Activity of faropenem against resistant isolates of Streptococcus pneumoniae
J A Black1, E S Moland, S A Chartrand
1Center for Research in Anti-infectives and Biotechnology, Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, NE 68178, USA. jblack1@creighton.edu
Abstract:
An in vitro study of the activity of 9 agents against 181 US pediatric isolates of Streptococcus pneumoniae identified imipenem and faropenem as the most active agents. Overall, faropenem was the most potent oral agent inhibiting 98% of isolates at 1 microg/mL.
Insights
Imipenem and faropenem showed the most activity against pediatric Streptococcus pneumoniae isolates in an in vitro study. Faropenem was the most potent oral antibiotic, inhibiting 98% of strains at 1 microg/mL.
Area of Science:
- Microbiology
- Infectious Diseases
- Pharmacology
Background:
- Streptococcus pneumoniae is a leading cause of pediatric bacterial infections.
- Antibiotic resistance in Streptococcus pneumoniae is a growing public health concern.
- Understanding the in vitro activity of various agents is crucial for guiding treatment decisions.
Purpose of the Study:
- To evaluate the in vitro activity of nine antimicrobial agents against a collection of US pediatric isolates of Streptococcus pneumoniae.
- To identify the most potent agents, particularly oral options, for treating infections caused by these strains.
Main Methods:
- An in vitro study was conducted.
- Nine different antimicrobial agents were tested.
- 181 US pediatric isolates of Streptococcus pneumoniae were used.
Main Results:
- Imipenem and faropenem demonstrated the highest levels of activity against the tested Streptococcus pneumoniae isolates.
- Faropenem exhibited potent activity as an oral agent, inhibiting 98% of isolates at a concentration of 1 microg/mL.
Conclusions:
- Imipenem and faropenem are promising agents for treating pediatric Streptococcus pneumoniae infections.
- Faropenem represents a potent oral therapeutic option for susceptible strains.
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