DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci
Objectives: To analyse the effectiveness of dalbavancin (DBV) in clinical practice as consolidation therapy in patients with bloodstream infection (BSI) and/or infective endocarditis (IE) produced by gram-positive cocci (GPC), as well as its safety and pharmacoeconomic impact. Methods: A multicentre...
| Autores: | , , , , , , , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10230/46599 |
| Acceso en línea: | http://hdl.handle.net/10230/46599 http://dx.doi.org/10.1186/s12941-019-0329-6 |
| Access Level: | acceso abierto |
| Palabra clave: | Bloodstream infection Dalbavancin Endocarditis |
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DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocciHidalgo-Tenorio, CarmenVinuesa, DavidPlata Ciezar, AntonioMartín Dávila, PilarIftimie, Simona MihaelaSequera, SergioLoeches, BelénLopez-Cortés, Luis EduardoFariñas, Mari CarmenFernández-Roldan, ConcepciónJavier-Martinez, RosarioMuñoz-Millán, PatriciaArenas-Miras, María Del MarMartínez-Marcos, Francisco JavierMiró, José MaríaHerrero, CarmenBereciartua, Elenade Jesús, Samantha E.Pasquau, JuanBloodstream infectionDalbavancinEndocarditisObjectives: To analyse the effectiveness of dalbavancin (DBV) in clinical practice as consolidation therapy in patients with bloodstream infection (BSI) and/or infective endocarditis (IE) produced by gram-positive cocci (GPC), as well as its safety and pharmacoeconomic impact. Methods: A multicentre, observational and retrospective study was conducted of hospitalised patients with IE and/or BSI produced by GPC who received at least one dose of DBV. Clinical response was assessed during hospitalization, at 3 months and at 1 year. Results: Eighty-three patients with median age of 73 years were enrolled; 73.5% were male; 59.04% had BSI and 49.04% IE (44.04% prosthetic valve IE, 32.4% native IE, 23.5% pacemaker lead). The most frequently isolated microorganism was Staphylococcus aureus in BSI (49%) and coagulase-negative staphylococci in IE (44.1%). All patients with IE were clinically cured in hospital; at 12 months, there was 2.9% loss to follow-up, 8.8% mortality unrelated to IE, and 2.9% therapeutic failure rate. The percentage effectiveness of DBV to treat IE was 96.7%. The clinical cure rate for BSI was 100% during hospital stay and at 3 months; there were no recurrences or deaths during the follow-up. No patient discontinued treatment for adverse events. The saving in hospital stay was 636 days for BSI (315,424.20€) and 557 days for IE (283,187.45€). Conclusions: DBV is an effective consolidation antibiotic therapy in clinically stabilized patients with IE and/or BSI. It proved to be a cost-effective treatment, reducing the hospital stay, thanks to the pharmacokinetic/pharmacodynamic profile of this drug.BioMed Central202120212019info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/46599http://dx.doi.org/10.1186/s12941-019-0329-6reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésCopyright © The Author(s) 2019. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/465992026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| title |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| spellingShingle |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci Hidalgo-Tenorio, Carmen Bloodstream infection Dalbavancin Endocarditis |
| title_short |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| title_full |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| title_fullStr |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| title_full_unstemmed |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| title_sort |
DALBACEN cohort: dalbavancin as consolidation therapy in patients with endocarditis and/or bloodstream infection produced by gram-positive cocci |
| dc.creator.none.fl_str_mv |
Hidalgo-Tenorio, Carmen Vinuesa, David Plata Ciezar, Antonio Martín Dávila, Pilar Iftimie, Simona Mihaela Sequera, Sergio Loeches, Belén Lopez-Cortés, Luis Eduardo Fariñas, Mari Carmen Fernández-Roldan, Concepción Javier-Martinez, Rosario Muñoz-Millán, Patricia Arenas-Miras, María Del Mar Martínez-Marcos, Francisco Javier Miró, José María Herrero, Carmen Bereciartua, Elena de Jesús, Samantha E. Pasquau, Juan |
| author |
Hidalgo-Tenorio, Carmen |
| author_facet |
Hidalgo-Tenorio, Carmen Vinuesa, David Plata Ciezar, Antonio Martín Dávila, Pilar Iftimie, Simona Mihaela Sequera, Sergio Loeches, Belén Lopez-Cortés, Luis Eduardo Fariñas, Mari Carmen Fernández-Roldan, Concepción Javier-Martinez, Rosario Muñoz-Millán, Patricia Arenas-Miras, María Del Mar Martínez-Marcos, Francisco Javier Miró, José María Herrero, Carmen Bereciartua, Elena de Jesús, Samantha E. Pasquau, Juan |
| author_role |
author |
| author2 |
Vinuesa, David Plata Ciezar, Antonio Martín Dávila, Pilar Iftimie, Simona Mihaela Sequera, Sergio Loeches, Belén Lopez-Cortés, Luis Eduardo Fariñas, Mari Carmen Fernández-Roldan, Concepción Javier-Martinez, Rosario Muñoz-Millán, Patricia Arenas-Miras, María Del Mar Martínez-Marcos, Francisco Javier Miró, José María Herrero, Carmen Bereciartua, Elena de Jesús, Samantha E. Pasquau, Juan |
| author2_role |
author author author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Bloodstream infection Dalbavancin Endocarditis |
| topic |
Bloodstream infection Dalbavancin Endocarditis |
| description |
Objectives: To analyse the effectiveness of dalbavancin (DBV) in clinical practice as consolidation therapy in patients with bloodstream infection (BSI) and/or infective endocarditis (IE) produced by gram-positive cocci (GPC), as well as its safety and pharmacoeconomic impact. Methods: A multicentre, observational and retrospective study was conducted of hospitalised patients with IE and/or BSI produced by GPC who received at least one dose of DBV. Clinical response was assessed during hospitalization, at 3 months and at 1 year. Results: Eighty-three patients with median age of 73 years were enrolled; 73.5% were male; 59.04% had BSI and 49.04% IE (44.04% prosthetic valve IE, 32.4% native IE, 23.5% pacemaker lead). The most frequently isolated microorganism was Staphylococcus aureus in BSI (49%) and coagulase-negative staphylococci in IE (44.1%). All patients with IE were clinically cured in hospital; at 12 months, there was 2.9% loss to follow-up, 8.8% mortality unrelated to IE, and 2.9% therapeutic failure rate. The percentage effectiveness of DBV to treat IE was 96.7%. The clinical cure rate for BSI was 100% during hospital stay and at 3 months; there were no recurrences or deaths during the follow-up. No patient discontinued treatment for adverse events. The saving in hospital stay was 636 days for BSI (315,424.20€) and 557 days for IE (283,187.45€). Conclusions: DBV is an effective consolidation antibiotic therapy in clinically stabilized patients with IE and/or BSI. It proved to be a cost-effective treatment, reducing the hospital stay, thanks to the pharmacokinetic/pharmacodynamic profile of this drug. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019 2021 2021 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10230/46599 http://dx.doi.org/10.1186/s12941-019-0329-6 |
| url |
http://hdl.handle.net/10230/46599 http://dx.doi.org/10.1186/s12941-019-0329-6 |
| dc.language.none.fl_str_mv |
Inglés |
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Inglés |
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http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
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http://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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application/pdf application/pdf |
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BioMed Central |
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BioMed Central |
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