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Cost-effectiveness of treating infantile haemangioma with propranolol in an outpatient setting
Kanupriya Chaturvedi1, Joni S Steinberg2, Christopher S Snyder1
11The Congenital Heart Collaborative,Rainbow Babies and Children's Hospital,Case Western Reserve University School of Medicine,Cleveland,OH,USA.
Insights
Outpatient propranolol treatment for infantile haemangioma is more cost-effective than inpatient therapy. This approach offers significant savings while managing this common vascular tumor.
Area of Science:
- Pediatric Dermatology
- Vascular Biology
- Health Economics
Background:
- Infantile haemangioma affects 3-10% of infants, often requiring treatment for cosmetic or functional reasons.
- Propranolol is the preferred treatment, but protocols vary, lacking consensus guidelines.
- This study evaluates the cost-effectiveness of inpatient versus outpatient propranolol initiation.
Purpose of the Study:
- To compare the cost-effectiveness of initiating propranolol treatment for infantile haemangioma in an inpatient versus outpatient setting.
- To analyze the financial implications of adding a pretreatment echocardiogram to both treatment strategies.
Main Methods:
- A decision tree model was developed to compare inpatient and outpatient propranolol initiation strategies.
- Cost analysis focused on healthy, term-born infants without complicating factors.
- Sensitivity analysis assessed the impact of potential propranolol side effects.
Main Results:
- Inpatient propranolol treatment averaged $2603/day, rising to $2843 with an echocardiogram.
- Outpatient treatment averaged $138, increasing to $828 with an echocardiogram.
- Outpatient initiation demonstrated substantial cost savings.
Conclusions:
- Initiating propranolol for infantile haemangioma on an outpatient basis is more cost-effective.
- Outpatient management offers a financially advantageous approach to treating this common condition.
Background:
Infantile haemangioma is one of the most commonly known benign vascular tumours of infancy and childhood, having an incidence of 3-10%. Most lesions regress spontaneously; however, some may require treatment owing to their clinical and cosmetic effects. Propranolol has become the treatment of choice for infantile haemangioma, but treatment protocols are largely institutional based without any specific consensus guidelines. Our aim was to evaluate the cost-effectiveness of propranolol use as inpatient versus outpatient therapy.
Methods:
A decision tree model was created depicting alternate strategies for initiating propranolol treatment on an inpatient versus outpatient basis combined with the option of a pretreatment echocardiogram applied to both strategies. Cost analysis was assumed to be based on treatment of haemangioma in patients who were born at term, had no chronic illnesses, a non-life-threatening location of the haemangioma, and those who were not taking any other medications that could potentiate the side effects of propranolol. A sensitivity analysis was performed to evaluate the probability of side effects.
Results:
The average cost incurred for inpatient treatment of infantile haemangioma was approximately $2603 for a single hospital day and increased to $2843 with the addition of an echocardiogram. The expected cost of treatment in the outpatient setting was $138, which increased to $828 after the addition of an echocardiogram.
Conclusion:
Treating infantile haemangioma with propranolol is more cost-effective when initiated on an outpatient basis.
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