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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

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 (...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164057/
https://www.ncbi.nlm.nih.gov/pubmed/34050768
http://dx.doi.org/10.1007/s00134-021-06431-0
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author 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
author_facet 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
author_sort Vanderbeke, Lore
collection PubMed
description 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 (1:1) 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00134-021-06431-0.
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spelling pubmed-81640572021-06-01 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 Intensive Care Med Original 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 (1:1) 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00134-021-06431-0. Springer Berlin Heidelberg 2021-05-29 2021 /pmc/articles/PMC8164057/ /pubmed/34050768 http://dx.doi.org/10.1007/s00134-021-06431-0 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original
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
Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title_full Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title_fullStr Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title_full_unstemmed Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title_short Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial
title_sort posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (posa-flu): a randomised, open-label, proof-of-concept trial
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164057/
https://www.ncbi.nlm.nih.gov/pubmed/34050768
http://dx.doi.org/10.1007/s00134-021-06431-0
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