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Propranolol in the management of periorbital infantile haemangioma
Jin Fong Cheng1, Glen A Gole, Timothy J Sullivan
1Royal Children's Hospital, Brisbane, Queensland, Australia. jin_fong_cheng@nuhs.edu.sg
Insights
Propranolol effectively reduced the size and color of infantile haemangiomas in children. This treatment also showed positive results in reducing astigmatism, with no significant side effects observed.
Area of Science:
- Ophthalmology
- Pediatric Oncology
- Dermatology
Background:
- Infantile haemangiomas are the most common orbital tumors in children.
- Treatment is typically observational unless vision is threatened.
- Alternative treatments like steroids and surgery carry inherent risks.
Purpose of the Study:
- To review the safety and efficacy of propranolol for treating periorbital infantile haemangiomas.
- To assess the impact of propranolol on lesion size, color, and associated astigmatism.
Main Methods:
- Retrospective review of 10 patients treated by two ophthalmologists.
- Data collected included lesion characteristics, treatment duration, and side effects.
- Outcomes measured were changes in lesion size, color, and astigmatism.
Main Results:
- All 10 patients showed reduced lesion color and size after treatment with propranolol.
- Mean lesion size decreased from 756.7 to 543.2 mm² (P=0.075).
- 60% of patients with astigmatism experienced successful reduction.
Conclusions:
- Propranolol is a safe and effective treatment option for infantile haemangioma.
- The study supports propranolol's use in managing periorbital haemangiomas.
- No significant adverse events were reported in the patient cohort.
Background:
Infantile haemangiomas are the commonest tumours of the orbit in children. Treatment is usually expectant, unless they are visually threatening. Although steroids, other pharmacological and surgical treatment modalities have their place, there are risks involved. A previous case series reported the successful use of propranolol for infantile haemangioma. The safety and efficacy of propranolol in the treatment of periorbital haemangioma was reviewed in a serious of our patients.
Methods:
We performed a retrospective review of patients seen by two ophthalmologists (TJS and GAG), collecting data on colour, size of lesion, duration of treatment and side-effects of treatment. Our main outcome measures were colour and size of infantile haemangioma before and after treatment, the change in astigmatism of our patients and the incidence of complications from propranolol.
Results:
We reviewed 10 patients with infantile haemangioma. They were treated with propranolol oral syrup 2 mg/kg/day in divided doses for a mean duration of 32.8 (range 12-42) weeks. All our patients had a reduction in colour and size of the lesions. The mean lesion size decreased from 756.7 to 543.2 mm(2) after treatment (P = 0.075). Five patients had significant astigmatism and 60% had successful reduction of astigmatism after treatment. None of our patients suffered significant side-effects of propranolol.
Conclusion:
Propranolol appears to be a safe and effective treatment in the management of infantile haemangioma.
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