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Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study

OBJECTIVE: To determine the prevalence of active convulsive epilepsy (ACE) and describe the clinical characteristics and associated factors among a rural Ugandan population. METHODS: The entire population in Iganga/Mayuge Health Demographic Surveillance Site (IM‐HDSS) was screened using two question...

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Autores principales: Kakooza‐Mwesige, Angelina, Ndyomugyenyi, Donald, Pariyo, George, Peterson, Stefan Swartling, Waiswa, Paul Michael, Galiwango, Edward, Chengo, Eddie, Odhiambo, Rachael, Ssewanyana, Derrick, Bottomley, Christian, Ngugi, Anthony K., Newton, Charles R. J. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719853/
https://www.ncbi.nlm.nih.gov/pubmed/29588948
http://dx.doi.org/10.1002/epi4.12048
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author Kakooza‐Mwesige, Angelina
Ndyomugyenyi, Donald
Pariyo, George
Peterson, Stefan Swartling
Waiswa, Paul Michael
Galiwango, Edward
Chengo, Eddie
Odhiambo, Rachael
Ssewanyana, Derrick
Bottomley, Christian
Ngugi, Anthony K.
Newton, Charles R. J. C.
author_facet Kakooza‐Mwesige, Angelina
Ndyomugyenyi, Donald
Pariyo, George
Peterson, Stefan Swartling
Waiswa, Paul Michael
Galiwango, Edward
Chengo, Eddie
Odhiambo, Rachael
Ssewanyana, Derrick
Bottomley, Christian
Ngugi, Anthony K.
Newton, Charles R. J. C.
author_sort Kakooza‐Mwesige, Angelina
collection PubMed
description OBJECTIVE: To determine the prevalence of active convulsive epilepsy (ACE) and describe the clinical characteristics and associated factors among a rural Ugandan population. METHODS: The entire population in Iganga/Mayuge Health Demographic Surveillance Site (IM‐HDSS) was screened using two questions about seizures during a door‐to‐door census exercise. Those who screened positive were assessed by a clinician to confirm diagnosis of epilepsy. A case control study with the patients diagnosed with ACE as the cases and age/sex‐matched controls in a ratio of 1:1 was conducted. RESULTS: A total of 64,172 (92.8%) IM‐HDSS residents, with a median age of 15.0 years (interquartile range [IQR]: 8.0–29.0), were screened for epilepsy. There were 152 confirmed ACE cases, with a prevalence of 10.3/1,000 (95% confidence interval [CI]: 9.5–11.1) adjusted for nonresponse and screening sensitivity. Prevalence declined with age, with the highest prevalence in the 0–5 years age group. In an analysis of n = 241 that included cases not identified in the survey, nearly 70% were unaware of their diagnosis. Seizures were mostly of focal onset in 193 (80%), with poor electroencephalogram (EEG) agreement with seizure semiology. Antiepileptic drug use was rare, noted in 21.2% (95% CI: 16.5–25.8), and 119 (49.3%) reported using traditional medicines. History of an abnormal antenatal period (adjusted odds ratio [aOR] 10.28; 95%CI 1.26–83.45; p = 0.029) and difficulties in feeding, crying, breathing in the perinatal period (aOR 10.07; 95%CI 1.24–81.97; p = 0.031) were associated with ACE in children. In adults a family history of epilepsy (aOR 4.38 95%CI 1.77–10.81; p = 0.001) was the only factor associated with ACE. SIGNIFICANCE: There is a considerable burden of epilepsy, low awareness, and a large treatment gap in this population of rural sub‐Saharan Africa. The identification of adverse perinatal events as a risk factor for developing epilepsy in children suggests that epilepsy burden may be decreased by improving obstetric and postnatal care.
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spelling pubmed-57198532018-03-27 Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study Kakooza‐Mwesige, Angelina Ndyomugyenyi, Donald Pariyo, George Peterson, Stefan Swartling Waiswa, Paul Michael Galiwango, Edward Chengo, Eddie Odhiambo, Rachael Ssewanyana, Derrick Bottomley, Christian Ngugi, Anthony K. Newton, Charles R. J. C. Epilepsia Open Full‐length Original Research OBJECTIVE: To determine the prevalence of active convulsive epilepsy (ACE) and describe the clinical characteristics and associated factors among a rural Ugandan population. METHODS: The entire population in Iganga/Mayuge Health Demographic Surveillance Site (IM‐HDSS) was screened using two questions about seizures during a door‐to‐door census exercise. Those who screened positive were assessed by a clinician to confirm diagnosis of epilepsy. A case control study with the patients diagnosed with ACE as the cases and age/sex‐matched controls in a ratio of 1:1 was conducted. RESULTS: A total of 64,172 (92.8%) IM‐HDSS residents, with a median age of 15.0 years (interquartile range [IQR]: 8.0–29.0), were screened for epilepsy. There were 152 confirmed ACE cases, with a prevalence of 10.3/1,000 (95% confidence interval [CI]: 9.5–11.1) adjusted for nonresponse and screening sensitivity. Prevalence declined with age, with the highest prevalence in the 0–5 years age group. In an analysis of n = 241 that included cases not identified in the survey, nearly 70% were unaware of their diagnosis. Seizures were mostly of focal onset in 193 (80%), with poor electroencephalogram (EEG) agreement with seizure semiology. Antiepileptic drug use was rare, noted in 21.2% (95% CI: 16.5–25.8), and 119 (49.3%) reported using traditional medicines. History of an abnormal antenatal period (adjusted odds ratio [aOR] 10.28; 95%CI 1.26–83.45; p = 0.029) and difficulties in feeding, crying, breathing in the perinatal period (aOR 10.07; 95%CI 1.24–81.97; p = 0.031) were associated with ACE in children. In adults a family history of epilepsy (aOR 4.38 95%CI 1.77–10.81; p = 0.001) was the only factor associated with ACE. SIGNIFICANCE: There is a considerable burden of epilepsy, low awareness, and a large treatment gap in this population of rural sub‐Saharan Africa. The identification of adverse perinatal events as a risk factor for developing epilepsy in children suggests that epilepsy burden may be decreased by improving obstetric and postnatal care. John Wiley and Sons Inc. 2017-03-13 /pmc/articles/PMC5719853/ /pubmed/29588948 http://dx.doi.org/10.1002/epi4.12048 Text en © 2017 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full‐length Original Research
Kakooza‐Mwesige, Angelina
Ndyomugyenyi, Donald
Pariyo, George
Peterson, Stefan Swartling
Waiswa, Paul Michael
Galiwango, Edward
Chengo, Eddie
Odhiambo, Rachael
Ssewanyana, Derrick
Bottomley, Christian
Ngugi, Anthony K.
Newton, Charles R. J. C.
Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title_full Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title_fullStr Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title_full_unstemmed Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title_short Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda: A population‐based study
title_sort adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in uganda: a population‐based study
topic Full‐length Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719853/
https://www.ncbi.nlm.nih.gov/pubmed/29588948
http://dx.doi.org/10.1002/epi4.12048
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