Cost-effective treatment of patients with bacterial infections can bes
t be accomplished by facilitating a rapid response. Achieving a more r
apid cure of the infection should result in reduced utilisation of hea
lthcare resources. An innovative means of achieving a more rapid respo
nse to antibacterial therapy has been termed dual individualisation. D
ual individualisation allows for the simultaneous consideration of the
pharmacokinetic interaction between an antibacterial agent and a pati
ent, with the pharmacodynamic interaction between the antibacterial ag
ent and the bacterial pathogen. Integrating the pharmacokinetic parame
ter of area under the curve (AUC), with the pharmacodynamic measure of
minimum inhibitory concentration (MIC) yields a ratio called the area
under the inhibitory curve (AUIC). Clinical studies using dual indivi
dualisation to achieve a target AUIC(24h) of 125-250 have been perform
ed with cephalosporins and fluoroquinalones. Economic evaluation of th
e results demonstrate that dual individualisation is cost-effective. D
ual individualisation can be implemented in most practice settings usi
ng existing clinical data. Use of a computer model allows for cost-eff
ective calculation of AUIC(24h) without having to measure serum drug c
oncentrations of bacterial MIC. By adjusting antibacterial regimens to
achieve a target AUIC, optimisation of antibacterial therapy can be a
chieved with resultant economic benefits.