Can Hyoscine Be Given in Children?
Hyoscine (scopolamine) can be used in children, but with significant age-related restrictions and heightened safety concerns, particularly in children under 6 years who face the greatest risk of adverse events including acute psychosis and delirium.
Age-Specific Restrictions and Safety Profile
Transdermal Scopolamine (Motion Sickness)
- Transdermal scopolamine patches are NOT recommended for young children due to documented cases of severe toxicity, including a reported case of acute delirium with psychotic behaviors, hallucinations, and aggressive behavior in a 4-year-old boy 1
- The transdermal formulation delivers 0.5 mg over 72 hours with highly variable plasma concentrations (range 11-240 pg/mL), making dose control particularly problematic in pediatric patients 2
- Systemic anticholinergic toxicity manifests as flushing, bizarre actions, hallucinations, hyperactivity, and incoherent speech in children 1
Hyoscine Butylbromide (Abdominal Cramping)
- Hyoscine butylbromide has a more favorable safety profile for abdominal cramping due to minimal systemic absorption (bioavailability <1%) and inability to cross the blood-brain barrier 3
- This formulation exerts local spasmolytic effects on gastrointestinal smooth muscle without significant CNS penetration 3
- However, specific pediatric dosing guidelines and safety data are lacking in the available evidence
Critical Safety Considerations in Pediatric Sedation Context
High-Risk Age Groups
- Children younger than 6 years, particularly those under 6 months, are at greatest risk of adverse events during any sedation or medication administration 4
- The American Academy of Pediatrics emphasizes that young children are especially vulnerable to respiratory depression, airway obstruction, and loss of protective reflexes 5, 4
Anticholinergic Effects and Monitoring
- Anticholinergic agents like scopolamine produce dose-dependent adverse effects including hallucinations, vertigo, dry mouth, and drowsiness 2
- Drug-induced psychosis should be considered in any child with acute behavioral changes when anticholinergic agents have been administered 1
- The short plasma half-life and first-pass metabolism after oral administration limit predictability in pediatric dosing 2
Practical Clinical Algorithm
When Considering Hyoscine in Children:
For Motion Sickness:
- Avoid transdermal scopolamine in children under 12 years given documented toxicity cases and lack of pediatric safety data 1
- Consider alternative antiemetics with established pediatric safety profiles
- If used in adolescents, monitor continuously for CNS effects including behavioral changes 1, 2
For Abdominal Cramping:
- Hyoscine butylbromide may be considered due to minimal systemic absorption 3
- Ensure proper dosing calculations based on weight, recognizing that pediatric patients require individualized pharmacokinetic considerations 6
- Monitor for rare anticholinergic effects despite low bioavailability 3
For Pre-operative Use:
- Alternative agents are preferred - the American Academy of Pediatrics recommends pentobarbital (2-6 mg/kg IV) or midazolam (0.2-0.3 mg/kg IV) for procedural sedation with established pediatric safety profiles 4
- If scopolamine is used for antisialagogue effects, use minimal effective doses with continuous monitoring 5
Common Pitfalls to Avoid
- Failing to recognize that children are not simply "small adults" and require age-specific pharmacokinetic considerations including organ maturity and metabolic capacity 6
- Underestimating the risk of CNS toxicity from transdermal formulations, which can cause severe delirium even in young children 1
- Not having rescue protocols in place - practitioners must be able to manage one level deeper than intended sedation 5, 4
- Inadequate monitoring - continuous physiologic monitoring and presence of personnel not performing the procedure are essential when any sedating medication is used 4
Key Contraindications and Warnings
- Scopolamine crosses the placenta and should be used cautiously in pregnant adolescents 2
- The highly variable pharmacokinetic response to transdermal scopolamine reflects individual differences that are even more pronounced in developing pediatric patients 7, 2
- Symptoms resolve after removal of the patch and conservative management, but recognition of toxicity is critical 1