Epilepsy encompasses a range of neurological disorders marked by recurring seizures, stemming from abnormal electrical brain activity. These seizures vary in intensity and duration, from subtle episodes to prolonged shaking, potentially leading to physical injuries. A diagnosis of epilepsy typically requires two or more unprovoked seizures, although a single seizure might suffice in cases where recurrence is anticipated. These seizures are distinguished from isolated incidents triggered by specific causes like poisoning. The unpredictable nature of epileptic seizures can result in social stigma and varied treatment approaches globally.
In 1912, phenobarbital was developed as the first modern treatment for epilepsy.
In 1938, phenytoin was introduced as an anti-seizure medication.
Before 1971, epilepsy could be grounds for marriage annulment in the United Kingdom.
The ILAE presented a classification system for epilepsies and epileptic syndromes in 1989.
In 1990, epilepsy resulted in 125,000 deaths globally.
Around 2000 BC, the oldest known description of a seizure, from Mesopotamia, attributed the condition to spiritual causes, involving the influence of a moon god.
Between the 1970s and 2003 in developed nations, there was a decrease in new childhood epilepsy cases, but an increase in elderly cases. Increased survival rates after strokes in older adults are believed to be a factor.
In 2004, the economic costs of epilepsy in Europe amounted to approximately 15.5 billion euros.
In 2005, the ILAE defined epilepsy as "a disorder of the brain characterized by an enduring predisposition to generate epileptic seizures and by the neurobiologic, cognitive, psychological, and social consequences of this condition." It requires the occurrence of at least one epileptic seizure.
In 2005, the ILAE defined epilepsy with a focus on its practical application in clinical settings. This definition emphasizes when an "enduring predisposition" to seizures exists.
Purple Day, a global epilepsy awareness day, was created in 2008 by Cassidy Megan from Canada. It takes place each year on March 26th.
In 2010, the ILAE Commission for Classification of the Epilepsies tackled the issue of underlying causes, categorizing epilepsies into genetic, structural/metabolic, and unknown causes.
The ILAE further refined its epilepsy classification in 2011, expanding to four categories and several subcategories, reflecting advancements in technology and science.
In 2011, the ILAE addressed difficulties in classifying syndromes with unclear causes and where epilepsy wasn't the primary feature. They acknowledged that the classification would continue to evolve with ongoing research.
As of 2011, research on seizure prediction using EEG data had not yet yielded an effective prediction method, though progress was being made.
A 2012 review explored the connection between epilepsy and celiac disease, estimating that 1-6% of individuals with epilepsy also have celiac disease, compared to 1% in the general population. The review also mentioned a specific syndrome involving celiac disease, epilepsy, and brain calcifications.
In 2012, active epilepsy, defined as having at least one seizure in the past five years, was estimated to affect 3-10 per 1,000 people. Poverty was identified as a risk factor.
In 2012, gene therapy and immune-altering medications were being studied for epilepsy treatment. Additionally, noninvasive stereotactic radiosurgery was being compared with traditional surgery for specific epilepsy types.
The International League Against Epilepsy (ILAE) clarified its 2005 definition of epilepsy in 2014. The clarified definition focuses on the clinical presentation of epilepsy, designed for practical use in diagnosing and managing the condition.
International Epilepsy Day, also known as World Epilepsy Day, was established in 2015 and is observed annually on the second Monday of February.
As of 2016, there's no reliable evidence to support the use of alternative medicine, like acupuncture or yoga, for epilepsy. Evidence regarding melatonin use was also insufficient.
In 2017, the International League Against Epilepsy (ILAE) introduced updated guidelines for classifying seizures and epilepsies, including their causes and associated conditions.
In 2018, the FDA approved cannabidiol as an add-on therapy for specific epilepsy syndromes (Lennox-Gastaut and Dravet syndromes) in children who don't respond well to other medications.
As of 2021, approximately 50 million people worldwide were affected by epilepsy, representing 1% of the population by age 20 and 3% by age 75. A greater number of males experience the disorder compared to females.
In 2021, around 51 million people globally were affected by epilepsy, with the majority of cases (80%) occurring in developing countries. This resulted in 140,000 deaths, an increase from 125,000 deaths in 1990.
A 2022 Cochrane review indicated that high-level vagus nerve stimulation (h-VNS) could reduce seizure frequency in children and adults with drug-resistant epilepsy who haven't responded to other treatments, compared with low-level VNS.
A 2022 systematic review found evidence suggesting that ketogenic and modified Atkins diets can reduce seizures in some infants with epilepsy and children with drug-resistant epilepsy.
A 2023 systematic review showed that surgery can significantly reduce or eliminate seizures in children aged 1-36 months with drug-resistant epilepsy.
A 2024 study found 64.8% of relatives of epilepsy patients experienced moderate stigma. Higher stigma levels correlated with more negative attitudes towards epilepsy, especially among relatives of patients with frequent seizures or poor medication adherence.