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.
Background:
Febrile convulsion and sickle cell disease are common in tropical countries and both are associated with significant morbidity and mortality. Worldwide, Nigeria has the highest prevalence of sickle cell disease. However, there is a dearth of knowledge on the haemoglobin electrophoresis in patients with febrile convulsions.
Methods:
This was a hospital based, descriptive, cross-sectional study of the relationship between haemoglobin genotype and febrile convulsion at the University of Ilorin Teaching Hospital over a period of 12 months. A self-designed pretested questionnaire was administered on the subjects, and necessary examinations and investigations were conducted.
Results:
Of a total of 1675 children admitted into the emergency paediatric unit during the study period, children aged 6 months-5 years that presented with febrile convulsions were 167(10%). Of this, 1,212 were aged 6 months-5 years. Thus, the age specific, hospital-based prevalence was 13.8%. The M:F was 1.1:1. Their Haemoglobin genotype distribution was AA 131(78.4%), AS 23(13.8%), AC 6(3.6%), SS 6(3.6%), and 1(0.6%) SC. The mean age of the sickle cell disease patients was higher at 46.0±13.5 months compared to 29.2±15.4 months in the non-sickle cell disease patients (p=0.005). The mean packed cell volume in subjects with sickle cell anaemia was 8.8±1.5%; the only case of haemoglobin SC had packed cell volume of 20%, while the non-sickle cell disease patients had a normal PCV. Malaria was present in 80.4% of them.
Conclusion:
Febrile convulsion remains a common cause of hospitalisation. It is uncommon in haemoglobin SS where severe anaemia is always an accompanying derangement. The packed cell volume is nearly normal in children with normal haemoglobin genotype.
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