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Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria.

Publication ,  Journal Article
Stryjewski, ME; O'Riordan, WD; Lau, WK; Pien, FD; Dunbar, LM; Vallee, M; Fowler, VG; Chu, VH; Spencer, E; Barriere, SL; Kitt, MM; Cabell, CH ...
Published in: Clin Infect Dis
June 1, 2005

BACKGROUND: Telavancin, a novel lipoglycopeptide, exerts concentration-dependent, rapid bactericidal activity on account of its multiple mechanisms of action. Telavancin is highly active against gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-intermediate, and vancomycin-resistant strains. METHODS: We conducted a randomized, double-blind, controlled, phase-2 clinical trial. Patients > or = 18 years of age with a diagnosis of complicated skin and soft-tissue infection caused by suspected or confirmed gram-positive organisms were randomized to receive either intravenously administered telavancin once daily or standard therapy (antistaphylococcal penicillin 4 times daily or vancomycin twice daily). RESULTS: For the study, 167 patients were randomized and received at least 1 dose of study medication. Success rates were similar in all analysis populations at the test-of-cure evaluation. Of patients with S. aureus infection at baseline (n = 102), 80% of the telavancin group were cured and 77% of the standard therapy group were cured. For patients with MRSA infection at baseline (n = 48), cure rates were 82% for the telavancin group and 69% for the standard therapy group. Microbiologic eradication in patients with MRSA infection was 84% for the telavancin group versus 74% for the standard therapy group. MIC90 values were lower for telavancin in all tested strains of S. aureus (< or = 0.25 ug/mL) compared with the MIC90 values for vancomycin and oxacillin. Similar proportions of patients discontinued therapy for adverse events in both treatment groups (approximately 5%). Fewer serious adverse events were reported in the telavancin group (4 events) than were for the standard therapy group (9). CONCLUSION: Clinical and microbiological results of this study support the further development of telavancin, especially for treatment of infection due to MRSA.

Duke Scholars

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Published In

Clin Infect Dis

DOI

EISSN

1537-6591

Publication Date

June 1, 2005

Volume

40

Issue

11

Start / End Page

1601 / 1607

Location

United States

Related Subject Headings

  • Vancomycin
  • Soft Tissue Infections
  • Skin Diseases, Bacterial
  • Penicillins
  • Middle Aged
  • Microbiology
  • Male
  • Lipoglycopeptides
  • Humans
  • Gram-Positive Bacterial Infections
 

Citation

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Stryjewski, M. E., O’Riordan, W. D., Lau, W. K., Pien, F. D., Dunbar, L. M., Vallee, M., … FAST Investigator Group, . (2005). Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria. Clin Infect Dis, 40(11), 1601–1607. https://doi.org/10.1086/429914
Stryjewski, Martin E., William D. O’Riordan, William K. Lau, Francis D. Pien, Lala M. Dunbar, Marc Vallee, Vance G. Fowler, et al. “Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria.Clin Infect Dis 40, no. 11 (June 1, 2005): 1601–7. https://doi.org/10.1086/429914.
Stryjewski ME, O’Riordan WD, Lau WK, Pien FD, Dunbar LM, Vallee M, et al. Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria. Clin Infect Dis. 2005 Jun 1;40(11):1601–7.
Stryjewski, Martin E., et al. “Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria.Clin Infect Dis, vol. 40, no. 11, June 2005, pp. 1601–07. Pubmed, doi:10.1086/429914.
Stryjewski ME, O’Riordan WD, Lau WK, Pien FD, Dunbar LM, Vallee M, Fowler VG, Chu VH, Spencer E, Barriere SL, Kitt MM, Cabell CH, Corey GR, FAST Investigator Group. Telavancin versus standard therapy for treatment of complicated skin and soft-tissue infections due to gram-positive bacteria. Clin Infect Dis. 2005 Jun 1;40(11):1601–1607.
Journal cover image

Published In

Clin Infect Dis

DOI

EISSN

1537-6591

Publication Date

June 1, 2005

Volume

40

Issue

11

Start / End Page

1601 / 1607

Location

United States

Related Subject Headings

  • Vancomycin
  • Soft Tissue Infections
  • Skin Diseases, Bacterial
  • Penicillins
  • Middle Aged
  • Microbiology
  • Male
  • Lipoglycopeptides
  • Humans
  • Gram-Positive Bacterial Infections