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.
Abstract

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