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Sickle cell disease-related pediatric medical expenditures in the U.S
Djesika D Amendah1, Mercy Mvundura, Patricia L Kavanagh
1Division of Blood Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia 30333, USA. damendah@cdc.gov
Insights
Children with sickle cell disease (SCD) incurred significantly higher medical costs. The study estimated total SCD-attributable medical expenditures for children in the U.S. to be approximately $335 million in 2005.
Area of Science:
- Pediatric Hematology
- Health Economics
- Public Health
Background:
- Sickle cell disease (SCD) is associated with high healthcare utilization.
- Previous expenditure estimates for SCD often focused narrowly on inpatient care or limited geographic data.
Purpose of the Study:
- To determine the incremental healthcare expenditures per child with SCD compared to children without the condition.
- To estimate the total economic burden of SCD among children in the United States.
Main Methods:
- Utilized MarketScan Medicaid and Commercial Claims databases from 2005.
- Calculated SCD-attributable expenditures by comparing age-adjusted mean costs for children with and without SCD.
Main Results:
- Children with SCD had higher medical expenditures: $9,369 (Medicaid) and $13,469 (private insurance) more than their peers.
- Expenditure multiples were 6x for Medicaid and 11x for private insurance compared to children without SCD.
Conclusions:
- SCD-attributable medical costs for children in the U.S. were estimated at $335 million in 2005.
- This estimate, derived from a large, multi-state, multi-payer sample, is considered conservative.
Background:
Although it is known that people with sickle cell disease (SCD) have relatively high utilization of medical care, most previous estimates of SCD-attributable expenditures have been limited to either inpatient care or single-state data.
Purpose:
To extend known findings by measuring the attributable or incremental expenditures per child with SCD compared to children without this illness and to thereby estimate SCD-attributable expenditures among children in the U.S.
Methods:
MarketScan Medicaid and Commercial Claims databases for 2005 were used to estimate total medical expenditures of children with and without SCD. Expenditures attributable to SCD were calculated as the difference in age-adjusted mean expenditures during 2005 for children with SCD relative to children without SCD in the two databases.
Results:
Children with SCD incurred medical expenditures that were $9369 and $13,469 higher than those of children without SCD enrolled in Medicaid and private insurance, respectively. In other words, expenditures of children with SCD were 6 and 11 times those of children without SCD enrolled in Medicaid and private insurance, respectively.
Conclusions:
Using a large, multistate, multipayer patient sample, SCD-attributable medical expenditures in children were conservatively and approximately estimated at $335 million in 2005.
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