Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs

dc.contributor.authorBenavent Palomares, Eva
dc.contributor.authorMorata, Laura
dc.contributor.authorEscrihuela Vidal, Francesc
dc.contributor.authorReynaga, Esteban Alberto
dc.contributor.authorSoldevila-Boixader, Laura
dc.contributor.authorAlbiach, Laia
dc.contributor.authorPedro Botet, Maria Luisa
dc.contributor.authorPadullés Zamora, Ariadna
dc.contributor.authorSoriano Viladomiu, Alex
dc.contributor.authorMurillo Rubio, Óscar
dc.date.accessioned2021-02-24T14:42:21Z
dc.date.available2021-02-24T14:42:21Z
dc.date.issued2021-01-01
dc.date.updated2021-02-08T10:34:17Z
dc.description.abstractBackground: To evaluate the efficacy and safety of long-term use of tedizolid in osteoarticular infections. Methods: Multicentric retrospective study (January 2017–March 2019) of osteoarticular infection cases treated with tedizolid. Failure: clinical worsening despite antibiotic treatment or the need of suppressive treatment. Results: Cases (n = 51; 59% women, mean age of 65 years) included osteoarthritis (n = 27, 53%), prosthetic joint infection (n = 17, 33.3%), and diabetic foot infections (n = 9, 18%); where, 59% were orthopedic device-related. Most frequent isolates were Staphylococcus spp. (65%, n = 47; S. aureus, 48%). Reasons for choosing tedizolid were potential drug-drug interaction (63%) and cytopenia (55%); median treatment duration was 29 days (interquartile range -IQR- 15–44), 24% received rifampicin (600 mg once daily) concomitantly, and adverse events were scarce (n = 3). Hemoglobin and platelet count stayed stable throughout treatment (from 108.6 g/L to 116.3 g/L, p = 0.079; and 240 × 109/L to 239 × 109/L, p = 0.942, respectively), also in the subgroup of cases with cytopenia. Among device-related infections, 33% were managed with implant retention. Median follow-up was 630 days and overall cure rate 83%; among failures (n = 8), 63% were device-related infections. Conclusions: Long-term use of tedizolid was effective, showing a better safety profile with less myelotoxicity and lower drug-drug interaction than linezolid. Confirmation of these advantages could make tedizolid the oxazolidinone of choice for most of osteoarticular infections.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec720016
dc.identifier.pmid33429902
dc.identifier.urihttps://hdl.handle.net/2445/174217
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/antibiotics10010053
dc.relation.ispartofAntibiotics, 2021, vol. 10, num. 1
dc.relation.urihttps://doi.org/10.3390/antibiotics10010053
dc.rightscc by (c) Benavent Palomares et al., 2021
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.classificationDiabetis
dc.subject.classificationInteraccions dels medicaments
dc.subject.otherDiabetes
dc.subject.otherDrug interactions
dc.titleLong-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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