A comparison of two amikacin dosing regimens in paediatric surgical patients
N B Forsyth1, J H Botha, G P Hadley
1Department of Experimental and Clinical Pharmacology, Faculty of Medicine, University of Natal, Durban, South Africa.
Insights
This study compared once-daily versus twice-daily amikacin dosing in pediatric surgical patients. Both regimens showed similar efficacy and low toxicity, suggesting flexibility in amikacin administration for critically ill children.
Area of Science:
- Pediatric Surgery
- Pharmacology
- Critical Care Medicine
Background:
- Amikacin is a crucial antibiotic for treating serious bacterial infections in critically ill patients.
- Optimizing amikacin dosing is essential to balance efficacy and minimize toxicity in pediatric surgical populations.
Purpose of the Study:
- To compare the efficacy and toxicity of once-daily versus twice-daily intravenous amikacin regimens.
- To evaluate clinical outcomes, nephrotoxicity, and ototoxicity in pediatric surgical patients receiving different amikacin schedules.
Main Methods:
- A comparative study involving pediatric surgical patients (0.6-12 years) receiving amikacin intravenously.
- Two groups were formed: once-daily (15 mg/kg) and twice-daily (7.5 mg/kg) dosing.
- Efficacy assessed via temperature, clinical improvement, and white cell counts; toxicity evaluated by serum creatinine and audiometry.
Main Results:
- Mean peak serum amikacin levels were significantly higher in the once-daily group (37.7 mg/l) compared to the twice-daily group (19.5 mg/l).
- Favorable outcomes were observed in 18/24 (once-daily) and 22/25 (twice-daily) patients, with no statistically significant difference.
- No significant nephrotoxicity was detected; mild, reversible high-frequency hearing deficits occurred in a small percentage of patients in both groups.
Conclusions:
- Both once-daily and twice-daily amikacin regimens demonstrated comparable efficacy and acceptable safety profiles in seriously ill pediatric surgical patients.
- The findings suggest potential flexibility in amikacin dosing strategies for this patient population.
- Further research is warranted to definitively establish the optimal amikacin dosing approach in pediatric patients.
Abstract:
This investigation aimed to compare the efficacy and toxicity of two amikacin dosing regimens in seriously ill paediatric surgical patients. Children (0.6-12 years old) received amikacin intravenously either once daily (15 mg/kg, n = 27) or twice daily (7.5 mg/kg, n = 27). Concomitant medication was given as prescribed. Mean (SD) peak serum amikacin levels were significantly different (p < 0.05) between the once and twice daily groups (37.7 (6.9) mg/l and 19.5 (3.7) mg/l, respectively). Cumulative dose and duration of therapy were also significantly higher in the once-daily group. Regimen efficacy (favourable, unfavourable or indeterminate outcome) was assessed by patient temperatures, clinical improvement and white cell counts. Serum creatinine measurements and post-therapy, pure tone air conduction audiometry assessed nephro- and ototoxicity, respectively. No statistically significant differences were found between the groups in terms of outcome (18/24 and 22/25 patients in the once- and twice-daily groups had favourable outcomes; there were no unfavourable outcomes), nephrotoxicity (none of the patients assessed developed nephrotoxicity) or ototoxicity (2/20 and 5/20 patients, respectively, had mild high frequency hearing deficits which were predominantly unilateral and reversible). Although the regimens were similar in this study, other investigations will further clarify the optimal dosing approach in paediatric patients.
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