The aim of antibiotic therapy is pathogen eradication, which is often assum
ed on the basis of the alleviation of the signs and symptoms of the disease
. Pharmacokinetic/pharmacodymamic in vitro and animal models have now been
developed to predict bacteriological efficacy and to establish dosing regim
ens that are effective and control the development of resistance. These mod
els may be applied to the evaluation of new short-course dosing regimens, l
asting no longer than 3 - 5 days. Single-dose therapy, using agents with a
prolonged duration of action, is currently employed for streptococcal phary
ngitis, uncomplicated gonorrhoea and uncomplicated lower urinary tract infe
ctions in women. The use of short-course therapy in immunocompetent patient
s for the treatment of community-acquired infections that have a low bacter
ial load is feasible. Such regimens may have a number of advantages over th
ose currently employed, which typically involve dosing for 7 - 10 days. The
se advantages include improved tolerability: reduction in healthcare costs,
enhanced patient compliance and the prevention of the emergence of resista
nce.