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. 2012 Mar;18(2):276-83.
doi: 10.1111/j.1365-2516.2011.02713.x. Epub 2011 Dec 21.

Health care expenditures for Medicaid-covered males with haemophilia in the United States, 2008

Affiliations

Health care expenditures for Medicaid-covered males with haemophilia in the United States, 2008

S Guh et al. Haemophilia. 2012 Mar.

Abstract

Although haemophilia is an expensive disorder, no studies have estimated health care costs for Americans with haemophilia enrolled in Medicaid as distinct from those with employer-sponsored insurance (ESI). The objective of this study is to provide information on health care utilization and expenditures for publicly insured people with haemophilia in the United States in comparison with people with haemophilia who have ESI. Data from the MarketScan Medicaid Multi-State, Commercial and Medicare Supplemental databases were used for the period 2004-2008 to identify cases of haemophilia and to estimate medical expenditures during 2008. A total of 511 Medicaid-enrolled males with haemophilia were identified, 435 of whom were enrolled in Medicaid for at least 11 months during 2008. Most people with haemophilia qualified for Medicaid based on 'disability'. Average Medicaid expenditures in 2008 were $142,987 [median, $46,737], similar to findings for people with ESI. Average costs for males with haemophilia A and an inhibitor were 3.6 times higher than those for individuals without an inhibitor. Average costs for 56 adult Medicaid enrollees with HCV or HIV infection were not statistically different from those for adults without the infection, but median costs were 1.6 times higher for those treated for blood-borne infections. Haemophilia treatment can lead to high costs for payers. Further research is needed to understand the effects of public health insurance on haemophilia care and expenditures, to evaluate treatment strategies and to implement strategies that may improve outcomes and reduce costs of care.

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Conflict of interest statement

SM is currently an employee of Biogen Idec. CMK receives research funding (paid directly to his university with his salary set aside) from Octapharma, Baxter Immuno, Grifols, Pfizer, Bayer and NovoNordisk. He has received honoraria as a consultant on advisory boards for Octapharma, Baxter Immuno, Bayer, CSL Behring, NovoNordisk and Pfizer. All other authors have declared no conflicting interests.

Figures

Fig 1
Fig 1
Flow chart of sample selection. C, child; HA, haemophilia A; HB, haemophilia B; B+, treatment for an inhibitor with bypassing agents; B, no treatment for an inhibitor with bypassing agents; A, adult; H, haemophilia; V+, with blood-borne viral infection; V, without blood-borne viral infection. *Five adults with both viral infection and inhibitors were included in the AHB+ group.
Fig 2
Fig 2
Annual average health care costs of people with haemophilia who had Medicaid insurance by 10-year age group and type of care (clotting factors and all other costs) in 2008 (N = 435).

References

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