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Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa

PURPOSE: Epilepsy is common in sub-Saharan Africa (SSA), but the clinical features and consequences are poorly characterized. Most studies are hospital-based, and few studies have compared different ecological sites in SSA. We described active convulsive epilepsy (ACE) identified in cross-sectional...

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Autores principales: Kariuki, Symon M, Matuja, William, Akpalu, Albert, Kakooza-Mwesige, Angelina, Chabi, Martin, Wagner, Ryan G, Connor, Myles, Chengo, Eddie, Ngugi, Anthony K, Odhiambo, Rachael, Bottomley, Christian, White, Steven, Sander, Josemir W, Neville, Brian G R, Newton, Charles R J C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074306/
https://www.ncbi.nlm.nih.gov/pubmed/24116877
http://dx.doi.org/10.1111/epi.12392
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author Kariuki, Symon M
Matuja, William
Akpalu, Albert
Kakooza-Mwesige, Angelina
Chabi, Martin
Wagner, Ryan G
Connor, Myles
Chengo, Eddie
Ngugi, Anthony K
Odhiambo, Rachael
Bottomley, Christian
White, Steven
Sander, Josemir W
Neville, Brian G R
Newton, Charles R J C
author_facet Kariuki, Symon M
Matuja, William
Akpalu, Albert
Kakooza-Mwesige, Angelina
Chabi, Martin
Wagner, Ryan G
Connor, Myles
Chengo, Eddie
Ngugi, Anthony K
Odhiambo, Rachael
Bottomley, Christian
White, Steven
Sander, Josemir W
Neville, Brian G R
Newton, Charles R J C
author_sort Kariuki, Symon M
collection PubMed
description PURPOSE: Epilepsy is common in sub-Saharan Africa (SSA), but the clinical features and consequences are poorly characterized. Most studies are hospital-based, and few studies have compared different ecological sites in SSA. We described active convulsive epilepsy (ACE) identified in cross-sectional community-based surveys in SSA, to understand the proximate causes, features, and consequences. METHODS: We performed a detailed clinical and neurophysiologic description of ACE cases identified from a community survey of 584,586 people using medical history, neurologic examination, and electroencephalography (EEG) data from five sites in Africa: South Africa; Tanzania; Uganda; Kenya; and Ghana. The cases were examined by clinicians to discover risk factors, clinical features, and consequences of epilepsy. We used logistic regression to determine the epilepsy factors associated with medical comorbidities. KEY FINDINGS: Half (51%) of the 2,170 people with ACE were children and 69% of seizures began in childhood. Focal features (EEG, seizure types, and neurologic deficits) were present in 58% of ACE cases, and these varied significantly with site. Status epilepticus occurred in 25% of people with ACE. Only 36% received antiepileptic drugs (phenobarbital was the most common drug [95%]), and the proportion varied significantly with the site. Proximate causes of ACE were adverse perinatal events (11%) for onset of seizures before 18 years; and acute encephalopathy (10%) and head injury prior to seizure onset (3%). Important comorbidities were malnutrition (15%), cognitive impairment (23%), and neurologic deficits (15%). The consequences of ACE were burns (16%), head injuries (postseizure) (1%), lack of education (43%), and being unmarried (67%) or unemployed (57%) in adults, all significantly more common than in those without epilepsy. SIGNIFICANCE: There were significant differences in the comorbidities across sites. Focal features are common in ACE, suggesting identifiable and preventable causes. Malnutrition and cognitive and neurologic deficits are common in people with ACE and should be integrated into the management of epilepsy in this region. Consequences of epilepsy such as burns, lack of education, poor marriage prospects, and unemployment need to be addressed.
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spelling pubmed-40743062014-10-08 Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa Kariuki, Symon M Matuja, William Akpalu, Albert Kakooza-Mwesige, Angelina Chabi, Martin Wagner, Ryan G Connor, Myles Chengo, Eddie Ngugi, Anthony K Odhiambo, Rachael Bottomley, Christian White, Steven Sander, Josemir W Neville, Brian G R Newton, Charles R J C Epilepsia Full-Length Original Research PURPOSE: Epilepsy is common in sub-Saharan Africa (SSA), but the clinical features and consequences are poorly characterized. Most studies are hospital-based, and few studies have compared different ecological sites in SSA. We described active convulsive epilepsy (ACE) identified in cross-sectional community-based surveys in SSA, to understand the proximate causes, features, and consequences. METHODS: We performed a detailed clinical and neurophysiologic description of ACE cases identified from a community survey of 584,586 people using medical history, neurologic examination, and electroencephalography (EEG) data from five sites in Africa: South Africa; Tanzania; Uganda; Kenya; and Ghana. The cases were examined by clinicians to discover risk factors, clinical features, and consequences of epilepsy. We used logistic regression to determine the epilepsy factors associated with medical comorbidities. KEY FINDINGS: Half (51%) of the 2,170 people with ACE were children and 69% of seizures began in childhood. Focal features (EEG, seizure types, and neurologic deficits) were present in 58% of ACE cases, and these varied significantly with site. Status epilepticus occurred in 25% of people with ACE. Only 36% received antiepileptic drugs (phenobarbital was the most common drug [95%]), and the proportion varied significantly with the site. Proximate causes of ACE were adverse perinatal events (11%) for onset of seizures before 18 years; and acute encephalopathy (10%) and head injury prior to seizure onset (3%). Important comorbidities were malnutrition (15%), cognitive impairment (23%), and neurologic deficits (15%). The consequences of ACE were burns (16%), head injuries (postseizure) (1%), lack of education (43%), and being unmarried (67%) or unemployed (57%) in adults, all significantly more common than in those without epilepsy. SIGNIFICANCE: There were significant differences in the comorbidities across sites. Focal features are common in ACE, suggesting identifiable and preventable causes. Malnutrition and cognitive and neurologic deficits are common in people with ACE and should be integrated into the management of epilepsy in this region. Consequences of epilepsy such as burns, lack of education, poor marriage prospects, and unemployment need to be addressed. Blackwell Publishing Ltd 2014-01 2013-10-07 /pmc/articles/PMC4074306/ /pubmed/24116877 http://dx.doi.org/10.1111/epi.12392 Text en Wiley Periodicals, Inc. © 2013 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of the International League Against Epilepsy. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full-Length Original Research
Kariuki, Symon M
Matuja, William
Akpalu, Albert
Kakooza-Mwesige, Angelina
Chabi, Martin
Wagner, Ryan G
Connor, Myles
Chengo, Eddie
Ngugi, Anthony K
Odhiambo, Rachael
Bottomley, Christian
White, Steven
Sander, Josemir W
Neville, Brian G R
Newton, Charles R J C
Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title_full Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title_fullStr Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title_full_unstemmed Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title_short Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa
title_sort clinical features, proximate causes, and consequences of active convulsive epilepsy in africa
topic Full-Length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074306/
https://www.ncbi.nlm.nih.gov/pubmed/24116877
http://dx.doi.org/10.1111/epi.12392
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