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Secondary pneumonia in critically ill ventilated patients with COVID-19
Mailis Maes; Ellen Higginson; Joana Pereira Dias; Martin D Curran; Surendra Parmar; Fahad Khokhar; Delphine Cuchet-Lourenço; Janine Lux; Sapna Sharma-Hajela; Benjamin Ravenhill; Razeen Mahroof; Amelia Solderholm; Sally Forrest; Sushmita Sridhar; Nicholas M Brown; Stephen Baker; Vilas Navapurkar; Gordon Dougan; Josefin Bartholdson Scott; Andrew Conway Morris.
Afiliación
  • Mailis Maes; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Ellen Higginson; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Joana Pereira Dias; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Martin D Curran; Public Health England, Clinical Microbiology and Public Health Laboratory, Addenbrookes Hospital, Cambridge, United Kingdom
  • Surendra Parmar; Public Health England, Clinical Microbiology and Public Health Laboratory, Addenbrookes Hospital, Cambridge, United Kingdom
  • Fahad Khokhar; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Delphine Cuchet-Lourenço; Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Janine Lux; Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Sapna Sharma-Hajela; John Farman ICU, Addenbrookes Hospital, Cambridge, United Kingdom
  • Benjamin Ravenhill; John Farman ICU, Addenbrookes Hospital, Cambridge, United Kingdom
  • Razeen Mahroof; John Farman ICU, Addenbrookes Hospital, Cambridge, United Kingdom
  • Amelia Solderholm; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Sally Forrest; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Sushmita Sridhar; Wellcome Sanger Insitute, Hinxton, United Kingdom
  • Nicholas M Brown; Public Health England, Clinical Microbiology and Public Health Laboratory, Addenbrookes Hospital, Cambridge, United Kingdom
  • Stephen Baker; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Vilas Navapurkar; John Farman ICU, Addenbrookes Hospital, Cambridge, United Kingdom
  • Gordon Dougan; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Josefin Bartholdson Scott; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Department of Medicine, University of Cambridge, Cambridge, United Kingdom
  • Andrew Conway Morris; University of Cambridge
Preprint en Inglés | medRxiv | ID: ppmedrxiv-20139873
ABSTRACT
BackgroundPandemic COVID-19 caused by the coronavirus SARS-CoV-2 has a high incidence of patients with severe acute respiratory syndrome (SARS). Many of these patients require admission to an intensive care unit (ICU) for invasive artificial ventilation and are at significant risk of developing a secondary, ventilator-associated pneumonia (VAP). ObjectivesTo study the incidence of VAP, as well as differences in secondary infections, and bacterial lung microbiome composition of ventilated COVID-19 and non-COVID-19 patients. MethodsIn this prospective observational study, we compared the incidence of VAP and secondary infections using a combination of a TaqMan multi-pathogen array and microbial culture. In addition, we determined the lung microbime composition using 16S RNA analyisis. The study involved eighteen COVID-19 and seven non-COVID-19 patients receiving invasive ventilation in three ICUs located in a single University teaching hospital between April 13th 2020 and May 7th 2020. ResultsWe observed a higher percentage of confirmed VAP in COVID-19 patients. However, there was no statistical difference in the detected organisms or pulmonary microbiome when compared to non-COVID-19 patients. ConclusionCOVID-19 makes people more susceptible to developing VAP, partly but not entirely due to the increased duration of ventilation. The pulmonary dysbiosis caused by COVID-19, and the array of secondary infections observed are similar to that seen in critically ill patients ventilated for other reasons.
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Texto completo: Disponible Colección: Preprints Base de datos: medRxiv Tipo de estudio: Estudio observacional / Estudio pronóstico Idioma: Inglés Año: 2020 Tipo del documento: Preprint
Texto completo: Disponible Colección: Preprints Base de datos: medRxiv Tipo de estudio: Estudio observacional / Estudio pronóstico Idioma: Inglés Año: 2020 Tipo del documento: Preprint
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