The purpose of this study was to determine the safety and efficacy of
outpatient intravenous (IV) therapy with a third-generation cephalospo
rin, cefotaxime, in patients greater than or equal to 60 years of age
and to determine its effect on length of hospital stay. Subset analysi
s was performed with 62 patients with various infections who had been
enrolled in a prospective, multicenter, open-label trial of IV cefotax
ime delivered through a computerized ambulatory delivery system (ADS).
Initial treatment was given in hospital if required, followed by home
therapy. The overall clinical response rate among evaluable patients
was 98%, and the overall bacteriologic response rate was 93%. The mean
duration of inpatient therapy was 3.6 days less than the mean of 8.2
days allowed under diagnosis-related group (DRG) allotments. Outpatien
t therapy with cefotaxime via infusion pump is safe and effective and
may reduce hospitalization requirements.