Increased susceptibility to intensive care unit-acquired pneumonia in severe COVID-19 patients: a multicentre retrospective cohort study.

COVID-19 Immunosuppression Septic shock Ventilator-acquired pneumonia

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
29 Jan 2021
Historique:
received: 20 09 2020
accepted: 18 01 2021
entrez: 29 1 2021
pubmed: 30 1 2021
medline: 30 1 2021
Statut: epublish

Résumé

The aim of this study is to determine whether severe COVID-19 patients harbour a higher risk of ICU-acquired pneumonia. This retrospective multicentre cohort study comprised all consecutive patients admitted to seven ICUs for severe COVID-19 pneumonia during the first COVID-19 surge in France. Inclusion criteria were laboratory-confirmed SARS-CoV-2 infection and requirement for invasive mechanical ventilation for 48 h or more. Control groups were two historical cohorts of mechanically ventilated patients admitted to the ICU for bacterial or non-SARS-CoV-2 viral pneumonia. The outcome of interest was the development of ICU-acquired pneumonia. The determinants of ICU-acquired pneumonia were investigated in a multivariate competing risk analysis. One hundred and seventy-six patients with severe SARS-CoV-2 pneumonia admitted to the ICU between March 1st and 30th June of 2020 were included into the study. Historical control groups comprised 435 patients with bacterial pneumonia and 48 ones with viral pneumonia. ICU-acquired pneumonia occurred in 52% of COVID-19 patients, whereas in 26% and 23% of patients with bacterial or viral pneumonia, respectively (p < 0.001). Times from initiation of mechanical ventilation to ICU-acquired pneumonia were similar across the three groups. In multivariate analysis, the risk of ICU-acquired pneumonia remained independently associated with underlying COVID-19 (SHR = 2.18; 95 CI 1.2-3.98, p = 0.011). COVID-19 appears an independent risk factor of ICU-acquired pneumonia in mechanically ventilated patients with pneumonia. Whether this is driven by immunomodulatory properties by the SARS-CoV-2 or this is related to particular processes of care remains to be investigated.

Sections du résumé

BACKGROUND BACKGROUND
The aim of this study is to determine whether severe COVID-19 patients harbour a higher risk of ICU-acquired pneumonia.
METHODS METHODS
This retrospective multicentre cohort study comprised all consecutive patients admitted to seven ICUs for severe COVID-19 pneumonia during the first COVID-19 surge in France. Inclusion criteria were laboratory-confirmed SARS-CoV-2 infection and requirement for invasive mechanical ventilation for 48 h or more. Control groups were two historical cohorts of mechanically ventilated patients admitted to the ICU for bacterial or non-SARS-CoV-2 viral pneumonia. The outcome of interest was the development of ICU-acquired pneumonia. The determinants of ICU-acquired pneumonia were investigated in a multivariate competing risk analysis.
RESULT RESULTS
One hundred and seventy-six patients with severe SARS-CoV-2 pneumonia admitted to the ICU between March 1st and 30th June of 2020 were included into the study. Historical control groups comprised 435 patients with bacterial pneumonia and 48 ones with viral pneumonia. ICU-acquired pneumonia occurred in 52% of COVID-19 patients, whereas in 26% and 23% of patients with bacterial or viral pneumonia, respectively (p < 0.001). Times from initiation of mechanical ventilation to ICU-acquired pneumonia were similar across the three groups. In multivariate analysis, the risk of ICU-acquired pneumonia remained independently associated with underlying COVID-19 (SHR = 2.18; 95 CI 1.2-3.98, p = 0.011).
CONCLUSION CONCLUSIONS
COVID-19 appears an independent risk factor of ICU-acquired pneumonia in mechanically ventilated patients with pneumonia. Whether this is driven by immunomodulatory properties by the SARS-CoV-2 or this is related to particular processes of care remains to be investigated.

Identifiants

pubmed: 33512602
doi: 10.1186/s13613-021-00812-w
pii: 10.1186/s13613-021-00812-w
pmc: PMC7844782
doi:

Types de publication

Journal Article

Langues

eng

Pagination

20

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Auteurs

Jean-François Llitjos (JF)

3i Department, Team Pulmonary and Systemic Immune Responses During Acute and Chronic Bacterial Infections, Institut Cochin, INSERM U1016, CNRS UMR8104, Université de Paris, Paris, France. jeanfrancois.llitjos@gustaveroussy.fr.
Intensive care unit, Gustave Roussy, Université Paris-Saclay, Villejuif, France. jeanfrancois.llitjos@gustaveroussy.fr.

Swann Bredin (S)

Medical Intensive Care Unit, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, APHP, Centre, Paris, France.

Jean-Baptiste Lascarrou (JB)

Intensive Care Unit, Hôpital Hôtel-Dieu, Nantes, France.

Thibaud Soumagne (T)

Intensive Care Unit, Hôpital Jean Minjoz Hospital, Besançon, France.

Mariana Cojocaru (M)

Surgical Intensive Care Unit, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, APHP, Centre, Paris, France.

Maxime Leclerc (M)

Intensive Care Unit, Centre Hospitalier Mémorial France Etats-Unis, Saint-Lô, France.

Arnaud Lepetit (A)

Intensive Care Unit, Centre Hospitalier Mémorial France Etats-Unis, Saint-Lô, France.

Albin Gouhier (A)

Intensive Care Unit, Centre Hospitalier Intercommunal Alençon Mamers, Alençon, France.

Julien Charpentier (J)

Medical Intensive Care Unit, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, APHP, Centre, Paris, France.

Gaël Piton (G)

Intensive Care Unit, Hôpital Jean Minjoz Hospital, Besançon, France.

Matthieu Faron (M)

Department of Biostatistics and Epidemiology, Inserm UNIT 1018 CESP Oncostat Team, Gustave Roussy Cancer Campus, Villejuif, France.

Annabelle Stoclin (A)

Intensive care unit, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Frédéric Pène (F)

3i Department, Team Pulmonary and Systemic Immune Responses During Acute and Chronic Bacterial Infections, Institut Cochin, INSERM U1016, CNRS UMR8104, Université de Paris, Paris, France.
Medical Intensive Care Unit, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, APHP, Centre, Paris, France.

Classifications MeSH