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.