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Non-Selective Beta-Blocker (Infantile Haemangioma / SVT / Hypertension) Pregnancy: Avoid first trimester — beta-blockers associated with IUGR, neonatal bradycardia. If essential for maternal indication (arrhythmia, hypertension) — use with foetal monitoring. Paediatric indication not applicable in pregnancy.

Propranolol (Infantile Haemangioma / Paediatric Arrhythmias)

Brand names: Hemangiol (infantile haemangioma), Inderal (general)

Adult dose

Dose: Arrhythmia: 40 mg two to four times daily. Hypertension: 80–160 mg daily in divided doses. Thyrotoxicosis: 10–40 mg three times daily
Route: Oral
Frequency: Two to four times daily
Max: 320 mg/day
Adult indications for reference. Main paediatric focus — infantile haemangioma and SVT. Source: BNF 90.

Paediatric dose

Dose: Infantile haemangioma (Hemangiol): start 1.5 mg/kg/day in 2 divided doses for 1 week → 3 mg/kg/day in 2 divided doses. SVT: 0.25–0.5 mg/kg/dose IV under cardiac monitoring; oral 1–4 mg/kg/day in 3–4 divided doses. Hypertension: 1–4 mg/kg/day in 2–4 divided doses mg/day/kg
Route: Oral (Hemangiol oral solution 3.75 mg/mL). IV (SVT emergency only)
Frequency: Twice daily (haemangioma); three to four times daily (SVT/hypertension)
Max: 3 mg/kg/day (haemangioma); 4 mg/kg/day (SVT/hypertension)
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.

Dose adjustments

Renal

No dose adjustment required in paediatric renal impairment.

Hepatic

Severe hepatic impairment: reduce dose — first-pass metabolism reduced → higher systemic exposure.

Paediatric weight-based calculator

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.