TY - JOUR
T1 - Electroencephalographic features of convulsive epilepsy in Africa
T2 - A multicentre study of prevalence, pattern and associated factors
AU - on behalf of SEEDS investigators
AU - Kariuki, Symon M.
AU - White, Steven
AU - Chengo, Eddie
AU - Wagner, Ryan G.
AU - Ae-Ngibise, Kenneth A.
AU - Kakooza-Mwesige, Angelina
AU - Ngugi, Anthony K.
AU - Sander, Josemir W.
AU - Neville, Brian G.
AU - Newton, Charles R.
AU - Twine, Rhian
AU - Connor, Myles
AU - Olivé, F. Xavier Gómez
AU - Collinson, Mark
AU - Kahn, Kathleen
AU - Tollman, Stephen
AU - Masanja, Honratio
AU - Masanja, Honratio
AU - Kakooza, Angelina
AU - Pariyo, George
AU - Peterson, Stefan
AU - Ndyomughenyi, Donald
AU - Odhiambo, Rachael
AU - Chabi, Martin
AU - Bauni, Evasius
AU - Kamuyu, Gathoni
AU - Odera, Victor Mung ala
AU - Mageto, James O.
AU - Ae-Ngibise, Ken
AU - Akpalu, Bright
AU - Akpalu, Albert
AU - Agbokey, Francis
AU - Adjei, Patrick
AU - Owusu-Agyei, Seth
AU - Bottomley, Christian
AU - Kleinschmidt, Immo
AU - Doku, Victor C.K.
AU - Odermatt, Peter
AU - Neville, Brian
AU - Nutman, Thomas
AU - Wilkins, Patricia
AU - Noh, John
N1 - Publisher Copyright:
© 2015 International Federation of Clinical Neurophysiology.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Objective: We investigated the prevalence and pattern of electroencephalographic (EEG) features of epilepsy and the associated factors in Africans with active convulsive epilepsy (ACE). Methods: We characterized electroencephalographic features and determined associated factors in a sample of people with ACE in five African sites. Mixed-effects modified Poisson regression model was used to determine factors associated with abnormal EEGs. Results: Recordings were performed on 1426 people of whom 751 (53%) had abnormal EEGs, being an adjusted prevalence of 2.7 (95% confidence interval (95% CI), 2.5-2.9) per 1000. 52% of the abnormal EEG had focal features (75% with temporal lobe involvement). The frequency and pattern of changes differed with site. Abnormal EEGs were associated with adverse perinatal events (risk ratio (RR) = 1.19 (95% CI, 1.07-1.33)), cognitive impairments (RR = 1.50 (95% CI, 1.30-1.73)), use of anti-epileptic drugs (RR = 1.25 (95% CI, 1.05-1.49)), focal seizures (RR = 1.09 (95% CI, 1.00-1.19)) and seizure frequency (RR = 1.18 (95% CI, 1.10-1.26) for daily seizures; RR = 1.22 (95% CI, 1.10-1.35) for weekly seizures and RR = 1.15 (95% CI, 1.03-1.28) for monthly seizures)). Conclusions: EEG abnormalities are common in Africans with epilepsy and are associated with preventable risk factors. Significance: EEG is helpful in identifying focal epilepsy in Africa, where timing of focal aetiologies is problematic and there is a lack of neuroimaging services.
AB - Objective: We investigated the prevalence and pattern of electroencephalographic (EEG) features of epilepsy and the associated factors in Africans with active convulsive epilepsy (ACE). Methods: We characterized electroencephalographic features and determined associated factors in a sample of people with ACE in five African sites. Mixed-effects modified Poisson regression model was used to determine factors associated with abnormal EEGs. Results: Recordings were performed on 1426 people of whom 751 (53%) had abnormal EEGs, being an adjusted prevalence of 2.7 (95% confidence interval (95% CI), 2.5-2.9) per 1000. 52% of the abnormal EEG had focal features (75% with temporal lobe involvement). The frequency and pattern of changes differed with site. Abnormal EEGs were associated with adverse perinatal events (risk ratio (RR) = 1.19 (95% CI, 1.07-1.33)), cognitive impairments (RR = 1.50 (95% CI, 1.30-1.73)), use of anti-epileptic drugs (RR = 1.25 (95% CI, 1.05-1.49)), focal seizures (RR = 1.09 (95% CI, 1.00-1.19)) and seizure frequency (RR = 1.18 (95% CI, 1.10-1.26) for daily seizures; RR = 1.22 (95% CI, 1.10-1.35) for weekly seizures and RR = 1.15 (95% CI, 1.03-1.28) for monthly seizures)). Conclusions: EEG abnormalities are common in Africans with epilepsy and are associated with preventable risk factors. Significance: EEG is helpful in identifying focal epilepsy in Africa, where timing of focal aetiologies is problematic and there is a lack of neuroimaging services.
KW - Active convulsive epilepsy
KW - Africa
KW - Electroencephalographic features
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=84957941221&partnerID=8YFLogxK
U2 - 10.1016/j.clinph.2015.07.033
DO - 10.1016/j.clinph.2015.07.033
M3 - Article
C2 - 26337840
AN - SCOPUS:84957941221
SN - 1388-2457
VL - 127
SP - 1099
EP - 1107
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
IS - 2
ER -