Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study

Objectives: To describe the determinants of outcome of infections due to oxacillinase-48 (OXA-48) carbapenemase-producing Klebsiella pneumoniae (OXA-48-Kp). Methods: A retrospective cohort study of 117 episodes of OXA-48-Kp infection were conducted. Multivariate Cox models identified factors predict...

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Main Authors: Laura Corbella, Mario Fernández-Ruiz, María Ruiz-Ruigómez, Isabel Rodríguez-Goncer, José Tiago Silva, Pilar Hernández-Jiménez, Francisco López-Medrano, Manuel Lizasoain, Jennifer Villa, Octavio Carretero, José María Aguado, Rafael San-Juan
Format: Article
Language:English
Published: Elsevier 2022-06-01
Series:International Journal of Infectious Diseases
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1201971222001667
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author Laura Corbella
Mario Fernández-Ruiz
María Ruiz-Ruigómez
Isabel Rodríguez-Goncer
José Tiago Silva
Pilar Hernández-Jiménez
Francisco López-Medrano
Manuel Lizasoain
Jennifer Villa
Octavio Carretero
José María Aguado
Rafael San-Juan
author_facet Laura Corbella
Mario Fernández-Ruiz
María Ruiz-Ruigómez
Isabel Rodríguez-Goncer
José Tiago Silva
Pilar Hernández-Jiménez
Francisco López-Medrano
Manuel Lizasoain
Jennifer Villa
Octavio Carretero
José María Aguado
Rafael San-Juan
author_sort Laura Corbella
collection DOAJ
description Objectives: To describe the determinants of outcome of infections due to oxacillinase-48 (OXA-48) carbapenemase-producing Klebsiella pneumoniae (OXA-48-Kp). Methods: A retrospective cohort study of 117 episodes of OXA-48-Kp infection were conducted. Multivariate Cox models identified factors predicting 14-day clinical response and 30-day all-cause mortality. Results: A total of 77 (65.8%) isolates were susceptible to imipenem/meropenem. The 14-day clinical response and 30-day mortality rates were 41.9% and 28.2%. Catheter-related bloodstream infection (adjusted hazard ratio [aHR]: 8.33; 95% confidence interval [95%CI]: 3.19-21.72; P-value <0.001), urinary tract infection (aHR: 3.04; 95%CI: 1.39-6.66; P-value = 0.006) and early appropriate treatment (aHR: 1.77; 95%CI: 0.97-3.22; P-value = 0.064) predicted clinical response, whereas severe sepsis had a deleterious impact (aHR: 0.22; 95%CI: 0.10-0.50; P-value <0.001). Lower respiratory tract infection (aHR: 6.58; 95%CI: 2.83-15.29; P-value <0.001) and bloodstream infection (aHR: 2.33; 95%CI: 1.05-5.15; P-value = 0.037) were associated with 30-day mortality, whereas definitive therapy including ≥1 active agent (aHR: 0.26; 95%CI: 0.11-0.63; P-value = 0.003) and source control (aHR: 0.35; 95%CI: 0.14-0.91; P-value = 0.030) were protective. Combination therapy did not seem to be associated with better outcomes. Conclusions: Appropriate antimicrobial treatment was protective for 30-day mortality in OXA-48-Kp infections. Carbapenems are usually active, whereas combination therapy appeared not to confer additional benefit.
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spelling doaj.art-8b16a62a9a8a49e986dd6d59a44ac8472022-12-22T02:23:42ZengElsevierInternational Journal of Infectious Diseases1201-97122022-06-011195968Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort studyLaura Corbella0Mario Fernández-Ruiz1María Ruiz-Ruigómez2Isabel Rodríguez-Goncer3José Tiago Silva4Pilar Hernández-Jiménez5Francisco López-Medrano6Manuel Lizasoain7Jennifer Villa8Octavio Carretero9José María Aguado10Rafael San-Juan11Unit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Corresponding author: Laura Corbella, MD. Unit of Infectious Diseases, Hospital Universitario ''12 de Octubre''. Centro de Actividades Ambulatorias, 2ª planta, bloque D. Avda. de Córdoba, s/n. Postal code 28041. Madrid, Spain. Phone: +34 913908000. Fax: +34 914695775.Unit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFECT), Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFECT), Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFECT), Madrid, SpainDepartment of Microbiology, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFECT), Madrid, SpainUnit of Infectious Diseases, Hospital Universitario ''12 de Octubre'', Instituto de Investigación Sanitaria Hospital ''12 de Octubre'' (imas12), Madrid, Spain; Department of Medicine, Complutense University, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFECT), Madrid, SpainObjectives: To describe the determinants of outcome of infections due to oxacillinase-48 (OXA-48) carbapenemase-producing Klebsiella pneumoniae (OXA-48-Kp). Methods: A retrospective cohort study of 117 episodes of OXA-48-Kp infection were conducted. Multivariate Cox models identified factors predicting 14-day clinical response and 30-day all-cause mortality. Results: A total of 77 (65.8%) isolates were susceptible to imipenem/meropenem. The 14-day clinical response and 30-day mortality rates were 41.9% and 28.2%. Catheter-related bloodstream infection (adjusted hazard ratio [aHR]: 8.33; 95% confidence interval [95%CI]: 3.19-21.72; P-value <0.001), urinary tract infection (aHR: 3.04; 95%CI: 1.39-6.66; P-value = 0.006) and early appropriate treatment (aHR: 1.77; 95%CI: 0.97-3.22; P-value = 0.064) predicted clinical response, whereas severe sepsis had a deleterious impact (aHR: 0.22; 95%CI: 0.10-0.50; P-value <0.001). Lower respiratory tract infection (aHR: 6.58; 95%CI: 2.83-15.29; P-value <0.001) and bloodstream infection (aHR: 2.33; 95%CI: 1.05-5.15; P-value = 0.037) were associated with 30-day mortality, whereas definitive therapy including ≥1 active agent (aHR: 0.26; 95%CI: 0.11-0.63; P-value = 0.003) and source control (aHR: 0.35; 95%CI: 0.14-0.91; P-value = 0.030) were protective. Combination therapy did not seem to be associated with better outcomes. Conclusions: Appropriate antimicrobial treatment was protective for 30-day mortality in OXA-48-Kp infections. Carbapenems are usually active, whereas combination therapy appeared not to confer additional benefit.http://www.sciencedirect.com/science/article/pii/S1201971222001667carbapenemasesOXA-48Klebsiella pneumoniaecombination therapyprognostic factors
spellingShingle Laura Corbella
Mario Fernández-Ruiz
María Ruiz-Ruigómez
Isabel Rodríguez-Goncer
José Tiago Silva
Pilar Hernández-Jiménez
Francisco López-Medrano
Manuel Lizasoain
Jennifer Villa
Octavio Carretero
José María Aguado
Rafael San-Juan
Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
International Journal of Infectious Diseases
carbapenemases
OXA-48
Klebsiella pneumoniae
combination therapy
prognostic factors
title Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
title_full Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
title_fullStr Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
title_full_unstemmed Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
title_short Prognostic factors of OXA-48 carbapenemase-producing Klebsiella pneumoniae infection in a tertiary-care Spanish hospital: A retrospective single-center cohort study
title_sort prognostic factors of oxa 48 carbapenemase producing klebsiella pneumoniae infection in a tertiary care spanish hospital a retrospective single center cohort study
topic carbapenemases
OXA-48
Klebsiella pneumoniae
combination therapy
prognostic factors
url http://www.sciencedirect.com/science/article/pii/S1201971222001667
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