TY - JOUR
T1 - Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU)
T2 - a randomised, open-label, proof-of-concept trial
AU - the Dutch-Belgian Mycosis Study Group
AU - Vanderbeke, Lore
AU - Janssen, Nico A.F.
AU - Bergmans, Dennis C.J.J.
AU - Bourgeois, Marc
AU - Buil, Jochem B.
AU - Debaveye, Yves
AU - Depuydt, Pieter
AU - Feys, Simon
AU - Hermans, Greet
AU - Hoiting, Oscar
AU - van der Hoven, Ben
AU - Jacobs, Cato
AU - Lagrou, Katrien
AU - Lemiale, Virginie
AU - Lormans, Piet
AU - Maertens, Johan
AU - Meersseman, Philippe
AU - Mégarbane, Bruno
AU - Nseir, Saad
AU - van Oers, Jos A.H.
AU - Reynders, Marijke
AU - Rijnders, Bart J.A.
AU - Schouten, Jeroen A.
AU - Spriet, Isabel
AU - Thevissen, Karin
AU - Thille, Arnaud W.
AU - Van Daele, Ruth
AU - van de Veerdonk, Frank L.
AU - Verweij, Paul E.
AU - Wilmer, Alexander
AU - Brüggemann, Roger J.M.
AU - Wauters, Joost
AU - Rijnders, Bart
AU - Verweij, Paul
AU - van de Veerdonk, Frank
AU - Schauwvlieghe, Alexander
AU - Wolfs, Tom
AU - Wauters, Joost
N1 - Publisher Copyright:
© 2021, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2021/6
Y1 - 2021/6
N2 - 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.
AB - 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.
KW - Aspergillosis
KW - Critical illness
KW - Influenza
KW - Posaconazole
KW - Prophylaxis
UR - http://www.scopus.com/inward/record.url?scp=85107277749&partnerID=8YFLogxK
U2 - 10.1007/s00134-021-06431-0
DO - 10.1007/s00134-021-06431-0
M3 - Article
C2 - 34050768
AN - SCOPUS:85107277749
SN - 0342-4642
VL - 47
SP - 674
EP - 686
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 6
ER -