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Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis.

Authors :
Weber, Sarah
Magh, Aaron
Hogardt, Michael
Kempf, Volkhard A. J.
Vehreschild, Maria J. G. T.
Serve, Hubert
Scheich, Sebastian
Steffen, Björn
Source :
Annals of Hematology. Jun2021, Vol. 100 Issue 6, p1593-1602. 10p.
Publication Year :
2021

Abstract

Bloodstream infections (BSI) are a frequent complication in patients with hematological and oncological diseases. However, the impact of different bacterial species causing BSI and of multiple BSI remains incompletely understood. We performed a retrospective study profiling 637 bacterial BSI episodes in hematological and oncological patients. Based on the 30-day (30d) overall survival (OS), we analyzed different types of multiple BSI and grouped BSI-associated bacteria into clusters followed by further assessment of clinical and infection-related characteristics. We discovered that polymicrobial BSI (different organisms on the first day of a BSI episode) and sequential BSI (another BSI before the respective BSI episode) were associated with a worse 30d OS. Different bacterial groups could be classified into three BSI outcome clusters based on 30d OS: favorable (FAV) including mainly common skin contaminants, Escherichia spp. and Streptococcus spp.; intermediate (INT) including mainly Enterococcus spp., vancomycin-resistant Enterococcus spp., and multidrug-resistant gram-negative bacteria (MDRGN); and adverse (ADV) including MDRGN with an additional carbapenem-resistance (MDRGN+CR). A polymicrobial or sequential BSI especially influenced the outcome in the combination of two INT cluster BSI. The presence of a polymicrobial BSI and the assignment into the BSI outcome clusters were identified as independent risk factors for 30d mortality in a Cox multivariate regression analysis. The assignment to a BSI outcome cluster and the differentiated perspective of multiple BSI open new insights into the prognosis of patients with BSI and should be further validated in other patient cohorts. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09395555
Volume :
100
Issue :
6
Database :
Academic Search Index
Journal :
Annals of Hematology
Publication Type :
Academic Journal
Accession number :
150302164
Full Text :
https://doi.org/10.1007/s00277-021-04541-9