Assessing Patient Preferences for Treatment Options for Pediatric Sickle Cell Disease: A Critical Review of Quantitative and Qualitative Studies

Sickle cell disease (SCD) resulting from a mutation of the β-globin gene results in sickle deformation of the red blood cell with consequent vaso-occlusion and intravascular hemolysis. SCD results in substantial morbidity, with impaired quality of life and premature mortality. Comprehensive and supp...

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Detalles Bibliográficos
Autores principales: Katoch, Deeksha, Krishnamurti, Lakshmanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493010/
https://www.ncbi.nlm.nih.gov/pubmed/34629865
http://dx.doi.org/10.2147/PPA.S264918

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493010/
https://www.ncbi.nlm.nih.gov/pubmed/34629865
http://dx.doi.org/10.2147/PPA.S264918

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