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Review

Epidemiology, aetiology, and clinical management of


epilepsy in Asia: a systematic review
Tu Luong Mac, Duc-Si Tran, Fabrice Quet, Peter Odermatt, Pierre-Marie Preux, Chong Tin Tan

Epilepsy is a significant, but often underappreciated, health problem in Asia. Here, we systematically review the Lancet Neurol 2007; 6: 533–43
literature on epidemiology, aetiology, and management of epilepsy in 23 Asian countries. Prevalence estimates are Institute of Neurological
available for only 11 countries from door-to-door surveys and are generally low. Figures for annual incidence in China Epidemiology and Tropical
Neurology, Limoges, France
and India are similar to those in the USA and Europe but lower than those reported from Africa and Latin America.
(T L Mac, F Quet, P-M Preux);
There is a peak in incidence and prevalence in childhood, but a second peak in elderly people, as seen in developed French-Speaking Institute for
countries, has not been documented. The main causes are head injuries, cerebrovascular disease, CNS infections, Tropical Medicine, Vientiane,
and birth trauma. Availability of epilepsy care depends largely on economic factors. Imaging and neurophysiological Laos (D-S Tran); Department of
Public Health and
facilities are available in most countries, but often only in urban centres. Costly drugs, a large treatment gap, limited
Epidemiology, Swiss Tropical
epilepsy surgery, and negative public attitude to epilepsy are other notable features of management in Asia. An Institute, Basel, Switzerland
understanding of the psychosocial, cultural, economic, organisational, and political factors influencing epilepsy (P Odermatt); and Division of
causation, management, and outcome should be of high priority for future investigations. Neurology, University of
Malaya, Kuala Lumpur,
Malaysia (C T Tan)
Introduction Mongolia, Burma, Nepal, Pakistan, the Philippines,
Correspondence to:
Epilepsy is a disorder of the brain that is characterised by South Korea, Singapore, Sri Lanka, Thailand, East Timor, Pierre-Marie Preux, Institut
an enduring predisposition to generate seizures and by and Vietnam. All issues of Neurology Asia and of the d’Epidémiologie Neurologique et
its neurobiological, cognitive, psychological, and social national medical journals of Korea (Journal of Korean de Neurologie Tropicale,
(EA3174), Faculté de Médecine,
consequences.1 WHO estimates that eight people per Medical Science), Singapore (Singapore Medical Journal)
2 rue du Docteur Marcland,
1000 worldwide have this disease.2 The prevalence of and India (Neurology India) were hand-searched with the 87025 Limoges Cedex, France
epilepsy in developing countries is usually higher than in same criteria. Articles were included if they had at least pierre-marie.preux@unilim.fr
developed countries.3–5 an abstract in English or French. We included only
Although substantial economic development and studies reaching the recommendations of the
improvement of health services have occurred, Asia is a International League Against Epilepsy (ILAE) 1993
heterogeneous and resource-constrained continent. Over Commission.8 Background references were identified
half of the 50 million people with epilepsy worldwide are through these searches and through searches of the
estimated to live in Asia. Although much research is authors’ own files.
done in Asia, information about the recognition of the
burden created by the disease is scarce. In 1997, Jallon6 Data collection and analysis
reviewed studies from Asia, mostly done in the 1980s, A total of 1348 articles from 20 countries were found
and showed a prevalence varying from 1·5 per 1000 in using PubMed. No publications were found from Bhutan,
Japan to 10·0 per 1000 in Pakistan. Here, we provide an Brunei, or North Korea. Most articles originated from
update on prevalence, incidence, demographic data, Japan (460 articles), India (343 articles), and China
types of epilepsy, aetiology, treatment, and prognosis in (165 articles). Articles were assessed by the first two
recent years to give a comprehensive view of epilepsy in authors searching in each survey for methods and results
this region. on prevalence, incidence, demography, classification,
causes, treatment, and knowledge, attitudes, and practice.
Methods Data from 119 articles were collected for this Review (see
Search strategy and selection criteria figure for more detail on the selection process).
We searched the PubMed database by using the keyword
“epilepsy”, combined with each of the following: Results
“epidemiology”, “prevalence”, “incidence”, “aetiology”, Prevalence
and “treatment” for each Asian country. Other words The lifetime prevalence of epilepsy varied among
were also used in association with the keywords. These countries from 1·5 to 14·0 per 1000 (table 1).9–30 This wide
were “malaria”, “neurocysticercosis”, “cysticercosis”, variation could partly result from the use of different
“encephalitis”, “classification”, “mortality”, “therapy”, methods and different types of questionnaire. Screening
“antiepileptic”, “AEDs”, “surgery”, “chirurgical”, questionnaires were mainly derived from WHO
“recurrence”, “prognosis”, “stigma”, “stigmatization”, questionnaires, but two studies used Limoges’
“knowledge”, and “awareness”. Asian countries (n=23) questionnaire.19,28 The median lifetime prevalence is
were defined as the countries of the WHO Western estimated at 6 per 1000, which is lower than in developing
Pacific region and WHO Southeast Asian region:7 countries in other areas of the world (15 per 1000 in sub-
Bangladesh, Bhutan, Brunei, Cambodia, China, North Saharan Africa and 18 per 1000 in Latin America).4,5 An
Korea, India, Indonesia, Japan, Laos, Malaysia, Maldives, understanding of these differences could generate

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Review

hypotheses for studies aimed at identifying ways to


Initial PubMed search prevent this disease: for example, is there a protective
factor in Asia or specific risk factors in Africa or Latin
America?
1348 articles

Incidence
1039 articles excluded:
228 not written in French or English
Incidence rates were available from only two countries,
143 no abstract China and India; of the five estimates, three were based
308 non-epilepsy studies* on retrospective analyses of collections of prevalence data
360 non-epidemiological studies†
(table 2).9,12,17,18,31 The epilepsy incidence rates reported from
China were low—from 28·8 per 100 000 person-years9 to
309 articles that may contain
relevant data 35·0 per 100 000 person-years in the general population.12
The results from India were higher, and reached 60·0 per
Full-text collection via: 100 000 person-years.31 Overall, the results were not
Hinari, Science Direct, Epilepsia, different from those in developed countries where the
The New England Journal of Medicine,
Medscape Infectious Diseases
age-adjusted incidence of epilepsy is 24–53 per 100 000
person-years.32 Some authors report an incidence rate in
190 articles excluded because the full text
developing countries that is as high as 190 per 100 000
was not available or because they did person-years.33,34 Confirmation of low incidence rates in
not contain information relevant to this Asia would be very important, and rigorous population-
systematic review
based prospective studies are needed.
Data collection from 119 references
Demographic indicators
Age
Figure: Study selection for the systematic review The publications included in this Review show one peak
*Articles that were not specifically on epilepsy in Asia, except analytical studies on age for incidence in children19,26 and one peak age for
epilepsy risk factors. †Articles that were not within the framework of this review.
prevalence in young adults.12–13,16,19,35–38 However, one study,
done in Shanghai, showed two prevalence age peaks: one
between 10 and 30 years old and one in people over
Reference Year N Prevalence/1000 Method
60 years old.11 These figures are summarised in
China (five provinces) 9,10 2002 and 55 000 7·0 Door-to-door survey
table 3.11,13,16,19,26,35–38
2003 4·6*
In developed countries, the incidence and prevalence
China (Shanghai) 11 2002 48 628 3·6* Door-to-door survey
of epilepsy both follow a bimodal distribution with a first
China (six cities) 12 1985 63 195 4·4 Door-to-door survey
peak in childhood and another in old age.32,39,40 The most
India (West Godavari) 15 2004 74 086 6·2 Door-to-door survey
probable reason for the missing peak in the older age
India (Kerala state) 16 2000 238 102 4·7† Door-to-door survey
groups in many Asian countries is the relatively young
India 18 1998 64 963 3·9† Door-to-door survey
population compared with that in more developed
India 29 2006 50 617 3·8† Door-to-door survey
regions.
Laos 19 2006 4310 7·7† Door-to-door survey
Turkey 26 1997 11 497 7·0† Door-to-door survey
Sex
Pakistan 21 1994 24 130 10·0† Door-to-door survey
Epilepsy is slightly more common in men than in women
Vietnam 28 2005 6617 10·7† Door-to-door survey but the sex-specific prevalence is not, in general,
Nepal 20 2003 4636 7·3 Community based significantly different (table 4).11,13,18–20,23,26,35,38
Taiwan 24 1997 10 058 2·4 Community based
Taiwan 30 2001 13 663 2·8† Community based Location
Thailand 25 2002 2069 7·2 Community based Two studies (in Pakistan and in India) indicated that the
Singapore 22 1997 20 542 5·0 Men at 18 years old prevalence was higher in rural areas than in urban areas.26,29
Singapore 23 1997 96 047 3·5 Review <9 years Although not significant, a meta-analysis of published and
Hong Kong 13 2003 NA 1·5 Estimation in adult non-published community-based studies in India showed
patients (≥15 years)
a higher prevalence of 5·5 per 1000 (95% CI 4·0–6·9) in
Vietnam 27 2003 NA 14·0 Estimation rural areas than that of 5·1 per 1000 (3·5–6·7) in urban
India 14 2003 NA 5·6 Review areas.35 Indeed, a higher prevalence in rural areas is a
India 17 2002 NA 5·0 Review common tendency in developing countries.6
N=sample size. NA=not available. *Active epilepsy (seizures within the previous year). †Active epilepsy (seizures within
the previous 5 years). Otherwise, details of disease duration were not available. Mortality
Data on mortality rate in Asian people with epilepsy are
Table 1: Prevalence of epilepsy in Asia
scarce, and those that are available indicate high rates in

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adequately treated and Laos is one of the least developed


Reference Year N Incidence/ Method
100 000 countries in this region. A recent study found a standardised
person-years mortality ratio of 3·9 among 2455 people with epilepsy
China (five 9 2002 55 616 28·8 Door-to-door who participated in an assessment of epilepsy management
provinces) survey at the primary health-care level in rural China.41 Mortality
China 12 1985 63 195 35·0 Door-to-door is also usually high in developing countries in other
survey regions of the world: 28·9 per 1000 person-years in a rural
India 18 1998 64 963 49·3 Door-to-door area of Cameroon42 and 31·6 per 1000 person-years in rural
survey
central Ethiopia.43 Other studies should be done to confirm
India 31 1999 NA 60·0 Estimation
this higher mortality rate in Asia, which might partly
India 17 2002 NA 38·0–49·3 Review
explain the low prevalence rate.
N=sample size. NA=not available. By contrast, mortality in the most developed countries
in Asia is low. A study of childhood epilepsy in a Japanese
Table 2: Incidence of epilepsy in Asia
general population showed a mortality of 45·0 per 1000
people accumulated over a long follow-up period (mean:
developing countries in this region. In one study in Laos, 18·9 years).44 Another study in adult Taiwanese patients
there was a very high case-fatality rate of 90·9 per 1000 showed a mortality of 9 per 1000 person-years.45 Patients
person-years.19 This study was in a mountainous region, in with epilepsy in Taiwan had a nearly 3·5 times higher
which very few people had access to antiepileptic drugs. risk of death than the general population (standardised
These data came from a management project after door-to- mortality ratio 3·47, 95% CI 2·46–4·91).46
door screening. The number of patients followed-up was Other researchers examined the outcome in convulsive
small, but the results might not be too far from the real disorders in a more indirect way: an analysis of 37 125 death
mortality rate, because almost all patients in Laos were not certificates in Sri Lanka since 1967 found death by

Reference Year Age peak (years) Mean age of % children N Method


onset (years) (<18 years)
China (Shanghai) 11 2002 10–30, >60 NA NA 151 Door-to-door survey
India 16 2000 10–19 NA NA 1175 Door-to-door survey
Laos 19 2006 11–20 NA NA 33 Door-to-door survey
Pakistan 26 1997 NA 13·3 74·3 241 Door-to-door survey
Turkey 26 1997 NA 12·9 72·0 81 Door-to-door survey
Hong Kong 13 2003 25–30 19·9 NA 736 Adult patients in hospital
India 37 1999 NA 14·3 NA 972 Hospital-registered patients
India 35 1999 10–19 NA NA 525 Review
Bangladesh 36 2004 16–31 NA NA NA Review
Hong Kong 38 1997 NA 18·8 NA 2952 Review of outpatient records

N=number of patients with epilepsy. NA=not available.

Table 3: Age distribution of patients with epilepsy in Asia

Reference Year Male (%) Female (%) Male prevalence Female prevalence N Method
(‰) (‰)
China (Shanghai) 11 2002 NA NA 3·6 2·5 151 Door-to-door survey
Turkey 26 1997 54·3 45·7 8·7 6·3 81 Door-to-door survey
India 18 1998 NA NA 4·4 3·4 254 Door-to-door survey
Laos 19 2006 60·6 39·4 NA NA 33 Door-to-door survey
Pakistan 26 1997 49·8 50·2 9·2 10·9 241 Door-to-door survey
Nepal 20 2003 NA NA 6·8 7·9 34 Community based
Hong Kong 13 2003 57·1 42·9 NA NA 736 Adult patients in hospital
Hong Kong 38 2001 54·3 45·7 NA NA 2952 Review of outpatient records
Singapore 23 1997 50·1 49·9 3·5 3·5 336 Review <9 years
India 35 1999 NA NA 5·9 5·5 3207 Meta-analysis

N=number of patients with epilepsy. NA=not available.

Table 4: Gender proportions and gender-adjusted prevalence in patients with epilepsy in Asia

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Review

convulsions in 23·7 per 1000.47 The most common cause, epilepsy (relative risk 2·86, 95% CI 2·35–3·48) and a
febrile convulsions, was documented in 396 (44·9%) higher number of seizures before seizure control (1·50,
deaths. Neonatal and infantile convulsions accounted for 1·30–1·73) increased the risk of recurrence. Seizure-free
186 (21·1%) deaths. Other causes of death associated with duration before beginning drug withdrawal (2 years vs
seizures included chest complications (60; 6·8%), drowning 4 years) did not significantly influence this risk.54
(28; 3·2%), asphyxia (20; 2·3%), status epilepticus (19; Surgery for intractable temporal-lobe epilepsy led to
2·2%), burns (7; 0·8%), and poisoning (2; 0·2%).47 In this good results in a study in Indonesia.55 Of 56 patients
study, deaths due to convulsive disorders showed a decrease who had anterior temporal lobectomy with amygdalo-
from 37·3 per 1000 people in 1967 to 9·5 per 1000 people in hippocampectomy, 46 patients (82·0%) were seizure-free
1987.47 Mortality from status epilepticus in patients in a large (Engel I). Six patients (11%) had fewer than two seizures
community hospital in Hong Kong from 1996 to 2001 was per year (Engel II), and seizures decreased by more than
16·0%. Predictors of mortality were older age (OR 1·04, 75% (Engel III) in four patients (7%). Complications
95% CI 1·01–1·07), a delay in starting treatment (3·52, included extradural empyema in five patients (9%),
1·01–12·18), status epilepticus due to cerebrovascular depression in two patients (4%), and transient
disease (9·73, 1·58–59·96), and CNS infection (30·27, hemiparesis in one patient (2%). 31 patients were able to
3·14–292·19).48 Complications related to steroid treatment stop taking antiepileptic drugs. The follow-up varied
in West syndrome were also an important cause of death as between 12 and 76 months. This is the only description
seen in Hong Kong.49 Specific mortality rates for the main found in Asia on epilepsy surgery, an efficient solution
causes of death must be estimated in Asia to enable better for intractable epilepsy. Few patients in Asia can benefit
prevention. from this therapy even if it is available in several countries
(see Surgery section).
Prognosis
In general, a third to two-thirds of patients will have Clinical classification
recurrent seizures within 5 years of the first unprovoked Numerous clinical studies have been published but few
seizure.50,51 Similar recurrence rates are seen in Asia. A have described the distribution of seizure types in
study in Thai children showed a cumulative risk of community-based studies. In addition, comparison of
recurrence of 25% at 14 days, 50% at 4 months, 51% at the results from different studies is difficult because
6 months, and 66% at 12 months.52 In children treated for classifications used are not homogeneous. Here, we
epilepsy, follow-up after withdrawal of antiepileptic drugs present only the results based on the 1981 ILAE
(average duration 43·5 months) showed a cumulative classification (table 5).13,16,19,22,38,49,56–59
risk of recurrence of 10% at 12 months and 12% at The range of patients with generalised seizures was
36 months.53 The need for two AEDs to control seizures 50–69%, and 31–50% had partial seizures.16,19,22,56 The
was a risk factor for recurrence (incidence 0·025 vs 0·002, prevalence rates of symptomatic, idiopathic, and
p=0·001).53 Another study in India noted seizure cryptogenic epilepsy were 22–53%, 4–42%, and 13–60%,
recurrence in 31% of patients (of all ages) during a follow- respectively.13,19,38,49,56,59 The predominance of generalised
up period of 18 months. Longer duration of active epilepsy and wider range of cryptogenic epilepsy may be

Reference Year Seizure type classification Aetiological classification N Method


GS FS US IE CE SE
India 16 2000 58·8 30·6 NA NA NA NA 1175 Door-to-door survey
Laos 19 2006 63·6 27·3 9·1 27·3 48·5 24·2 33 Door-to-door survey
Hong Kong 13 2003 NA NA NA 38·7 13·6 38·7 736 Adult patients in hospital
Hong Kong 49 2001 NA NA NA 18·0 22·0 53·3 105 Children with West syndrome
Hong Kong 38 2001 NA NA NA 3·9 59·9 35·1 2952 Review of outpatient records
Hong Kong 56 2001 49·5 48·2 2·3 42·4 16·8 40·8 309 Child patients
India 57 2005 42·0 58·0 NA NA NA NA 112 PWE with follow-up >12 months at tertiary care
epilepsy centre and aged >16 years
Malaysia 58 1993 86·0 14·0 NA NA NA NA 593 Adult patients with EEG
Malaysia 58 1993 92·0 8·0 NA NA NA NA 593 Child patients with EEG
Malaysia 59 1999 NA NA NA 78·0* 22·0 165 Newly diagnosed epilepsy
Singapore 22 1997 69·0 31·0 NA NA NA NA 106 All epilepsy
Singapore 22 1997 29·0 64·0 7·0 NA NA NA 14 Refractory seizures

GS=generalised seizures. FS=focal seizures. US=unclassified seizures or multiple seizure types. IE=idiopathic epilepsy. CE=cryptogenic epilepsy. SE=symptomatic epilepsy.
N=number of patients with epilepsy. NA=not available. PWE= people with epilepsy. EEG=electroencephalogram. *This figure applies to IE and CE combined.

Table 5: Clinical classification of patients in studies on epilepsy in Asia

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due to differences in the extent of imaging studies and occur in 50–80% of patients with parenchymal
the lack of standardised classification and terminology in cysticercosis.65 In Asia, many studies report the presence
epilepsy research in Asia. Electroencephalographic data of cysticercosis (taeniasis).65–76 However, there are few
were often not available, which could also have influenced studies on the relation between neurocysticercosis and
the proportions of idiopathic epilepsy reported in several epilepsy in Asia, and their results vary widely.
studies. Population-based studies with electroencephalo- Neurocysticercosis is probably an important cause of
graphic recording are required to enable accurate clinical seizures and epilepsy in regions with a high prevalence
classification of epilepsy in Asia. of Taenia solium infection in human beings. In Asia, this
includes India, Nepal, Bali, Papua and Sulawesi in
Causes Indonesia, and parts of Vietnam and China. Cysticercosis
There are very few studies on the causes of epilepsy in is only rarely detected in the most economically advanced
Asian populations, and there are particularly few case– countries of Asia, such as South Korea,74 but the
control studies or cohort studies. From the available prevalence might also be low in poor regions.15,19,71 In a
literature, causes seem to be dominated by head injury, meta-analysis, seizures were the most common symptom
birth trauma, and intracranial infections, such as (56·2%) of cysticercosis in China.69 Another study noted
neurocysticercosis or meningoencephalitis. Where socio- that between 8·7% and 50·0% of cysticercosis-infected
economic development is better, head trauma and stroke patients had recent seizures.66 Single CT enhancing
are the leading causes of epilepsy. In China in the 1980s, lesions and neurocysticercosis together accounted for
brain injury, intracranial infection, and cerebrovascular 67% of the provoking factors of acute symptomatic
disease, in that order, were the leading putative causes of seizures.77 Conversely, in some studies, the cysticercosis
epilepsy.12 Cases reported from China during 1994–2003 seropositivity was not higher in patients with epilepsy in
allowed the estimation of an average incidence of 8·7% for regions with either a low prevalence (eg, Laos19) or a high
epilepsy with cerebrovascular disease and of 8% with post- prevalence (eg, Indonesia73).
traumatic epilepsy.60 In patients in Hong Kong, the Paragonimiasis is endemic in several Asian countries:
commonest causes were cerebrovascular disease (26·2%), China, South Korea, the Philippines, Japan, and
a history of CNS infection (26·0%), head trauma (11·4%), Vietnam.78,79 During migration, the causal lung fluke may
perinatal insult (9·7%), congenital brain malformation reach the brain and may cause seizures, epilepsy, and
(7·4%), hippocampal sclerosis (5·9%), and intracranial other neurological syndromes.80–82 However, no study has
neoplasm (5·6%).61 By contrast, in 300 incident cases of quantified the importance of Paragonimus infection in
epilepsy in Nepal 47% were caused by neurocysticercosis, epilepsy.
9% by tumour, 4% by vascular disease, and 2% by head Malaria is still widely endemic in Asia, with more than
injury.20 In this section, we elaborate on these causes of 3 million cases per year. India, Burma, Indonesia,
epilepsy in Asia. Pakistan, Cambodia, Papua New Guinea, and Bangladesh
each have more than 50 000 cases per year.83 Malaria
Head injury causes various symptoms, such as fever and convulsions.
In Asia, post-traumatic epilepsy is one of the most 7·7% of patients with childhood malaria (with or without
common complications of head injury. One study claimed the presence of cerebral malaria) in a retrospective survey
that post-traumatic epilepsy accounted for 5% of total in Thailand had convulsions.84 In cerebral malaria,
epilepsy and 20% of symptomatic epilepsy.60 A history of convulsions present in 60% of cases.85 However, we did
major brain trauma (20·9%) was also the leading cause not find any analytical study reporting the relation
of epilepsy in surgically treated patients in China.62 between malaria and epilepsy in Asia. Nevertheless, the
link between epilepsy and malaria was recently supported
CNS infections by a case–control study in Gabon and a cohort study in
In developing countries in other regions of the world, Mali in Africa.86,87
such as sub-Saharan Africa or Latin America, CNS Japanese encephalitis is one of the most common
infections seem to explain the high prevalence of epilepsy. encephalitic disorders worldwide. Most of China,
The Commission on Tropical Disease of the International southeast Asia, and the Indian subcontinent are affected.88
League Against Epilepsy listed several diseases as causes 65% of patients with Japanese encephalitis have acute
of epilepsy, including malaria, tuberculosis, schisto- symptomatic seizures and 13% have chronic epilepsy.89
somiasis, AIDS, and cysticercosis—among these, the In a study in India, 30 of 65 patients with Japanese
latter seems to be the most common cause of epilepsy.3 encephalitis had seizures in the first weeks of illness;
In Asia, there is a lack of rigorous analytical studies to 19 of them had two or more seizures.90
assess the effect of these infections in epilepsy.
An association between neurocysticercosis and epilepsy Genetic factors
was found in numerous studies in Africa5 and Latin Two studies in India found no relation between being a
America.63,64 Neurocysticercosis was the cause of epilepsy twin and epilepsy, and twins of people with epilepsy did not
in about 50% of patients in some studies,42,65 and seizures have a high risk of epilepsy.91,92 Case–control studies in

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China have found no relation between epilepsy and and educators rarely participate in the management of
susceptibility genes, such as GABABR1,93,94 KHDRBS3 epilepsy in Asia—another difference from epilepsy care
(T-STAR),95 and CACNA1G (calcium channel, voltage in Europe.103
dependent, T-type, alpha 1G subunit).96 However, numerous Technologies such as electroencephalography, CT, and
studies have confirmed familial history of epilepsy and MRI used in epilepsy diagnosis are widely available in
parental consanguinity as risk factors. In Kerala, south Asian countries, but their accessibility varies in the
India, a family history of epilepsy was three times more different geographical regions. In developed economies,
common in patients with epilepsy than in controls (OR such as Japan, South Korea, Singapore, and Taiwan,
3·2, 95% CI 2·1–4·7)97 and two times higher in another sophisticated facilities are highly accessible to most of the
study in north India (2·1, 1·1–4·3).31 Family history was also population, whereas almost no electroencephalography
a risk factor for epilepsy in studies in Laos19 and China.98 or imaging facilities are available in other countries, such
This level of risk is similar to that in studies from Africa.5 as Cambodia, East Timor, Laos, or Mongolia. In addition,
In Asia, consanguineous marriage is common in many of these facilities are privately operated and available
certain cultures, in particular among Indian and Muslim only in big cities, with MRI being mainly used for
populations. Consanguinity of parents was significantly assessments for epilepsy surgery.100 However, the
more common among patients than among controls development of these facilities is changing rapidly.
(13·1% vs 6·6%).97 The odds ratio for parental Currently, there are 15 ILAE chapters in Asia. They are
consanguinity was higher in patients with generalised located in Bangladesh, China and Hong Kong, India,
epilepsy than for controls (2·6; 95% CI 1·5–4·4).97 Indonesia, Japan, South Korea, Malaysia, Mongolia,
Another study of 316 patients with epilepsy of Indian Nepal, Pakistan, the Philippines, Taiwan, Thailand, and
origin in Malaysia showed that 29·5% of them had a Singapore. These chapters are absent in the less
parental consanguineous marriage, and that there was a developed nations.
significant association with parental consanguinity in
idiopathic and cryptogenic epilepsies.99 Consanguinity Antiepileptic drugs
could be a target for a campaign to prevent epilepsy. Antiepileptic drugs are the simplest and the safest means
of controlling epilepsy. Various first-generation anti-
Epilepsy care epileptic drugs—phenytoin, carbamazepine, valproic
Typically, there is great variability in the case management acid, phenobarbital, clonazepam, primidone, and
of epilepsy among different countries. In southeast Asia, ethosuximide—are used widely in Asian countries104
this variability depends on factors such as the economic (table 6),20,39,61,105–112 and monotherapy is common. The
status, the quality of the health system and peripheral particular drug used depends on the medical culture and
services, rural or urban residence, and the cultural practices in each country.
frameworks of societies.33,100 Second-generation antiepileptic drugs, such as
lamotrigine, gabapentin, tiagabine, felbamate, vigabatrin,
Health-care facilities or topiramate, are used widely in Malaysia, China, and
According to WHO, the median number of hospital beds Singapore and in some of the economically less developed
for epilepsy care per 100 000 population is very low in countries, including the Philippines and Vietnam.7,113
Asia: 0·05 in southeast Asia and 0·46 in the Western Clobazam, oxcarbazepine, and levetiracetam are available
Pacific—fewer than in Africa (0·55) and far fewer than in in large Asian countries, such as India, but are
Europe (1·65).101 Similarly, the number of neurologists is prohibitively expensive. Access to drugs is probably easier
extremely low in most Asian countries. In 2004, in India, in Asia than in Africa but this varies widely according to
Laos, and Bangladesh, WHO estimated that there was the context (degree of development, urbanisation, etc).
fewer than one neurologist per million inhabitants. In Although first-generation antiepileptic drugs are
Japan, there are between one and 50 neurologists per predominant, there are availability and accessibility
million people,101,102 and a proportion of these neurologists problems in several places. In 2003, a study in Long Xuyen,
work in the private sector.100 In 2001, a comparative study Vietnam, showed that drugs were available but only for a
of epilepsy reference centres in Europe and Asia showed short period of time. Moreover, these antiepileptic drugs
that medical specialists in Asia examined more patients were sold in pharmacies that were located in only a small
per day in walk-in clinics than did their European area in the city centres.114 In most parts of Asia, there are
counterparts.103 The development of epilepsy care is limited amounts of or no subsidised antiepileptic drugs.
commonly driven by epileptologists—neurologists with a The patients and families have to pay beyond their means
special interest in epilepsy. If an epileptologist is defined for even the most common first-generation drugs. For
practically as someone who has had a period of fellowship example, the yearly cost of 100 mg daily phenobarbital, one
after training in general neurology, only Japan, South of the cheapest drugs, is about US$30 in Laos, which is
Korea, Singapore, and Taiwan have at least one about the monthly salary of a school teacher; in north
epileptologist per million people. Paramedical India, this cost is US$11. In consequence, almost all
professionals, such as nurses, occupational therapists, patients would not be able to have long-term treatment if it

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Reference First or second- Monotherapy or AEDs used Comments


generation AEDs polytherapy
Hong Kong 61 First and second Monotherapy: 57·4% Phenytoin used in 38·7%
India 39 First Polytherapy: 57·8% (entry) Carbamazepine used at entry
and monotherapy: 76·4% and at follow-up
(follow-up)
India (secondary level hospital) 105 NA Polytherapy: 20·8% Phenytoin used in 93·0%
India (university medical 106 First and second Polytherapy: 24·5% and Carbamazepine used in 47·4%
centres) monotherapy 75·5%
Indonesia 107 First and second NA NA Availability of AEDs depending on urban or rural area
Nepal (hospital) 20 First NA NA AEDs used depending on geographical location. Monotherapy:
with carbamazepine used at 92·0% in one hospital
Sri Lanka 108 First Monotherapy: 75·0% Carbamazepine used in 48·0%
Sri Lanka (hospital) 109 First Monotherapy: 70·8% Carbamazepine Second-generation AEDs are available in private clinic
Taiwan 110 First and second Polytherapy: 0·6% and Carbamazepine used in 78·4%
monotherapy: 29·4%
Taiwan 111 First Monotherapy: 61·0% Carbamazepine used in 56·9%
Thailand 112 NA Polytherapy: 58·6% NA

First-generation antiepileptic drugs (AEDs): phenytoin, carbamazepine, valproic acid, phenobarbital, clonazepam, primidone, ethosuximide. Second-generation AEDs: lamotrigine, gabapentin, tiagabine,
felbamate, vigabatrin, topiramate. NA=not available.

Table 6: Use of antiepileptic drugs in Asian countries

is not funded. The average annual cost (direct and indirect) with active epilepsy (defined in this case as two or more
of outpatient treatment of epilepsy is US$47 per patient. In unprovoked seizures on different days in the previous
general, the cost of phenobarbital in southeast Asia is 2·7 year) and the number whose seizures are being
times higher than in Europe,101 and two to six times higher appropriately treated in a given population at a given
than in sub-Saharan Africa. The annual cost incurred in point in time, expressed as a percentage.33,117 In
emergency and inpatient management in India is developing countries in sub-Saharan Africa and Latin
estimated to be US$810·50 and US$168·30, respectively, America, up to 90% of people with epilepsy receive
for all the patients attending a secondary hospital.105 In inadequate treatment or no treatment at all.33,118,119 In
general, the cost of treatment is much lower than Asian countries, the treatment gap was 29–98%, with
productivity losses, and it would be cost efficient for values for most countries between 50% and 80%. The
governments or societies to invest in epilepsy treatment.105 treatment gap was higher in rural areas than in urban
areas (table 7).9,10,16,17,21,26,35,120–126 In rural areas, lack of
Epilepsy control assessment antiepileptic drugs and knowledge of epilepsy contribute
Treatment with phenobarbital was assessed in 2455 to the treatment gap.
Chinese patients from rural areas in a community-based
intervention trial. In 68% of patients who completed
12 months’ treatment, seizure frequency was decreased References Year Treatment
gap (%)
by at least 50%, and a third of patients were seizure-free.
72% of patients who completed 24 months’ treatment China 9,10 2002 (and 2003) 62·6

had at least 50% reduction in seizure frequency and a India 120 2003 50·0–70·0
quarter of patients remained seizure-free. 597 patients India 17 2002 73·0–78·0
discontinued treatment before the end of the study. Many India (semi-urban) 16 2000 38·0
of those withdrew because of a misunderstanding that India (rural) 35 1999 >70·0
they were cured on becoming seizure-free (28%); others India (rural) 121 1999 54·0
withdrew because they perceived the treatment to be India (rural) 122 1997 78·0
ineffective (16%). Only 5% discontinued the treatment India (semi-urban) 123 1997 57·0
because of adverse events.115 Another study in India India (rural) 124 1988 74·5
showed that strict drug compliance and early treatment India (urban) 125 1988 29·0
(with phenobarbital or phenytoin or both) were important Nepal 126 2004 >70·0
predictors of a 2 year terminal remission.116 Pakistan (rural) 21,26 1994 (and 1997) 98·0
Pakistan (urban) 21,26 1994 (and 1997) >72·0
Treatment gap Turkey 26 1997 70·0
The treatment gap was defined by a workshop of the
Table 7: Treatment gap for epilepsy in Asia
ILAE as the difference between the number of people

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Review

Surgery reported from Taiwan that 50% of their patients used


The ILAE reported the presence of epilepsy surgery Chinese traditional medicine, and 47% sought folk
centres in 26 countries worldwide from 1980 to 1990; at healing methods including Qian interpretation, fortune
that time, only four Asian countries were on the list: telling, Qigong, geomancy, and shamanism. The use of
Japan, China, Taiwan, and Vietnam.127 More recent reports these traditional treatment modalities is probably related
revealed some others in Hong Kong, India, Iran, North to the large treatment gap in large parts of Asia. Some of
Korea and South Korea, the Philippines, Singapore, the so-called traditional preparations are adulterated with
Thailand, and Turkey.128,129 A cohort study of patients with conventional antiepileptic drugs, which complicates the
medically refractory temporal-lobe epilepsy in India management of these patients.133 This situation is
showed a significantly better outcome of surgery (77·0% comparable to that in sub-Saharan Africa.5 As long as
seizure-free, 32·7% off medication) compared with traditional beliefs exist, patients with epilepsy are not
medical treatment (11·5% seizure-free, 0·8% off likely to be correctly treated.
medication). There was no statistically significant
difference in mortality between the two groups.130 Knowledge, attitudes, and practice
Numerous studies on knowledge, attitudes, and practice
Concepts of disease and use of traditional, complementary, and have been done, particularly in Chinese communities
alternative medicine within and outside China (table 8).16,134–144 Stigma was least
There are few dedicated studies on the concepts of important but evident in some advanced regions, such as
disease and use of traditional, complementary, and Hong Kong or Singapore.131,137,138 In Hong Kong, 94·1% of
alternative medicine among patients with epilepsy in respondents thought that people with epilepsy could be
Asia, although many clinicians practising in the region married, but only 67·8% would allow their child to marry a
have reported widespread use of traditional medicine person with epilepsy;138 from the reports discussed in this
and spiritual medium, particularly in rural areas.20,100,131 Review, it seems that people in Hong Kong have the most
Tan and Lim100 reported prevalence of syncretism (ie, open-minded attitudes towards epilepsy. In another study
simultaneously holding to concepts from different in China, only 13·0% of the respondents would allow their
schools of thought) in concepts and practice among the child to marry a person with epilepsy.141 Lack of awareness
ethnic Chinese patients with chronic epilepsy in Kuala may be a factor explaining stigma. In almost all studies, a
Lumpur, with some patients attributing the illness to third to a half of responding people thought that a person
epilepsy as well as to the traditional concepts of with epilepsy cannot work like other people, and a quarter
“weakness” (xu), “hotness” (re), “wind” (feng), and thought that epilepsy is a mental illness or a form of
“supernatural cause” (xie). Rajbhandari20 reported that insanity. As in other parts of the world, epilepsy is believed
69% of the newly diagnosed patients with epilepsy in to be a contagious disease,123,145 and some people avoid
Kathmandu worshipped family gods, 66% wore mantra touching patients, especially during seizures, when some
butti, jantar, and beets (items believed to protect patients simple forms of help may avoid dangerous situations.
from evil spirits), and 58% made animal sacrifices. Tsai132 Health education campaigns are necessary to rehabilitate

Reference Year N Proportion of affirmative answers Population interviewed


Q1 (%) Q2 (%) Q3 (%) Q4 (%) Q5 (%)
Malaysia 134 1999 379 99·0 9·0* 13·0 91·0 57·0 Public
Malaysia 135 2000 839 91·0 24·0 58·0 80·0 52·0 Public
Burma 136 2002 296 82·0 25·0* 86·0 56·0 29·0 Public
Hong Kong 137 2004 233 96·0 10·0* 10·0 89·0 56·0 Public
Hong Kong 138 2002 1128 58·2 10·4 22·5† 88·8 67·8 Public
India 16 2000 1118 98·7 27·3 45·6 89·2 71·3‡ Public
Korea 140 2003 820 93·0 34·0 52·0 49·0 4·0 Public
Taiwan 141 1995 2610 87·0 7·0* 31·0 82·0 28·0 Public
Vietnam 143 2005 523 68·0 25·0 NA NA 14·0 Public
Vietnam 144 2006 1000 54·6 23·8* 57·9 81·3 44·0 Public
Indonesia 139 2002 84 100·0 57·0 43·0 75·0 44·0 School teacher
Thailand 142 1999 284 57·8 18·2 NA 94·7 41·2 School teacher

Q1=have you ever heard about epilepsy? Q2=do you think that epilepsy is a mental illness? Q3=do you think that people with epilepsy would not be employed like others?
Q4=would you allow your child to associate with a child with epilepsy at school or in play? Q5=would you allow your child to marry a person with epilepsy? N=number of
respondents. NA=not available. *Epilepsy is a form of insanity. †Employers would terminate the employment contract after an epileptic seizure in an employee with
unreported epilepsy. ‡Patient with epilepsy can lead a married life.

Table 8: Awareness, attitudes and understanding towards epilepsy in Asia

540 http://neurology.thelancet.com Vol 6 June 2007


Review

patients with epilepsy in the community and to improve 7 WHO-Regional Office for the Western Pacific. Epilepsy in the
their quality of life. Western Pacific Region: a call to action: Global Campaign Against
Epilepsy. Geneva: WHO, 2004.
8 Commission on epidemiology and prognosis, International League
Conclusion Against Epilepsy. Guidelines for epidemiologic studies on epilepsy.
There have been significant advances in the Epilepsia 1993; 34: 592–96.
9 Wang W, Wu J, Wang D, et al. Epidemiological survey on epilepsy
understanding of the epidemiology of epilepsy in Asia among rural populations in five provinces in China.
over the past 20 years. The median lifetime prevalence Zhonghua Yi Xue Za Zhi 2002; 82: 449–52.
rate is estimated to be six per 1000 people, which is lower 10 Wang WZ, Wu JZ, Wang DS, et al. The prevalence and treatment
gap in epilepsy in China: an ILAE/IBE/WHO study. Neurology 2003;
than in other developing regions. However, the number 60: 1544–45.
of affected patients in the region is large and much 11 Huang M, Hong Z, Zeng J, et al. The prevalence of epilepsy in rural
remains poorly documented or unknown. There are few Jinshan in Shanghai. Zhonghua Liu Xing Bing Xue Za Zhi 2002;
data on incidence and mortality (in particular in elderly 23: 345–46.
12 Li SC, Schoenberg BS, Wang CC, et al. Epidemiology of epilepsy in
people), the treatment gap, public understanding and urban areas of the People’s Republic of China. Epilepsia 1985;
attitudes, patients’ concepts of disease, and help-seeking 26: 391–94.
behaviour. What distinguishes epilepsy in Asia from 13 Fong GCY, Mak W, Cheng TS, et al. A prevalence study of epilepsy
in Hong Kong. Hong Kong Med J 2003; 9: 252–57.
other regions is probably not so much genetics or
14 Bharucha NE. Epidemiology of epilepsy in India. Epilepsia 2003;
biological differences of Asians or environmental factors 44: 9–11.
that influence the causes of symptomatic epilepsy, but 15 Murthy JMK, Vijay S, Ravi Raju C, et al. Acute symptomatic
most likely, the psychosocial, cultural, economic, seizures associated with neurocysticercosis: A community-based
prevalence study and comprehensive rural epilepsy study in South
organisational, and political factors that influence India. Neurol Asia 2004; 9: 86.
epilepsy causation, management, and outcome. These 16 Radhakrishnan K, Pandian JD, Santhoshkuma T, et al. Prevalence,
areas should be the focus of further study, and knowledge, attitude and practice of epilepsy in Kerala, South India.
Epilepsia 2000; 41: 1027–35.
governments must give a higher priority to the fight 17 Ray BK, Bhattacharya S, Kundu TN, et al. Epidemiology of epilepsy-
against epilepsy in Asia. Some of the countries included Indian perspective. J Indian Med Assoc 2002; 100: 322–26.
in this Review are no longer poor, and could make free 18 Mani KS, Rangan G, Srinivas HV, et al. The Yelandur study: a
or subsidised antiepileptic drugs available to the general community-based approach to epilepsy in rural South India—
epidemiological aspects. Seizure 1998; 7: 281–88.
public, as the cost of even phenobarbital can be a burden 19 Tran DS, Odermatt P, Le TO, et al. Prevalence of epilepsy in a rural
on some of these communities. Nurturing of district of central Lao PDR. Neuroepidemiology 2006; 26: 199–206.
epileptologists who can spearhead improvements in 20 Rajbhandari KC. Epilepsy in Nepal. Neurol J Southeast Asia 2003;
8: 1–4.
epilepsy care in the community is also important.
21 Aziz H, Ali SM, Frances P, et al. Epilepsy in Pakistan: a community
Moreover, governments should give high priority to the based epidemiologic study. Epilepsia 1994; 35: 950–58.
development of epilepsy surgery to treat drug-resistant 22 Loh NK, Lee WL, Yew WW, et al. Refractory seizures in a young
epilepsy and should identify centres to be equipped with army cohort. Ann Acad Med Singap 1997; 26: 471–74.
23 Lee WL, Low PS, Murugasu B, et al. Epidemiology of epilepsy in
physical facilities such as video-electroencephalography Singapore children. Neurol J Southeast Asia 1997; 2: 31–35.
and MRI. 24 Su CL, Chang SF, Chen ZY, et al. Prevalence of epilepsy in Ilan,
Contributors Taiwan. Taiwan Epileps Soc Bull 1997; 7: 47.
TLM and DST contributed equally in reviewing all the publications and 25 Asawavichienjinda T, Sitthi-Amorn C, Tanyanont W. Prevalence
analysing data, FQ and PO participated in interpretation, and the work of epilepsy in rural Thailand: a population-based study.
J Med Assoc Thai 2002; 85: 1066–73.
was coordinated by PMP and CTT. All authors contributed to the writing
of the paper. 26 Aziz H, Guvener A, Akhtar SW, et al. Comparative epidemiology of
epilepsy in Pakistan and Turkey: population based studies using
Conflicts of interest identical protocols. Epilepsia 1997; 38: 716–22.
We have no conflicts of interest. 27 Mori P. Combattre l’épilepsie au Vietnam. Pulsations 2003; 4: 10.
Acknowledgments 28 Cuong LQ, Doanh NV, Jallon P. Prevalence of epilepsy in Thai Bao-
Bac Ninh, a region in Vietnam affected by neurocysticercosis.
We thank Sandra Gresiak for her help typing the paper and obtaining
Epilepsia 2005; 46: 132.
references. We have received an unrestricted grant from Sanofi Aventis.
29 Rajshekhar V, Raghava MV, Prabhakaran V, et al. Active epilepsy as
References an index of burden of neurocysticercosis in Vellore district, India.
1 Fisher RS, van Emde Boas W, Blume W, et al. Epileptic seizures and Neurology 2006; 67: 2135–39.
epilepsy: definitions proposed by the International League Against 30 Chen CC, Chen TF, Hwang YC, et al. Population-based survey on
Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE). prevalence of adult patients with epilepsy in Taiwan (Keelung
Epilepsia 2005; 46: 470–72. community-based integrated screening no.12). Epilepsy Res 2006;
2 World Health Organization: epilepsy: epidemiology, aetiology and 72: 67–74.
prognosis. WHO Factsheet, 2001: number 165. 31 Sawhney IM, Singh A, Kaur P, et al. A case control study and one
3 Commission on Tropical Diseases of the International League year follow-up of registered epilepsy cases in a resettlement colony
Against Epilepsy. Relationship between epilepsy and tropical of North India, a developing tropical country. J Neurol Sci 1999;
diseases. Epilepsia 1994; 35: 89–93. 165: 31–35.
4 Burneo JG, Tellez-Zenteno J, Wiebe S. Understanding the burden 32 Jallon P. Epilepsy and epileptic disorders, an epidemiological
of epilepsy in Latin America: a systematic review of its prevalence marker? Contribution of descriptive epidemiology. Epileptic Disord
and incidence. Epilepsy Res 2005; 66: 63–74. 2002; 4: 1–13.
5 Preux PM, Druet-Cabanac M: Epidemiology of epilepsy in sub- 33 Scott RA, Lhatoo SD, Sander JWAS. The treatment of epilepsy
Saharan Africa. Lancet Neurol 2005; 4: 21–31. in developing countries: where do we go from here?
6 Jallon P. Epilepsy in developing countries. Epilepsia 1997; 38: 1143–51. Bull World Health Organ 2001; 79: 344–51.

http://neurology.thelancet.com Vol 6 June 2007 541


Review

34 Singhal BS. Neurology in developing countries: a population 62 Xiao B, Huang ZL, Zhang H, et al. Aetiology of epilepsy in
perspective. Arch Neurol 1998; 55: 1019–21. surgically treated patients in China. Seizure 2004; 13: 322–27.
35 Sridharan R, Murthy BM. Prevalence and pattern of epilepsy in 63 Del Brutto OH, Santibanez R, Idrovo L, et al. Epilepsy and
India. Epilepsia 1999; 40: 631–36. Neurocysticercosis in Atahualpa: a door-to-door survey in rural
36 Mannan MA. Epilepsy in Bangladesh. Neurol Asia 2004; 9: 18. coastal Ecuador. Epilepsia 2005; 46: 583–87.
37 Radhakrishnan K, Nayak SD, Kumar SP, et al. Profile of 64 Garcia HH, Del Brutto OH, and the Cysticercosis working group in
antiepileptic pharmacotherapy in a tertiary referral center in South Peru. Neurocysticercosis: updated concepts about an old disease.
India: a pharmacoepidemiologic and pharmacoeconomic study. Lancet Neurol 2005; 4: 653–61.
Epilepsia 1999, 40: 179–85. 65 Rajshekhar V, Joshi DD, NQ Doanh, et al. Taenia solium taeniosis/
38 Ng KK, Ng PW, Tsang KL, et al. Clinical characteristics of adult cysticercosis in Asia: epidemiology, impact and issues. Acta Trop
epilepsy patients in the 1997 Hong Kong epilepsy registry. 2003; 87: 53–60.
Chin Med J (Engl) 2001; 114: 84–87. 66 Rajshekhar V. Epidemiology of Taenia solium taeniasis/cysticercosis
39 Lim SH. Seizures and epilepsy in the elderly: epidemiology and in India and Nepal. Southeast Asian J Trop Med Public Health 2004;
etiology of seizures and epilepsy in the elderly in Asia. Neurol Asia 35: 247–51.
2004; 9: 31–32. 67 Ito A, Nakao M, Wandra T. Human taeniasis and cysticercosis in
40 Sander JWAS, Hart YM, Johnson AL, et al. National general practice Asia. Lancet 2003; 362: 1918–20.
study of epilepsy: newly diagnosed epileptic seizures in general 68 Joshi DD, Maharjan M, Johnsen MV, et al. Taeniasis/cysticercosis
population. Lancet 1990; 336: 1267–71. situation in Nepal. Southeast Asian J Trop Med Public Health 2004;
41 Ding D, Wang W, Wu J, et al. Premature mortality in people with 35: 252–58.
epilepsy in rural China: a prospective study. Lancet Neurol 2006; 69 Chen YD, Xu LQ, Zhou XN. Distribution and disease burden of
5: 823–27. cysticercosis in China. Southeast Asian J Trop Med Public Health
42 Kamgno J, Pion SDS, Boussinesq M. Demographic impact of 2004; 35: 231–39.
epilepsy in Africa: result of a 10 year cohort study in a rural area of 70 Willingham AL III, De NV, Doanh NQ, et al. Current status of
Cameroon. Epilepsia 2003; 44: 956–63. cysticercosis in Vietnam. Southeast Asian J Trop Med Public Health
43 Tekle-Haimanot R, Forsgren L, Abebe M, et al. Clinical and 2003; 34 (suppl 1): S35–50.
electroencephalographic characteristics of epilepsy in rural 71 Kuruvilla A, Pandian JD, Radhakrishnan VV, et al.
Ethiopia: a community-based study. Epilepsy Res 1990; 7: 230–39. Neurocysticercosis: a clinical and radiological appraisal from Kerala
44 Wakamoto H, Nagao H, Hayashi M, et al. Long-term medical, State, South India. Singapore Med J 2001; 42: 297–303.
educational, and social prognoses of childhood-onset epilepsy: a 72 Erhart A, Dorny P, Van De N, et al. Taenia solium cysticercosis in a
population-based study in a rural district of Japan. Brain Dev 2000; village in northern Viet Nam: seroprevalence study using an ELISA
22: 246–55. for detecting circulating antigen. Trans R Soc Trop Med Hyg 2002;
45 Tsai JJ. Mortality of epilepsy from national vital statistics and 96: 270–72.
university epilepsy clinic in Taiwan. Epilepsia 2005; 46: 8–10. 73 Theis JH, Goldsmith RS, Flisser A, et al. Detection by immunoblot
46 Chen RC, Chang YC, Chen TH, et al. Mortality in adult patients assay of antibodies to Taenia solium cysticerci in sera from residents
with epilepsy in Taiwan. Epileptic Disord 2005; 7: 215–19. of rural communities and from epileptic patients in Bali, Indonesia.
47 Senanayake N, Peiris H. Mortality related to convulsive disorders in Southeast Asian J Trop Med Public Health 1994; 25: 464–68.
a developing country in Asia: trends over 20 years. Seizure 1995; 74 Chung CK, Lee SK, Chi JG. Temporal lobe epilepsy caused by
4: 273–77. intrahippocampal calcified cysticercus. J Korean Med Sci 1998;
48 Hui AC, Joynt GM, Li H, et al. Status epilepticus in Hong Kong 13: 445–48.
Chinese: aetiology, outcome and predictors of death and morbidity. 75 Dorny P, Somers R, Cam-Thach D, et al. Cysticercosis in Cambodia,
Seizure 2003; 12: 478–82. Lao PDR and Vietnam. Southeast Asian J Trop Med Public Health
49 Wong V. West syndrome—The University of Hong Kong experience 2004; 35: 223–26.
(1970–2000). Brain Dev 2001; 23: 609–15. 76 Veliath AJ, Ratnakar C, Thakur LC. Cysticercosis in South India.
50 Hauser WA, Rich SS, Annegers JF, et al. Seizure recurrence after a J Trop Med Hyg 1985; 88: 25–29.
1st unprovoked seizure: an extended follow-up. Neurology 1990; 77 Murthy JM, Yangala R. Acute symptomatic seizures—incidence and
40: 1163–70. etiological spectrum: a hospital-based study from south India.
51 Berg AT, Shinnar S. The risk of seizure recurrence following a first Seizure 1999; 8: 162–65.
unprovoked seizure: a quantitative review. Neurology 1991; 78 Strobel M, Veasna D, Saykham M, et al. Pleuro-pulmonary
41: 965–72. paragonimiasis. Med Mal Infect 2005; 35: 476–81.
52 Boonluksiri P. Risk of recurrence following a first unprovoked 79 Tran DS, Nanthapone S, Odermatt P, et al. A village cluster of
seizure in Thai children. Neurol J Southeast Asia 2003; 8: 25–29. paragonimiasis in Vientiane province, Lao PDR. Southeast Asian
53 Boonluksiri P. Risk of seizure recurrence after antiepileptic drug J Trop Med Public Health 2004; 35: 323–26.
withdrawal in Thai children with epilepsy. Neurol Asia 2006; 11: 80 Higashi K, Aoki H, Tatebayashi K, et al. Cerebral paragonimiasis.
25–29. J Neurosurg 1971; 34: 115–27.
54 Verma A, Misra S. Risk of seizure recurrence after antiepileptic 81 Kaw GJL, Sitoh YY. Clinic in diagnostic imaging. Singapore Med J
drug withdrawal, an Indian study. Neurol Asia 2006; 11: 19–23. 2001; 42: 89–91.
55 Muttaqin Z. Surgery for temporal lobe epilepsy in Semarang, 82 Choo JK, Suh BS, Lee HS, et al. Chronic cerebral paragonimiasis
Indonesia: the first 56 patients with follow up longer than combined with aneurismal subarachnoid hemorrhage.
12 months. Neurol Asia 2006; 11: 31–36. Am J Trop Med Hyg 2003; 69: 466–69.
56 Kwong KL, Chak WK, Wong SN, et al. Epidemiology of childhood 83 WHO, UNICEF. Roll Back Malaria: World Malaria Report. Geneva:
epilepsy in a cohort of 309 Chinese children. Pediatr Neurol 2001; WHO, 2005.
24: 276–82. 84 Wattanagoon Y, Srivilairit S, Looareesuwan S, et al. Convulsions in
57 Thomas SV, Koshy S, Nair CR, et al. Frequent seizures and childhood malaria. Trans R Soc Trop Med Hyg 1994; 88: 426–28.
polytherapy can impair quality of life in persons with epilepsy. 85 Faiz MA, Rahman MR, Hossain MA, et al. Cerebral malaria—a
Neurol India 2005; 53: 46–50. study of 104 cases. Bangladesh Med Res Counc Bull 1998; 24: 35–42.
58 Win MN. The EEG and epilepsy in Kelantan—a hospital/laboratory- 86 Ngoungou EB, Dulac O, Poudiougou B, et al. Epilepsy as a
based study. Med J Malaysia 1993; 48: 153–59. consequence of cerebral malaria in area in which malaria is
59 Manonmani V, Tan CT. A study of newly diagnosed epilepsy in endemic in Mali, West Africa. Epilepsia 2006; 47: 873–79.
Malaysia. Singapore Med J 1999; 40: 32–35. 87 Ngoungou EB, Koko J, Druet-Cabanac M, et al. Cerebral malaria
60 Li S, Wang X, Wang J, et al. Cerebrovascular disease and and sequelar epilepsy: first matched case–control study in Gabon.
posttraumatic epilepsy. Neurol Asia 2004; 9 (suppl): 12–13. Epilepsia 2006; 47: 2147–53.
61 Hui AC, Kwan P. Epidemiology and management of epilepsy in 88 Solomon T, Dung NM, Kneen R, et al. Japanese encephalitis.
Hong Kong: an overview. Seizure 2004; 13: 244–46. J Neurol Neurosurg Psychiatry 2000; 68: 405–15.

542 http://neurology.thelancet.com Vol 6 June 2007


Review

89 Murthy JMK. Some problems and pitfalls in developing countries. 118 Anonymous. In the shadow of epilepsy. Lancet 1997; 349: 1851.
Epilepsia 2003: 44 (suppl 1): 38–42. 119 Shorvon SD, Farmer PJ. Epilepsy in developing countries: a review
90 Misra UK, Kalita J. Seizures in Japanese encephalitis. J Neurol Sci of epidemiological, sociocultural and treatment aspects. Epilepsia
2001; 190: 57–60. 1988: 29 (suppl 1): S36–45.
91 Jain S, Padma MV, Puri A, et al. Twin birth and epilepsy: an 120 Gourie-Devi M, Satishchandra P, Gururaj G. Epilepsy control
expanded India study. Neurol J Southeast Asia 1999; 4: 19–23. program in India: a district model. Epilepsia 2003; 44: 58–62.
92 Sharma K. Genetic epidemiology of epilepsy: a twin study. 121 Pal DK. Methodologic issues in assessing risk factors for epilepsy in
Neurol India 2005; 53: 93–98. an epidemiologic study in India. Neurology 1999; 53: 2058–63.
93 Lu J, Chen Y, Pan H, et al. The gene encoding GABBR1 is not 122 Mani KS. Epidemiology of epilepsy in Karnataka, India.
associated with childhood absence epilepsy in the Chinese Han Neurosci Today 1997; 1: 167–74.
population. Neurosci Lett 2003; 343: 151–54. 123 Bharucha NE, Weiss MG, Bharucha EP, et al. Sociocultural aspects
94 Ren L, Jin L, Zhang B, et al. Lack of GABABR1 gene variation of epilepsy in developing countries: presented at the 22nd Epilepsy
(G1465A) in a Chinese population with temporal lobe epilepsy. congress, Dublin, Ireland, July 1997.
Seizure 2005; 14: 611–13. 124 Koul R, Razdan S, Motta A. Prevalence and pattern of epilepsy (Lath/
95 Chen YC, Zhang YH, Lu JJ, et al. Association of child absence epilepsy Mirgi/Laran) in rural Kashmir, India. Epilepsia 1988; 29: 116–22.
with T-STAR gene. Zhonghua Yi Xue Za Zhi 2003; 83: 1134–37. 125 Bharucha NE, Bharucha EP, Bharucha AE, et al. Prevalence of
96 Chen Y, Lu J, Zhang Y, et al. T-type calcium channel gene alpha (1G) epilepsy in the Parsi community of Bombay. Epilepsia 1988; 29: 111–15.
is not associated with childhood absence epilepsy in the Chinese 126 Rajbhandari KC: Epilepsy in Nepal. Can J Neurol Sci 2004; 31: 257–60.
Han population. Neurosci Lett. 2003; 341: 29–32. 127 ILAE commission report. A global survey on epilepsy surgery,
97 Nair RR, Thomas SV. Genetic liability to epilepsy in Kerala State, 1980–1990. A report by the Commission on Neurosurgery of Epilepsy,
India. Epilepsy Res 2004; 62: 157–64. International League Against Epilepsy. Epilepsia 1997; 38: 249–55.
98 Zeng J, Hong Z, Huang MS, et al. A case-control study on the risk 128 Wieser HG, Silfvenius H. Overview: epilepsy surgery in developing
factors and other socio-psychological factors of epilepsy. countries. Epilepsia 2000; 41: 83–89.
Zhonghua Liu Xing Bing Xue Za Zhi 2003; 24: 116–18. 129 Lee BI. Current status and future direction of epilepsy surgery in
99 Ramasundrum V, Tan CT. Consanguinity and risk of epilepsy. Asia. Neurol Asia 2004; 9: 47–48.
Neurol Asia 2004; 9: 10–11. 130 Panda S, Radhakrishnan K, Sarma PS. Mortality in surgically versus
100 Tan CT, Lim SH. Epilepsy in Southeast Asia. Neurol J Southeast Asia medically treated patients with medically refractory temporal lobe
1997; 2: 11–15. epilepsy. Neurol Asia 2004; 9: 129.
101 WHO, International Bureau for Epilepsy, International League 131 Pan APS, Lim SH. Public awareness, attitudes and understanding
Against Epilepsy. Atlas—epilepsy care in the world 2005. Geneva: toward epilepsy among Singaporean Chinese.
WHO, 2005. Neurol J Southeast Asia 2000; 5: 5–10.
102 World Health Organization. Neurology Atlas 2004: http://www.who. 132 Tsai JJ. Help-seeking behavior among patients with epilepsy.
int/mental_health/neurology/neurogy_atlas_results6-8.pdf Epilepsia 1991; 32: 32.
(accessed Feb 28, 2007). 133 Goh KJ, Ma WT, Ali Mohd M, et al. Case reports of covert use of
103 Seino M. Comprehensive epilepsy care: Contributions from para- Phenobarbital in patients taking Diankexing and Diankening,
medical professionals. Neurol J Southeast Asia 2001; 6: 1–5. traditional herbal medicine for epilepsy. Neurol Asia 2004; 9: 55–57.
104 Commission on Tropical Diseases of the International League 134 Lim KS, Tan LP, Lim KT, et al. Survey of public awareness,
Against Epilepsy. Availability and distribution of antiepileptic drugs understanding and attitudes toward epilepsy among Chinese in
in developing countries. Epilepsia 1985; 26: 117–21. Malaysia. Neurol J Southeast Asia 1999; 4: 31–36.
105 Krishnan A, Sahariah SU, Kumar Kapoor S. Cost of epilepsy in 135 Ramasundrum V, Mohd Hussin ZA, Tan CT. Public awareness,
patients attending a secondary-level hospital in India. Epilepsia attitudes and understanding towards epilepsy in Kelantan, Malaysia.
2004; 45: 289–91. Neurol J Southeast Asia 2000; 5: 55–60.
106 Thomas SV, Sarma PS, Alexander M, et al. Economic burden of 136 Win NN, Soe C. Public awareness, attitude and understanding
epilepsy in India: Epilepsia 2001; 42: 1052–60. toward epilepsy among Myanmar people. Neurol J Southeast Asia
107 Gunawan D. Epilepsy management with limited resources, 2002; 7: 81–88.
Indonesian experience. Neurology Asia 2004; 9 (suppl 1): 16–17. 137 Wong V, Chung B, Wong R. Pilot survey of public awareness,
108 Seneviratne U, Rajapakse P, Pathirana R, et al. Knowledge, attitude, attitudes and understanding towards epilepsy in Hong Kong.
and practice of epilepsy in rural Sri Lanka. Seizure 2002; 11: 40–43. Neurol Asia 2004; 9: 21–27.
109 Kariyawasam SH, Bandara N, Koralagama A, et al. Challenging 138 Fong CY, Hung A. Public awareness, attitude, and understanding of
epilepsy with antiepileptic pharmacotherapy in a tertiary teaching epilepsy in Hong Kong Special Administrative Region, China.
hospital in Sri Lanka. Neurol India 2004; 52: 233–37. Epilepsia 2002; 43: 311–16.
110 Lillian L, Chun-Hing Y, Der-Jen Y, et al. Medication education for 139 Rambe AS, Sjahrir H. Awareness, attitudes and understanding
patients with epilepsy in Taiwan. Seizure 2003; 12: 473–77. towards epilepsy among school teachers in Medan, Indonesia.
111 Chen LC, Chen YF, Yang LL, et al. Drug utilization pattern of Neurol J Southeast Asia 2002; 7: 77–80.
antiepileptic drugs and traditional Chinese medicines in a 140 Kim MK, Kim IK, Kim BC, et al. Positive trends of public attitudes
general hospital in Taiwan—a pharmaco-epidemiologic study. toward epilepsy after public education campaign among rural
J Clin Pharm Ther 2000; 25: 125–29. Korean residents. J Korean Med Sci 2003; 18: 248–54.
112 Silpakit O, Silpakit C. A Thai version of a health-related quality of 141 Chung MY, Chang YC, Lai CW. Survey of public awareness,
life instrument for epilepsy. Neurol J Southeast Asia 2003; 8: 103–07. understanding and attitudes towards epilepsy in Taiwan. Epilepsia
113 Nassiri R, Stelmasiak Z. Pharmacotherapy of epilepsy. 1995; 36: 488–93.
Neurol Neurochir Pol 2000; 34: 47–58. 142 Kankirawatana P. Epilepsy awareness among schoolteachers in
114 Mac TL, Le VT, Vu AN, et al. AEDs availability and professional Thailand. Epilepsia 1999; 40: 497–501.
practice in delivery outlets in a city centre in southern Vietnam. 143 Tuan NA, Tomson T, Cuong LQ, et al. Public awareness
Epilepsia 2006; 47: 330–34. understanding and attitudes towards epilepsy in Bavi, Vietnam: first
115 Wang WZ, Wu JZ, Ma GY, et al. Efficacy assessment of Report from the APIBAVI study. Epilepsia 2005; 46: 192.
phenobarbital in epilepsy: a large community-based intervention 144 Cuong LQ, Thien DD, Jallon P. Survey of public awareness,
trial in rural China. Lancet Neurol 2006; 5: 46–52. attitudes and understanding toward epilepsy in Nhan Chinh,
116 Mani KS, Rangan G, Srinivas HV, et al. Epilepsy control with Hanoi, Vietnam, in 2003. Epilepsy Behav 2006; 8: 176–80.
phenobarbital or phenytoin in rural south India: the Yelandur study. 145 Ab Rahman AF. Awareness and knowledge of epilepsy among
Lancet 2001; 357: 1316–20. students in a Malaysian university. Seizure 2005; 14: 593–96.
117 Meinardi H, Scott RA, Reis R, et al. ILAE Commission on the
Developing World: the treatment gap in epilepsy: the current
situation and ways forward. Epilepsia 2001; 42: 136–49.

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