Discriminatory Ability of Gas Chromatography-Ion Mobility Spectrometry to Identify Patients Hospitalized With COVID-19 and Predict Prognosis.

COVID-19 diagnosis respiratory virus volatile organic compounds

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 07 06 2022
accepted: 30 09 2022
entrez: 8 11 2022
pubmed: 9 11 2022
medline: 9 11 2022
Statut: epublish

Résumé

Rapid diagnostic and prognostic tests for coronavirus disease (COVID-19) are urgently required. We aimed to evaluate the diagnostic and prognostic ability of breath analysis using gas chromatography-ion mobility spectrometry (GC-IMS) in hospitalized patients with COVID-19. Between February and May 2021, we took 1 breath sample for analysis using GC-IMS from participants who were admitted to the hospital for COVID-19, participants who were admitted to the hospital for other respiratory infections, and symptom-free controls, at the University Hospitals of Leicester NHS Trust, United Kingdom. Demographic, clinical, and radiological data, including requirement for continuous positive airway pressure (CPAP) ventilation as a marker for severe disease in the COVID-19 group, were collected. A total of 113 participants were recruited into the study. Seventy-two (64%) were diagnosed with COVID-19, 20 (18%) were diagnosed with another respiratory infection, and 21 (19%) were healthy controls. Differentiation between participants with COVID-19 and those with other respiratory tract infections with GC-IMS was highly accurate (sensitivity/specificity, 0.80/0.88; area under the receiver operating characteristics curve [AUROC], 0.85; 95% CI, 0.74-0.96). GC-IMS was also moderately accurate at identifying those who subsequently required CPAP (sensitivity/specificity, 0.62/0.80; AUROC, 0.70; 95% CI, 0.53-0.87). GC-IMS shows promise as both a diagnostic tool and a predictor of prognosis in hospitalized patients with COVID-19 and should be assessed further in larger studies.

Sections du résumé

Background UNASSIGNED
Rapid diagnostic and prognostic tests for coronavirus disease (COVID-19) are urgently required. We aimed to evaluate the diagnostic and prognostic ability of breath analysis using gas chromatography-ion mobility spectrometry (GC-IMS) in hospitalized patients with COVID-19.
Methods UNASSIGNED
Between February and May 2021, we took 1 breath sample for analysis using GC-IMS from participants who were admitted to the hospital for COVID-19, participants who were admitted to the hospital for other respiratory infections, and symptom-free controls, at the University Hospitals of Leicester NHS Trust, United Kingdom. Demographic, clinical, and radiological data, including requirement for continuous positive airway pressure (CPAP) ventilation as a marker for severe disease in the COVID-19 group, were collected.
Results UNASSIGNED
A total of 113 participants were recruited into the study. Seventy-two (64%) were diagnosed with COVID-19, 20 (18%) were diagnosed with another respiratory infection, and 21 (19%) were healthy controls. Differentiation between participants with COVID-19 and those with other respiratory tract infections with GC-IMS was highly accurate (sensitivity/specificity, 0.80/0.88; area under the receiver operating characteristics curve [AUROC], 0.85; 95% CI, 0.74-0.96). GC-IMS was also moderately accurate at identifying those who subsequently required CPAP (sensitivity/specificity, 0.62/0.80; AUROC, 0.70; 95% CI, 0.53-0.87).
Conclusions UNASSIGNED
GC-IMS shows promise as both a diagnostic tool and a predictor of prognosis in hospitalized patients with COVID-19 and should be assessed further in larger studies.

Identifiants

pubmed: 36345428
doi: 10.1093/ofid/ofac509
pii: ofac509
pmc: PMC9619573
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofac509

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. A.S. and E.B. report provision of materials, consumables, and training only, with no payment from IMSPEX Diagnostics Ltd, Abercynon, UK. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

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Auteurs

Joshua Nazareth (J)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Daniel Pan (D)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Jee Whang Kim (JW)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Respiratory Biomedical Research Centre, University of Leicester, Leicester, United Kingdom.

Jack Leach (J)

University of Leicester Medical School, Leicester, United Kingdom.

James G Brosnan (JG)

University of Leicester Medical School, Leicester, United Kingdom.

Adam Ahmed (A)

University of Leicester Medical School, Leicester, United Kingdom.

Emma Brodrick (E)

IMSPEX Diagnostics Ltd, Abercynon, United Kingdom.

Paul Bird (P)

Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Alfian Wicaksono (A)

School of Engineering, University of Warwick, Coventry, United Kingdom.

Emma Daulton (E)

School of Engineering, University of Warwick, Coventry, United Kingdom.

Julian W Tang (JW)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Department of Clinical Microbiology, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Caroline Williams (C)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Pranabashis Haldar (P)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Respiratory Biomedical Research Centre, University of Leicester, Leicester, United Kingdom.

James A Covington (JA)

School of Engineering, University of Warwick, Coventry, United Kingdom.

Manish Pareek (M)

Department of Respiratory Sciences, University of Leicester, Leicester, United Kingdom.
Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Amandip Sahota (A)

Department of Infectious Diseases and HIV Medicine, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.

Classifications MeSH