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Microbial Volatiles as Diagnostic Biomarkers of Bacterial Lung Infection in Mechanically Ventilated Patients.
Ahmed, Waqar M; Fenn, Dominic; White, Iain R; Dixon, Breanna; Nijsen, Tamara M E; Knobel, Hugo H; Brinkman, Paul; Van Oort, Pouline M P; Schultz, Marcus J; Dark, Paul; Goodacre, Royston; Felton, Timothy; Bos, Lieuwe D J; Fowler, Stephen J.
Afiliación
  • Ahmed WM; Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, and Manchester Academic Health Science Centre and National Institute for Health Research Biomedical Research Centre, Manchester University Hospi
  • Fenn D; Department of Respiratory Medicine, Amsterdam UMC-location AMC, University of Amsterdam, Amsterdam, The Netherlands.
  • White IR; Laboratory of Experimental Intensive Care and Anaesthesiology, Amsterdam University Medical Center (UMC), Academic Medical Center (AMC), Amsterdam, The Netherlands.
  • Dixon B; Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, and Manchester Academic Health Science Centre and National Institute for Health Research Biomedical Research Centre, Manchester University Hospi
  • Nijsen TME; Laboratory for Environmental and Life Science, University of Nova Gorica, Nova Gorica, Slovenia.
  • Knobel HH; Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, and Manchester Academic Health Science Centre and National Institute for Health Research Biomedical Research Centre, Manchester University Hospi
  • Brinkman P; Philips Research, Philips BV, Eindhoven, The Netherlands.
  • Van Oort PMP; Eurofins Materials Science Netherlands BV, High Tech Campus, Eindhoven, The Netherlands.
  • Schultz MJ; Department of Respiratory Medicine, Amsterdam UMC-location AMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Dark P; Department of Anaesthesiology, Amsterdam UMC Location VU Medical Center, Amsterdam, The Netherlands.
  • Goodacre R; Intensive Care, Amsterdam UMC Location AMC, Amsterdam, The Netherlands.
  • Felton T; Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.
  • Bos LDJ; Department of Clinical Affairs, Hamilton Medical AG, Chur, Switzerland.
  • Fowler SJ; Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, and Manchester Academic Health Science Centre and National Institute for Health Research Biomedical Research Centre, Manchester University Hospi
Clin Infect Dis ; 76(6): 1059-1066, 2023 03 21.
Article en En | MEDLINE | ID: mdl-36310531
ABSTRACT

BACKGROUND:

Early and accurate recognition of respiratory pathogens is crucial to prevent increased risk of mortality in critically ill patients. Microbial-derived volatile organic compounds (mVOCs) in exhaled breath could be used as noninvasive biomarkers of infection to support clinical diagnosis.

METHODS:

In this study, we investigated the diagnostic potential of in vitro-confirmed mVOCs in the exhaled breath of patients under mechanical ventilation from the BreathDx study. Samples were analyzed by thermal desorption-gas chromatography-mass spectrometry.

RESULTS:

Pathogens from bronchoalveolar lavage (BAL) cultures were identified in 45 of 89 patients and Staphylococcus aureus was the most commonly identified pathogen (n = 15). Of 19 mVOCs detected in the in vitro culture headspace of 4 common respiratory pathogens (S. aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli), 14 were found in exhaled breath samples. Higher concentrations of 2 mVOCs were found in the exhaled breath of patients infected with S. aureus compared to those without (3-methylbutanal P < .01, area under the receiver operating characteristic curve [AUROC] = 0.81-0.87; and 3-methylbutanoic acid P = .01, AUROC = 0.79-0.80). In addition, bacteria identified from BAL cultures that are known to metabolize tryptophan (E. coli, Klebsiella oxytoca, and Haemophilus influenzae) were grouped and found to produce higher concentrations of indole compared to breath samples with culture-negative (P = .034) and other pathogen-positive (P = .049) samples.

CONCLUSIONS:

This study demonstrates the capability of using mVOCs to detect the presence of specific pathogen groups with potential to support clinical diagnosis. Although not all mVOCs were found in patient samples within this small pilot study, further targeted and qualitative investigation is warranted using multicenter clinical studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía / Infecciones Estafilocócicas / Compuestos Orgánicos Volátiles Tipo de estudio: Diagnostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neumonía / Infecciones Estafilocócicas / Compuestos Orgánicos Volátiles Tipo de estudio: Diagnostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article