High burden of COVID-19-associated pulmonary aspergillosis (CAPA) in severely immunocompromised patients requiring mechanical ventilation.

CAPA COVID-19 COVID-19-associated pulmonary aspergillosis aspergillosis critical care immunocompromised intensive care invasive pulmonary aspergillosis vaccination

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
11 Sep 2023
Historique:
received: 05 06 2023
revised: 18 08 2023
accepted: 07 09 2023
medline: 11 9 2023
pubmed: 11 9 2023
entrez: 11 9 2023
Statut: aheadofprint

Résumé

COVID-19-associated pulmonary aspergillosis (CAPA) is a frequent superinfection in critically ill COVID-19 patients and is associated with increased mortality. The increasing proportion of severely immunocompromised patients among COVID-19 patients who require mechanical ventilation warrants research into the incidence and impact of CAPA during the vaccination era. We performed a retrospective, monocentric, observational study. We collected data from adult patients with severe COVID-19 requiring mechanical ventilation admitted to the ICU of University Hospitals Leuven, a tertiary referral center, between March 1st, 2020 and November 14th, 2022. Diagnosis of probable or proven CAPA was made according to the 2020 ECMM/ISHAM criteria. We included 335 patients. Bronchoalveolar lavage (BAL) sampling was performed in 300 (90%) patients. CAPA was diagnosed in 112 (33%) patients. CAPA incidence was 62% (50/81 patients) in EORTC/MSGERC host factor positive patients, compared to 24% (62/254) in host factor negative patients. CAPA incidence was significantly higher in the vaccination era, increasing from 24% (57/241) to 59% (55/94) in patients admitted to ICU before and since October 2021 respectively. Both EORTC/MSGERC host factors and ICU admission in the vaccination era were independently associated with CAPA development. CAPA remained an independent risk factor associated with mortality during the vaccination era. Presence of EORTC/MSGERC host factors for invasive mold disease is associated with increased CAPA incidence and worse outcome parameters, and is the main driver for the significantly higher incidence of CAPA in the vaccination era. Our findings warrant investigation of antifungal prophylaxis in critically ill COVID-19 patients.

Sections du résumé

BACKGROUND BACKGROUND
COVID-19-associated pulmonary aspergillosis (CAPA) is a frequent superinfection in critically ill COVID-19 patients and is associated with increased mortality. The increasing proportion of severely immunocompromised patients among COVID-19 patients who require mechanical ventilation warrants research into the incidence and impact of CAPA during the vaccination era.
METHODS METHODS
We performed a retrospective, monocentric, observational study. We collected data from adult patients with severe COVID-19 requiring mechanical ventilation admitted to the ICU of University Hospitals Leuven, a tertiary referral center, between March 1st, 2020 and November 14th, 2022. Diagnosis of probable or proven CAPA was made according to the 2020 ECMM/ISHAM criteria.
RESULTS RESULTS
We included 335 patients. Bronchoalveolar lavage (BAL) sampling was performed in 300 (90%) patients. CAPA was diagnosed in 112 (33%) patients. CAPA incidence was 62% (50/81 patients) in EORTC/MSGERC host factor positive patients, compared to 24% (62/254) in host factor negative patients. CAPA incidence was significantly higher in the vaccination era, increasing from 24% (57/241) to 59% (55/94) in patients admitted to ICU before and since October 2021 respectively. Both EORTC/MSGERC host factors and ICU admission in the vaccination era were independently associated with CAPA development. CAPA remained an independent risk factor associated with mortality during the vaccination era.
CONCLUSIONS CONCLUSIONS
Presence of EORTC/MSGERC host factors for invasive mold disease is associated with increased CAPA incidence and worse outcome parameters, and is the main driver for the significantly higher incidence of CAPA in the vaccination era. Our findings warrant investigation of antifungal prophylaxis in critically ill COVID-19 patients.

Identifiants

pubmed: 37691392
pii: 7267431
doi: 10.1093/cid/ciad546
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Auteurs

Simon Feys (S)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Katrien Lagrou (K)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Department of Laboratory Medicine and National Reference Center for Mycosis, University Hospitals Leuven, Leuven, Belgium.

Hanne Moon Lauwers (HM)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.

Koen Haenen (K)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.

Cato Jacobs (C)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.

Marius Brusselmans (M)

Leuven Biostatistics and Statistical Bioinformatics Center (L-BioStat), KU Leuven, Leuven, Belgium.

Yves Debaveye (Y)

Department of Intensive Care Medicine, University Hospitals Leuven, Leuven, Belgium.
Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.

Greet Hermans (G)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.

Martin Hoenigl (M)

Division of Infectious Diseases, ECMM Excellence Center, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Bio TechMed, Graz, Austria.
Translational Medical Mycology Research Group, Medical University of Graz, Graz, Austria.

Johan Maertens (J)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Department of Hematology, University Hospitals Leuven, Leuven, Belgium.

Philippe Meersseman (P)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Marijke Peetermans (M)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Isabel Spriet (I)

Pharmacy Department, University Hospitals Leuven, Leuven, Belgium.
Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

Christophe Vandenbriele (C)

Department of Cardiovascular Diseases, University Hospitals Leuven, Leuven, Belgium.
Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.

Lore Vanderbeke (L)

Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.

Robin Vos (R)

Department of Respiratory Diseases, University Hospitals Leuven, Leuven, Belgium.
Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.

Eric Van Wijngaerden (E)

Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Department of General Internal Medicine, University Hospitals Leuven, Leuven, Belgium.

Alexander Wilmer (A)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Joost Wauters (J)

Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Classifications MeSH