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Co-Infection and Ventilator-Associated Pneumonia in Critically Ill COVID-19 Patients Requiring Mechanical Ventilation: A Retrospective Cohort Study.

Benjamine SartonMarion GrareFanny Vardon-BounesAnna GaubertStein SilvaLaure CrognierBéatrice RiuThierry SeguinBernard GeorgesVincent MinvilleStéphanie Ruiz
Published in: Biomedicines (2022)
Considering virus-related and drug-induced immunocompromised status of critically ill COVID-19 patients, we hypothesize that these patients would more frequently develop ventilator-associated pneumonia (VAP) than patients with ARDS from other viral causes. We conducted a retrospective observational study in two intensive care units (ICUs) from France, between 2017 and 2020. We compared bacterial co-infection at ICU admission and throughout the disease course of two retrospective longitudinally sampled groups of critically ill patients, who were admitted to ICU for either H1N1 or SARS-CoV-2 respiratory infection and depicted moderate-to-severe ARDS criteria upon admission. Sixty patients in the H1N1 group and 65 in the COVID-19 group were included in the study. Bacterial co-infection at the endotracheal intubation time was diagnosed in 33% of H1N1 and 16% COVID-19 patients ( p = 0.08). The VAP incidence per 100 days of mechanical ventilation was 3.4 (2.2-5.2) in the H1N1 group and 7.2 (5.3-9.6) in the COVID-19 group ( p < 0.004). The HR to develop VAP was of 2.33 (1.34-4.04) higher in the COVID-19 group ( p = 0.002). Ten percent of H1N1 patients and 30% of the COVID-19 patients had a second episode of VAP ( p = 0.013). COVID-19 patients have fewer bacterial co-infections upon admission, but the incidence of secondary infections increased faster in this group compared to H1N1 patients.
Keyphrases
  • sars cov
  • mechanical ventilation
  • intensive care unit
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • drug induced
  • coronavirus disease
  • liver injury
  • patient reported outcomes
  • high intensity