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Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial.
Vanderbeke, Lore; Janssen, Nico A F; Bergmans, Dennis C J J; Bourgeois, Marc; Buil, Jochem B; Debaveye, Yves; Depuydt, Pieter; Feys, Simon; Hermans, Greet; Hoiting, Oscar; van der Hoven, Ben; Jacobs, Cato; Lagrou, Katrien; Lemiale, Virginie; Lormans, Piet; Maertens, Johan; Meersseman, Philippe; Mégarbane, Bruno; Nseir, Saad; van Oers, Jos A H; Reynders, Marijke; Rijnders, Bart J A; Schouten, Jeroen A; Spriet, Isabel; Thevissen, Karin; Thille, Arnaud W; Van Daele, Ruth; van de Veerdonk, Frank L; Verweij, Paul E; Wilmer, Alexander; Brüggemann, Roger J M; Wauters, Joost.
Afiliação
  • Vanderbeke L; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
  • Janssen NAF; Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • Bergmans DCJJ; Department of Internal Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Bourgeois M; Center of Expertise in Mycology Radboudumc/CWZ, Radboudumc Center for Infectious Diseases (RCI), Nijmegen, The Netherlands.
  • Buil JB; Department of Intensive Care Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.
  • Debaveye Y; Department of Intensive Care, Algemeen Ziekenhuis Sint-Jan Brugge-Oostende, Brugge, Belgium.
  • Depuydt P; Center of Expertise in Mycology Radboudumc/CWZ, Radboudumc Center for Infectious Diseases (RCI), Nijmegen, The Netherlands.
  • Feys S; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Hermans G; Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Hoiting O; Department of Intensive Care Medicine, University Hospitals Leuven, Leuven, Belgium.
  • van der Hoven B; Department of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
  • Jacobs C; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
  • Lagrou K; Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • Lemiale V; Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • Lormans P; Department of Cellular and Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Maertens J; Department of Intensive Care Medicine, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
  • Meersseman P; Department of Intensive Care Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Mégarbane B; Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • Nseir S; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
  • van Oers JAH; Department of Laboratory Medicine and National Reference Center for Mycosis, University Hospitals Leuven, Leuven, Belgium.
  • Reynders M; Department of Intensive Care Medicine, Saint-Louis Hospital, Paris, France.
  • Rijnders BJA; Department of Anesthesiology and Intensive Care Medicine, Algemeen Ziekenhuis Delta, Roeselare, Belgium.
  • Schouten JA; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
  • Spriet I; Department of Haematology, University Hospitals Leuven, Leuven, Belgium.
  • Thevissen K; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
  • Thille AW; Medical Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • Van Daele R; Department of Medical and Toxicological Critical Care, Lariboisière Hospital, INSERM UMRS-1144, University of Paris, Paris, France.
  • van de Veerdonk FL; Department of Intensive Care Medicine, Critical Care Center, University Hospital Lille, INSERM U995-E2, Lille Inflammation Research International Center, University of Lille, Lille, France.
  • Verweij PE; Department of Intensive Care Medicine, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.
  • Wilmer A; Department of Laboratory Medicine, Algemeen Ziekenhuis Sint-Jan Brugge-Oostende, Brugge, Belgium.
  • Brüggemann RJM; Department of Internal Medicine, Section of Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Wauters J; Department of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Intensive Care Med ; 47(6): 674-686, 2021 06.
Article em En | MEDLINE | ID: mdl-34050768
ABSTRACT

PURPOSE:

Influenza-associated pulmonary aspergillosis (IAPA) is a frequent complication in critically ill influenza patients, associated with significant mortality. We investigated whether antifungal prophylaxis reduces the incidence of IAPA.

METHODS:

We compared 7 days of intravenous posaconazole (POS) prophylaxis with no prophylaxis (standard-of-care only, SOC) in a randomised, open-label, proof-of-concept trial in patients admitted to an intensive care unit (ICU) with respiratory failure due to influenza (ClinicalTrials.gov, NCT03378479). Adult patients with PCR-confirmed influenza were block randomised (11) within 10 days of symptoms onset and 48 h of ICU admission. The primary endpoint was the incidence of IAPA during ICU stay in patients who did not have IAPA within 48 h of ICU admission (modified intention-to-treat (MITT) population).

RESULTS:

Eighty-eight critically ill influenza patients were randomly allocated to POS or SOC. IAPA occurred in 21 cases (24%), the majority of which (71%, 15/21) were diagnosed within 48 h of ICU admission, excluding them from the MITT population. The incidence of IAPA was not significantly reduced in the POS arm (5.4%, 2/37) compared with SOC (11.1%, 4/36; between-group difference 5.7%; 95% CI - 10.8 to 21.7; p = 0.32). ICU mortality of early IAPA was high (53%), despite rapid antifungal treatment.

CONCLUSION:

The higher than expected incidence of early IAPA precludes any definite conclusion on POS prophylaxis. High mortality of early IAPA, despite timely antifungal therapy, indicates that alternative management strategies are required. After 48 h, still 11% of patients developed IAPA. As these could benefit from prophylaxis, differentiated strategies are likely needed to manage IAPA in the ICU.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Influenza Humana / Aspergilose Pulmonar Invasiva Limite: Adult / Humans Idioma: En Ano de publicação: 2021

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Influenza Humana / Aspergilose Pulmonar Invasiva Limite: Adult / Humans Idioma: En Ano de publicação: 2021