The Role of Vancomycin in the Treatment Paradigm

Vancomycin was introduced in the United States in 1956 as a possible treatment for infections due to penicillin-resistant Staphylococcus aureus, but it was not used widely because of toxicity and the nearly simultaneous development of semisynthetic antibiotics and cephalosporins. Thus, its main indi...

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Published inClinical infectious diseases Vol. 42; no. Supplement-1; pp. S51 - S57
Main Author Stevens, Dennis L
Format Journal Article
LanguageEnglish
Published United States The University of Chicago Press 01.01.2006
University of Chicago Press
Oxford University Press
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Abstract Vancomycin was introduced in the United States in 1956 as a possible treatment for infections due to penicillin-resistant Staphylococcus aureus, but it was not used widely because of toxicity and the nearly simultaneous development of semisynthetic antibiotics and cephalosporins. Thus, its main indication was the treatment of serious gram-positive infections in penicillin-allergic patients. For susceptible strains of S. aureus, vancomycin was more rapidly bactericidal than penicillin, nafcillin, or cefazolin, and, in a rabbit model of S. aureus endocarditis, sterilization of vegetations was more rapid with vancomycin. In clinical practice, however, nafcillin remained the treatment of choice for staphylococcal bacteremia, largely because it had failure rates of only 4%. With the appearance of methicillin-resistant S. aureus and coagulase-negative staphylococci, vancomycin became the drug of choice for these infections. Recently, the efficacy of vancomycin has been questioned because of vancomycin's increasing minimum inhibitory concentrations among staphylococci, poor tissue penetration, and apparently slower bacterial killing than previously was recognized.
AbstractList Vancomycin was introduced in the United States in 1956 as a possible treatment for infections due to penicillin-resistant Staphylococcus aureus, but it was not used widely because of toxicity and the nearly simultaneous development of semisynthetic antibiotics and cephalosporins. Thus, its main indication was the treatment of serious gram-positive infections in penicillin-allergic patients. For susceptible strains of S. aureus, vancomycin was more rapidly bactericidal than penicillin, nafcillin, or cefazolin, and, in a rabbit model of S. aureus endocarditis, sterilization of vegetations was more rapid with vancomycin. In clinical practice, however, nafcillin remained the treatment of choice for staphylococcal bacteremia, largely because it had failure rates of only 4%. With the appearance of methicillin-resistant S. aureus and coagulase-negative staphylococci, vancomycin became the drug of choice for these infections. Recently, the efficacy of vancomycin has been questioned because of vancomycin's increasing minimum inhibitory concentrations among staphylococci, poor tissue penetration, and apparently slower bacterial killing than previously was recognized.
Vancomycin was introduced in the United States in 1956 as a possible treatment for infections due to penicillin-resistant Staphylococcus aureus, but it was not used widely because of toxicity and the nearly simultaneous development of semisynthetic antibiotics and cephalosporins. Thus, its main indication was the treatment of serious gram-positive infections in penicillin-allergic patients. For susceptible strains of S. aureus, vancomycin was more rapidly bactericidal than penicillin, nafcillin, or cefazolin, and, in a rabbit model of S. aureus endocarditis, sterilization of vegetations was more rapid with vancomycin. In clinical practice, however, nafcillin remained the treatment of choice for staphylococcal bacteremia, largely because it had failure rates of only 4%. With the appearance of methicillin-resistant S. aureus and coagulase-negative staphylococci, vancomycin became the drug of choice for these infections. Recently, the efficacy of vancomycin has been questioned because of vancomycin's increasing minimum inhibitory concentrations among staphylococci, poor tissue penetration, and apparently slower bacterial killing than previously was recognized. [PUBLICATION ABSTRACT]
Author Dennis L. Stevens
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  organization: Infectious Disease Section, Veterans Affairs Medical Center, Boise, Idaho 83702, USA. dlsteven@mindspring.com
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Snippet Vancomycin was introduced in the United States in 1956 as a possible treatment for infections due to penicillin-resistant Staphylococcus aureus, but it was not...
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SubjectTerms Anti-Bacterial Agents - blood
Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - therapeutic use
Antibacterials
Antibiotics
Bacteremia
Bacteremia - complications
Bacteremia - drug therapy
Bacteremia - microbiology
Bacteriology
Clinical outcomes
Dosage
Drug Therapy, Combination
Effectiveness
Endocarditis
Endocarditis, Bacterial - complications
Endocarditis, Bacterial - drug therapy
Endocarditis, Bacterial - microbiology
Gram-positive bacteria
Humans
Infections
Microbial Sensitivity Tests
Patients
Pneumonia, Staphylococcal - drug therapy
Soft Tissue Infections - drug therapy
Soft Tissue Infections - microbiology
Staphylococcal Infections - complications
Staphylococcal Infections - drug therapy
Staphylococcal pneumonia
Staphylococcal Skin Infections - drug therapy
Staphylococcal Skin Infections - microbiology
Staphylococcus
Staphylococcus aureus
Staphylococcus aureus - drug effects
Treatment Failure
Vancomycin - blood
Vancomycin - pharmacology
Vancomycin - therapeutic use
Ventilator associated pneumonia
Title The Role of Vancomycin in the Treatment Paradigm
URI https://api.istex.fr/ark:/67375/HXZ-0KXB9H8N-H/fulltext.pdf
https://www.jstor.org/stable/4484544
https://www.ncbi.nlm.nih.gov/pubmed/16323121
https://www.proquest.com/docview/219958568/abstract/
https://search.proquest.com/docview/17107438
Volume 42
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