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Updated: Mar 23, 2026

Intravenous Injections in Neonatal Mice
Published on: November 11, 2014
Serum concentrations of amoxicillin in neonates during continuous intravenous infusion
A van Boekholt1, H Fleuren1, J Mouton1
1Canisius Wilhelmina Hospital, Nijmegen, Netherlands.
Insights
Continuous infusion amoxicillin achieved therapeutic, non-toxic serum concentrations in neonates during the first three days of life. Further research is needed to compare continuous infusion (CI) versus intermittent dosing (ID) for neonatal bacterial infections.
Area of Science:
- Neonatal pharmacology
- Infectious disease treatment
- Pharmacokinetics and pharmacodynamics
Background:
- Amoxicillin is a primary treatment for neonatal bacterial infections using intermittent dosing (ID).
- Increasing bacterial resistance and a lack of new antibiotics necessitate optimizing current therapies.
- Continuous infusion (CI) of beta-lactam antibiotics shows promise in adults, but CI guidelines for amoxicillin in neonates are lacking.
Purpose of the Study:
- To characterize the pharmacokinetics and pharmacodynamics of amoxicillin administered via continuous infusion (CI) during the initial three days of life.
- To identify an optimal dosing regimen for amoxicillin CI in neonates.
- To evaluate the safety and efficacy of amoxicillin CI in a neonatal population.
Main Methods:
- Study included neonates (gestational age > 34 weeks) at risk for infection requiring amoxicillin therapy.
- Serum amoxicillin concentrations were measured on days 1 and 3 of life during steady-state CI.
- Analysis of 22 serum samples from 11 patients.
Main Results:
- All neonates achieved and maintained therapeutic amoxicillin serum concentrations within the target range (Day 1: 55.4 mg/l; Day 3: 48.8 mg/l).
- Concentrations remained below toxic levels throughout the study period.
- No significant decline in amoxicillin concentration was observed between Day 1 and Day 3 (p=0.38).
Conclusions:
- Continuous infusion amoxicillin is safe and achieves therapeutic concentrations in neonates within the first three days of life.
- Further randomized controlled trials are warranted to compare the clinical efficacy of amoxicillin CI versus ID regimens.
- Optimizing amoxicillin dosing through CI may be a viable strategy to combat neonatal bacterial infections and emerging resistance.
Abstract:
Amoxicillin is commonly used for the treatment of neonatal bacterial infection with intermittent dosing (ID) regimens. However, increasing bacterial resistance, in addition to a lack of new antimicrobial agents, urges the optimization of current therapeutic options. Clinical studies in adults suggest continuous infusion (CI) regimens of beta-lactam antibiotics to be superior to ID. There are as yet no guidelines concerning the CI dosing of amoxicillin. The present study was developed to describe the CI pharmacokinetics and -dynamics of amoxicillin during the first 3 days of life in search of the optimal dosing regimen. Neonates with a gestational age above 34 weeks, at risk of neonatal infection and requiring amoxicillin therapy, were included. Serum concentrations of amoxicillin were measured during CI on days 1 and 3 in the steady state. Twenty-two serum samples of 11 patients were collected. All patients reached and retained serum concentrations of amoxicillin within the therapeutic range without exceeding the toxic concentration (serum concentrations on day 1 mean 55.4 mg/l, range 30.9-69.5, SD 10.5, and on day 3 48.8 mg/l, range 25.5-92.4, SD 18.4). There was no significant decrease in concentration from day 1 to day 3 (p = 0.38). This study showed therapeutic, nontoxic concentrations of amoxicillin in neonates on CI of amoxicillin in the first 3 days of life. Randomized controlled trials should reveal whether the clinical benefits of the CI of amoxicillin exceed those of ID regimens.
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