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ABSTRACT: Background and objective
The disease burden of sickle cell anemia (SCA) in sub-Saharan African (SSA) countries is substantial, with many children dying without an established diagnosis or proper treatment. The global burden of SCA is increasing each year, making therapeutic intervention a high priority. Hydroxyurea is the only disease-modifying therapy with proven feasibility and efficacy suitable for SSA; however, no one has quantified the health economic implications of its use. Therefore, from the perspective of the health care provider, we estimated the incremental cost-effectiveness of hydroxyurea as a fixed-dose regimen or maximum tolerated dose (MTD) regimen, versus SCA care without hydroxyurea.Methods
We estimated the cost of providing outpatient treatment at a pedi
SUBMITTER: Teigen D
PROVIDER: S-EPMC10635957 | biostudies-literature | 2023 Dec
REPOSITORIES: biostudies-literature