Quality of life in adults with sickle cell disease: an integrative review of the literature
Felix de Freitas, Sandra Luzinete
Ivo, Maria Lucia
Figueiredo, Maria Stella [UNIFESP]
de Souza Gerk, Maria Auxiliadora
Nunes, Cristina Brandt
Monteiro, Fernando de Freitas
Is part ofRevista Brasileira De Enfermagem
MetadataShow full item record
Objective: To identify the available evidence in the literature on health-related quality of life in adults with sickle cell disease. Method: integrative review of MEDLINE, CUMED, LILACS and SciELO databases, from articles developed in this area, published between 2005 and 2015, in English, Portuguese or Spanish. Results: 22 articles were included, six scales were used to evaluate health-related quality of life scores: three generic and three specific. No specific scale for adults with sickle cell disease has been adapted to Brazilian Portuguese so far. Patients affected by frequent painful crises, with low adherence to treatment, had a compromised quality of life. Conclusion: Selected studies have shown that patients with sickle cell disease have worse scores than the general population. These indicators should be instrumental to the nurse in the proposal of interventions and strategies of assistance and socio-educational, with a view to improving the quality of life of this clientele.
CitationRevista Brasileira De Enfermagem. Brasilia Df, v. 71, n. 1, p. 195-205, 2018.
SponsorshipFoundation for Support to the Development of Education, Science and Technology of the State of Mato Grosso do Sul - FUNDECT
Coordination for the Improvement of Higher Education Personnel - CAPES
- EPM - Artigos