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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.
Afiliación
  • Weber S; Department of Medicine, Hematology/Oncology, University Hospital Frankfurt, Frankfurt am Main, Germany. sarah.weber@kgu.de.
  • Magh A; University Center for Infectious Diseases, University Hospital Frankfurt, Frankfurt, Germany. sarah.weber@kgu.de.
  • Hogardt M; Department of Medicine, Hematology/Oncology, University Hospital Frankfurt, Frankfurt am Main, Germany.
  • Kempf VAJ; University Center for Infectious Diseases, University Hospital Frankfurt, Frankfurt, Germany.
  • Vehreschild MJGT; Institute of Medical Microbiology and Infection Control, University Hospital Frankfurt, Frankfurt, Germany.
  • Serve H; University Center of Competence for Infection Control, Frankfurt, State of Hesse, Germany.
  • Scheich S; University Center for Infectious Diseases, University Hospital Frankfurt, Frankfurt, Germany.
  • Steffen B; Institute of Medical Microbiology and Infection Control, University Hospital Frankfurt, Frankfurt, Germany.
Ann Hematol ; 100(6): 1593-1602, 2021 Jun.
Article en En | MEDLINE | ID: mdl-33942127
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacteriemia / Neoplasias Hematológicas / Enfermedades Hematológicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Hematol Asunto de la revista: HEMATOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bacteriemia / Neoplasias Hematológicas / Enfermedades Hematológicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Hematol Asunto de la revista: HEMATOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Alemania