SciELO - Scientific Electronic Library Online

 
vol.24 número2Formación de la habilidad entrevistar en la asignatura Introducción a la Medicina General IntegralEstrategia para el perfeccionamiento de la asignatura Elementos de Investigación Cualitativa en Salud índice de autoresíndice de assuntospesquisa de artigos
Home Pagelista alfabética de periódicos  

Serviços Personalizados

Artigo

Indicadores

  • Não possue artigos citadosCitado por SciELO

Links relacionados

  • Não possue artigos similaresSimilares em SciELO

Compartilhar


Revista de Ciencias Médicas de Pinar del Río

versão On-line ISSN 1561-3194

Resumo

SUAREZ CRESPO, Maidelyn; HERNANDEZ TRIGUERO, Yanet; LICOURT OTERO, Deysi  e  CABRERA RODRIGUEZ, Niurka. Program for the prevention of sickle cell anemia: a preventive strategy. Rev Ciencias Médicas [online]. 2020, vol.24, n.2, pp. 205-214.  Epub 01-Mar-2020. ISSN 1561-3194.

Introduction:

hemoglobinopathies, including sickle cell disease, are the most frequent monogenic alterations in the world, with an autosomal recessive inheritance pattern. In Cuba, it is the most frequent molecular disease. The Program for the Prevention of Hemoglobinopathies is based on research through the study of hemoglobin electrophoresis in all pregnant women and has been applied in Cuba since 1983.

Objective:

to design a preventive educational strategy for couples at risk based on the results of the program for the prevention of hemoglobinopathies in Pinar del Río province during the period of 2013-2018.

Methods:

a descriptive, retrospective and longitudinal study was carried out with all pregnant women who had undergone hemoglobin electrophoresis during 2013-2018, along with those whose condition was known from previous pregnancies. The percentage of carriers was calculated, as well as the homozygous for S and C allele, to all these cases the couple was studied. The results were presented in tables.

Results:

the frequency of carriers of hemoglobin S and C was 1,49 % and 0,30 % respectively, 95.1 % of the spouses were studied, there were 34 couples at risk who underwent fetal molecular study, after genetic counseling.

Conclusions:

genetic counseling and fetal molecular study were provided to high-risk couples, corroborating the need to improve the education of the population regarding this disease.

Palavras-chave : ANEMIA, SICKLE CELL; ELECTROPHORESIS; GENETIC COUSELING.

        · resumo em Espanhol     · texto em Espanhol     · Espanhol ( pdf )