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dc.rights.licenseopenen_US
hal.structure.identifierCentre Hospitalier Universitaire de Nice [CHU Nice]
dc.contributor.authorCOURJON, Johan
hal.structure.identifierEvaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]
dc.contributor.authorSENNEVILLE, Eric
hal.structure.identifierCHU Mont de Marsan
dc.contributor.authorILLES, Hajnal-Gabriela
hal.structure.identifierCentre Hospitalier Universitaire [CHU Grenoble] [CHUGA]
dc.contributor.authorPAVESE, Patricia
hal.structure.identifierCentre d'investigation clinique (CIC) de Nantes -CIC Plurithématique [CIC 0004 - Nantes]
dc.contributor.authorBOUTOILLE, David
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDAOUD-PINEAU, Frederic
dc.contributor.authorDUNKEL, Nathalie
hal.structure.identifierARN régulateurs bactériens et médecine [BRM]
hal.structure.identifierCentre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
dc.contributor.authorTATTEVIN, Pierre
dc.date.accessioned2024-10-30T12:42:20Z
dc.date.available2024-10-30T12:42:20Z
dc.date.issued2023-08-04
dc.identifier.issn0924-8579en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202992
dc.description.abstractEnOBJECTIVES: Dalbavancin is a lipoglycopeptide antibiotic approved for the treatment of acute bacterial skin and skin structure infections. However, several studies have suggested that it is used mostly for off-label indications. We aimed to describe the use of dalbavancin in patients who received at least one dose of the antibiotic in France. METHODS: Prospective, observational, multicentre study conducted in France from September 2018 to April 2020. The primary outcome was the clinical response at 30 days after the last dalbavancin dose. RESULTS: A total of 151 patients in 16 centres were included in this study. The main infection sites were bone and joint infections (55.0%), multisite infections (15.9%), and vascular infections (14.6%), and the primary pathogens were coagulase-negative staphylococci (N = 82), Staphylococcus aureus (N = 51), and enterococci (N = 27). Most patients (71.5%) received three previous antibiotic treatments. The number of dalbavancin injections per patient was 1 in 26 patients (17.2%), 2 in 95 patients (62.9%), 3 in 17 patients (11.3%), and more than 3 in 13 patients (8.6%), with a mean cumulative dose of 3089 ± 1461 mg per patient. Among the 129 patients with a complete follow-up, clinical success was achieved in 119 patients (92.2%). At least 1 adverse event was reported in 67 patients (44.4%), including 12 (7.9%) patients with dalbavancin-related adverse events. CONCLUSIONS: The results of the study showed that dalbavancin is used mostly for off-label indications and in heavily pretreated patients in France. The clinical response at 30 days after the last dose was favourable in most patients, with a good safety profile.
dc.language.isoENen_US
dc.subject.enAntibiotics
dc.subject.enDalbavancin
dc.subject.enEffectiveness
dc.subject.enOff-label
dc.subject.enSafety
dc.title.enEffectiveness and safety of dalbavancin in France: a prospective, multicentre cohort study
dc.title.alternativeInt J Antimicrob Agentsen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.ijantimicag.2023.106945en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
bordeaux.journalInternational Journal of Antimicrobial Agentsen_US
bordeaux.page106945en_US
bordeaux.volume62en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue4en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamAHEAD_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-04196650
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=International%20Journal%20of%20Antimicrobial%20Agents&rft.date=2023-08-04&rft.volume=62&rft.issue=4&rft.spage=106945&rft.epage=106945&rft.eissn=0924-8579&rft.issn=0924-8579&rft.au=COURJON,%20Johan&SENNEVILLE,%20Eric&ILLES,%20Hajnal-Gabriela&PAVESE,%20Patricia&BOUTOILLE,%20David&rft.genre=article


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