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Treatment of respiratory tract infections with ciprofloxacin
The Journal of Antimicrobial Chemotherapy
|November 1, 1986
Abstract:
The efficacy and safety of ciprofloxacin in an oral dose of 750 mg twice daily, in the treatment of respiratory infections was studied in 129 patients. Ciprofloxacin showed broad in-vitro antibacterial activity and was highly effective in both Gram-negative and Gram-positive infections with a clinical cure rate of 96%. The major side effect was an interaction with theophylline particularly in the elderly patients.
Insights
Ciprofloxacin, an antibiotic, effectively treated respiratory infections in 96% of patients. Caution is advised due to potential theophylline interactions, especially in elderly individuals.
Area of Science:
- Pharmacology
- Infectious Diseases
- Clinical Medicine
Background:
- Respiratory infections pose a significant health burden.
- Broad-spectrum antibiotics are crucial for treating diverse bacterial pathogens.
- Ciprofloxacin is a fluoroquinolone antibiotic with known antibacterial properties.
Purpose of the Study:
- To evaluate the efficacy and safety of oral ciprofloxacin for respiratory infections.
- To assess the clinical cure rates associated with ciprofloxacin treatment.
- To identify potential adverse drug reactions and interactions.
Main Methods:
- A study involving 129 patients with respiratory infections.
- Oral administration of ciprofloxacin at 750 mg twice daily.
- In-vitro testing to determine antibacterial spectrum.
- Clinical monitoring for treatment outcomes and side effects.
Main Results:
- Ciprofloxacin demonstrated broad in-vitro activity against Gram-negative and Gram-positive bacteria.
- A high clinical cure rate of 96% was achieved.
- The primary adverse event noted was interaction with theophylline, particularly in elderly patients.
Conclusions:
- Oral ciprofloxacin is highly effective in treating respiratory infections.
- The drug exhibits a favorable safety profile, with theophylline interaction being the main concern.
- Further research may be warranted to explore management strategies for drug interactions in specific populations.