The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea

OBJECTIVE: To assess the burden and quality of life of caregivers of patients with sickle cell anemia taking hydroxyurea versus those of patients not taking hydroxyurea. METHODS: A cross-sectional study was performed of caregivers of outpatients with sickle cell anemia in two public hospitals in Cam...

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Detalles Bibliográficos
Autores principales: da Silva, Luiz Bernardino Lima, Ivo, Maria Lúcia, de Souza, Albert Schiaveto, Pontes, Elenir Rose Jardim Cury, Pinto, Alexandra Maria Almeida Carvalho, de Araujo, Olinda Maria Rodrigues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Hematologia e Hemoterapia 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460397/
https://www.ncbi.nlm.nih.gov/pubmed/23049439
http://dx.doi.org/10.5581/1516-8484.20120070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460397/
https://www.ncbi.nlm.nih.gov/pubmed/23049439
http://dx.doi.org/10.5581/1516-8484.20120070

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