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Characteristics and Outcomes of Bloodstream Infections in a Tertiary-Care Pediatric Hematology-Oncology Unit: A 10-Year Study

Bloodstream infections (BSIs) after chemotherapy or hematopoietic stem cell transplantation (HSCT) are a leading cause of morbidity and mortality. Data on 154 BSIs that occurred in 111 onco-hematological patients (57 hematological malignancies, 28 solid tumors, and 26 non-malignant hematological dis...

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Published in:Journal of clinical medicine 2022-02, Vol.11 (3), p.880
Main Authors: Mattei, Davide, Baretta, Valentina, Mazzariol, Annarita, Maccacaro, Laura, Balter, Rita, Zaccaron, Ada, Bonetti, Elisa, Chinello, Matteo, Vitale, Virginia, Caddeo, Giulia, Esposto, Maria Pia, Pezzella, Vincenza, Gibellini, Davide, Tridello, Gloria, Cesaro, Simone
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Language:English
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Summary:Bloodstream infections (BSIs) after chemotherapy or hematopoietic stem cell transplantation (HSCT) are a leading cause of morbidity and mortality. Data on 154 BSIs that occurred in 111 onco-hematological patients (57 hematological malignancies, 28 solid tumors, and 26 non-malignant hematological diseases) were retrospectively collected and analyzed. Monomicrobial Gram-positive (GP), Gram-negative (GN), and fungal BSIs accounted for 50% (77/154), 38.3% (59/144), and 3.2% (5/154) of all episodes. Polymicrobial infections were 7.8% (12/154), while mixed bacterial-fungal infections were 0.6% (1/154). The most frequent GN isolates were (46.9%), followed by (21.9%), species (18.8%), and species (6.3%). Overall, 18.8% (12/64) of GN organisms were multidrug-resistant (seven , three , and two ), whereas GP resistance to glycopeptides was observed in 1% (1/97). Initial empirical antibiotic therapy was deemed inappropriate in 12.3% of BSIs (19/154). The 30-day mortality was 7.1% (11/154), while the bacteremia-attributable mortality was 3.9% (6/154). In multivariate analysis, septic shock was significantly associated with 30-day mortality ( = 0.0001). Attentive analysis of epidemiology and continuous microbiological surveillance are essential for the appropriate treatment of bacterial infections in pediatric onco-hematological patients.
ISSN:2077-0383
2077-0383
DOI:10.3390/jcm11030880