| dc.description.abstract | Introduction: Sickle cell disease is the most common hereditary disease known to cause
death in children under five in Africa. Sickle cell trait is the benign form of the sickle cell
disease. Individuals with sickle cell anemia manifest a lot of complications such as pain
crisis; while those with trait remain asymptomatic, until exposed to adverse conditions that
can trigger hemoglobin polymerization. In South Sudan, there is scarcity of data regarding
the occurrence of sickle cell anemia or trait. Therefore this study was conducted with the aim
of determining the prevalence of sickle cell trait among patients attending Juba Teaching
Hospital.
Methodology: This was a cross-sectional study that recruited 384patients attending Juba
Teaching Hospital. Solubility screening technique was used. Venous blood samples were
picked and analyzed at the hospital laboratory. Interviews were conducted by the principle
investigator to assess knowledge, distribution and complications by self-reporting. Approval
was obtained from the Research and Ethics Committee at the Ministry of health, South-
Sudan. Data was analyzed using SPSS software program.
Results: The study reported a prevalence of 9%, seen high in males (11.6%) than females
(2.5%) and more prominent among the Bari and Dinka tribes. Knowledge was rated poor
among respondents.. Clinical history by self-reporting revealed 14.25% had severe pain, 20% had severe anemia, 55.6% had bloody urine, and 40.4% with urinary tract infection and
71.4% had abdominal pain at high altitude.
Conclusion: The study outcome gave a hint on the perception of South Sudanese of sickle
cell. This calls for massive awareness to improve understanding of sickle cell and
management of those with disease or trait. Screening programs can be established to enable
individuals know their sickle cell status. | en_US |
