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Lung Microbiota of Critically Ill Patients with COVID-19 Are Associated with Nonresolving Acute Respiratory Distress Syndrome.
Kullberg, Robert F J; de Brabander, Justin; Boers, Leonoor S; Biemond, Jason J; Nossent, Esther J; Heunks, Leo M A; Vlaar, Alexander P J; Bonta, Peter I; van der Poll, Tom; Duitman, JanWillem; Bos, Lieuwe D J; Wiersinga, W Joost.
Affiliation
  • Kullberg RFJ; Center for Experimental and Molecular Medicine.
  • de Brabander J; Center for Experimental and Molecular Medicine.
  • Boers LS; Department of Intensive Care Medicine.
  • Biemond JJ; Laboratory of Experimental Intensive Care and Anesthesiology.
  • Nossent EJ; Center for Experimental and Molecular Medicine.
  • Heunks LMA; Department of Pulmonary Medicine.
  • Vlaar APJ; Department of Intensive Care Medicine.
  • Bonta PI; Department of Intensive Care Medicine.
  • van der Poll T; Laboratory of Experimental Intensive Care and Anesthesiology.
  • Duitman J; Department of Pulmonary Medicine.
  • Bos LDJ; Center for Experimental and Molecular Medicine.
  • Wiersinga WJ; Division of Infectious Diseases, and.
Am J Respir Crit Care Med ; 206(7): 846-856, 2022 10 01.
Article in En | MEDLINE | ID: mdl-35616585
Rationale: Bacterial lung microbiota are correlated with lung inflammation and acute respiratory distress syndrome (ARDS) and altered in severe coronavirus disease (COVID-19). However, the association between lung microbiota (including fungi) and resolution of ARDS in COVID-19 remains unclear. We hypothesized that increased lung bacterial and fungal burdens are related to nonresolving ARDS and mortality in COVID-19. Objectives: To determine the relation between lung microbiota and clinical outcomes of COVID-19-related ARDS. Methods: This observational cohort study enrolled mechanically ventilated patients with COVID-19. All patients had ARDS and underwent bronchoscopy with BAL. Lung microbiota were profiled using 16S rRNA gene sequencing and quantitative PCR targeting the 16S and 18S rRNA genes. Key features of lung microbiota (bacterial and fungal burden, α-diversity, and community composition) served as predictors. Our primary outcome was successful extubation adjudicated 60 days after intubation, analyzed using a competing risk regression model with mortality as competing risk. Measurements and Main Results: BAL samples of 114 unique patients with COVID-19 were analyzed. Patients with increased lung bacterial and fungal burden were less likely to be extubated (subdistribution hazard ratio, 0.64 [95% confidence interval, 0.42-0.97]; P = 0.034 and 0.59 [95% confidence interval, 0.42-0.83]; P = 0.0027 per log10 increase in bacterial and fungal burden, respectively) and had higher mortality (bacterial burden, P = 0.012; fungal burden, P = 0.0498). Lung microbiota composition was associated with successful extubation (P = 0.0045). Proinflammatory cytokines (e.g., tumor necrosis factor-α) were associated with the microbial burdens. Conclusions: Bacterial and fungal lung microbiota are related to nonresolving ARDS in COVID-19 and represent an important contributor to heterogeneity in COVID-19-related ARDS.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome / Microbiota / COVID-19 Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2022 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome / Microbiota / COVID-19 Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Am J Respir Crit Care Med Journal subject: TERAPIA INTENSIVA Year: 2022 Type: Article