TY - JOUR
T1 - Adverse perinatal events, treatment gap, and positive family history linked to the high burden of active convulsive epilepsy in Uganda
T2 - A population-based study
AU - the SEEDS Writing Group
AU - Kakooza-Mwesige, Angelina
AU - Ndyomugyenyi, Donald
AU - Pariyo, George
AU - Peterson, Stefan Swartling
AU - Waiswa, Paul Michael
AU - Galiwango, Edward
AU - Chengo, Eddie
AU - Odhiambo, Rachael
AU - Ssewanyana, Derrick
AU - Bottomley, Christian
AU - Ngugi, Anthony K.
AU - Newton, Charles R.J.C.
AU - Wagner, Ryan
AU - Twine, Rhian
AU - Connor, Myles
AU - Gómez-Olivé, F. Xavier
AU - Collinson, Mark
AU - Kahn, Kathleen
AU - Tollman, Stephen
AU - Masanja, Honorati
AU - Mathew, Alexander
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 - Kleinschmidt, Immo
AU - Doku, Victor C.K.
AU - Odermatt, e. Peter
AU - Neville, Brian
AU - Sander, Josemir W.
AU - White, Stev
AU - Nutman, Thomas
AU - Wilkins, Patricia
AU - Noh, John
N1 - Publisher Copyright:
© 2017 The Authors. Epilepsia Open published by Wiley Periodicals Inc. on behalf of International League Against Epilepsy.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - 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.
AB - 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.
KW - Adverse perinatal events
KW - Population study of epilepsy
KW - Risk factors
KW - Treatment gap
KW - Uganda
UR - http://www.scopus.com/inward/record.url?scp=85071002900&partnerID=8YFLogxK
U2 - 10.1002/epi4.12048
DO - 10.1002/epi4.12048
M3 - Article
AN - SCOPUS:85071002900
SN - 2470-9239
VL - 2
SP - 188
EP - 198
JO - Epilepsia Open
JF - Epilepsia Open
IS - 2
ER -