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2012, Number s1

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Mediciego 2012; 18 (s1)

Current status of programme for prenatal prevention of Sicklemia in Ciego de Ávila municipality during 2011

Estrada NM, Machado FG, Estenoz HY
Full text How to cite this article

Language: Spanish
References: 11
Page:
PDF size: 43.32 Kb.


Key words:

national health programs, anemia, sickle cell.

ABSTRACT

The hemoglobin is a protein coded genetically that after the 6 months of life when fetal hemoglobin, the type of identified hemoglobin has disappeared through the electrophoretic study it is for a lifetime and it doesn't change, it means, that a pregnant woman once studied in its first pregnancy it should not be studied in successive pregnancies, and it has observed that profecionals of the primary attention indicate this study to the reception of all the pregnant ones, without keeping in mind if they are primiparous or multiparous showing a total lack of sense of the saving and rational use of resources. As answer to the necessity of saving of resources that our political leaders have expressed as urgent measure, necessary for sustaining the social system, a descriptive, longitudinal observational, retrospective study was carried out in the municipal service of community genetics with the objective of knowing which is the current situation of programme for prenatal prevention of Sicklemia in Ciego de Avila, in order to implement a strategy to counteract the indiscriminate indication of this study and this way to achieve saving of resources and an appropriate handling of the program.


REFERENCES

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  3. Castro Ruz F. Discurso. La Habana: 1ro de mayo de 2001.

  4. Castro Ruz R. Clausura del IX Congreso de la Unión de Jóvenes Comunistas. 4 de abril del 2010.

  5. Lineamientos de la política económica y social del partido y la revolución. Aprobado 18 de Abril 2001. Cap. VI. Tema Salud. Lineamiento 154.

  6. Hemoglobinas y hemoglobinopatías. En: Emery´s. Genética Médica. 10ma edición. Madrid. Editorial Marban. 2001. p. 137-148.

  7. Mueller RF, Young IY. Emery´s Genética Médica. 10ma ed. Madrid: Marban Libros, SL; 2001.

  8. Álvarez GE, Fernández GA. La anemia de hematíes falciformes dos puntos; investigaciones para el diagnostico y tratamiento. Rev Elec Univ Oriente. 2007 [citado 4 Ene 2009]; 4. Disponible en: http://www.santiago.cu/cienciaapc/numeros/2007/4/

  9. 19 de Junio: Día de la sicklemia o drepanocitosis, se celebra por primera vez en Cuba. La Habana: MINSAP; 2011.

  10. Martín Ruiz MR, Beltrán Blanes Y, Castro García M, Fuentes Smith LE. Tasas de incidencia de la anemia de células falciformes y de la enfermedad de la hemoglobina SC en Ciudad de la Habana, Cuba, de 1995 a 2004. Rev Cubana Gen Com. 2007; 1(1):45-50.

  11. Martín RM. Anemias de células falciformes. Un programa del nivel primario de atención. Ciudad de la Habana: MINSAP; 2006.




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C?MO CITAR (Vancouver)

Mediciego. 2012;18