The challenge of treating infections caused by metallo-β-lactamase-producing gram-negative bacteria: a narrative review

UDC.coleccionInvestigaciónes_ES
UDC.departamentoFisioterapia, Medicina e Ciencias Biomédicases_ES
UDC.endPage1539es_ES
UDC.grupoInvInvestigación en Microbiología (INIBIC)es_ES
UDC.institutoCentroINIBIC - Instituto de Investigacións Biomédicas de A Coruñaes_ES
UDC.issue12es_ES
UDC.journalTitleDrugses_ES
UDC.startPage1519es_ES
UDC.volume84es_ES
dc.contributor.authorHidalgo-Tenorio, Carmen
dc.contributor.authorBou, Germán
dc.contributor.authorOliver, Antonio
dc.contributor.authorRodríguez Aguirregabiria, Montserrat Aránzazu
dc.contributor.authorSalavert, Miguel
dc.contributor.authorMartínez-Martínez, Luis
dc.date.accessioned2025-02-06T08:57:40Z
dc.date.available2025-02-06T08:57:40Z
dc.date.issued2024-10-28
dc.descriptionReviewes_ES
dc.description.abstract[Abstract] Gram-negative multidrug-resistant (MDR) bacteria, including Enterobacterales, Acinetobacter baumannii, and Pseudomonas aeruginosa, pose a significant challenge in clinical practice. Infections caused by metallo-β-lactamase (MBL)-producing Gram-negative organisms, in particular, require careful consideration due to their complexity and varied prevalence, given that the microbiological diagnosis of these pathogens is intricate and compounded by challenges in assessing the efficacy of anti-MBL antimicrobials. We discuss both established and new approaches in the treatment of MBL-producing Gram-negative infections, focusing on 3 strategies: colistin; the recently approved combination of aztreonam with avibactam (or with ceftazidime/avibactam); and cefiderocol. Despite its significant activity against various Gram-negative pathogens, the efficacy of colistin is limited by resistance mechanisms, while nephrotoxicity and acute renal injury call for careful dosing and monitoring in clinical practice. Aztreonam combined with avibactam (or with avibactam/ceftazidime if aztreonam plus avibactam is not available) exhibits potent activity against MBL-producing Gram-negative pathogens. Cefiderocol in monotherapy is effective against a wide range of multidrug-resistant organisms, including MBL producers, and favorable clinical outcomes have been observed in various clinical trials and case series. After examining scientific evidence in the management of infections caused by MBL-producing Gram-negative bacteria, we have developed a comprehensive clinical algorithm to guide therapeutic decision making. We recommend reserving colistin as a last-resort option for MDR Gram-negative infections. Cefiderocol and aztreonam/avibactam represent favorable options against MBL-producing pathogens. In the case of P. aeruginosa with MBL-producing enzymes and with difficult-to-treat resistance, cefiderocol is the preferred option. Further research is needed to optimize treatment strategies and minimize resistance.es_ES
dc.identifier.citationHidalgo-Tenorio C, Bou G, Oliver A, Rodríguez-Aguirregabiria M, Salavert M, Martínez-Martínez L. The challenge of treating infections caused by metallo-β-lactamase-producing gram-negative bacteria: a narrative review. Drugs. 2024 Dec;84(12):1519-1539.es_ES
dc.identifier.doi10.1007/s40265-024-02102-8
dc.identifier.issn0012-6667
dc.identifier.urihttp://hdl.handle.net/2183/41079
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.relation.urihttps://doi.org/10.1007/s40265-024-02102-8es_ES
dc.rightsCreative Commons Attribution-NonCommercial 4.0 International License (CC-BY-NC 4.0)es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.subjectAnti-bacterial agentses_ES
dc.subjectAzabicyclo compoundses_ES
dc.subjectColistines_ES
dc.subjectDrug resistance, multiple, bacteriales_ES
dc.subjectGram-negative bacteriaes_ES
dc.subjectGram-negative bacterial infectionses_ES
dc.subjectBeta-lactamaseses_ES
dc.titleThe challenge of treating infections caused by metallo-β-lactamase-producing gram-negative bacteria: a narrative reviewes_ES
dc.typejournal articlees_ES
dspace.entity.typePublication
relation.isAuthorOfPublication909e08d1-6ed1-4b99-9e9e-c64eb72e7dea
relation.isAuthorOfPublication.latestForDiscovery909e08d1-6ed1-4b99-9e9e-c64eb72e7dea

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