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Published on: April 28, 2023
Oral propranolol administration is effective for infantile hemangioma in late infancy: A retrospective cohort study
Khalaf Kridin1, Nadav Pam1, Reuven Bergman1,2
1Department of Dermatology, Rambam Health Care Campus, Haifa, Israel.
Insights
Oral propranolol effectively treats infantile hemangioma (IH) beyond its proliferative phase. This study shows significant clinical resolution and a favorable safety profile in infants treated after 9 months of age.
Area of Science:
- Pediatric Dermatology
- Pharmacology
Background:
- Infantile hemangioma (IH) treatment efficacy is highest during the proliferative phase.
- Limited data exists on oral propranolol effectiveness in late-infancy IH management.
Purpose of the Study:
- To evaluate the clinical outcomes of oral propranolol for infantile hemangioma (IH) initiated after the proliferative phase.
- To assess the safety and efficacy of propranolol in infants older than 9 months with IH.
Main Methods:
- Retrospective cohort study at a tertiary care center.
- Included 28 pediatric patients with IH receiving oral propranolol after 9 months of age.
- Dosage: 2-3 mg/kg/day.
Main Results:
- All patients showed clinical resolution, averaging 77.1% improvement.
- Efficacy was comparable in patients treated between 9-12 months and those over 12 months.
- No serious adverse events were recorded.
Conclusions:
- Oral propranolol is a safe and effective treatment for infantile hemangioma (IH) initiated beyond the proliferative phase.
- Treatment initiated after 9 months of age yields significant clinical resolution.
Abstract:
The highest efficacy of oral propranolol is for infantile hemangioma (IH) in the proliferative phase. Evaluation of the effectiveness of oral propranolol is less established when it is administered in late infancy following the proliferative phase. We aimed to assess the clinical outcomes of pediatric patients managed by oral propranolol beyond the proliferative phase of IH. A retrospective cohort study in a tertiary health care referral center was conducted to track all patients with IH receiving systemic propranolol following the proliferative phase. Twenty-eight eligible patients were managed by 2 to 3 mg/kg per day of oral propranolol for IH beyond the proliferative phase, defined at 9 months of age. The mean age at the initiation of propranolol was estimated at 11.25 (SD 2.24) months. All eligible patients experienced some degree of clinical resolution, with the average improvement rate being estimated at 77.1% (SD 16.1). Comparable results were achieved among patients who were placed on propranolol at an age older than 12 months and those managed between the age of 9 and 12 months. No serious adverse events were observed during the follow-up duration. In conclusion, oral propranolol is a safe and effective treatment for patients with IH initiating this agent beyond the proliferative phase.
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