COVID-19-associated pulmonary aspergillosis in mechanically ventilated patients: a prospective, multicentre UK study.

COVID-19 aspergillus lung disease critical care viral infection

Journal

Thorax
ISSN: 1468-3296
Titre abrégé: Thorax
Pays: England
ID NLM: 0417353

Informations de publication

Date de publication:
01 Sep 2023
Historique:
received: 11 01 2023
accepted: 22 06 2023
medline: 2 9 2023
pubmed: 2 9 2023
entrez: 1 9 2023
Statut: aheadofprint

Résumé

Invasive pulmonary aspergillosis is a complication of severe COVID-19, with regional variation in reported incidence and mortality. We describe the incidence, risk factors and mortality associated with COVID-19-associated pulmonary aspergillosis (CAPA) in a prospective, multicentre UK cohort. From March 2020 to March 2021, 266 mechanically ventilated adults with COVID-19 were enrolled across 5 UK hospital intensive care units (ICUs). CAPA was defined using European Confederation for Medical Mycology and the International Society for Human and Animal Mycology criteria and fungal diagnostics performed on respiratory and serum samples. Twenty-nine of 266 patients (10.9%) had probable CAPA, 14 (5.2%) possible CAPA and none proven CAPA. Probable CAPA was diagnosed a median of 9 (IQR 7-16) days after ICU admission. Factors associated with probable CAPA after multivariable logistic regression were cumulative steroid dose given within 28 days prior to ICU admission (adjusted OR (aOR) 1.16; 95% CI 1.01 to 1.43 per 100 mg prednisolone-equivalent), receipt of an interleukin (IL)-6 inhibitor (aOR 2.79; 95% CI 1.22 to 6.48) and chronic obstructive pulmonary disease (COPD) (aOR 4.78; 95% CI 1.13 to 18.13). Mortality in patients with probable CAPA was 55%, vs 46% in those without. After adjustment for immortal time bias, CAPA was associated with an increased risk of 90-day mortality (HR 1.85; 95% CI 1.07 to 3.19); however, this association did not remain statistically significant after further adjustment for confounders (adjusted HR 1.57; 95% CI 0.88 to 2.80). There was no difference in mortality between patients with CAPA prescribed antifungals (9 of 17; 53%) and those who were not (7 of 12; 58%) (p=0.77). In this first prospective UK study, probable CAPA was associated with corticosteroid use, receipt of IL-6 inhibitors and pre-existing COPD. CAPA did not impact mortality following adjustment for prognostic variables.

Sections du résumé

BACKGROUND BACKGROUND
Invasive pulmonary aspergillosis is a complication of severe COVID-19, with regional variation in reported incidence and mortality. We describe the incidence, risk factors and mortality associated with COVID-19-associated pulmonary aspergillosis (CAPA) in a prospective, multicentre UK cohort.
METHODS METHODS
From March 2020 to March 2021, 266 mechanically ventilated adults with COVID-19 were enrolled across 5 UK hospital intensive care units (ICUs). CAPA was defined using European Confederation for Medical Mycology and the International Society for Human and Animal Mycology criteria and fungal diagnostics performed on respiratory and serum samples.
RESULTS RESULTS
Twenty-nine of 266 patients (10.9%) had probable CAPA, 14 (5.2%) possible CAPA and none proven CAPA. Probable CAPA was diagnosed a median of 9 (IQR 7-16) days after ICU admission. Factors associated with probable CAPA after multivariable logistic regression were cumulative steroid dose given within 28 days prior to ICU admission (adjusted OR (aOR) 1.16; 95% CI 1.01 to 1.43 per 100 mg prednisolone-equivalent), receipt of an interleukin (IL)-6 inhibitor (aOR 2.79; 95% CI 1.22 to 6.48) and chronic obstructive pulmonary disease (COPD) (aOR 4.78; 95% CI 1.13 to 18.13). Mortality in patients with probable CAPA was 55%, vs 46% in those without. After adjustment for immortal time bias, CAPA was associated with an increased risk of 90-day mortality (HR 1.85; 95% CI 1.07 to 3.19); however, this association did not remain statistically significant after further adjustment for confounders (adjusted HR 1.57; 95% CI 0.88 to 2.80). There was no difference in mortality between patients with CAPA prescribed antifungals (9 of 17; 53%) and those who were not (7 of 12; 58%) (p=0.77).
INTERPRETATION CONCLUSIONS
In this first prospective UK study, probable CAPA was associated with corticosteroid use, receipt of IL-6 inhibitors and pre-existing COPD. CAPA did not impact mortality following adjustment for prognostic variables.

Identifiants

pubmed: 37657925
pii: thorax-2023-220002
doi: 10.1136/thorax-2023-220002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical Research Council
ID : MR/N006364/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V033417/1
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: MPW, WH and TB have received speaker fees from Gilead Sciences. JY has received honoraria from Pfizer for contributing to a CAPA working group. TB has received Advisory Board fees from Gilead Sciences and Mundipharma and funding from MSD and Pfizer. DRJ is the president of the British Society for Antimicrobial Chemotherapy and has received honoraria from Pfizer, Shionogi, Menarini and Tillots. SS has received honoraria from Pfizer and Gilead for educational purposes. PLW performed diagnostic evaluations and received meeting sponsorship from Associates of Cape Cod, Bruker, Dynamiker and Launch Diagnostics; speaker fees, expert advice fees and meeting sponsorship from Gilead; and speaker and expert advice fees from Pfizer and expert advice fees from F2G.

Auteurs

William Hurt (W)

Institute of Infection and Immunity, St George's University of London, London, UK whurt@sgul.ac.uk.
Clinical Infection Unit, St George's University Hospitals NHS Foundation Trust, London, UK.
Medical Research Council Centre for Medical Mycology, University of Exeter, Exeter, UK.

Jonathan Youngs (J)

Institute of Infection and Immunity, St George's University of London, London, UK.
Clinical Infection Unit, St George's University Hospitals NHS Foundation Trust, London, UK.

Jonathan Ball (J)

Adult Critical Care, St George's University Hospitals NHS Foundation Trust, London, UK.

Jonathan Edgeworth (J)

Clinical Infection and Microbiology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Philip Hopkins (P)

Adult Critical Care, King's College Hospital NHS Foundation Trust, London, UK.

David R Jenkins (DR)

Clinical Microbiology, University Hospitals of Leicester NHS Trust, Leicester, UK.

Susannah Leaver (S)

Adult Critical Care, St George's University Hospitals NHS Foundation Trust, London, UK.

Andrea Mazzella (A)

Institute of Infection and Immunity, St George's University of London, London, UK.

Síle F Molloy (SF)

Institute of Infection and Immunity, St George's University of London, London, UK.

Silke Schelenz (S)

Medical Microbiology, King's College Hospital NHS Foundation Trust, London, UK.

Matt P Wise (MP)

Adult Critical Care, University of Wales Hospital, Cardiff, UK.

P Lewis White (PL)

Microbiology, Public Health Wales, Cardiff, UK.

Hakeem Yusuff (H)

Adult Critical Care, University Hospitals of Leicester NHS Trust, Leicester, UK.

Duncan Wyncoll (D)

Adult Critical Care, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Tihana Bicanic (T)

Institute of Infection and Immunity, St George's University of London, London, UK.
Clinical Infection Unit, St George's University Hospitals NHS Foundation Trust, London, UK.
Medical Research Council Centre for Medical Mycology, University of Exeter, Exeter, UK.

Classifications MeSH