Dalbavancin in clinical practice in Spain: a 2 year retrospective study

dc.contributor.authorMorata, Laura
dc.contributor.authorAguado, José María
dc.contributor.authorSalavert, Miguel
dc.contributor.authorPasquau, Juan
dc.contributor.authorMíguez, Enrique
dc.contributor.authorMuñoz, Patricia
dc.contributor.authorRosselló, Irantzu
dc.contributor.authorAlmirante, Benito
dc.date.accessioned2023-02-06T08:51:55Z
dc.date.available2023-02-06T08:51:55Z
dc.date.issued2022-11-03
dc.date.updated2023-02-01T16:34:10Z
dc.description.abstractObjectives Dalbavancin is approved for the treatment of acute bacterial skin and skin-structure infections (ABSSSIs) in adults. Its unique pharmacokinetic properties allow daily dosing to be avoided. The objective was to describe the sociodemographic and clinical characteristics of patients treated with dalbavancin in Spain, and to evaluate its effectiveness and safety in real-world settings. Patients and methods This non-interventional, retrospective, observational and multicentre study included patients who received at least one dose between 2018 and 2019 in seven Spanish hospitals. Results In total, 187 patients were included. The most common comorbidities were cardiovascular disease (27.4%) and diabetes mellitus (23.5%). Dalbavancin was used to treat osteoarticular infections (28.3%), ABSSSIs (22.5%), cardiovascular infections (20.9%) and catheter-related infections (18.2%). The most prevalent pathogens were Staphylococcus aureus (34.2%), CoNS (32.6%), and enterococci (12.8%). The main reason for use was early hospital discharge (65.8%). Most patients were treated with 1500 mg in a single dose (35.3%) and the median duration of treatment was 2 weeks. The treatment was clinically successful in 91.4% of cases. Six patients (3.2%) reported adverse events. Physicians agreed on the potential reduction of hospitalization days (85.3%). A subanalysis of patient characteristics and type of pathogen showed similar results in terms of efficacy and safety. Conclusions Dalbavancin seems to be effective and safe as second-line treatment in severe Gram-positive infections. It improves treatment adherence and allows outpatient management. Furthermore, the effectiveness and safety profile are maintained against diverse microorganisms in Gram-positive infections and regardless of the patients' comorbidities at baseline, or age.
dc.format.mimetypeapplication/pdf
dc.identifier.issn2632-1823
dc.identifier.pmid36570687
dc.identifier.urihttps://hdl.handle.net/2445/193142
dc.language.isoeng
dc.publisherOxford University Press (OUP)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1093/jacamr/dlac120
dc.relation.ispartofJAC-Antimicrobial Resistance, 2022, vol. 4, num. 6, p. dlac120
dc.relation.urihttps://doi.org/10.1093/jacamr/dlac120
dc.rightscc by (c) Morata, Laura et al., 2022
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationMalalties bacterianes grampositives
dc.subject.classificationMedicaments antibacterians
dc.subject.classificationMedicina clínica
dc.subject.otherGram-positive bacterial infections
dc.subject.otherAntibacterial agents
dc.subject.otherClinical medicine
dc.titleDalbavancin in clinical practice in Spain: a 2 year retrospective study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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