Literature DB >> 8310270

[Sickle cell disease as a public health problem in Brazil].

R B de Paiva e Silva1, A S Ramalho, R M Cassorla.   

Abstract

Sickle cell anemia is the most prevalent hereditary disease in Brazil. However, the Brazilian literature registers no investigations into the public health aspects of the disease. This present study investigates the way of life of 80 adult patients (49 women and 31 men) with a diagnosis of sickle cell anemia, at a blood center in Brazil. The late diagnosis of the disease was one of the most significant aspects observed in this group of patients. It was also observed that the dominant problem faced by adult patients with sickle cell anemia is of an economic nature, mainly due to lack of professional opportunities. However, patients can well undertake economic activities under adequate medical supervision, according to their own limitations and potentialities. The psychotherapeutic orientation was well accepted by patients regardless of sex. It is concluded that there exists need for the establishment of community programs for early diagnosis and medical, social and psychological orientation for sickle cell anemia patients in Brazil.

Entities:  

Mesh:

Year:  1993        PMID: 8310270

Source DB:  PubMed          Journal:  Rev Saude Publica        ISSN: 0034-8910            Impact factor:   2.106


  7 in total

1.  Sociodemographic aspects and quality of life of patients with sickle cell anemia.

Authors:  Juliana Pereira Dos Santos; Mansueto Gomes Neto
Journal:  Rev Bras Hematol Hemoter       Date:  2013

2.  Socioeconomic and demographic characteristics of sickle cell disease patients from a low-income region of northeastern Brazil.

Authors:  Thales Allyrio Araújo de Medeiros Fernandes; Tereza Maria Dantas de Medeiros; Jayra Juliana Paiva Alves; Christiane Medeiros Bezerra; José Veríssimo Fernandes; Édvis Santos Soares Serafim; Maria Zélia Fernandes; Maria de Fatima Sonati
Journal:  Rev Bras Hematol Hemoter       Date:  2015-04-14

3.  Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders.

Authors:  Sônia Aparecida Dos Santos Pereira; Stela Brener; Clareci Silva Cardoso; Anna Bárbara de Freitas Carneiro Proietti
Journal:  Rev Bras Hematol Hemoter       Date:  2013

4.  Anti-Toxoplasma gondii antibodies in patients with beta-hemoglobinopathies: the first report in the Americas.

Authors:  Marina Neves Ferreira; Claudia Regina Bonini-Domingos; Isabeth Fonseca Estevão; Clarice Lopes de Castro Lobo; Gisele Cristina Souza Carrocini; Aparecida Perpétuo Silveira-Carvalho; Octávio Ricci; Luiz Carlos de Mattos; Cinara Cássia Brandão de Mattos
Journal:  BMC Res Notes       Date:  2017-06-14

5.  Impact of sickle cell disease on work activity.

Authors:  Rosana Paula Pires; Mário Cézar Oliveira; Lucio Borges Araújo; João Carlos Oliveira; Tânia Machado Alcântara
Journal:  Rev Bras Med Trab       Date:  2022-06-30

6.  Craniofacial bone abnormalities and malocclusion in individuals with sickle cell anemia: a critical review of the literature.

Authors:  Cyrene Piazera Silva Costa; Halinna Larissa Cruz Correia de Carvalho; Erika Bárbara Abreu Fonseca Thomaz; Soraia de Fátima Carvalho Sousa
Journal:  Rev Bras Hematol Hemoter       Date:  2012

7.  The importance of hemoglobin A2 determination.

Authors:  Maria Stella Figueiredo
Journal:  Rev Bras Hematol Hemoter       Date:  2015-07-21
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.