We searched Medline (1966 to May, 2012), ISI Web of Science (1966 to May, 2012), and Cochrane Reviews (1966 to May, 2012) with the search terms (‘epilepsy” AND “resource poor”) OR (“developing countries”) OR (“low income countries”). Searches were restricted to human studies. We found 646 references.
SeriesEpilepsy in poor regions of the world
Introduction
Over 85% of the global burden of epilepsy occurs in the 49% of the population living in low-income and lower-middle-income countries (LLMIC; table).1, 2 Most of these countries are in Africa, where the yearly expenditure on health care is often less than US$50 per person (5·1% of the gross national income; figure 1). However, these mean data often belie the large disparities found within these countries, particularly between the poorer areas (rural or urban settlement) and more affluent urban areas and between the scarcity of health facilities and personnel in the government sector and those in the private medical sector. These disparities contribute to the enormous treatment gap (ie, the proportion of people with epilepsy who have active epilepsy but who are not taking antiepileptic drugs [AEDs] or are inadequately treated): over 60% of people with epilepsy do not access biomedical treatment for epilepsy in LLMIC,3 and if they do, they often do not or are not able to adhere to the prescribed regimens.
Section snippets
The burden of epilepsy
Epilepsy was estimated to account for 0·5% of the global burden of disease, accounting for 7 307 975 disability-adjusted life-years, in 2005.4 These figures did not take into account the limited data from the LLMIC or that the disability weights of epilepsy are not based on measurements in poor areas. Deriving accurate figures on the epidemiology of epilepsy in LLMIC is very difficult since most data have to be derived from cross-sectional surveys, of which there are few and which are expensive
Risk factors
Risk factors for seizure disorders and epilepsy differ between LLMIC and HIC, at least in their frequencies. The most marked difference relates to the age of onset, which in HIC follows a bimodal curve with markedly higher incidence in early childhood and later life (people older than 65 years) than at other ages.17, 18 In LLMIC the incidence is increased in older children and young adults compared with other age groups, probably because of the high incidence of infections and trauma as
Prevention
Since preventable epilepsies arise from well-defined causative agents or situations, most interventions are directed towards the underlying disease or risk factor itself rather than towards preventing the development of epilepsy (ie, epileptogenesis in affected individuals). Improvements in perinatal care should decrease neonatal brain damage. Interventions against some infectious diseases or traumatic brain injury should decrease the incidence of epilepsy.
Stigma
Epilepsy, like many other mental health disorders, is often associated with substantial stigma, particularly in poor areas. Most people with epilepsy in these regions are less likely to be sent to school, find employment, or marry.47, 48, 49 Some of these impediments might be related to the underlying brain disorder, manifesting as cognitive impairment or psychiatric illness. In those studies that have measured stigma, the evidence suggests that most stigma is enacted (ie, discrimination
Treatment gap
Although the International League Against Epilepsy (ILAE) defines active epilepsy as a seizure within the past 5 years, in many LLMIC it is defined as one or two seizures within the past year, since this is the criteria used to start treatment with AEDs and to measure the treatment gap.55 The epilepsy treatment gap has two components: those not accessing or unable to access biomedical facilities for diagnosis and treatment and, if accessing biomedical treatment, those not adhering to the
Services for epilepsy
In LLMIC there are substantial disparities in the care that is available for epilepsy. Most neurologists and psychiatrists work in the urban private sector, where they provide care similar to that found in developed countries, with access to the newer AEDs, sophisticated neuroimaging, and epilepsy surgery programmes. However, in the poorer urban areas, government facilities, and rural areas this level of care is rarely available. To address these disparities, epilepsy needs to be integrated
Initiatives to reduce the burden and treatment gap of epilepsy
The Global Campaign Against Epilepsy was started in 1997 as a result of a collaboration between WHO, ILAE, and the International Bureau for Epilepsy (IBE) to address many of these issues. The first phase aimed to raise awareness, develop regional declarations on epilepsy, and encourage prioritisation of epilepsy services. The second phase was launched in 2001, with demonstration projects set up to support ministries of health in identifying needs and promoting education, training, treatment,
Conclusions
The burden of epilepsy can be reduced in poor parts of the world by alleviating poverty, but perhaps more easily by reducing the preventable causes, namely perinatal insults, parasitic diseases, and head injuries. Community sensitisation, with identification of people with epilepsy in poor areas and education that epilepsy is a controllable disorder, would provide an opportunity for these people to access treatment. Empowering primary health-care workers to diagnose and start treatment might
Search strategy and selection criteria
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