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Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis
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 episode...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116230/ https://www.ncbi.nlm.nih.gov/pubmed/33942127 http://dx.doi.org/10.1007/s00277-021-04541-9 |
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author | Weber, Sarah Magh, Aaron Hogardt, Michael Kempf, Volkhard A. J. Vehreschild, Maria J. G. T. Serve, Hubert Scheich, Sebastian Steffen, Björn |
author_facet | Weber, Sarah Magh, Aaron Hogardt, Michael Kempf, Volkhard A. J. Vehreschild, Maria J. G. T. Serve, Hubert Scheich, Sebastian Steffen, Björn |
author_sort | Weber, Sarah |
collection | PubMed |
description | 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04541-9. |
format | Online Article Text |
id | pubmed-8116230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-81162302021-05-13 Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis Weber, Sarah Magh, Aaron Hogardt, Michael Kempf, Volkhard A. J. Vehreschild, Maria J. G. T. Serve, Hubert Scheich, Sebastian Steffen, Björn Ann Hematol Original Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00277-021-04541-9. Springer Berlin Heidelberg 2021-05-03 2021 /pmc/articles/PMC8116230/ /pubmed/33942127 http://dx.doi.org/10.1007/s00277-021-04541-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Weber, Sarah Magh, Aaron Hogardt, Michael Kempf, Volkhard A. J. Vehreschild, Maria J. G. T. Serve, Hubert Scheich, Sebastian Steffen, Björn Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title | Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title_full | Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title_fullStr | Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title_full_unstemmed | Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title_short | Profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
title_sort | profiling of bacterial bloodstream infections in hematological and oncological patients based on a comparative survival analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116230/ https://www.ncbi.nlm.nih.gov/pubmed/33942127 http://dx.doi.org/10.1007/s00277-021-04541-9 |
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