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Published on: March 2, 2020
In vitro activity of ciprofloxacin compared with other agents against recent hospital isolates
Abstract:
Ciprofloxacin's in vitro activity was tested against 385 hospital isolates originating from three geographically distinct regions. Of all strains tested, only three (1 Acinetobacter sp. and 2 Pseudomonas aeruginosa) were ciprofloxacin resistant. Ciprofloxacin was more active against Escherichia coli, Enterobacter cloacae, Enterobacter aerogenes, Acinetobacter sp., Proteus sp., Shigella sp. than gentamicin, mezlocillin and cefotaxime. It was more active than azlocillin and cefsulodin against P. aeruginosa. It was more active than cloxacillin and cefamandole against staphylococci. It was as active as cefotaxime against Klebsiella pneumoniae, Citrobacter freundii and Serratia marcescens. Ciprofloxacin demonstrated similar activity in broth and solid agar. The minimal inhibitory concentrations (MIC's) of all strains were similar to the minimal bactericidal concentrations (MBC's). Ciprofloxacin's MIC was not influenced by increase of the inoculum or addition of human serum and only slightly influenced by anaerobic conditions. Decrease of the medium pH increased the MIC substantially. Ciprofloxacin exhibited a rapid bactericidal effect and had only a minimal post-antibiotic effect. These favorable in vitro characteristics of ciprofloxacin warrant further studies.
Insights
Ciprofloxacin demonstrated broad in vitro activity against most hospital bacterial isolates, showing high efficacy compared to other antibiotics. Its effectiveness remained consistent across various conditions, supporting further clinical investigation.
Area of Science:
- Microbiology
- Pharmacology
- Infectious Diseases
Background:
- Antibiotic resistance is a growing global health concern.
- Evaluating the in vitro efficacy of broad-spectrum antibiotics is crucial for guiding treatment strategies.
Purpose of the Study:
- To assess the in vitro antibacterial activity of ciprofloxacin against a diverse range of hospital bacterial isolates.
- To compare ciprofloxacin's efficacy with other commonly used antibiotics.
Main Methods:
- In vitro susceptibility testing of 385 hospital bacterial isolates from three distinct geographical regions.
- Determination of minimal inhibitory concentrations (MICs) and minimal bactericidal concentrations (MBCs).
- Evaluation of ciprofloxacin's activity under varying conditions (inoculum size, serum presence, anaerobic environment, pH).
Main Results:
- Ciprofloxacin exhibited potent in vitro activity against most tested strains, with only 3 out of 385 isolates showing resistance.
- It demonstrated superior or comparable activity against Gram-negative and Gram-positive bacteria when compared to gentamicin, mezlocillin, cefotaxime, azlocillin, cefsulodin, cloxacillin, and cefamandole.
- Activity was consistent in broth and agar, with MICs similar to MBCs, and minimal impact from inoculum size, serum, or anaerobic conditions. However, decreased pH significantly increased MICs.
- Ciprofloxacin showed rapid bactericidal effects and a minimal post-antibiotic effect.
Conclusions:
- Ciprofloxacin possesses favorable in vitro characteristics, including broad-spectrum activity and rapid bactericidal action.
- Its consistent performance across various conditions suggests potential clinical utility.
- Further clinical studies are warranted to confirm these promising in vitro findings.
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