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Propranolol was effective in treating cutaneous infantile haemangiomas in Thai children
Leelawadee Techasatian1, Patcharee Komwilaisak2, Sunee Panombualert2
1Division of Dermatology, Department of Pediatric, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Insights
Propranolol effectively treats infantile haemangiomas, with rapid responses observed. Combining propranolol with prednisolone showed no significant difference in outcomes, but monitoring for side effects like hypoglycemia is crucial.
Area of Science:
- Pediatric Dermatology
- Vascular Biology
- Pharmacology
Background:
- Infantile haemangiomas are common benign vascular tumors in children.
- Early intervention is key for optimal treatment outcomes.
- Propranolol has emerged as a primary treatment option.
Purpose of the Study:
- To evaluate the efficacy and safety of propranolol for infantile haemangiomas.
- To compare propranolol monotherapy with combination therapy including prednisolone.
Main Methods:
- Retrospective chart review of 53 patients with infantile haemangiomas.
- Analysis of treatment response and adverse events following oral propranolol administration.
- Comparison of outcomes between monotherapy and combination therapy.
Main Results:
- 91.5% of patients showed treatment response within two weeks of propranolol initiation.
- All patients achieved desired treatment outcomes by two months.
- No significant difference in efficacy between propranolol monotherapy and combination therapy with prednisolone.
- Adverse events (hypoglycemia, hypotension) occurred in 5.6% of cases with dose escalation.
Conclusions:
- Oral propranolol is an effective treatment for infantile haemangiomas.
- Combination therapy with prednisolone does not offer significant advantages over monotherapy.
- Close monitoring for hypoglycemia and hypotension is recommended during propranolol treatment.
- Further long-term studies are needed to fully understand propranolol's role in infantile haemangioma management.
Aim:
The aim of this study was to explore the efficacy and safety of propranolol in treating infantile haemangiomas, the most common benign vascular tumours in children.
Methods:
We carried out a retrospective chart review of infantile haemangioma patients admitted to the Faculty of Medicine, Khon Kaen University, Thailand, from January 2009 to January 2015.
Results:
There were 53 infantile haemangioma cases treated with oral propranolol. Treatment responses occurred as early as two weeks after propranolol administration in 91.5% of the follow-up patients, with all 53 cases achieving the desired treatment responses two months after propranolol was initiated. No significant differences in treatment responses were found between propranolol as a mono-therapy or as a combination therapy with prednisolone at the two-week (p value 0.13) and one-month follow-ups (p value 0.98). Complications were documented in three cases (5.6%) when the propranolol dose was increased, and these were asymptomatic hypoglycaemia in two cases and one case of hypotension.
Conclusion:
Propranolol was effective in treating infantile haemangiomas, and combining it with prednisolone achieved no significant differences in treatment outcome. Cases should be monitored for hypoglycaemia and hypotension. More data on using propranolol for infantile haemangiomas are needed, including long-term follow-up studies.
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