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[Cefixime treatment in different bacterial infections in the ENT region]
W W Schlenter1, R Blessing, K Pelz
1Klinik für Hals-Nasen-Ohrenheilkunde, Medizinische Universität, Lübeck, Germany.
Abstract:
The clinical efficacy and tolerance of cefixime were evaluated in an open uncontrolled clinical trial including 37 patients suffering from ENT-infections. The MIC90 values of this new oral cephalosporin against gram-negative pathogens are less than 1 mg/l. The antibacterial activity of cefixime against gram-negative pathogens is stronger than that of other oral cephalosporins. Cefixime was administered for five to twelve days twice daily in a dose of 200 mg. In one patient the treatment with cefixime was discontinued after five days due to perioral dermatitis. In 33 of 36 patients cure or distinct improvement was observed after cefixime treatment, showing a clinical success rate of 91.7%. Causative organisms were isolated in 17 of 37 patients (47.2%). After the cefixime therapy the causative organisms were eradicated in 13 of 17 patients (76.5%). The tolerance of cefixime is comparable with that of other oral cephalosporins.
Insights
Cefixime, a new oral cephalosporin, demonstrated high clinical efficacy (91.7% success rate) and good tolerance in treating ear, nose, and throat (ENT) infections. Its potent antibacterial activity against gram-negative pathogens supports its use.
Area of Science:
- Pharmacology
- Infectious Diseases
- Otolaryngology
Background:
- Ear, nose, and throat (ENT) infections are common, necessitating effective antibiotic treatments.
- Oral cephalosporins are widely used, but newer agents with improved efficacy and safety profiles are continually sought.
- Cefixime represents a novel oral cephalosporin with potential advantages in treating bacterial infections.
Purpose of the Study:
- To evaluate the clinical efficacy and tolerance of cefixime in patients with ENT infections.
- To assess the in vitro activity of cefixime against common gram-negative pathogens.
- To compare the clinical outcomes and safety profile of cefixime with existing oral cephalosporins.
Main Methods:
- An open, uncontrolled clinical trial was conducted involving 37 patients with ENT infections.
- Patients received cefixime 200 mg twice daily for 5 to 12 days.
- Minimum Inhibitory Concentration (MIC90) values were determined for gram-negative pathogens; clinical outcomes and adverse events were recorded.
Main Results:
- Cefixime exhibited strong in vitro activity against gram-negative pathogens (MIC90 < 1 mg/l), outperforming other oral cephalosporins.
- A high clinical success rate of 91.7% was observed, with 33 of 36 patients showing cure or improvement.
- Bacterial eradication was achieved in 76.5% of patients with isolated causative organisms.
- The drug was generally well-tolerated, with adverse effects comparable to other oral cephalosporins; one case of perioral dermatitis led to discontinuation.
Conclusions:
- Cefixime is a clinically effective and well-tolerated oral antibiotic for treating ENT infections.
- Its potent antibacterial activity against gram-negative pathogens makes it a valuable therapeutic option.
- Cefixime offers a favorable efficacy and safety profile comparable to existing oral cephalosporins.
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