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Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales
INTRODUCTION: 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)...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436381/ https://www.ncbi.nlm.nih.gov/pubmed/37592268 http://dx.doi.org/10.1186/s12941-023-00624-9 |
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author | Ávila-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, MT. |
author_facet | Ávila-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, MT. |
author_sort | Ávila-Núñez, M. |
collection | PubMed |
description | INTRODUCTION: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-023-00624-9. |
format | Online Article Text |
id | pubmed-10436381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104363812023-08-19 Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales Ávila-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, MT. Ann Clin Microbiol Antimicrob Research INTRODUCTION: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-023-00624-9. BioMed Central 2023-08-17 /pmc/articles/PMC10436381/ /pubmed/37592268 http://dx.doi.org/10.1186/s12941-023-00624-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ávila-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, MT. Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title | Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title_full | Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title_fullStr | Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title_full_unstemmed | Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title_short | Carbapenem alternatives for treatment of bloodstream infections due to AmpC producing enterobacterales |
title_sort | carbapenem alternatives for treatment of bloodstream infections due to ampc producing enterobacterales |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436381/ https://www.ncbi.nlm.nih.gov/pubmed/37592268 http://dx.doi.org/10.1186/s12941-023-00624-9 |
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