Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?

Background. Daptomycin has become a front-line antibiotic for multidrug-resistant Enterococcus faecium bloodstream infections (BSIs). We previously showed that E. faecium strains with daptomycin minimum inhibitory concentrations (MICs) in the higher end of susceptibility frequently harbor mutations...

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Autores:
Shukla, Bhavarth S.
Shelburne, Samuel A.
Reyes, Katherine C.
Kamboj, Mini
Lewis, Jessica D.
Rincon Núñez, Sandra
Reyes, Jinnethe
Carvajal Ortiz, Lina Paola
panesso, diana
Sifri, Costi
Zervos, Marcus John
Pamer, Eric G.
Tran, Truc T.
Adachi, Javier
Munita, Jose M.
Hasbun, Rodrigo
Arias, César A.
Tipo de recurso:
Article of journal
Fecha de publicación:
2016
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/3522
Acceso en línea:
http://hdl.handle.net/20.500.12495/3522
https://doi.org/10.1093/cid/ciw173
https://repositorio.unbosque.edu.co
Palabra clave:
Antibacterianos
Enterococcus faecium
Desnutrición
E. faecium
Daptomycin
MIC
Rights
openAccess
License
Acceso abierto
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dc.title.spa.fl_str_mv Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
dc.title.translated.spa.fl_str_mv Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
title Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
spellingShingle Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
Antibacterianos
Enterococcus faecium
Desnutrición
E. faecium
Daptomycin
MIC
title_short Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
title_full Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
title_fullStr Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
title_full_unstemmed Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
title_sort Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?
dc.creator.fl_str_mv Shukla, Bhavarth S.
Shelburne, Samuel A.
Reyes, Katherine C.
Kamboj, Mini
Lewis, Jessica D.
Rincon Núñez, Sandra
Reyes, Jinnethe
Carvajal Ortiz, Lina Paola
panesso, diana
Sifri, Costi
Zervos, Marcus John
Pamer, Eric G.
Tran, Truc T.
Adachi, Javier
Munita, Jose M.
Hasbun, Rodrigo
Arias, César A.
dc.contributor.author.none.fl_str_mv Shukla, Bhavarth S.
Shelburne, Samuel A.
Reyes, Katherine C.
Kamboj, Mini
Lewis, Jessica D.
Rincon Núñez, Sandra
Reyes, Jinnethe
Carvajal Ortiz, Lina Paola
panesso, diana
Sifri, Costi
Zervos, Marcus John
Pamer, Eric G.
Tran, Truc T.
Adachi, Javier
Munita, Jose M.
Hasbun, Rodrigo
Arias, César A.
dc.contributor.orcid.none.fl_str_mv Panesso, Diana [0000-0002-4049-9702]
Rincon Núñez, Sandra [0000-0002-8482-4554]
Carvajal Ortiz, Lina Paola [0000-0001-8301-8836]
dc.subject.decs.spa.fl_str_mv Antibacterianos
Enterococcus faecium
Desnutrición
topic Antibacterianos
Enterococcus faecium
Desnutrición
E. faecium
Daptomycin
MIC
dc.subject.keywords.spa.fl_str_mv E. faecium
Daptomycin
MIC
description Background. Daptomycin has become a front-line antibiotic for multidrug-resistant Enterococcus faecium bloodstream infections (BSIs). We previously showed that E. faecium strains with daptomycin minimum inhibitory concentrations (MICs) in the higher end of susceptibility frequently harbor mutations associated with daptomycin resistance. We postulate that patients with E. faecium BSIs exhibiting daptomycin MICs of 3–4 µg/mL treated with daptomycin are more likely to have worse clinical outcomes than those exhibiting daptomycin MICs ≤2 µg/mL. Methods. We conducted a multicenter retrospective cohort study that included adult patients with E. faecium BSI for whom initial isolates, follow-up blood culture data, and daptomycin administration data were available. A central laboratory performed standardized daptomycin MIC testing for all isolates. The primary outcome was microbiologic failure, defined as clearance of bacteremia ≥4 days after the index blood culture. The secondary outcome was all-cause in-hospital mortality. Results. A total of 62 patients were included. Thirty-one patients were infected with isolates that exhibited daptomycin MICs of 3–4 µg/mL. Overall, 34 patients had microbiologic failure and 25 died during hospitalization. In a multivariate logistic regression model, daptomycin MICs of 3–4 µg/mL (odds ratio [OR], 4.7 [1.37–16.12]; P = .014) and immunosuppression (OR, 5.32 [1.20–23.54]; P = .028) were significantly associated with microbiologic failure. Initial daptomycin dose of ≥8 mg/kg was not significantly associated with evaluated outcomes. Conclusions. Daptomycin MICs of 3–4 µg/mL in the initial E. faecium blood isolate predicted microbiological failure of daptomycin therapy, suggesting that modification in the daptomycin breakpoint for enterococci should be considered.
publishDate 2016
dc.date.issued.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2020-07-16T14:48:43Z
dc.date.available.none.fl_str_mv 2020-07-16T14:48:43Z
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dc.type.local.none.fl_str_mv Artículo de revista
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dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
format http://purl.org/coar/resource_type/c_6501
dc.identifier.issn.none.fl_str_mv 1537-6591
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/3522
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1093/cid/ciw173
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
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identifier_str_mv 1537-6591
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
url http://hdl.handle.net/20.500.12495/3522
https://doi.org/10.1093/cid/ciw173
https://repositorio.unbosque.edu.co
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Clinical infectious diseases, 1537-6591, Vol. 62, Nro. 12. 2016, p. 1514-1520
dc.relation.uri.none.fl_str_mv https://academic.oup.com/cid/article/62/12/1514/1745220
dc.rights.local.spa.fl_str_mv Acceso abierto
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Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2016-04-03
rights_invalid_str_mv Acceso abierto
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2016-04-03
eu_rights_str_mv openAccess
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Oxford University Press
dc.publisher.journal.spa.fl_str_mv Clinical infectious diseases
institution Universidad El Bosque
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spelling Shukla, Bhavarth S.Shelburne, Samuel A.Reyes, Katherine C.Kamboj, MiniLewis, Jessica D.Rincon Núñez, SandraReyes, JinnetheCarvajal Ortiz, Lina Paolapanesso, dianaSifri, CostiZervos, Marcus JohnPamer, Eric G.Tran, Truc T.Adachi, JavierMunita, Jose M.Hasbun, RodrigoArias, César A.Panesso, Diana [0000-0002-4049-9702]Rincon Núñez, Sandra [0000-0002-8482-4554]Carvajal Ortiz, Lina Paola [0000-0001-8301-8836]2020-07-16T14:48:43Z2020-07-16T14:48:43Z20161537-6591http://hdl.handle.net/20.500.12495/3522https://doi.org/10.1093/cid/ciw173instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquehttps://repositorio.unbosque.edu.coapplication/pdfengOxford University PressClinical infectious diseasesClinical infectious diseases, 1537-6591, Vol. 62, Nro. 12. 2016, p. 1514-1520https://academic.oup.com/cid/article/62/12/1514/1745220Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?Influence of minimum inhibitory concentration in clinical outcomes of Enterococcus faecium bacteremia treated with daptomycin: Is it Time to change the breakpoint?Artículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85AntibacterianosEnterococcus faeciumDesnutriciónE. faeciumDaptomycinMICBackground. Daptomycin has become a front-line antibiotic for multidrug-resistant Enterococcus faecium bloodstream infections (BSIs). We previously showed that E. faecium strains with daptomycin minimum inhibitory concentrations (MICs) in the higher end of susceptibility frequently harbor mutations associated with daptomycin resistance. We postulate that patients with E. faecium BSIs exhibiting daptomycin MICs of 3–4 µg/mL treated with daptomycin are more likely to have worse clinical outcomes than those exhibiting daptomycin MICs ≤2 µg/mL. Methods. We conducted a multicenter retrospective cohort study that included adult patients with E. faecium BSI for whom initial isolates, follow-up blood culture data, and daptomycin administration data were available. A central laboratory performed standardized daptomycin MIC testing for all isolates. The primary outcome was microbiologic failure, defined as clearance of bacteremia ≥4 days after the index blood culture. The secondary outcome was all-cause in-hospital mortality. Results. A total of 62 patients were included. Thirty-one patients were infected with isolates that exhibited daptomycin MICs of 3–4 µg/mL. Overall, 34 patients had microbiologic failure and 25 died during hospitalization. In a multivariate logistic regression model, daptomycin MICs of 3–4 µg/mL (odds ratio [OR], 4.7 [1.37–16.12]; P = .014) and immunosuppression (OR, 5.32 [1.20–23.54]; P = .028) were significantly associated with microbiologic failure. Initial daptomycin dose of ≥8 mg/kg was not significantly associated with evaluated outcomes. Conclusions. Daptomycin MICs of 3–4 µg/mL in the initial E. faecium blood isolate predicted microbiological failure of daptomycin therapy, suggesting that modification in the daptomycin breakpoint for enterococci should be considered.Acceso abiertohttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessAcceso abierto2016-04-03THUMBNAILBhavarth S. Shukla,Samuel Shelburne,Katherine Reyes_2016.pdf.jpgBhavarth S. 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