Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach
Stenotrophomonas maltophilia is an opportunistic, multidrug-resistant non-fermentative Gram-negative bacillus, posing a significant challenge in clinical treatment due to its numerous intrinsic and acquired resistance mechanisms. This study aimed to evaluate the adequacy of antibiotics used for the...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Universidad del País Vasco |
| Repositorio: | Addi. Archivo Digital para la Docencia y la Investigación |
| OAI Identifier: | oai:addi.ehu.eus:10810/68696 |
| Acceso en línea: | http://hdl.handle.net/10810/68696 |
| Access Level: | acceso abierto |
| Palabra clave: | Stenotrophomonas maltophilia PK/PD cotrimoxazole levofloxacin minocycline tigecycline aztreonam/avibactam cefiderocol |
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Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approachBarrasa González, HelenaMorán Rodríguez, Miguel ÁngelFernández Ciriza, LeireIsla Ruiz, ArantxazuSolinís Aspiazu, María ÁngelesCanut Blasco, AndrésRodríguez Gascón, AliciaStenotrophomonas maltophiliaPK/PDcotrimoxazolelevofloxacinminocyclinetigecyclineaztreonam/avibactamcefiderocolStenotrophomonas maltophilia is an opportunistic, multidrug-resistant non-fermentative Gram-negative bacillus, posing a significant challenge in clinical treatment due to its numerous intrinsic and acquired resistance mechanisms. This study aimed to evaluate the adequacy of antibiotics used for the treatment of S. maltophilia infections in critically ill patients using a pharmacokinetic/pharmacodynamic (PK/PD) approach. The antibiotics studied included cotrimoxazole, levofloxacin, minocycline, tigecycline, cefiderocol, and the new combination aztreonam/avibactam, which is not yet approved. By Monte Carlo simulations, the probability of target attainment (PTA), the PK/PD breakpoints, and the cumulative fraction of response (CFR) were estimated. PK parameters and MIC distributions were sourced from the literature, the European Committee on Antimicrobial Susceptibility Testing (EUCAST), and the SENTRY Antimicrobial Surveillance Program collection. Cefiderocol 2 g q8h, minocycline 200 mg q12h, tigecycline 100 mg q12h, and aztreonam/avibactam 1500/500 mg q6h were the best options to treat empirically infections due to S. maltophilia. Cotrimoxazole provided a higher probability of treatment success for the U.S. isolates than for European isolates. For all antibiotics, discrepancies between the PK/PD breakpoints and the clinical breakpoints defined by EUCAST (or the ECOFF) and CLSI were detected.This research was funded by the Basque Government (IT1587-22).MDPI2024202420242024info:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10810/68696reponame:Addi. Archivo Digital para la Docencia y la Investigacióninstname:Universidad del País VascoIngléshttps://www.mdpi.com/2079-6382/13/6/553info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/es/© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/ 4.0/).oai:addi.ehu.eus:10810/686962026-06-18T09:23:17Z |
| dc.title.none.fl_str_mv |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| title |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| spellingShingle |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach Barrasa González, Helena Stenotrophomonas maltophilia PK/PD cotrimoxazole levofloxacin minocycline tigecycline aztreonam/avibactam cefiderocol |
| title_short |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| title_full |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| title_fullStr |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| title_full_unstemmed |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| title_sort |
Optimizing antibiotic therapy for stenotrophomonas maltophilia infections in critically Ill patients: A pharmacokinetic/pharmacodynamic approach |
| dc.creator.none.fl_str_mv |
Barrasa González, Helena Morán Rodríguez, Miguel Ángel Fernández Ciriza, Leire Isla Ruiz, Arantxazu Solinís Aspiazu, María Ángeles Canut Blasco, Andrés Rodríguez Gascón, Alicia |
| author |
Barrasa González, Helena |
| author_facet |
Barrasa González, Helena Morán Rodríguez, Miguel Ángel Fernández Ciriza, Leire Isla Ruiz, Arantxazu Solinís Aspiazu, María Ángeles Canut Blasco, Andrés Rodríguez Gascón, Alicia |
| author_role |
author |
| author2 |
Morán Rodríguez, Miguel Ángel Fernández Ciriza, Leire Isla Ruiz, Arantxazu Solinís Aspiazu, María Ángeles Canut Blasco, Andrés Rodríguez Gascón, Alicia |
| author2_role |
author author author author author author |
| dc.subject.none.fl_str_mv |
Stenotrophomonas maltophilia PK/PD cotrimoxazole levofloxacin minocycline tigecycline aztreonam/avibactam cefiderocol |
| topic |
Stenotrophomonas maltophilia PK/PD cotrimoxazole levofloxacin minocycline tigecycline aztreonam/avibactam cefiderocol |
| description |
Stenotrophomonas maltophilia is an opportunistic, multidrug-resistant non-fermentative Gram-negative bacillus, posing a significant challenge in clinical treatment due to its numerous intrinsic and acquired resistance mechanisms. This study aimed to evaluate the adequacy of antibiotics used for the treatment of S. maltophilia infections in critically ill patients using a pharmacokinetic/pharmacodynamic (PK/PD) approach. The antibiotics studied included cotrimoxazole, levofloxacin, minocycline, tigecycline, cefiderocol, and the new combination aztreonam/avibactam, which is not yet approved. By Monte Carlo simulations, the probability of target attainment (PTA), the PK/PD breakpoints, and the cumulative fraction of response (CFR) were estimated. PK parameters and MIC distributions were sourced from the literature, the European Committee on Antimicrobial Susceptibility Testing (EUCAST), and the SENTRY Antimicrobial Surveillance Program collection. Cefiderocol 2 g q8h, minocycline 200 mg q12h, tigecycline 100 mg q12h, and aztreonam/avibactam 1500/500 mg q6h were the best options to treat empirically infections due to S. maltophilia. Cotrimoxazole provided a higher probability of treatment success for the U.S. isolates than for European isolates. For all antibiotics, discrepancies between the PK/PD breakpoints and the clinical breakpoints defined by EUCAST (or the ECOFF) and CLSI were detected. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 2024 2024 2024 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
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article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10810/68696 |
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http://hdl.handle.net/10810/68696 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
https://www.mdpi.com/2079-6382/13/6/553 |
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info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/es/ |
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openAccess |
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http://creativecommons.org/licenses/by/4.0/es/ |
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application/pdf |
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MDPI |
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MDPI |
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reponame:Addi. Archivo Digital para la Docencia y la Investigación instname:Universidad del País Vasco |
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Universidad del País Vasco |
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Addi. Archivo Digital para la Docencia y la Investigación |
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Addi. Archivo Digital para la Docencia y la Investigación |
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