Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial.
Aspergillosis
Critical illness
Influenza
Posaconazole
Prophylaxis
Journal
Intensive care medicine
ISSN: 1432-1238
Titre abrégé: Intensive Care Med
Pays: United States
ID NLM: 7704851
Informations de publication
Date de publication:
06 2021
06 2021
Historique:
received:
08
03
2021
accepted:
05
05
2021
pubmed:
30
5
2021
medline:
9
7
2021
entrez:
29
5
2021
Statut:
ppublish
Résumé
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. 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). 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. 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.
Identifiants
pubmed: 34050768
doi: 10.1007/s00134-021-06431-0
pii: 10.1007/s00134-021-06431-0
pmc: PMC8164057
doi:
Substances chimiques
Triazoles
0
posaconazole
6TK1G07BHZ
Banques de données
ClinicalTrials.gov
['NCT03378479']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
674-686Investigateurs
Bart Rijnders
(B)
Paul Verweij
(P)
Frank van de Veerdonk
(F)
Alexander Schauwvlieghe
(A)
Tom Wolfs
(T)
Joost Wauters
(J)
Katrien Lagrou
(K)
Commentaires et corrections
Type : CommentIn
Type : CommentIn
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