The common adverse
effects of transmucosal midazolam are sedation, ataxia, irritability or
euphoria, and mild respiratory depression. Intranasal administration may also
produce local irritation, stinging, sometimes with eyes watering and a runny
nose.
Avoid using the
intranasal route in children with any awareness during seizures because of the
irritation. We recommend using a reusable mucosal atomisation device for
intranasal administration, delivering half the dose into each nostril. Mucosal
atomisation devices may be available through hospitals or the ambulance service
and can be purchased privately.
Major complications of
treatment are unlikely when the guidelines for midazolam are followed.12 With
a single dose, respiratory depression is rare. Cumulative subsequent doses are
much safer if given where expert airway support is available.
When midazolam is
provided for use by carers, we recommend nominating only one prescriber and one
dispenser for each child in order to avoid confusion. This is most often the
treating neurologist and the hospital pharmacy because of the restricted
availability of the plastic ampoules. Midazolam is available in a range of
concentrations and volumes so we restrict prescription to 5 mg in 1 mL plastic
ampoules, wherever possible, to avoid dosing errors. Having a single prescriber
and dispenser also reduces the potential for abuse and stockpiling. In a review
of four years of pre-hospital use we found only two out of 197 families with
circumstantial evidence of carers abusing the drug.13
Parents used to using
plastic ampoules may struggle without extra instruction if glass ampoules are
dispensed. It is always best to review parental understanding and techniques
periodically. Frequent problems include:
- loss
of dose from ‘salivary washout’ in dribbly children
- dose swallowing in partially
aware children
- blocked noses
- confusion between ‘mL’
and ‘mg’ and the risk of accidental overdosing
- failure to adjust doses
for growing children.