Objective: To evaluate the economic benefit associated with the early conversion of therapy from intravenous ceftriaxone to the comparable oral third-generation cephalosporin, cefpodoxime proxetil. Design: Open-label, unblind, nonrandomized clinical trial. Setting: A 360-bed Veterans Affairs Medical Center. Patients: Forty patients who began receiving intravenous ceftriaxone for either a community-acquired pneumonia or a complicated urinary tract infection. Intervention: Twenty patients were selected, based on clinical assessment, to be converted from intravenous ceftriaxone to oral cefpodoxime proxetil. Twenty other comparable patients, who would have been appropriate for step-down therapy, did not receive pharmacy intervention and were used as a control group. Measurements: Both groups were assessed and compared for length of ceftriaxone therapy, length of oral follow-up therapy (if any), length of hospitalization, results of culture and sensitivity testing, treatment success and readmissions, and cost of respective therapeutic regimens. Results: In the cefpodoxime study group, the average time receiving intravenous and oral antibiotics was 9.1 days at a total cost of $3040.26 for the 20 patients. In the control group, the average time receiving intravenous and oral antibiotics was 11.9 days at a total cost of $3961.26. A savings of $46.05 per patient was achieved. Patients receiving step-down therapy averaged 1 fewer day of hospitalization. Conclusions: Pharmacist intervention and cefpodoxime step-down therapy were associated with decreased overall antibiotic costs in our intravenous-to-oral program.
[1]
R. Jones,et al.
Prediction of bacterial susceptibility to cefpodoxime by using the ceftriaxone minimum inhibitory concentration result.
,
1993,
Diagnostic microbiology and infectious disease.
[2]
Ronald N. Jones,et al.
In vitro activity of cefpodoxime compared with other oral cephalosporins tested against 5556 recent clinical isolates from five medical centers.
,
1993,
Diagnostic microbiology and infectious disease.
[3]
L. Gentry,et al.
Parenteral followed by oral ofloxacin for nosocomial pneumonia and community-acquired pneumonia requiring hospitalization.
,
1992,
The American review of respiratory disease.
[4]
J. Morris,et al.
Oral ofloxacin for the treatment of acute bacterial pneumonia: use of a nontraditional protocol to compare experimental therapy with "usual care" in a multicenter clinical trial.
,
1991,
The American journal of medicine.
[5]
L. Briceland,et al.
Economic impact of streamlining antibiotic administration.
,
1987,
The American journal of medicine.