Study of Hematological Parameters and Risk Factors for Febrile Seizure Among Sudanese Children
Esam-eddin Bakhei Mohamed Ahmed1, *, Nagah Abd Elwehab Ahmed Mohamed2, Faroug Bakheit Mohamed Ahmed3, Mashair Abdelgadir4, Safa Ahmed Ali5
1Department of ENT, Faculty of Medicine, Shendi University, Shendi, Sudan
2Department of Biochemistry, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey
3Department of Biochemistry, Faculty of Science and Technology, Shendi University, Shendi, Sudan
4Department of Pediatrics, Faculty of Medicine, El-Neelain University, Khartoum, Sudan
5Ministry of Health, Khartoum, Sudan
To cite this article:
Esam-eddin B. M. Ahmed, Nagah Abd Elwehab Ahmed Mohamed, Faroug B. M. Ahmed, Mashair Abdelgadir, Safa Ahmed Ali. Study of Hematological Parameters and Risk Factors for Febrile Seizure Among Sudanese Children. American Journal of Clinical and Experimental Medicine. Vol. 3, No. 6, 2015, pp. 332-334. doi: 10.11648/j.ajcem.20150306.12
Abstract: Current study aims to compare hematological parameters between children with febrile seizures and to find their common etiology among Sudanese children. In a case control study 150 children who were admitted to Gafar Ibn-Ouf pediatrics specialized hospital and Omdurman emergency pediatrics hospital during the period from Jun- Aug 2015 were studied. This study showed low levels of all hematological parameters in febrile seizures patients with exception of red distribution width (RDW), platelets and total iron binding capacity (TIBC) compared to their reference copartners. This evidence can be regarded as a risk factor for seizures in febrile children. The study also detected that children with low hematological levels of these parameters had a family history of febrile seizures and the consanguinity was associated with higher peak body temperature.
Keywords: Febrile Seizures, Children, Risk Factors and Iron Status
Febrile seizures is an event in infancy or childhood usually occurring between three months and five years of age, associated with fever but without evidence of intracranial infection or defined cause for the seizure [1,2,3]. The combination of fever and convulsions in infants is one of the most common emergency in the tropical countries [4,5,6]. It is not known how or why seizures are generated in response to fever; it may be due to fever-induced factors (e.g., interleukin-1beta) which are proconvulsants in individuals who are susceptible based upon the stage of brain development and genetic susceptibility [4,5]. Certain ion channels in the brain are temperature sensitive and may generate fever-associated synchronized neuronal activity [7,8]. There is also evidence to suggest that hyperthermia-induced hyperventilation and alkalosis may play a role [9,10].
The majority of children have their febrile seizures on the first day of illness and, in some cases; are the first manifestations of the child illness. The degree of fever associated with febrile convulsions is variable, and approximately 25 % of events occur when the temperature is between 38ºC and 39ºC.They are often seen as the temperature is increasing rapidly but may develop as the fever is declining .
Febrile seizures can occur during both viral and bacterial infections. The incidence of febrile seizures was similar with influenza, adenovirus, and parainfluenza infections and somewhat less common with respiratory syncytial virus and rotavirus. Hemoglobin, serum iron, ferritin levels were lower in febrile seizures patients than the control group [13,14].
There are many risk factors associated with febrile seizures and their recurrence. Researches of the association between iron deficiency and seizures have shown many controversies. This study aimed to compare between hematological parameters of children with a first seizure attack and control group and to detect the common diseases leading to febrile seizures among Sudanese children.
2. Patients and Methods
In a case control study 150 children who were admitted for febrile illnesses to Gafar Ibn Ouf pediatrics specialized hospital and Omdurman emergency pediatrics hospital during the period from Jun- Aug 2015 were studied. 75children with febrile seizure were considered as cases. The remaining 75 patients of the study sample taken as reference group from children who were admitted for febrile illnesses without convulsions. Age of cases and controls were (24.36+17.01, 25.19+17.97) months. Children with seizures due to central nervous system infection, metabolic cause, afebrile seizures, on recent iron therapy or have other causes of anemia, presence of any chronic systemic diseases and having neurodevelopmental delay, previous febrile seizures and acute central nervous system infection (meningitis, encephalitis) were excluded.
Body weight, height, mean of temperature peak at admission, and the underlying illness were recorded for all cases and controls, Blood samples were collected from all participants for hemoglobin (HB), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), red cell distribution width (RDW), serum ferritin (SF), serum iron (SI), and total iron binding capacity (TIBC). SF, SI, TIBC were done on the referral lab at Khartoum Teaching Hospital. SF level was measured by using the IMx Ferritin assay in micro particle enzyme immunoassay (MEIA) for quantitative determination of human SF. While, SI, and TIBC were measured by using analyzer, spectrophotometer (BT5- 305).
The data was processed statistically by using statistical package for social science (SPSS). Paired T test was conducted; results were expressed in frequency and percentage and Mean ±SD. P. value < 0.05 was considered to indicate significant.
At P≤0.05 body temperature were statically significant P value 0.001 with mean (39.07±0.60, 38.70±0.59) for case and control. While, body weight and height showed no significant between both groups P values 0.233 and 0.702 with Mean (10.42±3.09, 11.03±3.10) and (82.96±1.18, 83.72±1.2) respectively Table 1. Also this study revealed significant differences (P value 0.001, 0.003) in all hematological parameters between case and control group with mean of Hb (9.94±1.85, 11.14±1.81)g/dl Mean Corpuscular Volume (MCV) (70.06±8.10, 75.94±8.88) fl, Mean Corpuscular Hemoglobin (MCH) (22.74±3.67, 25.41±4.06) pg, mean corpuscular hemoglobin concentration (MCHC) (28.54 ±4.78, 31.12±4.95) g/dl, serum Ferritin (SF) (16.57±13.84, 19.76±10.45) µg/ml, serum Iron (SI) (38.97±32.92, 52.39±30.40) mcg/dl. While, Red Distribution width (RDW) (16.22±3.61, 13.94±3.67), Platelet (424.57±136.21, 363.31±91.84), Total Iron Binding Capacity (TIBC) (4.17±8.66, 3.69±9.00) mcg/dl were significantly higher among case group (Table2)
|Case Mean± SD||Control Mean± SD||P. Value|
|Case mean± SD||Control Mean± SD||P value|
|Mean Corpuscular Volume (MCV) fl||70.06±8.10||75.94±8.88||0.001|
|Mean Corpuscular Hemoglobin (MCH) pg||22.74±3.67||25.41±4.06||0.001|
|Mean Corpuscular Hemoglobin Concentration. (MCHC) g/dl||28.54±4.78||31.12±4.95||0.003|
|Red Distribution width(RDW)||16.22±3.61||13.94±3.67||0.001|
|Serum Ferritin (SF) ng/ml||16.57±13.84||19.76±10.45||0.003|
|Serum Iron (SI) mcg/dl||38.97±32.92||52.39±30.40||0.001|
|Total Iron Binding Capacity (TIBC) mcg/dl||4.17±8.66||3.69±9.00||0.001|
Underlying illnesses among cases and controls are detailed in table 3. Consanguinity was found in 44.2% of control group compared to 55.5% of the cases, Table 4.
|Disease||Gastroenteritis||Lower respiratory tract infections||Lymphadenitis||Measles||Otitis media||Tonsillitis||Upper respiratory tract infections||Urinary Tract infection||Nonspecific underlying illness|
|Family history of febrile seizure %||48||52|
The mean peak temperature is significantly high among cases. This can be explained by Eun, et al , prolonged febrile seizures (FS) have both acute and long-lasting because they are often associated with peripheral infection. Peripheral inflammation appears to work synergistically with hyperthermia to potentiate seizures and to exacerbate seizure-induced immune responses. This study showed low levels of all hematological parameters in febrile seizure patients with exception of red distribution width (RDW), platelet and total iron binding capacity (TIBC) compared to their reference copartners and this might be a risk factor for development seizures in children. Our study revealed that although anemia was not common among febrile seizures patients, iron deficiency was more frequent in these patients.
Upper respiratory tract infections (URTI) found to be the most common illness leading to febrile seizures among study sample children. Patients with febrile seizures were significantly more likely to have URTI than febrile controls that did not have a seizure. This is not unexpected because viral illnesses causing URTI symptoms such as influenza A and human herpes virus 6 are more likely to be associated with febrile seizures.
A genetic susceptibility to seizures with fever and family history of epilepsy were higher among cases than controls in this study, but the differences were not statistically significant. Genetic and familial factors appear to be important factors in the expression of febrile convulsions and the subsequent development of epilepsy in some children . Our study found a family history of febrile seizures in 26% of cases compared to 13% of controls and no statistically significant differences in family history of febrile seizures between cases and controls.
The study showed low levels of all hematological parameters in febrile seizure patients with exception of red distribution width, platelet and total iron binding capacity (TIBC) compared to their reference copartners. It also revealed that children with low hematological levels had a family history of febrile seizures and prone to febrile seizures. Moreover consanguinity showed higher peak body temperature and upper respiratory tract infections are predominant causative factors for febrile seizure.