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1000 Titel
  • Pharmacokinetics and Pharmacodynamics of Tedizolid
1000 Autor/in
  1. Iqbal, Khalid |
  2. Milioudi, Aliki |
  3. Wicha, Sebastian G. |
1000 Verlag Springer International Publishing
1000 Erscheinungsjahr 2022
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2022-02-07
1000 Erschienen in
1000 Quellenangabe
  • 61(4):489-503
1000 Copyrightjahr
  • 2022
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s40262-021-01099-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686459/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Tedizolid is an oxazolidinone antibiotic with high potency against Gram-positive bacteria and currently prescribed in bacterial skin and skin-structure infections. The aim of the review was to summarize and critically review the key pharmacokinetic and pharmacodynamic aspects of tedizolid. Tedizolid displays linear pharmacokinetics with good tissue penetration. In in vitro susceptibility studies, tedizolid exhibits activity against the majority of Gram-positive bacteria (minimal inhibitory concentration [MIC] of ≤ 0.5 mg/L), is four-fold more potent than linezolid, and has the potential to treat pathogens being less susceptible to linezolid. Area under the unbound concentration-time curve (fAUC) related to MIC (fAUC/MIC) was best correlated with efficacy. In neutropenic mice, fAUC/MIC of ~ 50 and ~ 20 induced bacteriostasis in thigh and pulmonary infection models, respectively, at 24 h. The presence of granulocytes augmented its antibacterial effect. Hence, tedizolid is currently not recommended for immunocompromised patients. Clinical investigations with daily doses of 200 mg for 6 days showed non-inferiority to twice-daily dosing of linezolid 600 mg for 10 days in patients with acute bacterial skin and skin-structure infections. In addition to its use in skin and skin-structure infections, the high pulmonary penetration makes it an attractive option for respiratory infections including Mycobacterium tuberculosis. Resistance against tedizolid is rare yet effective antimicrobial surveillance and defining pharmacokinetic/pharmacodynamic targets for resistance suppression are needed to guide dosing strategies to suppress resistance development.
1000 Sacherschließung
lokal Oxazoles/therapeutic use [MeSH]
lokal Oxazoles/pharmacology [MeSH]
lokal Anti-Bacterial Agents/therapeutic use [MeSH]
lokal Humans [MeSH]
lokal Review Article
lokal Oxazolidinones/pharmacology [MeSH]
lokal Animals [MeSH]
lokal Tetrazoles/pharmacology [MeSH]
lokal Organophosphates/pharmacology [MeSH]
lokal Organophosphates/therapeutic use [MeSH]
lokal Mice [MeSH]
lokal Medical and Health Sciences
lokal Anti-Bacterial Agents/pharmacology [MeSH]
lokal Microbial Sensitivity Tests [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/SXFiYWwsIEtoYWxpZA==|https://frl.publisso.de/adhoc/uri/TWlsaW91ZGksIEFsaWtp|https://orcid.org/0000-0002-8773-4845
1000 Hinweis
  • DeepGreen-ID: 77fbdcb2555142ec93c3445db39844e8 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Universität Hamburg |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
  1. Pharmacokinetics and Pharmacodynamics of Tedizolid
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Universität Hamburg |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6486084.rdf
1000 Erstellt am 2024-10-02T23:58:29.768+0200
1000 Erstellt von 322
1000 beschreibt frl:6486084
1000 Zuletzt bearbeitet 2025-08-13T21:33:46.255+0200
1000 Objekt bearb. Wed Aug 13 21:33:46 CEST 2025
1000 Vgl. frl:6486084
1000 Oai Id
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