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 in | Clinical infectious diseases Vol. 42; no. Supplement-1; pp. S51 - S57 |
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Main Author | |
Format | Journal Article |
Language | English |
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. |
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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 |
Author_xml | – sequence: 1 givenname: Dennis L surname: Stevens fullname: Stevens, Dennis L email: dlsteven@mindspring.com organization: Infectious Disease Section, Veterans Affairs Medical Center, Boise, Idaho 83702, USA. dlsteven@mindspring.com |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/16323121$$D View this record in MEDLINE/PubMed |
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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 |
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