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Incidence, risk factors, and outcome of pulmonary invasive fungal disease after respiratory virus infection in allogeneic hematopoietic stem cell transplantation recipients
Author(s) -
Piñana José Luis,
Gómez María Dolores,
Montoro Juan,
Lorenzo Ignacio,
Pérez Ariadna,
Giménez Estela,
GonzálezBarberá Eva María,
Carretero Carlos,
Guerreiro Manuel,
Salavert Miguel,
Sanz Guillermo,
HernándezBoluda Juan Carlos,
Borrás Rafael,
Sanz Jaime,
Solano Carlos,
Navarro David
Publication year - 2019
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1111/tid.13158
Subject(s) - medicine , hematopoietic stem cell transplantation , cumulative incidence , transplantation , incidence (geometry) , odds ratio , immunology , physics , optics
Abstract Background There is growing evidence that community‐acquired respiratory virus (CARV) increases the risk of pulmonary invasive fungal disease (IFD) in the allogeneic hematopoietic stem cell transplantation (allo‐HSCT) setting. To date, there is a lack of knowledge regarding the risk factors (RFs), as well as the most critical period for subsequent onset of IFD after CARV infections in allo‐HSCT recipients. Methods In this prospective longitudinal observational CARV survey, we analyzed the effect of CARV on subsequent IFD development in 287 adult allo‐HSCT recipients diagnosed with 597 CARV episodes from December 2013 to December 2018. Multiplex PCR panel assays were used to test CARVs in respiratory specimens. Findings Twenty‐nine out of 287 allo‐HSCT recipients (10%) developed IFD after a CARV episode. The median time of IFD onset was 21 days (range, 0‐158 days) from day of the first CARV detection. Generalized estimating equation model identified 4 risk factors for IFD: ATG‐based conditioning regimen [odds ratio (OR) 2.34, 95% confidence interval (CI) 1.05‐5.2, P  = .038], CARV lower respiratory tract disease (OR 10.6, 95% CI 3.7‐30.8, P  < .0001), CARV infection during the first year after transplant (OR 5.34, 95% CI 1.3‐21.8, P  = .014), and corticosteroids during CARV (OR 2.6, 95% CI 1.1‐6.3, P  = .03). Conclusion Allo‐HSCT recipients conditioned with ATG and under corticosteroid therapy at the time of CARV LRTD during the first year after transplant may require close monitoring for subsequent IFD.

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