Prevalence and Incidence of Epilepsy in Ulanga, a Rural Tanzanian District: A Community‐Based Study

H. T. Rwiza(University of Dar es Salaam), Gad Kilonzo(University of Dar es Salaam), J O Haule(University of Dar es Salaam), W. B. P. Matuja(University of Dar es Salaam), Ibrahim Mteza(University of Dar es Salaam), P. Mbena(Muslim University of Morogoro), P M Kilima(University of Dar es Salaam), Gabriel Mwaluko(University of Dar es Salaam), R.L. Mwango’mbola(Muslim University of Morogoro), Francis Mwaijande(University of Dar es Salaam), G. Rweyemamu(University of Dar es Salaam), A. Matowo(University of Dar es Salaam), Louise Jilek‐Aall(University of British Columbia)
Epilepsia
November 1, 1992
Cited by 227

Abstract

A random cluster sample survey of approximately 18,000 people in 11 villages was performed in Ulanga, a Tanzanian district with a population of approximately 139,000 people. Well-instructed fourth-year medical students and neurologic and psychiatry nurses identified persons with epilepsy using a screening questionnaire and sent them to a neurologist for detailed evaluation. Identified were 207 subjects (88 male, 119 female) with epilepsy; of these, 185 (89.4%) (80 male, 105 female) had active epilepsy. The prevalence of active epilepsy was 10.2 in 1,000. Prevalence among villages varied, ranging from 5.1 to 37.1 in 1,000 (age-adjusted 5.8-37.0). In a 10-year period (1979-1988) 122 subjects living in the 11 villages developed epilepsy, with an annual incidence of 73.3 in 100,000. Generalized tonic-clonic seizures (GTCS) accounted for 58% and partial seizures accounted for 31.9%, whereas in 10.1% seizures were unclassifiable. Of the partial seizures, secondarily generalized seizures were the most common. Possible etiologic or associated factors were identifiable in only 25.3% of cases. Febrile convulsions were associated in 13.4 of cases. Other associated factors included unspecified encephalitis (4.7%), cerebral malaria (1.9%), birth injury (1.4%), and other (3%). In 38% of the cases, there was a positive family history of epilepsy.


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