Propranolol (Infantile Haemangioma / Paediatric Arrhythmias)
Brand names: Hemangiol (infantile haemangioma), Inderal (general)
Adult dose
Paediatric dose
Dose adjustments
No dose adjustment required in paediatric renal impairment.
Severe hepatic impairment: reduce dose — first-pass metabolism reduced → higher systemic exposure.
Hemangiol licensed for infantile haemangioma from 5 weeks corrected gestational age to 5 months (treatment start window). Duration: 6 months total. Take during or just after feeding — prevents hypoglycaemia. Withhold if infant is sick (vomiting/not feeding) — hypoglycaemia risk. Source: BNF for Children 2024; MHRA SPC Hemangiol.
Clinical pearls
- Infantile haemangioma — transformative indication: Hemangiol (propranolol 3.75 mg/mL solution) is licensed for proliferating infantile haemangioma (IH) requiring treatment. Before propranolol, IH treatment was limited to oral steroids (side effects) or laser. Propranolol causes rapid involution of IH via vasoconstriction + anti-angiogenic effects (reduces VEGF, bFGF). Response rate >95% — most haemangiomas regress within 4–8 weeks.
- MHRA hypoglycaemia warning for Hemangiol: propranolol blocks sympathetically mediated glycogenolysis — infants are particularly vulnerable. MANDATORY rule: ALWAYS give Hemangiol dose during or immediately after feeding. NEVER give if infant is sick, vomiting, or refusing feeds — withhold dose. Blood glucose testing before discharge from initiation visit. Parents must be counselled on hypoglycaemia signs in infants (jitteriness, pallor, sweating, seizures) and emergency glucose management (oral glucose gel).
- Treatment start window: Hemangiol should be started between 5 weeks and 5 months corrected gestational age — when haemangiomas are actively proliferating. Starting too late (after 5 months) misses the proliferative phase. Duration: 6 months. Most haemangiomas treated from 1–3 months corrected age show complete or near-complete resolution by 12 months.
- SVT management in infants: propranolol is used for prevention of SVT (particularly WPW-related SVT and AVNRT) in infants and young children. Onset of oral action is 30–60 minutes. For acute SVT — adenosine (vagal manoeuvre first) is first-line; propranolol IV is second-line in haemodynamically stable SVT. IV use requires continuous cardiac monitoring.
- Asthma absolute contraindication: non-selective beta-blockade in any degree of airway hyperresponsiveness can precipitate fatal bronchospasm — even at the low doses used for haemangioma. Always ask parents about family history of asthma, wheeze, atopy, or breathing difficulties in the infant before prescribing. Source: BNF for Children 2024; Léauté-Labrèze et al. NEJM 2008 (haemangioma discovery); Léauté-Labrèze et al. NEJM 2015 (HEMANGIOL trial); MHRA SPC Hemangiol.
Contraindications
- Asthma or bronchospasm (non-selective beta-blockade — absolute CI in asthma; avoid even in history of wheeze)
- Cardiogenic shock, decompensated heart failure
- Sinus bradycardia, AV block greater than first degree (without pacemaker)
- Phaeochromocytoma without adequate alpha-blockade
- Hypoglycaemia-prone infants (premature, IUGR — hypoglycaemia risk at Hemangiol doses)
Side effects
- Bradycardia (most common cardiovascular effect — monitor HR, especially in neonates)
- Hypoglycaemia (MHRA warning for Hemangiol — propranolol blocks glycogenolysis and gluconeogenesis; always give with or after feeding; withhold if not feeding)
- Hypotension
- Bronchospasm (avoid in any respiratory disease; even at low doses for haemangioma)
- Sleep disturbances, nightmares, vivid dreams (central CNS penetration)
- Cold extremities, Raynaud phenomenon (peripheral vasoconstriction)
Interactions
- Calcium channel blockers (verapamil, diltiazem): profound bradycardia and AV block — avoid combination or close monitoring
- Antidiabetic agents (insulin, sulphonylureas): propranolol masks hypoglycaemia symptoms (except sweating) — very dangerous in hypoglycaemia-prone infants on Hemangiol
- Lidocaine: beta-blockade reduces lidocaine clearance — monitor for lidocaine toxicity if used concomitantly
- NSAIDs: reduce antihypertensive effect of propranolol
- Adrenaline: risk of rebound hypertension if used (alpha-uncountered vasopressor effect)
Monitoring
- Heart rate and blood pressure before first dose and after dose increases
- Blood glucose at 1–2h after first dose (hypoglycaemia — Hemangiol indication)
- Feed tolerance at each dose (withhold if not feeding — hypoglycaemia protocol)
- Haemangioma response at 4, 8, 12 weeks (photographic documentation — size, colour, texture)
- Respiratory assessment (bronchospasm at each visit)
- ECG at baseline (SVT indication — assess for WPW, AV block)
Reference: BNF for Children 2024; Léauté-Labrèze et al. NEJM 2015 (HEMANGIOL trial); MHRA SPC Hemangiol; American Heart Association Paediatric Advanced Life Support 2020. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
- PICU Delirium Assessment (pCAM-ICU) · Delirium Assessment
- Vasoactive-Inotropic Score (VIS) · Inotropic Support
- REVEAL 2.0 Risk Score for Pulmonary Arterial Hypertension · Pulmonary Hypertension
- AUB-HAS2 Cardiovascular Risk Index · Cardiovascular Risk
- MAGGIC Heart Failure Risk Score · Heart Failure
- RV Systolic Pressure Estimation (RVSP) · Echocardiography