PLoS ONE (Jan 2021)

Invasive pulmonary aspergillosis in critically ill patients with severe COVID-19 pneumonia: Results from the prospective AspCOVID-19 study.

  • Tobias Lahmer,
  • Silja Kriescher,
  • Alexander Herner,
  • Kathrin Rothe,
  • Christoph D Spinner,
  • Jochen Schneider,
  • Ulrich Mayer,
  • Michael Neuenhahn,
  • Dieter Hoffmann,
  • Fabian Geisler,
  • Markus Heim,
  • Gerhard Schneider,
  • Roland M Schmid,
  • Wolfgang Huber,
  • Sebastian Rasch

DOI
https://doi.org/10.1371/journal.pone.0238825
Journal volume & issue
Vol. 16, no. 3
p. e0238825

Abstract

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BackgroundSuperinfections, including invasive pulmonary aspergillosis (IPA), are well-known complications of critically ill patients with severe viral pneumonia. Aim of this study was to evaluate the incidence, risk factors and outcome of IPA in critically ill patients with severe COVID-19 pneumonia.MethodsWe prospectively screened 32 critically ill patients with severe COVID-19 pneumonia for a time period of 28 days using a standardized study protocol for oberservation of developement of COVID-19 associated invasive pulmonary aspergillosis (CAPA). We collected laboratory, microbiological, virological and clinical parameters at defined timepoints in combination with galactomannan-antigen-detection from nondirected bronchial lavage (NBL). We used logistic regression analyses to assess if COVID-19 was independently associated with IPA and compared it with matched controls.FindingsCAPA was diagnosed at a median of 4 days after ICU admission in 11/32 (34%) of critically ill patients with severe COVID-19 pneumonia as compared to 8% in the control cohort. In the COVID-19 cohort, mean age, APACHE II score and ICU mortality were higher in patients with CAPA than in patients without CAPA (36% versus 9.5%; pInterpretationCAPA is highly prevalent and associated with a high mortality rate. COVID-19 is independently associated with invasive pulmonary aspergillosis. A standardized screening and diagnostic approach as presented in our study can help to identify affected patients at an early stage.