Publication Date: 04 Jan 2012
Type: Review
Journal: Clinical Medicine Reviews in Therapeutics
Citation: Clinical Medicine Reviews in Therapeutics 2012:4 31-40
doi: 10.4137/CMRT.S3109
Telavancin is a lipoglycopeptide antibiotic with a dual mechanism of action; it disrupts both cell wall synthesis and cell membrane integrity resulting in rapid bactericidal activity. It is active against a wide range of Gram-positive organisms, including methicillin-resistant, vancomycin-intermediate, linezolid-resistant and daptomycin-resistant Staphylococcus aureus strains. Resistance is uncommon and only occurs in vancomycin-resistant organisms of the VanA type. Its pharmacokinetic profile enables once daily administration, making it potentially suitable for use in the outpatient setting. Telavancin is renally excreted and requires dose adjustment in renal impairment. Clinical trials have demonstrated efficacy in the treatment of complicated skin and skin structure infections and nosocomial pneumonia caused by Gram-positive pathogens. This review outlines the mechanisms of action, antimicrobial spectrum, pharmacokinetics, clinical use and safety aspects of telavancin, and discusses its potential role in the antimicrobial armamentarium.
RIS citation (ENDNOTE, REFERENCE MANAGER, PROCITE, REFWORKS)
BibTex citation (BIBDESK, LATEX)
I am very impressed by the quick and user friendly reviewing process. The editorial team is very efficient and I highly recommend submitting research papers to Libertas!
All authors are surveyed after their articles are published. Authors are asked to rate their experience in a variety of areas, and their responses help us to monitor our performance. Presented here are their responses in some key areas. No 'poor' or 'very poor' responses were received; these are represented in the 'other' category.See Our Results
Copyright © 2013 Libertas Academica Ltd (except open access articles and accompanying metadata and supplementary files.)
Facebook Google+ Twitter
Pinterest Tumblr YouTube