Outcome and characteristics of invasive fungal infections in critically ill burn patients: A multicenter retrospective study.


Journal

Mycoses
ISSN: 1439-0507
Titre abrégé: Mycoses
Pays: Germany
ID NLM: 8805008

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 23 12 2019
revised: 16 02 2020
accepted: 18 02 2020
pubmed: 23 2 2020
medline: 30 1 2021
entrez: 21 2 2020
Statut: ppublish

Résumé

Characteristics and outcome of invasive fungal infection (IFI) in critically ill burn patients have been poorly explored. We report the factors associated with 90-day mortality in a multicentre retrospective European study. All burn patients with confirmed IFI admitted between 1 January 2010 to 31 December 2015 in 10 centres in France and Belgium were included. Ninety-four patients were enrolled with 110 cases of IFIs: 79 (71.8%) were yeasts IFI and 31 (28.2%) filamentous IFI. Incidence was 1% among admitted patients. The 90-day mortality was 37.2% for all IFIs combined, 52% for filamentous infection and 31.9% for yeast infection. Patients with more than one IFI had a higher 90-day mortality than patients with only one episode (61.5% vs 33.5% (P = .006)). In multivariate analysis, higher Simplified Acute Physiology Score II (OR = 1.05 (95% CI: 1.02-1.09) P = .003), bacterial co-infection (OR = 3.85 (95% CI: 1.23-12.01), P = .014) and use of skin allografts at the time of IFI diagnosis (OR = 3.87 (95% CI: 1.31-11.42), P = .021) were associated with 90-day mortality. Although rare, invasive fungal infections remain associated with poor outcome in burn patients. Bacterial co-infection and presence of allograft were potentially modifiable factors independently associated with outcome.

Sections du résumé

BACKGROUND BACKGROUND
Characteristics and outcome of invasive fungal infection (IFI) in critically ill burn patients have been poorly explored.
OBJECTIVES OBJECTIVE
We report the factors associated with 90-day mortality in a multicentre retrospective European study.
PATIENTS/METHODS METHODS
All burn patients with confirmed IFI admitted between 1 January 2010 to 31 December 2015 in 10 centres in France and Belgium were included.
RESULTS RESULTS
Ninety-four patients were enrolled with 110 cases of IFIs: 79 (71.8%) were yeasts IFI and 31 (28.2%) filamentous IFI. Incidence was 1% among admitted patients. The 90-day mortality was 37.2% for all IFIs combined, 52% for filamentous infection and 31.9% for yeast infection. Patients with more than one IFI had a higher 90-day mortality than patients with only one episode (61.5% vs 33.5% (P = .006)). In multivariate analysis, higher Simplified Acute Physiology Score II (OR = 1.05 (95% CI: 1.02-1.09) P = .003), bacterial co-infection (OR = 3.85 (95% CI: 1.23-12.01), P = .014) and use of skin allografts at the time of IFI diagnosis (OR = 3.87 (95% CI: 1.31-11.42), P = .021) were associated with 90-day mortality.
CONCLUSIONS CONCLUSIONS
Although rare, invasive fungal infections remain associated with poor outcome in burn patients. Bacterial co-infection and presence of allograft were potentially modifiable factors independently associated with outcome.

Identifiants

pubmed: 32077536
doi: 10.1111/myc.13068
doi:

Substances chimiques

Antifungal Agents 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

535-542

Subventions

Organisme : The Research group SPILF-CMIT (Société De Pathologie Infectieuse de Langue Française-Collègue des Universitaires de maladie infectieuses et Tropicales)

Informations de copyright

© 2020 Blackwell Verlag GmbH.

Références

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Auteurs

Véronique Maurel (V)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, St-Louis Hospital, Paris, France.

Blandine Denis (B)

Department of Infectious Diseases, AP-HP, St-Louis Hospital, Paris, France.

Matthieu Camby (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, St-Louis Hospital, Paris, France.

Mathieu Jeanne (M)

Department of Anesthesiology and Intensive Care, CHU Lille, Lille, France.

Aline Cornesse (A)

Department of Anesthesiology and Critical Care and Burn Unit, CHU Toulouse, Toulouse, France.

Boris Glavnik (B)

Department of Anesthesiology and Critical Care and Burn Unit, Mercy Hospital, Metz, France.

Alexandre Alanio (A)

Molecular Mycology Unit, Institut Pasteur, CNRS, UMR2000, Paris, France.
Laboratoire de Parasitologie-Mycologie, Groupe Hospitalier Saint-Louis-Lariboisière-Fernand-Widal, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Sorbonne Paris Cité, Université Paris Diderot, Paris, France.

Anne-Françoise Rousseau (AF)

Burn Intensive Center, CHU Sart-Tilman, Liège, Belgium.

Ronan Lefloch (R)

Burn Intensive Care Unit, CHU Nantes, Nantes, France.

Marie Lagrange-Xelot (M)

Department of Infectious Diseases, CHU Félix Guyon, La Reunion, France.

Julien Textoris (J)

Department of Anesthesiology and Intensive Care, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
EA7426 P13 "Pathophysiology of Injury-Induced Immunosuppression", Hospices Civils de Lyon, bioMérieux, Université Claude Bernard Lyon-1, Lyon, France.

Sandrine Wiramus (S)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HM, Conception Hospital, Marseille, France.

Christian de Tymowski (C)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, St-Louis Hospital, Paris, France.

Matthieu Legrand (M)

Department of Anesthesiology and Critical Care and Burn Unit, AP-HP, St-Louis Hospital, Paris, France.
Sorbonne Paris Cité, Université Paris Diderot, Paris, France.
UMR INSERM 942, Institut National de la Santé et de la Recherche Médicale (INSERM), F-CRIN INI-CRCT Network, Paris, France.

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