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Efficacy and Safety of Oral Fosfomycin for Asymptomatic Bacteriuria in Kidney Transplant Recipients: Results from a Spanish Multicenter Cohort

dc.contributor.authorRuiz Ruigómez, María
dc.contributor.authorFernández Ruiz, Mario
dc.contributor.authorOrigüen Sabater, Julia
dc.contributor.authorCandel González, Francisco Javier
dc.contributor.authorPérez Flores, Isabel María
dc.contributor.authorPascual Santos, Julio
dc.contributor.authorAndrés Belmonte, Amado
dc.contributor.authorAguado García, José María
dc.contributor.authorLópez Medrano, Francisco
dc.date.accessioned2026-01-22T10:06:15Z
dc.date.available2026-01-22T10:06:15Z
dc.date.issued2023-05-01
dc.descriptionFinanciados con Fondos FEDER
dc.description.abstractCurrent guidelines recommend against systematic screening 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 post-transplant 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 - 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 [95%CI]: 31.9 - 48.9) for the whole cohort and 42.3% (95%CI: 31.2 - 54.0) for episodes due to MDR pathogens. Previous urinary tract infection (odds ratio [OR]: 2.42; 95%CI: 1.11 - 5.29; P-value = 0.027) and use of fosfomycin as salvage therapy (OR: 8.31; 95%CI: 1.67 - 41.35; P-value = 0.010) were predictors of microbiological failure. No severe treatment-related adverse event 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.
dc.description.departmentDepto. de Medicina
dc.description.facultyFac. de Medicina
dc.description.refereedTRUE
dc.description.sponsorshipEuropean Commission
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.sponsorshipInstituto de Salud Carlos III (España)
dc.description.statuspub
dc.identifier.citationRuiz-Ruigómez M, Fernández-Ruiz M, Silva JT, Vidal E, Origüen J, Calvo-Cano A, et al. Efficacy and safety of oral fosfomycin for asymptomatic bacteriuria in kidney transplant recipients: results from a Spanish multicenter cohort. Antimicrob Agents Chemother. 2023;95(5):e02267-20. doi:10.1128/AAC.02267-20.
dc.identifier.doi10.1128/AAC.02267-20
dc.identifier.essn1098-6596
dc.identifier.issn0066-4804
dc.identifier.officialurlhttps://doi.org/10.1128/aac.02267-20
dc.identifier.pmid33558295
dc.identifier.relatedurlhttps://journals.asm.org/doi/10.1128/aac.02267-20
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/33558295/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/130787
dc.issue.number5
dc.journal.titleAntimicrobial Agents Chemotherapy
dc.language.isoeng
dc.publisherAmerican Society for Microbiology
dc.relation.projectIDRD16/0016
dc.relation.projectIDRD16/0009
dc.rights.accessRightsrestricted access
dc.subject.keywordFosfomycin
dc.subject.keywordAsymptomatic Bacteriuria
dc.subject.keywordKidney Transplantation
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titleEfficacy and Safety of Oral Fosfomycin for Asymptomatic Bacteriuria in Kidney Transplant Recipients: Results from a Spanish Multicenter Cohort
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number95
dspace.entity.typePublication
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