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dc.creatorRuiz-Ruigómez, Maríaes
dc.creatorFernández Ruiz, Marioes
dc.creatorSilva, José Tiagoes
dc.creatorVidal, Elisaes
dc.creatorOrigüen, Juliaes
dc.creatorCalvo Cano, Antoniaes
dc.creatorCordero Matia, María Elisaes
dc.creatorLópez Medrano, Franciscoes
dc.date.accessioned2023-01-10T14:05:14Z
dc.date.available2023-01-10T14:05:14Z
dc.date.issued2021-04-19
dc.identifier.citationRuiz-Ruigómez, M., Fernández Ruiz, M., Silva, J.T., Vidal, E., Origüen, J., Calvo Cano, A.,...,López Medrano, F. (2021). Efficacy and Safety of Oral Fosfomycin for Asymptomatic Bacteriuria in Kidney Transplant Recipients: Results from a Spanish Multicenter Cohort. Antimicrobial Agents and Chemotherapy, 65 (5), e02267-20. https://doi.org/10.1128/aac.02267-20.
dc.identifier.issn0066-4804;1098-6596es
dc.identifier.urihttps://hdl.handle.net/11441/141083
dc.description.abstractCurrent guidelines recommend against systematic screening for or treating asymptomatic bacteriuria (AB) among kidney transplant (KT) recipients, although the evidence regarding episodes occurring early after transplantation or in the presence of anatomical abnormalities is inconclusive. Oral fosfomycin may constitute a good option for the treatment of posttransplant AB, particularly due to the emergence of multidrug-resistant (MDR) uropathogens. Available clinical evidence supporting its use in this specific setting, however, remains scarce. We performed a retrospective study in 14 Spanish institutions from January 2005 to December 2017. Overall, 137 episodes of AB diagnosed in 133 KT recipients treated with oral fosfomycin (calcium and trometamol salts) with a test-of-cure urine culture within the first 30 days were included. Median time from transplantation to diagnosis was 3.1 months (interquartile range [IQR], 1.1 to 10.5). Most episodes (96.4% [132/137]) were caused by Gram-negative bacteria (GNB), and 56.9% (78/137) were categorized as MDR (extended‐spectrum β‐lactamase‐producing Enterobacterales [20.4%] and carbapenem‐resistant GNB [2.9%]). Rate of microbiological failure at month 1 was 40.1% (95% confidence interval [CI], 31.9% to 48.9%) for the whole cohort and 42.3% (95% CI, 31.2% to 54.0%) for episodes due to MDR pathogens. Previous urinary tract infection (odds ratio [OR], 2.42; 95% CI, 1.11 to 5.29; P value = 0.027) and use of fosfomycin as salvage therapy (OR, 8.31; 95% CI, 1.67 to 41.35; P value = 0.010) were predictors of microbiological failure. No severe treatment-related adverse events were detected. Oral fosfomycin appears to be a suitable and safe alternative for the treatment (if indicated) of AB after KT, including those episodes due to MDR uropathogens.es
dc.formatapplication/pdfes
dc.format.extent9 p.es
dc.language.isoenges
dc.publisherAmerican Society for Micrpbiologyes
dc.relation.ispartofAntimicrobial Agents and Chemotherapy, 65 (5), e02267-20.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectasymptomatic bacteriuriaes
dc.subjectfosfomycines
dc.subjectkidney transplantes
dc.titleEfficacy and Safety of Oral Fosfomycin for Asymptomatic Bacteriuria in Kidney Transplant Recipients: Results from a Spanish Multicenter Cohortes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Medicinaes
dc.relation.projectIDREIPI RD16/0016es
dc.relation.projectIDRD16/0009es
dc.relation.projectIDCP18/00073es
dc.relation.publisherversionhttps://journals.asm.org/doi/10.1128/AAC.02267-20es
dc.identifier.doi10.1128/aac.02267-20es
dc.journaltitleAntimicrobial Agents and Chemotherapyes
dc.publication.volumen65es
dc.publication.issue5es
dc.publication.initialPagee02267-20es
dc.contributor.funderInstituto de Salud Carlos IIIes
dc.contributor.funderMinisterio de Ciencia e Innovación. Red Española de Investigación en Enfermedades Infecciosas REIPI RD16/0016es
dc.contributor.funderRed Española de Investigación en Enfermedades Renales Enfermedades RD16/0009es
dc.contributor.funderMinisterio de Ciencia e Innovación. Contrato de investigación Miguel Servet, CP18/00073es

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