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Propranolol treatment for severe infantile hemangiomas: a single-centre 3-year experience
Anastasia Georgountzou1, Emmanouil Karavitakis, Alexandra Klimentopoulou
1First Department of Paediatrics, University of Athens, Aghia Sophia Children's Hospital, Athens, Greece. stacegee1@hotmail.com
Insights
Propranolol effectively treats infantile hemangiomas (IHs), showing significant regression in most patients. This treatment is well-tolerated, with good results even in cases of regrowth, though optimal duration requires further study.
Area of Science:
- Pediatric Dermatology
- Vascular Malformations
- Pharmacology
Background:
- Infantile hemangiomas (IHs) are common benign vascular tumors in infants.
- Proliferative-phase IHs can cause significant cosmetic and functional issues.
- Limited treatment options exist for problematic IHs.
Purpose of the Study:
- To assess the efficacy, safety, and tolerability of propranolol as a monotherapy for infantile hemangiomas.
- To evaluate propranolol's effectiveness in problematic, proliferative-phase IHs.
- To determine the clinical response and side effects of propranolol treatment.
Main Methods:
- 28 children with IHs received oral propranolol (2 mg/kg/day).
- Cardiologic evaluation, hemodynamic monitoring, and blood glucose monitoring were performed.
- Clinical response, tolerance, and photographic documentation were assessed monthly.
Main Results:
- All patients showed initial improvements in color and growth within one month.
- 24 patients achieved >90% regression after a mean of 7.56 months.
- Four patients experienced hypotension; no treatment interruptions occurred due to side effects.
Conclusions:
- Propranolol is an effective first-line treatment for infantile hemangiomas with excellent clinical tolerance.
- Propranolol appears effective in managing IH regrowth.
- Long-term studies are needed to determine optimal treatment duration.
Aim:
To evaluate the effectiveness, safety and tolerability of propranolol as single-agent treatment in patients with problematic, proliferative-phase, infantile hemangiomas (IHs).
Methods:
Oral propranolol was administered at a dose of 2 mg/kg/day to 28 children. Cardiologic evaluation was performed before treatment initiation. Hemodynamic variables and blood glucose levels were monitored during the first 24 h of treatment, while the children were hospitalized. Clinical response and tolerance were assessed every month, along with photographic documentation. Macroscopic regression was considered the reduction >90% in the size of the IHs.
Results:
Effects on colour and growth were observed within the first month in all cases. Twenty-four patients completed treatment after a mean duration of 7.56 months, and their hemangiomas were successfully regressed. Propranolol was administered again, with satisfactory results, in three patients (12.5%) because of hemangioma regrowth. Satisfactory response is noticeable in ongoing cases. Episodes of hypotension were noted in four patients. There were no treatment interruptions because of side effects.
Conclusions:
Propranolol, as first-line treatment, yielded excellent results with very good clinical tolerance and also seems to be effective in relapses. The optimal duration of the treatment remains to be defined by long-term observation.
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