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Efficacy and safety of propranolol as first-line treatment for infantile hemangiomas
Clemens Schiestl1, Kathrin Neuhaus, Silke Zoller
1Division of Plastic Surgery, University Children's Hospital Zurich, Zurich, Switzerland.
Insights
Propranolol is an effective first-line treatment for complicated infantile hemangiomas (IH), showing significant reduction in size and color. This beta-blocker demonstrates good tolerance and minimal hemodynamic impact in infants.
Area of Science:
- Pediatric Dermatology
- Vascular Anomalies
- Pharmacology
Background:
- Complicated infantile hemangiomas (IH) are a significant concern.
- Beta-blockers show promise for IH treatment, but data on propranolol as a first-line therapy is limited.
- Objective outcome measures and hemodynamic effects in infants require further investigation.
Purpose of the Study:
- To evaluate propranolol as a first-line treatment for proliferating complicated infantile hemangiomas.
- To assess objective outcomes using visual analogue scale (VAS), ultrasound, and ophthalmological review.
- To monitor tolerance and hemodynamic changes in infants receiving propranolol.
Main Methods:
- Retrospective evaluation of 25 infants with complicated IH treated with propranolol (2 mg/kg/day).
- Outcome assessment via blinded photographic evaluation (VAS), ultrasound, and ophthalmological review.
- In-patient monitoring for tolerance and hemodynamics during initial therapy.
Main Results:
- Significant reduction in IH color (VAS -9) and size (VAS -8) after 7 months.
- Ultrasound showed a decrease in lesion thickness from 14 mm to 10 mm (p < 0.01).
- Periocular IH cases resolved rapidly; overall tolerance was good with no significant hemodynamic changes.
Conclusions:
- Propranolol is highly effective for complicated infantile hemangiomas.
- The therapy is well-tolerated with a favorable safety profile in infants.
- Propranolol is proposed as a first-line treatment for infantile hemangiomas.
Unlabelled:
Beta-blockers are a highly promising treatment modality for complicated infantile hemangiomas (IH). However, data on propranolol as first-line treatment, objective outcome measures and impact on hemodynamics in young infants is limited. We retrospectively evaluated a homogenous group of infants with proliferating complicated IH treated with propranolol (2 mg/kg/day). Outcome was assessed by blinded evaluation of clinical photographs by visual analogue scale (VAS), ultrasound examination and ophthalmological review (if appropriate). Tolerance and hemodynamic variables were recorded over time, including a 2-day in-patient observation at the initiation of therapy. Twenty-five infants (median age 3.6 (1.5-9.1) months) were included in the study. The median follow-up-time was 14 (9-20) months and 14 patients completed treatment at a median age of 14.3 (11.4-22.1) months, after a duration of 10.5 (7.5-16) months. In all patients, there was significant fading of colour (with a VAS of -9 (-6 to -9) after 7 months) and significant decrease in size of the IH (with a VAS of -8 (-3 to -10) after 7 months). Median thickness of the lesions assessed by ultrasound at baseline and after 1 month was 14 (7-28) mm and 10 (5-23) mm, respectively (p < 0.01). In children with periocular involvement, astigmatism and amblyopia resolved rapidly within 8 weeks. The overall tolerance of propranolol was good, and no relevant hemodynamic changes were noted.
Conclusion:
Our report supports the excellent effect and good tolerance of this novel therapy, and we propose the use of propranolol as first-line treatment for IH.
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