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Ceftriaxone therapy in bacteremic typhoid fever
Antimicrobial Agents and Chemotherapy
|October 1, 1985
Summary
Ceftriaxone effectively treats bacteremic typhoid fever in patients, showing a rapid clinical response and a short treatment duration. This antibiotic demonstrated safety with no serious adverse drug reactions observed in the study.
Area of Science:
- Infectious Diseases
- Pharmacology
- Internal Medicine
Background:
- Typhoid fever, caused by Salmonella Typhi, remains a significant global health concern.
- Bacteremic typhoid fever requires effective antibiotic treatment to prevent complications and mortality.
- Ceftriaxone is a third-generation cephalosporin with broad-spectrum activity.
Purpose of the Study:
- To evaluate the efficacy and safety of ceftriaxone in treating patients with bacteremic typhoid fever.
- To determine optimal dosage and duration of ceftriaxone therapy for typhoid fever.
- To assess the clinical response and adverse effects of ceftriaxone treatment.
Main Methods:
- A study involving 14 patients diagnosed with bacteremic typhoid fever.
- Intravenous administration of ceftriaxone at 50-60 mg/kg/day in divided or single doses.
- Monitoring of clinical response, including defervescence, cure rates, and relapse rates.
- Measurement of peak and trough ceftriaxone concentrations against isolated Salmonella Typhi strains.
Main Results:
- A mean defervescence period of 4 days was observed after excluding specific patient cases.
- Five to eight days of ceftriaxone therapy proved adequate for patient cure.
- 13 out of 14 patients achieved cure, with one treatment failure and no relapses in monitored patients.
- Ceftriaxone levels consistently exceeded the Minimum Inhibitory Concentrations (MICs) for isolated Salmonella Typhi.
Conclusions:
- Ceftriaxone is a successful treatment option for bacteremic typhoid fever in select patients.
- Advantages include a rapid clinical response and a short treatment course.
- The antibiotic exhibits a favorable safety profile with a lack of serious adverse drug reactions.