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dc.contributor.authorÁvila Núñez, Marina*
dc.contributor.authorLima Rodriguez, Olalla*
dc.contributor.authorSousa Dominguez, Adrián *
dc.contributor.authorRepresa Montenegro, Marta*
dc.contributor.authorRubiñan Iglesias, Pablo*
dc.contributor.authorCelestino, P.*
dc.contributor.authorGarrido Ventin, Martin*
dc.contributor.authorGarcía Formoso, Lia*
dc.contributor.authorVasallo Vidal, Francisco José*
dc.contributor.authorMartínez Lamas, Lucía*
dc.contributor.authorPerez Landeiro, Antonio*
dc.contributor.authorRubianes Gonzalez, Martin*
dc.contributor.authorPerez Rodriguez, Maria Teresa*
dc.date.accessioned2025-09-08T11:49:02Z
dc.date.available2025-09-08T11:49:02Z
dc.date.issued2023
dc.identifier.citationÁvila-Núñez, Lima, Sousa, Represa, Rubiñán, Celestino, et al. Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales. Annals of Clinical Microbiology and Antimicrobials. 2023;22(1).
dc.identifier.issn1476-0711
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/64f6355866ccc641d10d6bab
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21180
dc.description.abstractIntroduction: Carbapenems (CR) have traditionally been the first line treatment for bacteremia caused by AmpC-producing Enterobacterales. However, CR have a high ecological impact, and carbapenem-resistant strains continue rising. Thus, other treatment alternatives like Piperacillin-Tazobactam (P-T) or Cefepime (CEF) and oral sequential therapy (OST) are being evaluated. Methods: We conducted a retrospective, single-centre observational study. All adult patients with AmpC-producing Enterobacterales bacteremia were included. The primary endpoint was clinical success defined as a composite of clinical cure, 14-day survival, and no adverse events. We evaluated the evolution of patients in whom OST was performed. Results: Seventy-seven patients were included, 22 patients in the CR group and 55 in the P-T/CEF group (37 patients received CEF and 18 P-T). The mean age of the patients was higher in the P-T/CEF group (71 years in CR group vs. 76 years in P-T/CEF group, p = 0.053). In the multivariate analysis, age ? 70 years (OR 0.08, 95% CI [0.007-0.966], p = 0.047) and a Charlson index ? 3 (OR 0.16, 95% CI [0.026-0.984], p = 0.048), were associated with a lower clinical success. Treatment with P-T/CEF was associated with higher clinical success (OR 7.75, 95% CI [1.273-47.223], p = 0.026). OST was performed in 47% of patients. This was related with a shorter in-hospital stay (OST 14 days [7-22] vs. non-OST 18 days [13-38], p = 0.005) without difference in recurrence (OST 3% vs. non-OST 5%, p = 0.999). Conclusions: Targeted treatment with P-T/CEF and OST could be safe and effective treatments for patients with AmpC-producing Enterobacterales bacteremia.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdult *
dc.subject.meshHumans *
dc.subject.meshAged *
dc.subject.meshRetrospective Studies *
dc.subject.meshSepsis *
dc.subject.meshCefepime *
dc.subject.meshBacteremia *
dc.subject.meshCarbapenems *
dc.subject.meshPiperacillin, Tazobactam Drug Combination *
dc.titleCarbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales
dc.typeArtigo
dc.authorsophosÁvila-Núñez, M.; Lima, O.; Sousa, A.; Represa, M.; Rubiñán, P.; Celestino, P.; Garrido-Ventín, M.; García-Formoso, L.; Vasallo-Vidal, F.; Martinez-Lamas, L.; Pérez-Landeiro, A.; Rubianes, M.; Pérez-Rodríguez, M.
dc.identifier.doi10.1186/s12941-023-00624-9
dc.identifier.sophos64f6355866ccc641d10d6bab
dc.issue.number1
dc.journal.titleAnnals of Clinical Microbiology and Antimicrobials*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Microbioloxía
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)::Microbioloxía
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Farmacia e farmacoloxía
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Vigo::Medicina interna
dc.relation.publisherversionhttps://doi.org/10.1186/s12941-023-00624-9
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Santiago
dc.subject.keywordIDIS
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.subject.keywordAS Vigo
dc.subject.keywordCHUVI
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number22


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)