THE COMPARATIVE EFFICACY AND SAFETY OF TEICOPLANIN AND VANCOMYCIN

Authors
Citation
Mj. Wood, THE COMPARATIVE EFFICACY AND SAFETY OF TEICOPLANIN AND VANCOMYCIN, Journal of antimicrobial chemotherapy, 37(2), 1996, pp. 209-222
Citations number
27
Categorie Soggetti
Microbiology,"Pharmacology & Pharmacy","Infectious Diseases
ISSN journal
03057453
Volume
37
Issue
2
Year of publication
1996
Pages
209 - 222
Database
ISI
SICI code
0305-7453(1996)37:2<209:TCEASO>2.0.ZU;2-1
Abstract
Glycopeptide antibiotics, such as teicoplanin and vancomycin, are acti ve against staphylococci (including methicillin resistant strains), st reptococci, enterococci and Clostridium spp. Vancomycin and teicoplani n are both widely used in the treatment of infections caused by Gram-p ositive organisms. Vancomycin can, however, provoke a number of side-e ffects, and serum concentrations should be monitored during treatment. Teicoplanin has a longer half-life than vancomycin, it can be given a s an intravenous bolus or by intramuscular injection, and nephrotoxici ty and ototoxicity are relatively uncommon. Treatment with teicoplanin might, therefore, offer advantages over treatment with vancomycin-pro vided that similar clinical efficacy can be shown. At least 11 clinica l trials comparing the efficacy and safety of teicoplanin and vancomyc in have been carried out worldwide. Meta-analysis of the combined resu lts from these studies indicates that more than three-quarters of the patients in each of the treatment groups had a clinical response to th erapy. Meta-analysis of the numbers of adverse events occurring in eac h treatment group shows significantly fewer reports of adverse events in patients receiving teicoplanin (13.9%) than in those receiving vanc omycin (21.9%). Direct comparisons are difficult because of inherent d ifferences between studies, but available data suggest that teicoplani n is as effective as vancomycin and that its superior tolerability tog ether with advantages such as once-daily bolus administration, intramu scular use and lack of requirement for routine serum monitoring, give it considerable potential for use in clinical practice.