A. Adu et Cl. Armour, DRUG UTILIZATION REVIEW (DUR) OF THE 3RD-GENERATION CEPHALOSPORINS - FOCUS ON CEFTRIAXONE, CEFTAZIDIME AND CEFOTAXIME, Drugs, 50(3), 1995, pp. 423-439
Six parenteral third generation cephalosporins have been introduced in
to clinical use in the past 10 years. The 3 most frequently available
agents are cefotaxime, ceftriaxone and ceftazidime. These 3 third gene
ration cephalosporins are characterised by a broad spectrum of activit
y and increased stability to beta-lactamases compared with the first a
nd second generation cephalosporins. However, there are growing number
s of reports of resistance to these agents with increasing use. The ma
jor differences in the properties of the 3 agents are the long half-li
fe of ceftriaxone and its dual route of elimination. Ceftazidime is be
st restricted to Pseudomonas aeruginosa infections where other agents
are contraindicated or ineffective. Cefotaxime and ceftriaxone can be
used in nosocomial Gram-negative infections where P. aeruginosa can be
ruled out. The types and incidences of adverse drug reactions are not
different for the 3 agents. A number of drug utilisation review (DUR)
studies of these agents in the hospital setting have reported a consi
derable incidence of inappropriate use and substantial avoidable costs
. There are methodological problems with most of the DUR studies, espe
cially the criteria and the methods of cost estimation. The use of pha
rmacoeconomic methodology could ensure more realistic cost estimation;
however, outcome data are, in most cases, not available.