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Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy

Multidrug resistance associated with extended-spectrum beta-lactamase (ESBL) and Klebsiella pneumoniae carbapenemase (KPC) among K. pneumoniae is endemic in southern Europe. We retrospectively analyzed the impact of resistance on the appropriateness of empirical therapy and treatment outcomes of K....

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Autores principales: Girometti, Nicolò, Lewis, Russell E., Giannella, Maddalena, Ambretti, Simone, Bartoletti, Michele, Tedeschi, Sara, Tumietto, Fabio, Cristini, Francesco, Trapani, Filippo, Gaibani, Paolo, Viale, Pierluigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602416/
https://www.ncbi.nlm.nih.gov/pubmed/25398065
http://dx.doi.org/10.1097/MD.0000000000000111
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author Girometti, Nicolò
Lewis, Russell E.
Giannella, Maddalena
Ambretti, Simone
Bartoletti, Michele
Tedeschi, Sara
Tumietto, Fabio
Cristini, Francesco
Trapani, Filippo
Gaibani, Paolo
Viale, Pierluigi
author_facet Girometti, Nicolò
Lewis, Russell E.
Giannella, Maddalena
Ambretti, Simone
Bartoletti, Michele
Tedeschi, Sara
Tumietto, Fabio
Cristini, Francesco
Trapani, Filippo
Gaibani, Paolo
Viale, Pierluigi
author_sort Girometti, Nicolò
collection PubMed
description Multidrug resistance associated with extended-spectrum beta-lactamase (ESBL) and Klebsiella pneumoniae carbapenemase (KPC) among K. pneumoniae is endemic in southern Europe. We retrospectively analyzed the impact of resistance on the appropriateness of empirical therapy and treatment outcomes of K. pneumoniae bloodstream infections (BSIs) during a 2-year period at a 1420-bed tertiary-care teaching hospital in northern Italy. We identified 217 unique patient BSIs, including 92 (42%) KPC-positive, 49 (23%) ESBL-positive, and 1 (0.5%) metallo-beta-lactamase-positive isolates. Adequate empirical therapy was administered in 74% of infections caused by non-ESBL non-KPC strains, versus 33% of ESBL and 23% of KPC cases (p < 0.0001). To clarify the impact of resistance on BSI treatment outcomes, we compared several different models comprised of non-antibiotic treatment-related factors predictive of patients’ 30-day survival status. Acute Physiology and Chronic Health Evaluation (APACHE) II score determined at the time of positive blood culture was superior to other investigated models, correctly predicting survival status in 83% of the study cohort. In multivariate analysis accounting for APACHE II, receipt of inadequate empirical therapy was associated with nearly a twofold higher rate of death (adjusted hazard ratio 1.9, 95% confidence interval 1.1–3.4; p = 0.02). Multidrug-resistant K. pneumoniae accounted for two-thirds of all K. pneumoniae BSIs, high rates of inappropriate empirical therapy, and twofold higher rates of patient death irrespective of underlying illness.
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spelling pubmed-46024162015-10-27 Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy Girometti, Nicolò Lewis, Russell E. Giannella, Maddalena Ambretti, Simone Bartoletti, Michele Tedeschi, Sara Tumietto, Fabio Cristini, Francesco Trapani, Filippo Gaibani, Paolo Viale, Pierluigi Medicine (Baltimore) Article Multidrug resistance associated with extended-spectrum beta-lactamase (ESBL) and Klebsiella pneumoniae carbapenemase (KPC) among K. pneumoniae is endemic in southern Europe. We retrospectively analyzed the impact of resistance on the appropriateness of empirical therapy and treatment outcomes of K. pneumoniae bloodstream infections (BSIs) during a 2-year period at a 1420-bed tertiary-care teaching hospital in northern Italy. We identified 217 unique patient BSIs, including 92 (42%) KPC-positive, 49 (23%) ESBL-positive, and 1 (0.5%) metallo-beta-lactamase-positive isolates. Adequate empirical therapy was administered in 74% of infections caused by non-ESBL non-KPC strains, versus 33% of ESBL and 23% of KPC cases (p < 0.0001). To clarify the impact of resistance on BSI treatment outcomes, we compared several different models comprised of non-antibiotic treatment-related factors predictive of patients’ 30-day survival status. Acute Physiology and Chronic Health Evaluation (APACHE) II score determined at the time of positive blood culture was superior to other investigated models, correctly predicting survival status in 83% of the study cohort. In multivariate analysis accounting for APACHE II, receipt of inadequate empirical therapy was associated with nearly a twofold higher rate of death (adjusted hazard ratio 1.9, 95% confidence interval 1.1–3.4; p = 0.02). Multidrug-resistant K. pneumoniae accounted for two-thirds of all K. pneumoniae BSIs, high rates of inappropriate empirical therapy, and twofold higher rates of patient death irrespective of underlying illness. Wolters Kluwer Health 2014-10-02 /pmc/articles/PMC4602416/ /pubmed/25398065 http://dx.doi.org/10.1097/MD.0000000000000111 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins
spellingShingle Article
Girometti, Nicolò
Lewis, Russell E.
Giannella, Maddalena
Ambretti, Simone
Bartoletti, Michele
Tedeschi, Sara
Tumietto, Fabio
Cristini, Francesco
Trapani, Filippo
Gaibani, Paolo
Viale, Pierluigi
Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title_full Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title_fullStr Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title_full_unstemmed Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title_short Klebsiella pneumoniae Bloodstream Infection: Epidemiology and Impact of Inappropriate Empirical Therapy
title_sort klebsiella pneumoniae bloodstream infection: epidemiology and impact of inappropriate empirical therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602416/
https://www.ncbi.nlm.nih.gov/pubmed/25398065
http://dx.doi.org/10.1097/MD.0000000000000111
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