Prevalence of sickle-cell anemia in two communities Omoa Cortés, during the year 2017

Authors

  • Tania Soledad Licona Rivera National Autonomous University of Honduras in the Sula Valley
  • José Raúl Arita Chávez National Autonomous University of Honduras in the Sula Valley
  • Julia María Gámez Alvarado National Autonomous University of Honduras in the Sula Valley
  • Silvia Laudelina Witty Norales National Autonomous University of Honduras in the Sula Valley
  • Carmen María Zúniga Valle National Autonomous University of Honduras in the Sula Valley
  • Carmen María Zúniga Valle National Autonomous University of Honduras in the Sula Valley
  • Kenneth Antonio Maradiaga Orellana National Autonomous University of Honduras in the Sula Valley
  • Roxana Martínez National Autonomous University of Honduras in the Sula Valley

DOI:

https://doi.org/10.5377/rceucs.v4i2.7103

Abstract

Sickle cell anemia (AD) is the most common congenital hemolytic anemia in the world. The frequency of carrier status of hemoglobin S (AS) covers a ranges from 5 to 15% of the world's population. Objective: To identify the prevalence of sickle cell anemia in the communities of Masca and Pueblo Nuevo, Omoa Cortés, during the year 2017. Patients and Methods: study with quantitative approach, non-experimental design, longitudinal and descriptive scope. A random probabilistic sample of 369 was calculated. The first phase of the study included the accomplishment of hemogram and 2% sodium metabisulphite, the second phase consisted in the electro- phoresis of hemoglobin to patients with positive metabisulphite. The tests were processed in a certified clinical laboratory. The data were analyzed with SPSS. Results Of the 369 participants, the ages ranged from 1-83 years, 250 (67.8%) were female, and 119 (32.2%) were male hemoglobin values ranged from 7.85 to 17.4 g / dl and 20 were positive metabisulfite prevalence of 5.4%. In the second phase of the study, 13 (65%) of the patients were female, 12 (60%) were asymptomatic. Hemoglobin electrophoresis was performed, with 18 (94.7%) with HbAS and 1 (5.3%) patients with 100% HbSS. 

Conclusion: is similar to other studies found, but it should be emphasized that the predominant race for heterozygotes was mestizo, not Afrodescendant.

Keywords

Anemia, Sickle Cell, Homozygote, Heterozygote, Prevalence

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Author Biographies

Tania Soledad Licona Rivera, National Autonomous University of Honduras in the Sula Valley

*Profesor Titular, Escuela Universitaria de las Ciencias de la Salud, Universidad Nacional Autónoma de Honduras, Valle de Sula. EUCS, UNAH-VS.

José Raúl Arita Chávez, National Autonomous University of Honduras in the Sula Valley

*Profesor Titular, Escuela Universitaria de las Ciencias de la Salud, Universidad Nacional Autónoma de Honduras, Valle de Sula. EUCS, UNAH-VS.

Julia María Gámez Alvarado, National Autonomous University of Honduras in the Sula Valley

*Profesor Titular, Escuela Universitaria de las Ciencias de la Salud, Universidad Nacional Autónoma de Honduras, Valle de Sula. EUCS, UNAH-VS.

Silvia Laudelina Witty Norales, National Autonomous University of Honduras in the Sula Valley

*Profesor Titular, Escuela Universitaria de las Ciencias de la Salud, Universidad Nacional Autónoma de Honduras, Valle de Sula. EUCS, UNAH-VS.

Carmen María Zúniga Valle, National Autonomous University of Honduras in the Sula Valley

**Profesor Titular, Carrera de Psicología. UNAH-VS.

Carmen María Zúniga Valle, National Autonomous University of Honduras in the Sula Valley

**Profesor Titular, Carrera de Psicología. UNAH-VS.

Kenneth Antonio Maradiaga Orellana, National Autonomous University of Honduras in the Sula Valley

***Estudiante de Medicina. EUCS, UNAH-VS.

Roxana Martínez, National Autonomous University of Honduras in the Sula Valley

****Hematooncóloga Pediatra, Hospital Nacional Mario Catarino Rivas. HMCR.

Published

2019-01-18

How to Cite

Licona Rivera, T. S., Arita Chávez, J. R., Gámez Alvarado, J. M., Witty Norales, S. L., Zúniga Valle, C. M., Zúniga Valle, C. M., Maradiaga Orellana, K. A., & Martínez, R. (2019). Prevalence of sickle-cell anemia in two communities Omoa Cortés, during the year 2017. Revista Científica De La Escuela Universitaria De Las Ciencias De La Salud, 4(2), 5–13. https://doi.org/10.5377/rceucs.v4i2.7103

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Original Articles