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Knowledge, attitudes, and practices with respect to epilepsy among primary and secondary school teachers in the city of Niamey, Niger

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AbstractObjectiveWe aimed firstly to evaluate knowledge, attitudes, and practices about epilepsy among primary and secondary school teachers in the city of Niamey and secondly to formulate targeted sensitization messages for these teachers.Materials and methodsA descriptive cross‐sectional survey was carried out among primary and secondary school teachers in the city of Niamey, capital of Niger, using a self‐administered questionnaire including questions related to knowledge, attitudes, and practices about epilepsy.ResultsOne hundred and forty‐five (145) teachers aged 27–69 (mean age: 39.57 ± 8.304 years) had answered the questionnaire (52 men and 93 women). In 62.1% of cases, respondents had a bachelor degree in education signifying a high level of education. Sixty‐one respondents (42.1%) considered epilepsy as a brain disease, whereas it was considered as a psychiatric illness by 15.9% of respondents and as an impurity by 38.9%. Sixteen respondents (11%) considered it as a hereditary disease. Epilepsy was considered as a contagious disease by 46.2% of teachers, and the main transmission routes reported were contact with places of crisis (26.2%), physical contact with an epileptic person (16.6%), and contact with saliva (6.9%). It was considered as an incurable disease by 6.9% of teachers. Of the 115 respondents (79.3%) who considered epilepsy as a treatable condition, 46 of them believe that epilepsy is treated by traditional medicine. When someone has an epileptic seizure, 28.3% of respondents think that physical contact with him should be avoided and that the places of the crisis should be avoided.ConclusionConsidering that epilepsy is common in school‐age, the study results suggest the need to train teachers with respect to epilepsy to change misconceptions about epilepsy and to promote positive attitudes toward epileptic people to avoid the rejection of these people by the society responsible for problems of social integration.
Title: Knowledge, attitudes, and practices with respect to epilepsy among primary and secondary school teachers in the city of Niamey, Niger
Description:
AbstractObjectiveWe aimed firstly to evaluate knowledge, attitudes, and practices about epilepsy among primary and secondary school teachers in the city of Niamey and secondly to formulate targeted sensitization messages for these teachers.
Materials and methodsA descriptive cross‐sectional survey was carried out among primary and secondary school teachers in the city of Niamey, capital of Niger, using a self‐administered questionnaire including questions related to knowledge, attitudes, and practices about epilepsy.
ResultsOne hundred and forty‐five (145) teachers aged 27–69 (mean age: 39.
57 ± 8.
304 years) had answered the questionnaire (52 men and 93 women).
In 62.
1% of cases, respondents had a bachelor degree in education signifying a high level of education.
Sixty‐one respondents (42.
1%) considered epilepsy as a brain disease, whereas it was considered as a psychiatric illness by 15.
9% of respondents and as an impurity by 38.
9%.
Sixteen respondents (11%) considered it as a hereditary disease.
Epilepsy was considered as a contagious disease by 46.
2% of teachers, and the main transmission routes reported were contact with places of crisis (26.
2%), physical contact with an epileptic person (16.
6%), and contact with saliva (6.
9%).
It was considered as an incurable disease by 6.
9% of teachers.
Of the 115 respondents (79.
3%) who considered epilepsy as a treatable condition, 46 of them believe that epilepsy is treated by traditional medicine.
When someone has an epileptic seizure, 28.
3% of respondents think that physical contact with him should be avoided and that the places of the crisis should be avoided.
ConclusionConsidering that epilepsy is common in school‐age, the study results suggest the need to train teachers with respect to epilepsy to change misconceptions about epilepsy and to promote positive attitudes toward epileptic people to avoid the rejection of these people by the society responsible for problems of social integration.

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