Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/201926
Title: Breakthrough invasive fungal infection among patients with haematologic malignancies: A national, prospective, and multicentre study
Author: Puerta Alcalde, Pedro
Monzó Gallo, Patricia
Aguilar-Guisado, Manuela
Ramos, Juan Carlos
Laporte Amargós, Júlia
Machado, Marina
Martín Davila, Pilar
Franch Sarto, Mireia
Sánchez Romero, Isabel
Badiola, Jon
Gómez, Lucia
Ruiz Camps, Isabel
Yáñez, Lucrecia
Vázquez, Lourdes
Chumbita, Mariana
Marco, Francesc
Soriano Viladomiu, Alex
González, Pedro
Fernández Cruz, Ana
Batlle, Montserrat
Fortún, Jesús
Guinea, Jesús
Gudiol, Carlota
García, Julio
Ruiz Pérez de Pipaón, Maite
Alastruey Izquierdo, Ana
García Vidal, Carolina
Keywords: Hematologia
Micosi
Hematology
Mycosis
Issue Date: 16-May-2023
Publisher: Elsevier BV
Abstract: Objectives: We describe the current epidemiology, causes, and outcomes of breakthrough invasive fungal infections (BtIFI) in patients with haematologic malignancies.Methods: BtIFI in patients with & GE; 7 days of prior antifungals were prospectively diagnosed (36 months across 13 Spanish hospitals) according to revised EORTC/MSG definitions.Results: 121 episodes of BtIFI were documented, of which 41 (33.9%) were proven; 53 (43.8%), probable; and 27 (22.3%), possible. The most frequent prior antifungals included posaconazole (32.2%), echinocandins (28.9%) and fluconazole (24.8%)-mainly for primary prophylaxis (81%). The most common haematologic malignancy was acute leukaemia (64.5%), and 59 (48.8%) patients had undergone a hematopoietic stem-cell transplantation. Invasive aspergillosis, principally caused by non-fumigatus Aspergillus, was the most fre-quent BtIFI with 55 (45.5%) episodes recorded, followed by candidemia (23, 19%), mucormycosis (7, 5.8%), other moulds (6, 5%) and other yeasts (5, 4.1%). Azole resistance/non-susceptibility was commonly found. Prior antifungal therapy widely determined BtIFI epidemiology. The most common cause of BtIFI in proven and probable cases was the lack of activity of the prior antifungal (63, 67.0%). At diagnosis, antifungal therapy was mostly changed (90.9%), mainly to liposomal amphotericin-B (48.8%). Overall, 10 0-day mor-tality was 47.1%; BtIFI was either the cause or an essential contributing factor to death in 61.4% of cases.Conclusions: BtIFI are mainly caused by non-fumigatus Aspergillus, non-albicans Candida, Mucorales and other rare species of mould and yeast. Prior antifungals determine the epidemiology of BtIFI. The exceed-ingly high mortality due to BtIFI warrants an aggressive diagnostic approach and early initiation of broad-spectrum antifungals different than those previously used.& COPY; 2023 The Author(s). Published by Elsevier Ltd on behalf of The British Infection Association. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Note: Reproducció del document publicat a: https://doi.org/10.1016/j.jinf.2023.05.005
It is part of: Journal of Infection, 2023, vol. 87, num. 1, p. 46-53
URI: http://hdl.handle.net/2445/201926
Related resource: https://doi.org/10.1016/j.jinf.2023.05.005
ISSN: 1532-2742
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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