Reproducibility study of the pharmacokinetics of amikacin, gentamicin and tobramycin; a three-way crossover study
A. Dyas, Robert A. Wise, J. Pijck, Th. Hallynck, J. F. Acar, Dieter Adam, R Cadórniga, Markus R. Wenk, H. Soep
Abstract
A. Dyas, Robert A. Wise, J. Pijck, Th. Hallynck, J. F. Acar, Dieter Adam, R Cadórniga, Markus R. Wenk, H. Soep
Abstract
The hypothesis that the pharmacokinetics of amikacin are more predictable than those of gentamicin or tobramycin was studied. In a three-way crossover design 58 volunteers received 7.5 mg/kg amikacin by iv infusion and either 1.5 mg/kg or 1 mg/kg gentamicin and tobramycin. The mean half-life and mean serum concentration at 1 h for each drug was determined. No consistent significant difference was found between the pharmacokinetics of amikacin and the other two drugs.
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The hypothesis that the pharmacokinetics of amikacin are more predictable than those of gentamicin or tobramycin was studied. In a three-way crossover design 58 volunteers received 7.5 mg/kg amikacin by iv infusion and either 1.5 mg/kg or 1 mg/kg gentamicin and tobramycin. The mean half-life and mean serum concentration at 1 h for each drug was determined. No consistent significant difference was found between the pharmacokinetics of amikacin and the other two drugs.
Key concepts: Amikacin, Tobramycin, Library science, Medicine, Gentamicin, History, Computer science, Antibiotics