Many childhood infections do not require antibiotics at all, including:
- common self-limiting infections
- viral infections
- bacterial infections that require drainage or other physical treatment (e.g. cutaneous abscess, dental infections requiring timely dental treatment).
Shared decision making with parents is an effective approach to appropriately using antibiotics and reducing antibiotic overuse.
‘Children are not little adults’ is a common comment from those working in paediatrics. The epidemiology, clinical presentation and prognosis of some infections differ in children compared to adults. Understanding this is key to timely diagnosis and good antimicrobial stewardship. In addition, pharmacokinetics can be different in children. This was evident with oral penicillins from the very beginning – gastric acid secretion, intestinal motility and drug pH all affect absorption. Depending on age and whether a child is unwell, these can result in net increased or decreased absorption compared to an adult. However, the magnitude of these effects are greatest during the first two years of life.4
In paediatric studies, dosage requirements often exceeded the expected dose for body size.4,5 Direct comparisons between paediatric studies were complicated by incomplete information about the age or weight of patients, use of different product strengths, teaspoon measures, and the ‘rounding’ of doses for convenient administration.4,6
Empiric prescribing should ideally be based on the likely pathogen and the pharmacokinetics and pharmacodynamics of the antibiotic. Dosing information for children is included in Therapeutic Guidelines, the AMH Children’s Dosing Companion, and guidelines from children’s hospitals.
When a penicillin is required, it should be prescribed at doses that are expected to safely maximise the time that the drug remains above the minimum inhibitory concentration for the pathogen. If available, reviewing cultures and the results of susceptibility testing ensures the correct drug with the narrowest spectrum is used.
Narrow-spectrum penicillins are active against Streptococcus pyogenes (Group A streptococcus). Phenoxymethylpenicillin has been used extensively for erysipelas, streptococcal tonsillitis and dental infections that require antibiotics.
Amoxicillin is active against susceptible Escherichia coli. Adding the beta-lactamase inhibitor clavulanic acid increases the ability to treat certain Gram-negative organisms.
For Streptococcus pneumoniae infections (other than meningitis) with reduced susceptibility to penicillin, increasing the penicillin or amoxicillin dose may be effective. Using amoxicillin/clavulanic acid does not provide additional benefit in this case, as penicillin resistance in Streptococcus pneumoniae is not mediated by a beta-lactamase.7 For mild to moderate pneumonia, oral amoxicillin is recommended in Therapeutic Guidelines at 25 mg/kg dose eight hourly and in World Health Organization guidelines8 at 40 mg/kg 12 hourly. It is non-inferior to parenteral options for this condition.
Amoxicillin/clavulanic acid is appropriate for treating beta-lactamase-producing strains of Haemophilus influenzae and Moraxella catarrhalis. If a higher amoxicillin dose is required, children aged two months and over should be prescribed a formulation with a lower dose of clavulanic acid.
Duration of therapy varies by indication. Many common, uncomplicated infections may be treated with shorter antibiotic courses than are commonly given.9