Risk of Coronavirus Disease 2019-Associated Pulmonary Aspergillosis Based on Corticosteroid Duration in Intensive Care Patients.

CAPA COVID-19 aspergillosis corticosteroids critically ill

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 20 10 2022
entrez: 7 3 2023
pubmed: 8 3 2023
medline: 8 3 2023
Statut: epublish

Résumé

Coronavirus disease 2019 (COVID-19)-associated pulmonary aspergillosis (CAPA) is a potential complication in critically ill COVID-19 patients. Corticosteroids are standard of care for hospitalized COVID-19 patients but carry an increased risk of secondary infections including CAPA. The objective of this study was to evaluate if duration of corticosteroid therapy ≤10 days versus >10 days affects the risk of developing CAPA. This was a retrospective cohort study of adult patients with severe COVID-19 pneumonia requiring mechanical ventilation who received at least 3 days of corticosteroid treatment. Incidence of CAPA and secondary outcomes were compared using appropriate bivariable analyses. Steroid duration was evaluated as an independent predictor in a logistic regression model. A total of 278 patients were included (n = 169 for ≤10 days' steroid duration; n = 109 for >10 days). CAPA developed in 20 of 278 (7.2%) patients. Patients treated with >10 days of corticosteroid therapy had significantly higher incidence of CAPA (11.9% vs 4.1%; Corticosteroid treatment >10 days in critically ill COVID-19 patients is associated with an increased risk of CAPA. Patients may require corticosteroids for reasons beyond COVID-19 and clinicians should be cognizant of risk of CAPA with prolonged courses.

Sections du résumé

Background UNASSIGNED
Coronavirus disease 2019 (COVID-19)-associated pulmonary aspergillosis (CAPA) is a potential complication in critically ill COVID-19 patients. Corticosteroids are standard of care for hospitalized COVID-19 patients but carry an increased risk of secondary infections including CAPA. The objective of this study was to evaluate if duration of corticosteroid therapy ≤10 days versus >10 days affects the risk of developing CAPA.
Methods UNASSIGNED
This was a retrospective cohort study of adult patients with severe COVID-19 pneumonia requiring mechanical ventilation who received at least 3 days of corticosteroid treatment. Incidence of CAPA and secondary outcomes were compared using appropriate bivariable analyses. Steroid duration was evaluated as an independent predictor in a logistic regression model.
Results UNASSIGNED
A total of 278 patients were included (n = 169 for ≤10 days' steroid duration; n = 109 for >10 days). CAPA developed in 20 of 278 (7.2%) patients. Patients treated with >10 days of corticosteroid therapy had significantly higher incidence of CAPA (11.9% vs 4.1%;
Conclusions UNASSIGNED
Corticosteroid treatment >10 days in critically ill COVID-19 patients is associated with an increased risk of CAPA. Patients may require corticosteroids for reasons beyond COVID-19 and clinicians should be cognizant of risk of CAPA with prolonged courses.

Identifiants

pubmed: 36879627
doi: 10.1093/ofid/ofad062
pii: ofad062
pmc: PMC9984984
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofad062

Informations de copyright

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

Déclaration de conflit d'intérêts

Potential conflicts of interest. The authors have no conlicts of interest related to this work.

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Auteurs

Meera Shah (M)

Department of Pharmacotherapy and Pharmacy Services, University Health, San Antonio, Texas, USA.
Division of Pharmacotherapy, College of Pharmacy, University of Texas at Austin, Austin, Texas, USA.
Pharmacotherapy Education and Research Center, UT Health San Antonio, San Antonio, Texas, USA.

Kelly Reveles (K)

Division of Pharmacotherapy, College of Pharmacy, University of Texas at Austin, Austin, Texas, USA.
Pharmacotherapy Education and Research Center, UT Health San Antonio, San Antonio, Texas, USA.

Rebecca Moote (R)

Department of Pharmacotherapy and Pharmacy Services, University Health, San Antonio, Texas, USA.
Division of Pharmacotherapy, College of Pharmacy, University of Texas at Austin, Austin, Texas, USA.
Pharmacotherapy Education and Research Center, UT Health San Antonio, San Antonio, Texas, USA.

Elizabeth Hand (E)

Department of Pharmacotherapy and Pharmacy Services, University Health, San Antonio, Texas, USA.
Pharmacotherapy Education and Research Center, UT Health San Antonio, San Antonio, Texas, USA.

Dean Kellogg Iii (D)

Division of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, Joe R. and Terry Lozano Long School of Medicine, UT Health San Antonio, San Antonio, Texas, USA.

Rebecca L Attridge (RL)

Feik School of Pharmacy, University of the Incarnate Word, San Antonio, Texas, USA.
The Craneware Group, Deerfield Beach, Florida, USA.

Diego J Maselli (DJ)

Division of Pulmonary Diseases and Critical Care Medicine, Department of Medicine, Joe R. and Terry Lozano Long School of Medicine, UT Health San Antonio, San Antonio, Texas, USA.

G Christina Gutierrez (GC)

Department of Pharmacotherapy and Pharmacy Services, University Health, San Antonio, Texas, USA.
Division of Pharmacotherapy, College of Pharmacy, University of Texas at Austin, Austin, Texas, USA.
Pharmacotherapy Education and Research Center, UT Health San Antonio, San Antonio, Texas, USA.

Classifications MeSH