Propranolol Dosing for Infantile Hemangioma
Start propranolol at 1 mg/kg/day divided into 2-3 doses, then increase after 24 hours to a maintenance dose of 2 mg/kg/day for uncomplicated cases, with a maximum of 3 mg/kg/day for non-responders. 1
Standard Dosing Protocol
Initial Dosing
- Starting dose: 1 mg/kg/day divided into 2-3 doses for term infants >4 weeks old with no comorbidities 1
- Escalate to maintenance dose after 24 hours: 2 mg/kg/day divided into 2-3 doses 1
- Target maintenance range: 2-3 mg/kg/day based on high-quality RCT data showing 60% complete/nearly complete resolution at 3 mg/kg/day for 6 months versus 4% with placebo 1, 2
- Maximum dose: 3 mg/kg/day for non-responders 1
Administration Guidelines
- Give with or after feeding to reduce hypoglycemia risk 1
- Hold doses during reduced oral intake or vomiting to prevent hypoglycemia 1
- Can divide into 2 or 3 daily doses at clinician discretion 1
Modified Dosing for High-Risk Patients
PHACE Syndrome (Segmental Facial Hemangiomas)
- Starting dose: 0.5 mg/kg/day before brain MRI/MRA completion 1
- Obtain brain MRI/MRA, echocardiogram, and ECG before full-dose propranolol 1
- If arterial stenosis/agenesis present, consult pediatric neurology before escalating dose 1
- Use lowest effective dose, titrate slowly, and give 3 times daily to minimize blood pressure fluctuations 1
Preterm/Low Weight/Comorbidities
- Starting dose: 0.5 mg/kg/day for preterm infants, low birthweight, faltering growth, or conditions predisposing to hypoglycemia (e.g., hyperinsulinism) 1
- Require hospital admission for 2-4 hours on initiation and dose increases >0.5 mg/kg/day 1
- Monitor heart rate and blood pressure every 30 minutes for 2-4 hours after first dose 1
- Check blood glucose only in at-risk patients 1
Treatment Duration
Continue treatment until at least 12 months of age to minimize rebound growth risk 1
- 6 months duration superior to 3 months (60% vs lower response rates) 1, 2
- Majority of patients don't need treatment beyond 17 months 1
- Rebound growth occurs in 10-25% of patients, highest risk when stopping <12 months (especially <9 months) 1
- Risk factors for rebound: mixed/deep morphology, female sex, early discontinuation 1
- Safe to stop abruptly rather than tapering 1
Pre-Treatment Assessment
Required for All Patients
- Thorough history and physical examination including auscultation, peripheral pulses, abdominal exam for hepatomegaly 1
- Heart rate and blood pressure measurement 1
- Baseline photographs 1
Selective Testing
ECG indicated if: 1
- Heart rate outside normal range for age
- Strong family history of sudden death/arrhythmia
- Episodes of loss of consciousness
- Maternal connective tissue disease
Echocardiogram indicated if: 1
- Heart rate outside normal range for age
- Heart murmur on auscultation
- Segmental hemangioma (PHACE risk)
Baseline glucose indicated if: 1
- Preterm infant
- Small for gestational age
- Feeding poorly
- History of hypoglycemic episodes
No Routine Testing Required
- Screening blood tests (CBC, renal, liver, thyroid function) not needed in otherwise healthy infants 1
Monitoring During Treatment
- Routine follow-up every 2-3 months for stable patients 1
- No routine vital sign monitoring between appointments if infant is well 1
- Adjust dose for weight at clinic visits 1
- Use drug dosing card to prevent errors 1
Critical Safety Considerations
When to Hold Propranolol
- Reduced oral intake or vomiting (hypoglycemia risk) 1
- Intercurrent illness affecting feeding 1
- Progressive ulceration while on therapy (rare—propranolol can worsen ulceration via peripheral ischemia; consider dose reduction) 1
Contraindications
- Heart block
- Decompensated heart failure
- Asthma/obstructive airway disease
- Cardiogenic shock
- Sinus node dysfunction without pacemaker 1
Common Adverse Effects
- Sleep disturbances (most common—10/71 patients in one series) 3
- Hypoglycemia, bradycardia, hypotension, bronchospasm (infrequent but serious) 1, 2
- Cool extremities 4
Special Populations
Vision-Threatening Periocular Hemangiomas
- Warrant early treatment to prevent amblyopia, refractive errors, strabismus (complications in up to 80% if untreated) 1
- Require ophthalmology co-management 1