Cp. Rains et al., CEFTAZIDIME - AN UPDATE OF ITS ANTIBACTERIAL ACTIVITY, PHARMACOKINETIC PROPERTIES AND THERAPEUTIC EFFICACY, Drugs, 49(4), 1995, pp. 577-617
Ceftazidime is a third generation cephalosporin antibacterial agent wh
ich, since its introduction in the early 1980s, has retained a broad s
pectrum of in vitro antimicrobial activity and clinical utility in ser
ious infections. However increasing resistance to ceftazidime and othe
r third generation cephalosporins, particularly among Enterobacteriace
ae, due to the emergence of plasmid-mediated extended spectrum beta-la
ctamases and the class I chromosomally mediated beta-lactamases, is of
concern. There is now a wealth of information on the pharmacokinetics
of the drug, enabling ceftazidime to be used predictably, and with a
low potential for adverse effects, in a diversity of patient populatio
ns. Overall, ceftazidime remains an effective agent for the treatment
of serious infection, particularly those due to major nosocomial patho
gens, and respiratory infections in patients with cystic fibrosis. Cef
tazidime-containing regimens also remain an important option for the e
mpirical therapy of febrile episodes in neutropenic patients. The tole
rability profile of ceftazidime makes the drug a useful option in seri
ously ill patients who are at risk of developing adverse events with o
ther antibacterial agents. Although patterns of bacterial resistance h
ave changed in the ensuing years since its introduction, judicious use
of this important agent will help maintain its present clinical utili
ty.