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Invasive aspergillosis in liver transplant recipients: Epidemiology, clinical characteristics, treatment, and outcomes in 116 cases
Author(s) -
Barchiesi Francesco,
Mazzocato Susanna,
Mazzanti Sara,
Gesuita Rosaria,
Skrami Edlira,
Fiorentini Alessandro,
Singh Nina
Publication year - 2015
Publication title -
liver transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.814
H-Index - 150
eISSN - 1527-6473
pISSN - 1527-6465
DOI - 10.1002/lt.24032
Subject(s) - medicine , voriconazole , aspergillosis , itraconazole , liver transplantation , amphotericin b , transplantation , confidence interval , proportional hazards model , gastroenterology , surgery , immunology , antifungal , dermatology
Invasive aspergillosis (IA) in liver transplant recipients is associated with grave outcomes. We reviewed 116 individual cases reported in the literature from 1985 to 2013. IA was diagnosed after a median of 25 days after transplantation and involved a single organ in 51% of the cases, whereas in the remaining cases, multiple sites were involved. The most common infecting Aspergillus species were Aspergillus fumigatus (73%), Aspergillus flavus (14%), and Aspergillus terreus (8%). Amphotericin B was the drug most frequently used, and it was followed by voriconazole and itraconazole. Combination regimens were used in 51% of the cases. The overall 1‐year cumulative survival probability was 35% [95% confidence interval (CI) = 24.6%‐49.6%]. Survival was significantly higher for patients reported from the year 2000 and thereafter ( P  < 0.001), for those diagnosed with IA more than 30 days after transplantation versus those diagnosed earlier ( P  = 0.019), and for patients without renal failure ( P  = 0.020). Additionally, the use of voriconazole was significantly associated with a higher probability of survival ( P  < 0.001). Cox regression analysis showed that subjects with the involvement of multiple sites had a 2.52 times higher risk of a negative outcome (95% CI = 1.08‐5.87) than those with the involvement of a single site. Thus, IA causes life‐threatening infections in liver transplant recipients. Predictors associated with poor outcomes may help clinicians to optimize the management of this infection. Liver Transpl 21:204‐212, 2015 . © 2014 AASLD.

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