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      Late diagnosis of human immunodeficiency virus infection is linked to higher rates of epilepsy in children in the Eastern Cape of South Africa

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          Abstract

          BACKGROUND: Human immunodeficiency virus (HIV)-positive children may present with a wide range of neurological disorders. Among these, epilepsy is of key concern because of its lifelong impact and potential for damage to the central nervous system (CNS). Few studies in developing regions have investigated the prevalence and aetiology of epilepsy in HIV-infected children as a key population. OBJECTIVES: We describe the prevalence of epilepsy, associated neurological disabilities, immunological status, clinical stage and history of CNS infection at epilepsy diagnosis in a cohort of HIV-infected children receiving antiretroviral therapy (ART) in the Eastern Cape of South Africa. METHODS: We conducted a retrospective study (2004-2014) at two major referral sites for HIV-infected children diagnosed with epilepsy aged 0-16 years. Eligible subjects were extracted from the electronic medicine bridging access to care in excellence (EMBRACE) Paediatric Cohort using the Paediatric ART Data Management Tool (PADMT). Fixed data fields were interrogated for exposures to antiepileptic drugs. Unstructured 'comments' fields were searched for the terms: epilepsy, seizures, fits and szs, as well as abbreviated versions of common antiepileptic drug names. Eligible subject folders were then retrieved to validate the digital data. RESULTS: From 2139 children enrolled in the two sites, 53 children were diagnosed with epilepsy (2.48%). In these, the median CD4 count was 591 cells/mm³, and the mean viral load was 4.9 log copies/mL, with undetectable viral loads in only seven children (14.0%). World Health Organization (WHO) clinical HIV stage was available for 46 patients of the sample, with 3, 6, 26 and 11 children graded at stages 1, 2, 3 and 4, respectively. Forty percent children had a history of CNS infection prior to the epilepsy diagnosis, and 55% children were reported to have school problems. CONCLUSIONS: In this descriptive study, the prevalence of epilepsy among children with HIV was 2.48%, mostly diagnosed in advanced HIV-disease stages. Our findings support the usefulness of early detection and initiation of ART in HIV-infected children in order to reduce the risk of epilepsy. In addition, our study demonstrates that novel techniques are effective in accessing cohort-level data that allow interrogation of both structured and unstructured clinical data.

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          Most cited references47

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          ILAE official report: a practical clinical definition of epilepsy.

          Epilepsy was defined conceptually in 2005 as a disorder of the brain characterized by an enduring predisposition to generate epileptic seizures. This definition is usually practically applied as having two unprovoked seizures >24 h apart. The International League Against Epilepsy (ILAE) accepted recommendations of a task force altering the practical definition for special circumstances that do not meet the two unprovoked seizures criteria. The task force proposed that epilepsy be considered to be a disease of the brain defined by any of the following conditions: (1) At least two unprovoked (or reflex) seizures occurring >24 h apart; (2) one unprovoked (or reflex) seizure and a probability of further seizures similar to the general recurrence risk (at least 60%) after two unprovoked seizures, occurring over the next 10 years; (3) diagnosis of an epilepsy syndrome. Epilepsy is considered to be resolved for individuals who either had an age-dependent epilepsy syndrome but are now past the applicable age or who have remained seizure-free for the last 10 years and off antiseizure medicines for at least the last 5 years. "Resolved" is not necessarily identical to the conventional view of "remission or "cure." Different practical definitions may be formed and used for various specific purposes. This revised definition of epilepsy brings the term in concordance with common use. A PowerPoint slide summarizing this article is available for download in the Supporting Information section here. Wiley Periodicals, Inc. © 2014 International League Against Epilepsy.
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            Developmental potential in the first 5 years for children in developing countries

            Summary Many children younger than 5 years in developing countries are exposed to multiple risks, including poverty, malnutrition, poor health, and unstimulating home environments, which detrimentally affect their cognitive, motor, and social-emotional development. There are few national statistics on the development of young children in developing countries. We therefore identified two factors with available worldwide data—the prevalence of early childhood stunting and the number of people living in absolute poverty—to use as indicators of poor development. We show that both indicators are closely associated with poor cognitive and educational performance in children and use them to estimate that over 200 million children under 5 years are not fulfilling their developmental potential. Most of these children live in south Asia and sub-Saharan Africa. These disadvantaged children are likely to do poorly in school and subsequently have low incomes, high fertility, and provide poor care for their children, thus contributing to the intergenerational transmission of poverty.
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              Epidemiology, causes, and treatment of epilepsy in sub-Saharan Africa.

              Epilepsy is a common neurological disease in tropical countries, particularly in sub-Saharan Africa. Previous work on epilepsy in sub-Saharan Africa has shown that many cases are severe, partly a result of some specific causes, that it carries a stigma, and that it is not adequately treated in many cases. Many studies on the epidemiology, aetiology, and management of epilepsy in sub-Saharan Africa have been reported in the past 10 years. The prevalence estimated from door-to-door studies is almost double that in Asia, Europe, and North America. The most commonly implicated risk factors are birth trauma, CNS infections, and traumatic brain injury. About 60% of patients with epilepsy receive no antiepileptic treatment, largely for economic and social reasons. Further epidemiological studies should be a priority to improve understanding of possible risk factors and thereby the prevention of epilepsy in Africa, and action should be taken to improve access to treatment.
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                Author and article information

                Journal
                sajhivmed
                Southern African Journal of HIV Medicine
                South. Afr. j. HIV med. (Online)
                Southern African HIV Clinicians Society (Johannesburg, Gauteng, South Africa )
                1608-9693
                2078-6751
                2020
                : 21
                : 1
                : 1-6
                Affiliations
                [07] London orgnameUniversity College London orgdiv1Faculty of Population Health Sciences orgdiv2Department of Medical Statistics and Epidemiology United Kingdom
                [04] orgnameQueen Elizabeth Central Hospital orgdiv1Department of Paediatrics
                [03] Liverpool orgnameUniversity of Liverpool orgdiv1Faculty of Clinical Infection, Immunology and Microbiology orgdiv2Institute of Infection and Global Health United Kingdom
                [01] Mthatha orgnameWalter Sisulu University orgdiv1Faculty of Paediatrics orgdiv2Department of Health South Africa
                [02] Blantyre orgnameFaculty of Infectious Disease orgdiv1Department of Paediatrics and Child Health Malawi
                [05] Oxford orgnameUniversity of Oxford orgdiv1Faculty of Sociology orgdiv2Department of Evidence- Based Social Intervention United Kingdom
                [06] Berlin orgnameFaculty of Paediatrics orgdiv1Department of Neuropaediatrics and Social Paediatrics Germany
                [08] Dublin orgnameUCD School of Medicine orgdiv1Faculty of Infectious Diseases and Genitourinary Medicine orgdiv2Department of Infectious Diseases Ireland
                Article
                S2078-67512020000100020 S2078-6751(20)02100100020
                10.4102/sajhivmed.v21i1.1047
                ffc5c79a-4e51-430e-bdee-86726d4ca83a

                This work is licensed under a Creative Commons Attribution 4.0 International License.

                History
                : 23 November 2019
                : 07 January 2020
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 43, Pages: 6
                Product

                SciELO South Africa

                Categories
                Original Research

                epilepsy,WHO staging,HIV-infection,paediatric ART data management tool,children

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