalized with LRTIs at a public tertiary care hospital in southern Sri Lanka from 2019 to 2021. Demographic and clinical data were collected, and a sputum sample for each patient was tested using the Pneumonia plus Panel. Assay results were compared with sputum culture results. Fisher's exact test was applied to identify association between the presence of viruses, bacteria, or antimicrobial resistant genes and the findings of the chest radiographs during hospitalization as well as associations between the genomic concentration identified through the panel and the bacteria known to cause typical pneumonia infection included in the panel.

resultsIn 267 patients tested, the most detected bacteria by the Pneumonia plus Panel were the Klebsiella pneumoniae group (41.9%), Staphylococcus aureus (34.5%), and the Acinetobacter calcoaceticus-baumannii complex (32.6%). The most detected viruses were the human rhinovirus/enterovirus (19.5%) and influenza A (10.9%). In total, 211 patients (79.0%) had at least one gram-negative bacterium and 139 patients (52.1%) had at least one gram-positive bacteria. As for Antimicrobial Resistance, 96 patients (40.0%) had at least one carbapenem resistant gene, 56 patients (21.0%) had an extended spectrum beta-lactamase related gene, and 42 patients (15.7%) had a methicillin resistant gene. Only 15 patients (5.6%) were identified to have Pneumonia plus Panel results matching with sputum culture results.

conclusionsOur findings suggest that patients with LRTI in Southern Province, Sri Lanka have a high prevalence of gram-negative bacteria and antibacterial resistance in their sputum samples. However, it remains difficult to differentiate isolates that are colonizers not leading to disease versus the true cause of infection via the use of the BIOFIRE

Indexed as

Multiplex Polymerase Chain ReactionPneumoniaRespiratory Tract InfectionsAdolescentAdultAgedBacteriaChildChild, PreschoolCommunity-Acquired InfectionsFemaleHospitalizationHumansInfantMaleMiddle AgedAntimicrobial resistanceBIOFIRE® FILMARRAY® Pneumonia plus PanelGram-Negative bacteriaLower respiratory tract infectionsSouthern Province, Sri Lanka

Identifiers

PMID41023658
PMCPMC12482574

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LicenceCC BY-NC-ND
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Registered trials

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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.