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dc.rights.licenseopenen_US
dc.contributor.authorSOUEGES, Sarah
dc.contributor.authorFAURE, Emmanuel
dc.contributor.authorPARIZE, Perrine
dc.contributor.authorLANTERNIER-DESSAP, Fanny
dc.contributor.authorLECUYER, Hervé
dc.contributor.authorHUYNH, Anne
dc.contributor.authorMARTIN-BLONDEL, Guillaume
dc.contributor.authorGABORIT, Benjamin
dc.contributor.authorBLOT, Mathieu
dc.contributor.authorMAGALLON, Arnaud
dc.contributor.authorBLANCHARD, Elodie
dc.contributor.authorBROUSSE, Xavier
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorLAHOUATI, Marin
dc.contributor.authorBRUNEL, Anne-Sophie
dc.contributor.authorLE BANNER, Eloise
dc.contributor.authorCAMELENA, François
dc.contributor.authorLARCHER, Romaric
dc.contributor.authorPANTEL, Alix
dc.contributor.authorMELICA, Giovanna
dc.contributor.authorRAZAZI, Keyvan
dc.contributor.authorDANION, François
dc.contributor.authorSCHRAMM, Frederic
dc.contributor.authorDUMITRESCU, Oana
dc.contributor.authorHOELLINGER, Baptiste
dc.contributor.authorADER, Florence
dc.date.accessioned2025-01-14T09:01:43Z
dc.date.available2025-01-14T09:01:43Z
dc.date.issued2025-01-01
dc.identifier.issn1532-2742en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/204253
dc.description.abstractEnThe increase in the population of immunocompromised patients due to advances in management of end-stage diseases and transplants poses challenges in treating infections caused by multi-drug resistant (MDR) pathogens. Cefiderocol (FDC), a siderophore cephalosporin, has shown efficacy against carbapenem-resistant Gram-negative bacteria. This retrospective multicentre study investigated the real-world use of FDC in 114 immunocompromised adults treated for MDR infections in 12 French hospitals (June 2020-November 2023). Clinical and microbiological outcomes, including infection cure, relapse, as well as mortality, and resistance acquisition, were assessed at days 28 and 90. Antibiotic prescription compliance with current guidelines was investigated. At day 28, clinical success was achieved in 53.3% of cases, and overall mortality was 37.7%, consistent with other studies (33-37%). Infection-related mortality accounted for 25.4%. Relapse occurred in 17.5% of patients by day 28, rising by an additional 9.8% among survivors by day 90. Resistance acquisition was observed in two cases at day 28 (Pseudomonas aeruginosa and Stenotrophomonas maltophilia) and in three additional cases by day 90. FDC was used as monotherapy in 49.1% of cases, with a median treatment duration of 10 days. Nearly 25% of strains collected in FDC-treated patients were susceptible to best-practice alternatives. These findings highlight FDC's utility in difficult-to-treat infections, particularly S. maltophilia, but the high relapse rate and resistance acquisition underscore the need for careful monitoring, adherence to guidelines, and reconsideration of empirical use to prevent resistance and improve outcomes in fragile populations.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enHumans
dc.subject.enCefiderocol
dc.subject.enRetrospective Studies
dc.subject.enMale
dc.subject.enImmunocompromised Host
dc.subject.enFemale
dc.subject.enGram-Negative Bacterial Infections
dc.subject.enDrug Resistance
dc.subject.enMultiple
dc.subject.enBacterial
dc.subject.enMiddle Aged
dc.subject.enAnti-Bacterial Agents
dc.subject.enAged
dc.subject.enGram-Negative Bacteria
dc.subject.enAdult
dc.subject.enCephalosporins
dc.subject.enTreatment Outcome
dc.subject.enFrance
dc.subject.enAged
dc.subject.en80 and over
dc.title.enReal-world multicentre study of cefiderocol treatment of immunocompromised patients with infections caused by multidrug-resistant Gram-negative bacteria: CEFI-ID.
dc.title.alternativeJ Infecten_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.jinf.2024.106376en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed39681233en_US
bordeaux.journalJournal of Infectionen_US
bordeaux.page106376en_US
bordeaux.volume90en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04885304
hal.version1
hal.date.transferred2025-01-14T09:01:47Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Infection&rft.date=2025-01-01&rft.volume=90&rft.issue=1&rft.spage=106376&rft.epage=106376&rft.eissn=1532-2742&rft.issn=1532-2742&rft.au=SOUEGES,%20Sarah&FAURE,%20Emmanuel&PARIZE,%20Perrine&LANTERNIER-DESSAP,%20Fanny&LECUYER,%20Herv%C3%A9&rft.genre=article


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