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      Epilepsy in Tanzanian children: Association with perinatal events and other risk factors

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          Abstract

          Purpose

          To define the prevalence and risk factors for epilepsy in children in a rural district of Tanzania by conducting a community-based case–control study.

          Methods

          Children aged 6–14 years with active epilepsy (at least two unprovoked seizures in the last 5 years) were identified in a cross-sectional survey in Tanzania. Cases were compared with age-matched controls.

          Key Findings

          Overall 112 children with epilepsy (CWE) were identified; the unadjusted prevalence of epilepsy was 2.91 per 1,000 (95% confidence interval [95% CI] 2.4–3.5). The main seizure types were focal motor with secondary generalization in 73 (65.2%) of 112 and generalized convulsive seizures in 19 (16.9%) of 112. Adverse perinatal events were present in 16 (14%) of 112 cases but in no controls. In multivariate analysis, epilepsy was associated with number of parents who were resident at home (odds ratio [OR] 6.2 for none vs. both resident, 95% CI 1.5–25.5), history of adverse perinatal events (OR 14.9, 95% CI 1.4–151.3), family history of afebrile seizures (OR 5.7, 95% CI 1.0–27.5), and poor scholastic attainment (OR 8.6, 95% CI 4.0–18.4). Electroencephalography (EEG) and computed tomography (CT) scans were abnormal in 44 (44%) of 101 and 26 (29%) of 90 cases, respectively. Overall, 98 (88%) of 112 cases had focal features on assessment.

          Significance

          In this study from sub-Saharan Africa, CWE predominantly had focal features that support the suggestion that most epilepsy in this region has a symptomatic etiology. Adverse perinatal events were strongly associated with epilepsy. Genetic and social factors may also be important. Epilepsy may be preventable in a significant proportion of children with better antenatal and perinatal care.

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          Most cited references71

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          Estimation of the burden of active and life-time epilepsy: A meta-analytic approach

          Purpose To estimate the burden of lifetime epilepsy (LTE) and active epilepsy (AE) and examine the influence of study characteristics on prevalence estimates. Methods We searched online databases and identified articles using prespecified criteria. Random-effects meta-analyses were used to estimate the median prevalence in developed countries and in urban and rural settings in developing countries. The impact of study characteristics on prevalence estimates was determined using meta-regression models. Results The median LTE prevalence for developed countries was 5.8 per 1,000 (5th–95th percentile range 2.7–12.4) compared to 15.4 per 1,000 (4.8–49.6) for rural and 10.3 (2.8–37.7) for urban studies in developing countries. The median prevalence of AE was 4.9 per 1,000 (2.3–10.3) for developed countries and 12.7 per 1,000 (3.5–45.5) and 5.9 (3.4–10.2) in rural and urban studies in developing countries. The estimates of burden for LTE and AE in developed countries were 6.8 million (5th–95th percentile range 3.2–14.7) and 5.7 million (2.7–12.2), respectively. In developing countries these were 45 (14–145) million LTE and 17 (10–133) million AE in rural areas and 17 (5–61) million LTE and 10 (5–17) million AE in urban areas. Studies involving all ages or only adults showed higher estimates than pediatric studies. Higher prevalence estimates were also associated with rural location and small study size. Conclusions This study estimates the global burden of epilepsy and the proportions with AE, which may benefit from treatment. There are systematic differences in reported prevalence estimates, which are only partially explained by study characteristics.
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            Guidelines for epidemiologic studies on epilepsy. Commission on Epidemiology and Prognosis, International League Against Epilepsy.

            (2015)
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              Standards for epidemiologic studies and surveillance of epilepsy.

              Worldwide, about 65 million people are estimated to have epilepsy. Epidemiologic studies are necessary to define the full public health burden of epilepsy; to set public health and health care priorities; to provide information needed for prevention, early detection, and treatment; to identify education and service needs; and to promote effective health care and support programs for people with epilepsy. However, different definitions and epidemiologic methods complicate the tasks of these studies and their interpretations and comparisons. The purpose of this document is to promote consistency in definitions and methods in an effort to enhance future population-based epidemiologic studies, facilitate comparison between populations, and encourage the collection of data useful for the promotion of public health. We discuss: (1) conceptual and operational definitions of epilepsy, (2) data resources and recommended data elements, and (3) methods and analyses appropriate for epidemiologic studies or the surveillance of epilepsy. Variations in these are considered, taking into account differing resource availability and needs among countries and differing purposes among studies. © 2011 International League Against Epilepsy.
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                Author and article information

                Journal
                Epilepsia
                Epilepsia
                epi
                Epilepsia
                Blackwell Publishing Ltd (Oxford, UK )
                0013-9580
                1528-1167
                April 2012
                06 February 2012
                : 53
                : 4
                : 752-760
                Affiliations
                [* ]Kilimanjaro Christian Medical Centre Moshi, Tanzania
                []Neurosciences Unit, Institute of Child Health, University College London London, United Kingdom
                []Northumbria Healthcare NHS Foundation Trust, North Tyneside General Hospital North Shields, United Kingdom
                [§ ]Great Ormond Street Hospital London, United Kingdom
                []Department of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Tropical Medicine London, United Kingdom
                [# ]National Institute for Medical Research Mwanza, Tanzania
                [** ]Department of Paediatrics, Muhimbili University of Health and Allied Sciences Dar-es-Salaam, Tanzania
                [†† ]Department of Psychiatry, University of Oxford Oxford, United Kingdom
                Author notes
                Address correspondence to Kathryn J. Burton, Kilimanjaro Christian Medical Centre, PO Box 2254, Moshi, Tanzania. E-mail: kjburton@ 123456doctors.org.uk

                Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://wileyonlinelibrary.com/onlineopen#OnlineOpen_Terms

                Article
                10.1111/j.1528-1167.2011.03395.x
                3467761
                22308971
                fbf76ed1-e749-4bbf-9d4f-d8dfc4eadaf9
                Wiley Periodicals, Inc. © 2012 International League Against Epilepsy

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 13 December 2011
                Categories
                Full-Length Original Research

                Neurology
                adverse perinatal events,africa,prevalence,epilepsy,etiology,children
                Neurology
                adverse perinatal events, africa, prevalence, epilepsy, etiology, children

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