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Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors
OBJECTIVE: We estimated premature mortality and identified causes of death and associated factors in people with active convulsive epilepsy (ACE) in rural Kenya. METHODS: In this prospective population-based study, people with ACE were identified in a cross-sectional survey and followed up regularly...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963418/ https://www.ncbi.nlm.nih.gov/pubmed/24443454 http://dx.doi.org/10.1212/WNL.0000000000000123 |
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author | Ngugi, Anthony K. Bottomley, Christian Fegan, Gregory Chengo, Eddie Odhiambo, Rachael Bauni, Evasius Neville, Brian Kleinschmidt, Immo Sander, Josemir W. Newton, Charles R. |
author_facet | Ngugi, Anthony K. Bottomley, Christian Fegan, Gregory Chengo, Eddie Odhiambo, Rachael Bauni, Evasius Neville, Brian Kleinschmidt, Immo Sander, Josemir W. Newton, Charles R. |
author_sort | Ngugi, Anthony K. |
collection | PubMed |
description | OBJECTIVE: We estimated premature mortality and identified causes of death and associated factors in people with active convulsive epilepsy (ACE) in rural Kenya. METHODS: In this prospective population-based study, people with ACE were identified in a cross-sectional survey and followed up regularly for 3 years, during which information on deaths and associated factors was collected. We used a validated verbal autopsy tool to establish putative causes of death. Age-specific rate ratios and standardized mortality ratios were estimated. Poisson regression was used to identify mortality risk factors. RESULTS: There were 61 deaths among 754 people with ACE, yielding a rate of 33.3/1,000 persons/year. Overall standardized mortality ratio was 6.5. Mortality was higher across all ACE age groups. Nonadherence to antiepileptic drugs (adjusted rate ratio [aRR] 3.37), cognitive impairment (aRR 4.55), and age (50+ years) (rate ratio 4.56) were risk factors for premature mortality. Most deaths (56%) were directly related to epilepsy, with prolonged seizures/possible status epilepticus (38%) most frequently associated with death; some of these may have been due to sudden unexpected death in epilepsy (SUDEP). Possible SUDEP was the likely cause in another 7%. CONCLUSION: Mortality in people with ACE was more than 6-fold greater than expected. This may be reduced by improving treatment adherence and prompt management of prolonged seizures and supporting those with cognitive impairment. |
format | Online Article Text |
id | pubmed-3963418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-39634182014-04-03 Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors Ngugi, Anthony K. Bottomley, Christian Fegan, Gregory Chengo, Eddie Odhiambo, Rachael Bauni, Evasius Neville, Brian Kleinschmidt, Immo Sander, Josemir W. Newton, Charles R. Neurology Article OBJECTIVE: We estimated premature mortality and identified causes of death and associated factors in people with active convulsive epilepsy (ACE) in rural Kenya. METHODS: In this prospective population-based study, people with ACE were identified in a cross-sectional survey and followed up regularly for 3 years, during which information on deaths and associated factors was collected. We used a validated verbal autopsy tool to establish putative causes of death. Age-specific rate ratios and standardized mortality ratios were estimated. Poisson regression was used to identify mortality risk factors. RESULTS: There were 61 deaths among 754 people with ACE, yielding a rate of 33.3/1,000 persons/year. Overall standardized mortality ratio was 6.5. Mortality was higher across all ACE age groups. Nonadherence to antiepileptic drugs (adjusted rate ratio [aRR] 3.37), cognitive impairment (aRR 4.55), and age (50+ years) (rate ratio 4.56) were risk factors for premature mortality. Most deaths (56%) were directly related to epilepsy, with prolonged seizures/possible status epilepticus (38%) most frequently associated with death; some of these may have been due to sudden unexpected death in epilepsy (SUDEP). Possible SUDEP was the likely cause in another 7%. CONCLUSION: Mortality in people with ACE was more than 6-fold greater than expected. This may be reduced by improving treatment adherence and prompt management of prolonged seizures and supporting those with cognitive impairment. Lippincott Williams & Wilkins 2014-02-18 /pmc/articles/PMC3963418/ /pubmed/24443454 http://dx.doi.org/10.1212/WNL.0000000000000123 Text en © 2014 American Academy of Neurology This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ngugi, Anthony K. Bottomley, Christian Fegan, Gregory Chengo, Eddie Odhiambo, Rachael Bauni, Evasius Neville, Brian Kleinschmidt, Immo Sander, Josemir W. Newton, Charles R. Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title | Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title_full | Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title_fullStr | Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title_full_unstemmed | Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title_short | Premature mortality in active convulsive epilepsy in rural Kenya: Causes and associated factors |
title_sort | premature mortality in active convulsive epilepsy in rural kenya: causes and associated factors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963418/ https://www.ncbi.nlm.nih.gov/pubmed/24443454 http://dx.doi.org/10.1212/WNL.0000000000000123 |
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