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Potential role for telavancin in bacteremic infections due to gram-positive pathogens: Focus on staphylococcus aureus

Corey, G. Ralph
•
Rubinstein, Ethan
•
Stryjewski, Martin E.
altro
BASSETTI, MATTEO
2015
  • journal article

Periodico
CLINICAL INFECTIOUS DISEASES
Abstract
Staphylococcus aureus bacteremia (SAB) is one of the most common serious bacterial infections and the most frequent invasive infection due to methicillin-resistant S. aureus (MRSA). Treatment is challenging, particularly for MRSA, because of limited treatment options. Telavancin is a bactericidal lipoglycopeptide antibiotic that is active against a range of clinically relevant gram-positive pathogens including MRSA. In experimental animal models of sepsis telavancin was shown to be more effective than vancomycin. In clinically evaluable patients enrolled in a pilot study of uncomplicated SAB, cure rates were 88% for telavancin and 89% for standard therapy. Among patients with infection due to only gram-positive pathogens enrolled in the 2 phase 3 studies of telavancin for treatment of hospital-acquired pneumonia, cure rates for those with bacteremic S. aureus pneumonia were 41% (9/22, telavancin) and 40% (10/25, vancomycin) with identical mortality rates. These data support further evaluation of telavancin in larger, prospective studies of SAB.
DOI
10.1093/cid/ciu971
WOS
WOS:000349766100020
Archivio
http://hdl.handle.net/11390/1101047
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84931068669
http://cid.oxfordjournals.org/content/by/year
Diritti
metadata only access
Soggetti
  • Bacteremia

  • Experimental

  • MRSA

  • Staphylococcus aureu

  • Telavancin

  • Aminoglycoside

  • Animal

  • Anti-Bacterial Agent

  • Bacteremia

  • Clinical Trials, Phas...

  • Clinical Trials, Phas...

  • Disease Models, Anima...

  • Human

  • Staphylococcal Infect...

  • Staphylococcus aureu

  • Treatment Outcome

  • Infectious Disease

  • Microbiology (medical...

Scopus© citazioni
21
Data di acquisizione
Jun 14, 2022
Vedi dettagli
Web of Science© citazioni
24
Data di acquisizione
Mar 26, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
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