Febrile Convulsion among Hospitalized Children Aged Six Months to Five Years and Its Association With Haemoglobin

M Adeboye1, A Ojuawo1, A Adeniyi1

  • 1Department of Paediatrics, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.

Insights

Febrile convulsions are common in Nigeria, but uncommon in children with sickle cell disease (Hb SS). Sickle cell disease patients had lower packed cell volume and higher mean age than those without the condition.

Area of Science:

  • Pediatrics
  • Hematology
  • Infectious Diseases

Background:

  • Febrile convulsions and sickle cell disease (SCD) are prevalent in tropical regions, causing significant morbidity and mortality.
  • Nigeria has the highest global prevalence of SCD.
  • Limited research exists on hemoglobin electrophoresis in febrile convulsion patients.

Purpose of the Study:

  • To investigate the relationship between hemoglobin genotype and febrile convulsions in Nigerian children.
  • To determine the prevalence of different hemoglobin genotypes in children presenting with febrile convulsions.

Main Methods:

  • A descriptive, cross-sectional study was conducted at the University of Ilorin Teaching Hospital over 12 months.
  • Data collected via questionnaires, examinations, and investigations.
  • Included children aged 6 months to 5 years admitted with febrile convulsions.

Main Results:

  • The hospital-based prevalence of febrile convulsions was 13.8% among children aged 6 months-5 years.
  • Hemoglobin genotype distribution: AA (78.4%), AS (13.8%), AC (3.6%), SS (3.6%), SC (0.6%).
  • Sickle cell disease patients (Hb SS and SC) were older and had lower packed cell volume; 80.4% had malaria.

Conclusions:

  • Febrile convulsions are a common reason for hospitalization.
  • Febrile convulsions are infrequent in patients with sickle cell disease (Hb SS) due to severe anemia.
  • Normal hemoglobin genotypes are associated with near-normal packed cell volume.
Abstract

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