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Propranolol as first-line treatment for rapidly proliferating infantile haemangiomas
W J M Holmes1, A Mishra, C Gorst
1Department of Plastic Surgery, Alder Hey Children's Hospital, Eaton Road, Liverpool L12 2AP, UK. willjmholmes@googlemail.com
Insights
Propranolol effectively halts infantile haemangioma proliferation and induces regression in most cases. This study supports propranolol as a well-tolerated first-line treatment for problematic infantile haemangiomas.
Area of Science:
- Pediatric Oncology
- Dermatology
- Pharmacology
Background:
- Infantile haemangioma is the most common childhood tumor, with about 10% requiring intervention.
- Recent studies indicate propranolol's high efficacy in treating rapidly proliferating haemangiomas.
Purpose of the Study:
- To prospectively evaluate propranolol's effectiveness as a first-line therapy for problematic infantile haemangiomas.
- To establish a standardized treatment protocol for propranolol administration.
Main Methods:
- 31 consecutive patients with rapidly proliferating infantile haemangioma causing functional impairment or cosmetic issues were enrolled.
- All patients underwent cardiovascular pre-treatment assessment and were initiated on propranolol at 3 mg/kg/day.
- The study prospectively monitored treatment response and side effects.
Main Results:
- 100% of patients experienced an immediate cessation of haemangioma proliferation.
- Significant regression of haemangioma was observed in 87% of patients.
- Propranolol treatment was well-tolerated with minimal adverse effects.
Conclusions:
- Propranolol demonstrates remarkable efficacy and safety as a first-line treatment for problematic infantile haemangiomas.
- The study's findings led to the adoption of propranolol as a standard first-line therapy for such cases in the unit.
- This approach offers a promising therapeutic option for infantile haemangioma management.
Abstract:
Infantile haemangioma is the commonest childhood tumour and approximately 10% requires treatment.(1,2) Recent reports have highlighted the impressive efficacy of propranolol in treating rapidly proliferating haemangioma. The aims of our study were to prospectively assess the efficacy of propranolol as a first line treatment for problematic haemangioma, and develop a treatment regime. 31 consecutive patients with rapidly proliferating infantile haemangioma with functional impairment or cosmetic disfigurement were treated with propranolol as a first line treatment. All patients had cardiovascular pre-treatment work-up and commenced on propranolol at 3 mg/kg/day. A rapid halt in haemangioma proliferation was seen in 100% of patients and significant regression in 87% of patients. This treatment is well tolerated and has little side effects. Since this study, our unit has adopted the policy of using propranolol as a first line treatment for all problematic proliferative infantile haemangiomas.
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