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Propranolol for severe infantile hemangiomas: follow-up report
Véronique Sans1, Eric Dumas de la Roque, Jérôme Berge
1National Reference Center for Rare Skin Diseases, Children's Hospital, Bordeaux, France.
Insights
Oral propranolol effectively controls infantile hemangiomas (IHs), the most common infant tumors. This treatment rapidly reduces IH growth and offers a safe, well-tolerated therapeutic option.
Area of Science:
- Pediatric Oncology
- Dermatology
- Pharmacology
Background:
- Infantile hemangiomas (IHs) are common vascular tumors in infants.
- Effective management strategies for IHs are crucial to prevent complications.
Purpose of the Study:
- To evaluate the efficacy and safety of oral propranolol in managing the growth phase of infantile hemangiomas.
Main Methods:
- 32 children with IHs received propranolol (2-3 mg/kg/day) after clinical and ultrasound assessment.
- Cardiac evaluations and vital sign monitoring were performed.
- Treatment outcomes and side effects were assessed over a mean duration of 6.1 months.
Main Results:
- All patients showed immediate improvement in IH color and growth.
- Ulcerated IHs healed within 2 months; significant regression observed by 2 months.
- Mild side effects were noted, with one case of wheezing.
Conclusions:
- Oral propranolol at 2-3 mg/kg/day demonstrates consistent and rapid therapeutic effects on IHs.
- The treatment significantly shortens the natural course of IHs with good clinical tolerance.
- Propranolol offers a safe and effective alternative to systemic corticosteroids.
Objective:
Infantile hemangiomas (IHs) are the most-common soft-tissue tumors of infancy. We report the use of propranolol to control the growth phase of IHs.
Methods:
Propranolol was given to 32 children (21 girls; mean age at onset of treatment: 4.2 months) after clinical and ultrasound evaluations. After electrocardiographic and echocardiographic evaluations, propranolol was administered with a starting dose of 2 to 3 mg/kg per day, given in 2 or 3 divided doses. Blood pressure and heart rate were monitored during the first 6 hours of treatment. In the absence of side effects, treatment was continued at home and the child was reevaluated after 10 days of treatment and then every month. Ultrasound measurements were performed after 60 days of treatment.
Results:
Immediate effects on color and growth were noted in all cases and were especially dramatic in cases of dyspnea, hemodynamic compromise, or palpebral occlusion. In ulcerated IHs, complete healing occurred in <2 months. Objective clinical and ultrasound evidence of longer-term regression was seen in 2 months. Systemic corticosteroid treatment could be stopped within a few weeks. Treatment was administered for a mean total duration of 6.1 months. Relapses were mild and responded to retreatment. Side effects were limited and mild. One patient discontinued treatment because of wheezing.
Conclusion:
Propranolol administered orally at 2 to 3 mg/kg per day has a consistent, rapid, therapeutic effect, leading to considerable shortening of the natural course of IHs, with good clinical tolerance.
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