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...
- 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 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.local.none.fl_str_mv |
Artículo de revista |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
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 |
dc.identifier.repourl.none.fl_str_mv |
https://repositorio.unbosque.edu.co |
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 |
dc.rights.accessrights.none.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 info:eu-repo/semantics/openAccess Acceso abierto |
dc.rights.creativecommons.none.fl_str_mv |
2016-04-03 |
rights_invalid_str_mv |
Acceso abierto http://purl.org/coar/access_right/c_abf2 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 |
bitstream.url.fl_str_mv |
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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. Shukla,Samuel Shelburne,Katherine Reyes_2016.pdf.jpgimage/jpeg5775https://repositorio.unbosque.edu.co/bitstreams/7d66f107-7dc6-46fe-9780-177a96c33734/download7210a811635d1799e7c05fee5d259be7MD53ORIGINALBhavarth S. Shukla,Samuel Shelburne,Katherine Reyes_2016.pdfBhavarth S. Shukla,Samuel Shelburne,Katherine Reyes_2016.pdfapplication/pdf272241https://repositorio.unbosque.edu.co/bitstreams/e62c2611-4c44-42ec-837e-27701bc3200d/download754d06c19544ba9ca0b9da03e8dae5f3MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.unbosque.edu.co/bitstreams/5457d1bd-6f35-42ad-a9b2-d6de349199a7/download8a4605be74aa9ea9d79846c1fba20a33MD52TEXTBhavarth S. Shukla,Samuel Shelburne,Katherine Reyes_2016.pdf.txtBhavarth S. 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