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

Background: 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 ne...

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Autores principales: Benavent, Eva, Morata, Laura, Escrihuela-Vidal, Francesc, Reynaga, Esteban Alberto, Soldevila, Laura, Albiach, Laia, Pedro-Botet, Maria Luisa, Padullés, Ariadna, Soriano, Alex, Murillo, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826593/
https://www.ncbi.nlm.nih.gov/pubmed/33429902
http://dx.doi.org/10.3390/antibiotics10010053
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author Benavent, Eva
Morata, Laura
Escrihuela-Vidal, Francesc
Reynaga, Esteban Alberto
Soldevila, Laura
Albiach, Laia
Pedro-Botet, Maria Luisa
Padullés, Ariadna
Soriano, Alex
Murillo, Oscar
author_facet Benavent, Eva
Morata, Laura
Escrihuela-Vidal, Francesc
Reynaga, Esteban Alberto
Soldevila, Laura
Albiach, Laia
Pedro-Botet, Maria Luisa
Padullés, Ariadna
Soriano, Alex
Murillo, Oscar
author_sort Benavent, Eva
collection PubMed
description Background: 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 × 10(9)/L to 239 × 10(9)/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.
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spelling pubmed-78265932021-01-25 Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs Benavent, Eva Morata, Laura Escrihuela-Vidal, Francesc Reynaga, Esteban Alberto Soldevila, Laura Albiach, Laia Pedro-Botet, Maria Luisa Padullés, Ariadna Soriano, Alex Murillo, Oscar Antibiotics (Basel) Article Background: 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 × 10(9)/L to 239 × 10(9)/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. MDPI 2021-01-08 /pmc/articles/PMC7826593/ /pubmed/33429902 http://dx.doi.org/10.3390/antibiotics10010053 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Benavent, Eva
Morata, Laura
Escrihuela-Vidal, Francesc
Reynaga, Esteban Alberto
Soldevila, Laura
Albiach, Laia
Pedro-Botet, Maria Luisa
Padullés, Ariadna
Soriano, Alex
Murillo, Oscar
Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title_full Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title_fullStr Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title_full_unstemmed Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title_short Long-Term Use of Tedizolid in Osteoarticular Infections: Benefits among Oxazolidinone Drugs
title_sort long-term use of tedizolid in osteoarticular infections: benefits among oxazolidinone drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826593/
https://www.ncbi.nlm.nih.gov/pubmed/33429902
http://dx.doi.org/10.3390/antibiotics10010053
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