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Amikacin therapy. Use against infections caused by gentamicin- and tobramycin-resistant organisms
Abstract:
Amikacin sulfate was used in 24 treatment courses for 25 serious infections caused by aerobic or facultative anaerobic Gram-negative organisms resistant to numerous drugs. Sites of infection included urinary tract (11 cases), pleuropulmonary (6 cases), primary bacteremia (5 cases), and miscellaneous (3 cases). Serratia marcescens and Pseudomonas sp accounted for 73% of the isolates. The mean minimal inhibitory concentration (MIC) of these organisms to amikacin was 3.6 microgram/ml; to gentamicin, 39 microgram/ml; and to tobramycin, 32 microgram/ml. The mean peak serum concentration of the drug was 20.8 microgram/ml. Eleven patients were critically ill at the onset of therapy, and seven patients were bacteremic. The overall favorable response rate was 80%. The most serious side effect was ototoxicity, which occurred in three of 15 patients examined by serial audiometry.
Insights
Amikacin sulfate effectively treated serious Gram-negative infections, showing an 80% favorable response rate. This antibiotic demonstrated potent activity against drug-resistant organisms like Serratia marcescens and Pseudomonas.
Area of Science:
- Infectious Diseases
- Pharmacology
- Microbiology
Background:
- Serious infections caused by Gram-negative organisms resistant to multiple drugs pose a significant clinical challenge.
- Aminoglycosides are crucial for treating such infections, but resistance patterns necessitate evaluating new therapeutic options.
Purpose of the Study:
- To evaluate the efficacy and safety of amikacin sulfate in treating serious infections caused by drug-resistant Gram-negative bacteria.
- To compare the in vitro activity of amikacin against gentamicin and tobramycin for the causative organisms.
Main Methods:
- A retrospective analysis of 24 treatment courses of amikacin sulfate in 25 patients with serious Gram-negative infections.
- In vitro susceptibility testing was performed, determining minimal inhibitory concentrations (MICs) for amikacin, gentamicin, and tobramycin.
- Clinical outcomes and adverse events, including ototoxicity assessed by serial audiometry, were monitored.
Main Results:
- Amikacin sulfate demonstrated an 80% favorable response rate across various infection sites, including urinary tract, pleuropulmonary, and bacteremia.
- The causative organisms, primarily Serratia marcescens and Pseudomonas sp (73% of isolates), showed significantly lower MICs to amikacin (3.6 µg/ml) compared to gentamicin (39 µg/ml) and tobramycin (32 µg/ml).
- Ototoxicity was observed in 3 of 15 patients evaluated by audiometry, highlighting a potential safety concern.
Conclusions:
- Amikacin sulfate is an effective therapeutic option for serious infections caused by multidrug-resistant Gram-negative organisms.
- Its in vitro activity against key pathogens like Serratia and Pseudomonas surpasses that of gentamicin and tobramycin.
- Careful monitoring for ototoxicity is warranted during amikacin sulfate treatment.
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