Socio-demographic, economic and health profile of adults with sickle-cell disease

• Autor(a) principal: Amaral, Júlia Lamese
• Data de Publicação: 2015
• Outros Autores: Almeida, Nívea Aparecida, Santos, Paula Silveira, Oliveira, Patrícia Peres de, Lanza, Fernanda Moura
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Rev Rene (Online)
• Texto Completo: http://periodicos.ufc.br/rene/article/view/2763
• topic: Anemia; Sickle Cell; Adult Health; Epidemiology.

Objective: to describe socio-demographic and economic characteristics, lifestyle, clinical manifestations, use of medicationsand monitoring of adults with sickle-cell disease. Methods: a descriptive study with quantitative approach, made with 20adults, registered in a Hematology and Hemotherapy Center, using, for data collection, interviews in the participant’s homeand medical records. In order to have the database, the EpiDatae analysis software through statistical program was used.Results: most of the population consisted of women, married, with complete high school, which used exclusively the UnifiedHealth System. The average age was 30.6 years, and 90.0% (95% CI 68.3-98.8) were black. All of them reported painful crisesand fatigue. They used folic acid daily 35.0% (95% CI 15.4-59.2). Conclusion: the implications of sickle-cell disease could bemitigated through primary, secondary and tertiary health care, according to the needs of those adults.