Table of Contents
History of Epilepsy
In all clinical departments, there is a recurrent group of disease etiologies, e.g., infectious, autoimmune, inflammatory, neoplastic, traumatic, metabolic or genetic causes for diseases. However, only the neurology department reserves a very special etiological group for itself: epilepsy.
Early in history, people were impressed by the spectacular clinical picture of epilepsy and interpreted it in the context of the divine. This is the reason why there is the old term of morbus sacer since in ancient Greece epilepsy was considered a ‘holy disease’.
Later, in medieval times, the divine character faded and epileptics were more and more considered to be possessed by demons. During the reign of national socialism in Germany, epileptics were seen as ‘unworthy’.
Definition of Epilepsy
During an epileptic seizure, a short synchronous discharge of neurons occurs. This results in sudden symptoms that vanish just as quickly and can affect all neuronal qualities (e.g., motor function, sensory, vegetative, and consciousness).
An epileptic seizure is no evidence for epilepsy. Roughly 5% of all people have an epileptic seizure at some point in their lives.
Epilepsy itself is a chronic disease of the brain which results in recurrent and unprovoked seizures.
If technical examinations result in the diagnosis of changes that are typical for epilepsy (see below), the diagnosis of epilepsy can be made after only 1 seizure. In this sense, it is important to remember the following vocabulary:
- Occasional seizure: epileptic seizure due to a clear trigger; no seizures if the trigger is avoided.
- Epileptic seizure: sudden, short, synchronous unloading of a group of neurons; can occur in every human being if the stimulus is strong enough.
- Status epilepticus: longer-lasting seizures (> 5 minutes) or repeated seizures between which consciousness is not regained.
Causes of Epilepsy
We distinguish between idiopathic, symptomatic, and cryptogenic forms of epilepsy: symptomatic means that a structural cerebral alteration that seems to be responsible for the epileptic discharge can be diagnosed. The cause is cryptogenic if such a structural alteration can be suspected but is not verifiable.
Pathophysiological etiologies are very heterogeneous: malformations, metabolic diseases, acquired brain lesions, radiation, early childhood hypoxia, encephalitis, etc.
Likewise, different provocation factors lead to increased readiness for seizure: fever, electrolyte derailment, uremia, hypoglycemia, hypoxia, alcohol (withdrawal), medicaments (withdrawal). Often, spontaneous epileptic seizures develop from a combination of (exogenous) stimuli, genetic predisposition, and metabolic processes.
General Symptoms and Clinical Relevance of Epileptic Seizures
The clinical presentation of epileptic seizures is very complex and extensive. It is best illustrated as a paroxysmal excitation of many neurons causing overshooting excitation in a certain region of the brain. Thus, focal frontal excitation results in clonic – occipital excitation to visual symptoms.
Generalized seizures can present as both a tonic (= stiff extension of the extremities) or clonic (= rhythmic convulsion), and also as absence (= empty, contactless gaze) or as individual generalized muscle twitches (= myoclonic seizure).
The ‘classical’ generalized grand mal seizure is often accompanied by an epileptic cry. Objectifying, one finds a lateral tongue bite, postictal muscle ache, and enuresis or encopresis on examination. After an epileptic discharge, intermittent palsies can occur (Todd’s palsy).
Monitoring keratin kinase is an important part of the laboratory procedures. The massive and generalized muscle contraction in combination with hypoxia results in diffuse muscle damages with the respective liberation of keratin kinase. If this parameter is significantly increased, the kidneys can be damaged. Therefore, hemodilution should be sought at high levels.
You should remember the following for the description of the clinical terms:
|Positive symptoms||Increased function|
|Negative symptoms||Decreased function|
|Ictal||During the seizure|
|Postictal||After the seizure, a normal neuronal function is not yet regained. In this period, the patients are very sleepy and are cognitively impaired.|
|Interictal||Between the seizures|
Differential diagnosis tips for clinical practice
Especially in emergency admission, it is important to differentiate the differential diagnoses: particularly in sleepy patients (with complicated anamnesis) with palsies, an acute ischemic event has to be ruled out.
Besides imaging, the clinical examination is also helpful: the visual angle deviates from the damaged side in ischemia and to the opposite side of the epileptic event in epilepsy. So, if there are left-sided hemiparesis and visual angle deviation to the right, ischemia is more likely.
When there is a lack of certainty in the diagnosis, diagnostic imaging tests should be done to rule out an ischemic event. Other considerations of differential diagnoses should include migraine attacks with aura, a (convulsive) syncope or a psychogenic seizure.
The psychogenic seizure is characterized by a very variable duration and can often last for several minutes. The type of seizure changes, and often there are very long presentiments – much longer than an epileptic aura. In a psychogenic seizure, the eyes are often tightly closed, especially if the examiner tries to open them. In an epileptic seizure, the eyes are mostly wide open. After a slow re-orientation, the patients often stutter.
Syndrome Classes of Epilepsy
The group of epileptic diseases is large and polymorphic. Classification in different syndrome classes serves the orientation and determines different approaches for therapy. The different diagnostic specificities, especially the respective electro-encephalogram (EEG) leads, are described later.
A common feature of focal epilepsies is the epileptogenic origin in a certain brain region with specific symptoms.
If impairments of consciousness occur during a focal seizure, it is referred to as complex-focal epilepsy. The epileptic aura (= perceptions a few seconds before the seizure) defines focal epilepsies. These are typical characteristics of focal epileptic areas:
|Temporal lobe epilepsy||The most frequent group of focal epilepsies; epigastric aura with the following externalizations: often hippocampus sclerosis, pharmacologically hard to adjust, and often neurosurgical therapy is needed. The following process is typical:
1. Aura: visceral, also déjà-vu or jamais-vu
|Frontal lobe epilepsy||Psychic aura, tonic/clonic seizures, Jackson seizure (= march of convulsion): the clonic movements march over different body areas, versive seizures, aphasic seizures|
|Parietal lobe epilepsy||Sensory aura, sensory (also marching) seizures, negative symptoms: apraxia, vertigo, and aphasia|
|Occipital lobe epilepsy||Visual aura, complex visual impressions or visual memories during the seizure; long-lasting|
|Benign focal epilepsy||Rolandic epilepsy, 1-sided clonic with strong salivation (especially at night), halting of the seizure before adolescence (thus benign). Therapy: sultiame, this form of epilepsy is idiopathic.|
In cases of generalized epilepsies, a generalized pathology has to be assumed. Accordingly, epileptic externalizations quickly affect the whole brain.
Idiopathic-generalized forms of epilepsy
The groups represent the greatest number of epilepsy occurrences. We distinguish between a series of individual diseases, of which the following are especially relevant for practice:
|Childhood absence epilepsy (pyknolepsy)||From the 3rd to 8th year of life onward, short absences, up to 100 seizures per day, good prognosis, therapy: ethosuximide.|
|Juvenile absence epilepsy||Similar to childhood absence epilepsy, but later onset and worse prognosis (roughly 40% are not permanently free of seizures); tonic-clonic grand mal seizures at waking up and especially later in the adult age|
|Juvenile myoclonic epilepsy ‘Janz syndrome’, ‘impulsive petit mal’||From the 12th to 20th year of life onward, myoclonic in the morning (especially at ungentle waking up), also bilateral myoclonic of the extremities (things are suddenly and jerkily thrown away), astatic, and tonic-clonic seizures|
|Grand mal epilepsy||Generalized tonic-clonic seizures with great irregularity|
Symptomatic or cryptogenic generalized forms of epilepsy
The main cause of symptomatic generalized epilepsies is early-childhood brain damages like hypoxia or metabolic diseases. Often, the patients have decreased intelligence and are severely affected. The following are 2 important forms:
- West syndrome: occurs in the first year of life. The seizure picture consists of infantile spasm (= short tonic cramp of the arms and legs in front of the body, former term: ‘Blitz-Neck-Salaam’); bad prognosis, frequently progresses into the Lennox-Gastaut syndrome; therapy: adrenocorticotropic hormone (ACTH), steroids or benzodiazepines.
- Lennox-Gastaut syndrome: an epileptic encephalopathy; develops out of West syndrome or due to late generalized brain damage; seizure picture: astatic (falling) seizures, absences, and generalized tonic-clonic externalizations.
Diagnosis of Epilepsy
An extensive anamnesis and especially 3rd-party anamnesis is important for detection and assessment. For instrument-based examination, electroencephalograms (EEGs), computerized axial tomography (CAT), and magnetic resonance imaging (MRI) are used.
With an EEG, decelerations or changes and patterns typical for epilepsy can be identified. Respectively, whole generalized epilepsies often show changes in the whole brain area, focal epilepsies only show them in some leads. The amplitude and frequency of the leads are assessed to detect spikes, spike-wave complexes or seizure patterns.
It takes a lot of training and experience to correctly interpret EEGs. Other than a rest EEG, provocation factors (flickering light, hyperventilation, and sleep deprivation) can be used to show epileptogenic potentials. Several important EEG findings with the respective epilepsy syndromes are:
- Childhood absence epilepsy: 3 Hz spike-wave complexes
- Juvenile absence epilepsy: 3 Hz spike-wave complexes and polyspike waves
- Juvenile myoclonic epilepsy: generalized polyspike waves
- West syndrome: hypsarrhythmia (= irregular, high-amplitude activity, interictal, and ictal flattening)
- Lennox-Gastaut syndrome: slow spike-wave complexes, slower than 2.5 Hz
- Creutzfeldt-Jakob disease: triphasic waves
For the evaluation of the 1st seizure, imaging should be sought for considerations of differential diagnoses. In an emergency, the computed tomography (CT) is quickly available. For better imaging of epileptogenic lesions, an MRI-examination can help.
Therapy of Epilepsy Forms
The therapy is based on different approaches. An important aspect is a lifestyle. On one hand, a decrease in seizure potential can be reached with good sleep hygiene or by quitting alcohol consumption. On the other hand, every epileptic has to be informed about a possible restructuring of everyday measures: can I perform my job as a window cleaner? Can I use my car or bike? What about swimming, cutting the hedge or working with the drilling machine?
Besides this, there are pharmacological, surgical, and interventional therapy possibilities. The indication for therapy is individual.
While some patients experience very little impaired epileptic externalization and face continuous medication intake rather reluctantly, others can be very scared after a grand mal seizure and urgently need therapy. The indication for therapy is available…
- …when diagnosing epilepsy.
- …in cases of a higher risk for seizure after a 1st seizure.
- …after the 1st seizure with quick necessary seizure protection.
- …after a 2nd seizure with intermediate seizure protection.
- …in cases of problematic seizures (e.g., status epilepticus).
- …with consent of the patient.
(according to Bauer & Neumann, 2008)
Medicamentous anticonvulsant therapy
The selection of the necessary anticonvulsant medication has to be deliberate and should follow the form of epilepsy, acuteness, possible comorbidity or pregnancy. Also, individual anticonvulsant medication options are differently tolerated. The following table gives a rough overview of the application areas of some frequently used anticonvulsants for seizure prophylaxis:
|Carbamazepine||400–1600 mg||Relatively secure in pregnancy; many side effects: enzyme induction, agranulocytosis, liver toxicity, hyponatremia, heat, reddening, swelling, and tenderness (HRST), and syndrome of inappropriate antidiuretic hormone secretion (SIADH)|
|Phenytoin||200–600 mg||As intravenous emergency medication; difficult dosage due to auto-induction; high risk for withdrawal seizures; prophylaxis with vitamin D and calcium is recommended|
|Focal and generalized epilepsies|
|Valproate||600–2000 mg||Broad-spectrum efficacy; CYP inhibition reinforces the effect of, e.g., Lamotrigine; side effects: liver toxicity, teratogenicity (neural tube defects); important for exams!!|
|Levetiracetam||1000–3000 mg||As intravenous emergency medication; quick effect; little interaction with other medicaments; side effects: fear, depression, and aggression|
|Lamotrigine||100–400 mg||Folate inhibitor, mood-elevating, can be prescribed during pregnancy; skin reactions (up to Stevens-Johnson syndrome) at too fast dosage increase.|
|Topiramate||100–400 mg||Carbonic anhydrase inhibitor (kidney stones), weight loss, and cognitive impairments|
During therapy, routine blood level controls at phenytoin and valproate are recommended. Also, you should remember the following medication for clinical routine: ethosuximide for absence epilepsies; sultiame for rolandic epilepsies or as additional medication for severe epileptic syndromes.
First aid for epileptic seizures
Acute epileptic seizures mostly terminate quickly and spontaneously. There is no special therapy needed. It is especially important to make sure that no collateral injuries develop due to surrounding objects or an uncontrolled fall.
Note: Renowned measures like the bite wedge or holding arms, legs or the head are obsolete nowadays.
If the seizure does not terminate spontaneously, the following level scheme is recommended:
- Benzodiazepines intravenously: The first resort medication is lorazepam, the 2nd 1 is diazepam. If intravenous medication is not possible, diazepam can be given rectally or lorazepam intranasally. Also, the intramuscular application is very effective (according to some studies even equally effective) and can be routinely useful, especially if intravenous injection fails.
- Phenytoin intravenously as an alternative: phenobarbital or valproate
- Narcotics with intensive care monitoring (thiopental and propofol)
Possibilities of epilepsy surgery
Surgical measures seek to eliminate the epileptogenic neuronal area. Of course, this can only work at focal epilepsies. Surgery is indicated if…
- …pharmacological resistance is present (= more seizures after 2 appropriate anticonvulsive therapy approaches).
- …the seizures are conceived as impairing and an increase in life quality is expected after the intervention.
- …appropriate motivation is present in the patient.
- …the epileptogenic focus is well-operable.
- …progressive neuronal disease is not present.
Besides the respective procedure, there are non-respective ones like callosotomy (sectioning of the corpus callosum). At first, a partial (usually the anterior 2/3rds) sectioning is attempted. At seizure persistence, the complete sectioning of the corpus callosum can be performed as well. The goal is to section the interhemispheric pathways to prevent a generalized spread of the seizure. This can be accompanied by severe cognitive deficits.
Interventional stimulus therapy of epilepsy
Via a pacemaker system, amygdala-hippocampal or anterior-thalamic stimulation can occur. This can achieve a seizure reduction of up to 50% (Vonck et al., 2002).
Even if an absolute therapy is not possible, many patients feel better if they are relieved from the pharmacological side effects, and the collateral psychiatric (e.g., depressive) impairments can be improved.
Therapy of status epilepticus
The status epilepticus is a neurological emergency. It is defined as an epileptic externalization that lasts longer than 5 minutes or presents as a series of seizures, between which consciousness is not regained.
Thus, status epilepticus can occur in every epileptic condition. There is the non-convulsive status epilepticus or the absence-status. The grand mal status is considered life-threatening.
The therapy of the status epilepticus generally follows the coherent level scheme, which was mentioned above, concerning the termination of an epileptic seizure. Only in cases of absences or myoclonic seizures, phenytoin should not be given since it can worsen the situation.
Epilepsy while Driving
The greatest fear of the people affected is the continuation of their usual life. Many fear the uncertainty of new seizures and the resulting impairments. Particularly, driving cars (of course also riding bikes, motorcycles or driving ships) is a relevant subject.
The treating physician must inform the patient about the respective impairments in traffic. Likewise, it is a medical duty to be familiar with the respective legal guidelines: when owners of a driver’s license are affected, usually, a preliminary withdrawal of the driver’s license occurs.
However, the driving ban is not absolute and definitive, but can be reversed depending on the further progression of the condition:
- If the first seizure occurred unprovoked, the driver’s license is returned after 3–6 months without seizures.
- If the 2nd seizure occurred symptomatically or provoked, the driver’s license is returned after 3 months without seizures.
- If there is a 2nd seizure, or if epilepsy has been diagnosed, the driver’s license is returned after a year without seizures (independently of the therapy course or the therapy type).
- If persisting epileptic seizures occur, the driver’s license is not returned as long as a significant risk for further seizures is present.
Commercial drivers with a truck driver’s license and/or for personal transportation usually undergo a definite withdrawal of their driver’s license. If necessary, the person affected must change his/her job. If it can be proven that there was no seizure within 5 years without anti-epileptic treatment, the driver’s license can be returned.
If there is a reason to believe that a driving ban is being violated, we have to consider reporting it to the police.