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Economic Burden of Thalassemia Major in Iran, 2015
Firooz Esmaeilzadeh1, Azita Azarkeivan2, Sara Emamgholipour3
1PhD Candidate of Health Economics, Department of Health Economics & Management, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. firooz.esmaeilzadeh@gmail.com.
Insights
The annual economic burden for major thalassemia patients is substantial, averaging $8,321.8 per person, highlighting the need for cost-management strategies and improved thalassemia screening.
Area of Science:
- Hematology
- Public Health
- Health Economics
Background:
- Major thalassemia is a severe autosomal recessive disorder.
- Increased life expectancy in patients necessitates lifelong care.
- Understanding patient costs is crucial for efficient management and treatment.
Purpose of the Study:
- To estimate the economic burden on patients with major thalassemia.
- To inform cost-control and management strategies for thalassemia care.
Main Methods:
- A prevalence-based, bottom-up approach was used from a social perspective.
- 198 major thalassemia patients were randomly selected in Tehran, Iran, in 2015.
- Economic burden was calculated including direct medical, direct non-medical, and indirect costs.
Main Results:
- The average annual cost per patient was $8,321.8 (excluding welfare loss).
- Direct medical costs constituted the largest portion ($7,286.8).
- Additional annual costs of $1,360.5 were attributed to disease-related distress.
Conclusions:
- High treatment costs for major thalassemia necessitate new cost-reduction policies.
- Enhanced thalassemia screening, even if initially more expensive, is recommended due to high treatment expenses.
- Policy interventions are needed to mitigate the financial impact on patients.
Background:
Major Thalassemia is an autosomal recessive disease with complications, mortality and serious pathology. Today, the life expectancy of patients with major thalassemia has increased along with therapeutic advances. Therefore, they need lifelong care, and caring for them would incur many costs. Being aware of the patients' costs can be effective for controlling and managing the costs and providing efficient treatments for the care of patients. Hence, this study was conducted to estimate the economic burden of the patients with major thalassemia.
Methods:
Totally, 198 patients with major thalassemia were randomly selected from among the patients with major thalassemia in Tehran, Iran in 2015. The economic burden of the patients was estimated from a social perspective and through a bottom-up, prevalence-based approach.
Results:
The average annual cost per patient was estimated $ 8321.8 regardless of the cost of lost welfare. Of this amount, $ 7286.8 was related to direct medical costs, $ 461.4 to direct non-medical costs, and $ 573.5 to indirect costs. In addition, the annual cost per patient was estimated $ 1360.5 due to the distress caused by the disease CONCLUSIONS: Considering the high costs of the treatment of patients with major thalassemia, adopting new policies to reduce the costs that patients have to pay seems necessary. In addition, making new decisions regarding thalassemia screening, even with higher costs than the usual screening costs, can be useful since the costs of treatment are high.
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