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Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens

Background. Telavancin is a lipoglycopeptide bactericidal against gram-positive pathogens. Methods. Two methodologically identical, double-blind studies (0015 and 0019) were conducted involving patients with hospital-acquired pneumonia (HAP) due to gram-positive pathogens, particularly methicillin-r...

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Autores principales: Rubinstein, Ethan, Lalani, Tahaniyat, Corey, G. Ralph, Kanafani, Zeina A., Nannini, Esteban C., Rocha, Marcelo G., Rahav, Galia, Niederman, Michael S., Kollef, Marin H., Shorr, Andrew F., Lee, Patrick C., Lentnek, Arnold L., Luna, Carlos M., Fagon, Jean-Yves, Torres, Antoni, Kitt, Michael M., Genter, Fredric C., Barriere, Steven L., Friedland, H. David, Stryjewski, Martin E.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060890/
https://www.ncbi.nlm.nih.gov/pubmed/21148517
http://dx.doi.org/10.1093/cid/ciq031
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author Rubinstein, Ethan
Lalani, Tahaniyat
Corey, G. Ralph
Kanafani, Zeina A.
Nannini, Esteban C.
Rocha, Marcelo G.
Rahav, Galia
Niederman, Michael S.
Kollef, Marin H.
Shorr, Andrew F.
Lee, Patrick C.
Lentnek, Arnold L.
Luna, Carlos M.
Fagon, Jean-Yves
Torres, Antoni
Kitt, Michael M.
Genter, Fredric C.
Barriere, Steven L.
Friedland, H. David
Stryjewski, Martin E.
author_facet Rubinstein, Ethan
Lalani, Tahaniyat
Corey, G. Ralph
Kanafani, Zeina A.
Nannini, Esteban C.
Rocha, Marcelo G.
Rahav, Galia
Niederman, Michael S.
Kollef, Marin H.
Shorr, Andrew F.
Lee, Patrick C.
Lentnek, Arnold L.
Luna, Carlos M.
Fagon, Jean-Yves
Torres, Antoni
Kitt, Michael M.
Genter, Fredric C.
Barriere, Steven L.
Friedland, H. David
Stryjewski, Martin E.
author_sort Rubinstein, Ethan
collection PubMed
description Background. Telavancin is a lipoglycopeptide bactericidal against gram-positive pathogens. Methods. Two methodologically identical, double-blind studies (0015 and 0019) were conducted involving patients with hospital-acquired pneumonia (HAP) due to gram-positive pathogens, particularly methicillin-resistant Staphylococcus aureus (MRSA). Patients were randomized 1:1 to telavancin (10 mg/kg every 24 h) or vancomycin (1 g every 12 h) for 7–21 days. The primary end point was clinical response at follow-up/test-of-cure visit. Results. A total of 1503 patients were randomized and received study medication (the all-treated population). In the pooled all-treated population, cure rates with telavancin versus vancomycin were 58.9% versus 59.5% (95% confidence interval [CI] for the difference, –5.6% to 4.3%). In the pooled clinically evaluable population (n = 654), cure rates were 82.4% with telavancin and 80.7% with vancomycin (95% CI for the difference, –4.3% to 7.7%). Treatment with telavancin achieved higher cure rates in patients with monomicrobial S. aureus infection and comparable cure rates in patients with MRSA infection; in patients with mixed gram-positive/gram-negative infections, cure rates were higher in the vancomycin group. Incidence and types of adverse events were comparable between the treatment groups. Mortality rates for telavancin-treated versus vancomycin-treated patients were 21.5% versus 16.6% (95% CI for the difference, –0.7% to 10.6%) for study 0015 and 18.5% versus 20.6% (95% CI for the difference, –7.8% to 3.5%) for study 0019. Increases in serum creatinine level were more common in the telavancin group (16% vs 10%). Conclusions. The primary end point of the studies was met, indicating that telavancin is noninferior to vancomycin on the basis of clinical response in the treatment of HAP due to gram-positive pathogens.
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spelling pubmed-30608902011-03-21 Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens Rubinstein, Ethan Lalani, Tahaniyat Corey, G. Ralph Kanafani, Zeina A. Nannini, Esteban C. Rocha, Marcelo G. Rahav, Galia Niederman, Michael S. Kollef, Marin H. Shorr, Andrew F. Lee, Patrick C. Lentnek, Arnold L. Luna, Carlos M. Fagon, Jean-Yves Torres, Antoni Kitt, Michael M. Genter, Fredric C. Barriere, Steven L. Friedland, H. David Stryjewski, Martin E. Clin Infect Dis Articles and Commentaries Background. Telavancin is a lipoglycopeptide bactericidal against gram-positive pathogens. Methods. Two methodologically identical, double-blind studies (0015 and 0019) were conducted involving patients with hospital-acquired pneumonia (HAP) due to gram-positive pathogens, particularly methicillin-resistant Staphylococcus aureus (MRSA). Patients were randomized 1:1 to telavancin (10 mg/kg every 24 h) or vancomycin (1 g every 12 h) for 7–21 days. The primary end point was clinical response at follow-up/test-of-cure visit. Results. A total of 1503 patients were randomized and received study medication (the all-treated population). In the pooled all-treated population, cure rates with telavancin versus vancomycin were 58.9% versus 59.5% (95% confidence interval [CI] for the difference, –5.6% to 4.3%). In the pooled clinically evaluable population (n = 654), cure rates were 82.4% with telavancin and 80.7% with vancomycin (95% CI for the difference, –4.3% to 7.7%). Treatment with telavancin achieved higher cure rates in patients with monomicrobial S. aureus infection and comparable cure rates in patients with MRSA infection; in patients with mixed gram-positive/gram-negative infections, cure rates were higher in the vancomycin group. Incidence and types of adverse events were comparable between the treatment groups. Mortality rates for telavancin-treated versus vancomycin-treated patients were 21.5% versus 16.6% (95% CI for the difference, –0.7% to 10.6%) for study 0015 and 18.5% versus 20.6% (95% CI for the difference, –7.8% to 3.5%) for study 0019. Increases in serum creatinine level were more common in the telavancin group (16% vs 10%). Conclusions. The primary end point of the studies was met, indicating that telavancin is noninferior to vancomycin on the basis of clinical response in the treatment of HAP due to gram-positive pathogens. Oxford University Press 2011-01-01 /pmc/articles/PMC3060890/ /pubmed/21148517 http://dx.doi.org/10.1093/cid/ciq031 Text en © The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. 2011. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles and Commentaries
Rubinstein, Ethan
Lalani, Tahaniyat
Corey, G. Ralph
Kanafani, Zeina A.
Nannini, Esteban C.
Rocha, Marcelo G.
Rahav, Galia
Niederman, Michael S.
Kollef, Marin H.
Shorr, Andrew F.
Lee, Patrick C.
Lentnek, Arnold L.
Luna, Carlos M.
Fagon, Jean-Yves
Torres, Antoni
Kitt, Michael M.
Genter, Fredric C.
Barriere, Steven L.
Friedland, H. David
Stryjewski, Martin E.
Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title_full Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title_fullStr Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title_full_unstemmed Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title_short Telavancin versus Vancomycin for Hospital-Acquired Pneumonia due to Gram-positive Pathogens
title_sort telavancin versus vancomycin for hospital-acquired pneumonia due to gram-positive pathogens
topic Articles and Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060890/
https://www.ncbi.nlm.nih.gov/pubmed/21148517
http://dx.doi.org/10.1093/cid/ciq031
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