| Literature DB >> 33925188 |
Carmine Liberatore1,2, Francesca Farina1, Raffaella Greco1, Fabio Giglio1, Daniela Clerici1, Chiara Oltolini3, Maria Teresa Lupo Stanghellini1, Federica Barzaghi4,5, Paolo Vezzulli6, Elena Orsenigo7, Consuelo Corti1, Fabio Ciceri1,2, Jacopo Peccatori1.
Abstract
Despite the recent introduction of mold-active antifungal prophylaxis (MAP), breakthrough invasive fungal infections (b-IFI) still represent a possible complication and a cause of morbidity and mortality in hematological patients and allogeneic hematopoietic stem-cell transplantation recipients (HSCT). Data on incidence and type of b-IFI are limited, although they are mainly caused by non-fumigatus Aspergillus and non-Aspergillus molds and seem to depend on specific antifungal prophylaxis and patients' characteristics. Herein, we described the clinical presentation and management of two cases of rare b-IFI which recently occurred at our institution in patients undergoing HSCT and receiving MAP. The management of b-IFI is challenging due to the lack of data from prospective trials and high mortality rates. A thorough analysis of risk factors, ongoing antifungal prophylaxis, predisposing conditions and local epidemiology should drive the choice of antifungal treatments. Early broad-spectrum preemptive therapy with a lipid formulation of amphotericin-B, in combination with a different mold-active azole plus/minus terbinafine, is advisable. The therapy would cover against rare azole-susceptible and -resistant fungal strains, as well as atypical sites of infections. An aggressive diagnostic work-up is recommended for species identification and subsequent targeted therapy.Entities:
Keywords: antifungal therapy; breakthrough invasive fungal infections; chemotherapy; diagnosis; hematology; invasive fungal infections; new risks; prophylaxis; resistance; transplantation
Year: 2021 PMID: 33925188 DOI: 10.3390/jof7050347
Source DB: PubMed Journal: J Fungi (Basel) ISSN: 2309-608X