Seizures and Epilepsy

Karl E. Misulis, MD, PhD



Seizure evaluation and management is a core function of the hospital neurologist. Most patients with seizures can be evaluated on outpatient basis, and admission purely for diagnosis of a single seizure is usually not needed. However, we do admit individuals in whom we fear an underlying cause that deserves rapid attention, if there is a prolonged postictal state, or if a patient fails to return to baseline.



OVERVIEW


Spectrum of Clinical Seizures


Classifications of seizures evolve, but generalized and focal seizures continue to be broad categories of interest at initial presentation. The International League Against Epilepsy (ILAE) classification of epilepsies is presented later in this chapter in the section entitled “Epilepsy.” The clinical description in the list presents the seizure types most commonly seen in the hospital setting:



Generalized tonic-clonic seizure


Generalized motor activity usually with generalized tonic posturing then clonic activity. This is usually followed by limp unresponsiveness and labored respiration at termination. There is no focal motor activity at onset. However, some asymmetry, including forced head turning at onset, could still be consistent with a generalized onset.


Focal seizure evolving to a bilateral, convulsive seizure


Focal seizure leading to bilateral motor activity, usually with tonic then clonic activity (but there could be preceding clonic activity). The transition usually includes tonic or clonic activity and forced head turning contralateral to the side where seizures start. The postictal state is similar to what is seen with a generalized onset tonic-clonic seizure.


Focal motor seizure without evolution to generalized tonic-clonic activity


Focal motor activity, usually clonic but could be tonic or dystonic in appearance. The term is usually used for seizures that do not affect consciousness.


Focal seizures with impairment of consciousness or awareness (complex partial seizures or discognitive seizures)


These may start with an aura or with altered awareness/consciousness. There could be total loss of awareness and responsiveness or only subtle confusion or slowing of responses. There may be motor manifestations such as lip smacking/chewing motions (with temporal involvement), fumbling/picking motions, and dystonic posturing of one or more extremities.


Differential Diagnosis of Seizure


The differential diagnosis of clinical seizures includes epileptic seizures versus nonepileptic psychogenic events versus nonepileptic physiological events. Syncope is the most common physiological event in the differential diagnosis.



Epileptic seizure


Seizures can vary considerably in clinical manifestations. If seizure is captured on electroencephalogram (EEG), there will be an associated ictal discharge, but EEG changes may not be seen with a focal motor seizure with preserved awareness. Diagnosis is supported by abnormal interictal EEG, but interictal abnormality is not necessary.


Nonepileptic psychogenic events (also called nonepileptic psychogenic seizures or pseudoseizures)


Atypical clinical features (below).


EEG during an episode is normal or only shows movement and muscle artifact. Long-term recording is sometimes needed.


Syncope


Commonly associated with multifocal myoclonus and even with tonic posturing. Myoclonus is usually of short duration, less than 15 seconds.


Movement disorder (tremor, myoclonus, asterixis, hemiballismus)


Movement disorders with positive motor manifestations can be mistaken for seizure if episodic or episodically worse (e.g., myoclonus from metabolic derangement, paroxysmal dyskinesia). Negative myoclonus can also be seen with toxic-metabolic encephalopathy, most commonly hepatic. Acute onset of a hemiballismus from infarction can also be mistaken for seizure.



Differentiation of epileptic seizure from psychogenic nonepileptic event is crucial and often difficult (see Table 19.1).




Table 19.1 Differentiation of epileptic seizure from psychogenic nonepileptic event



































Feature Epileptic seizure Psychogenic nonepileptic seizure
Motor activity Unilateral or bilateral synchronous. Often alternating or asynchronous extremity motions, forward pelvic thrusting, large amplitude side-to-side head motions
Consciousness May be partially or totally preserved with focal seizures, completely lost with generalized tonic-clonic seizures. May be responsive during generalized convulsive seizure. May resist eye opening while unresponsive.
Eye exam

Usually pupillary dilation.


Eyelids passive. No resistance to eye opening.


Normal or dilated pupils.


Often difficult to examine because of forced eye closure or upturning of the eyes. Almost always some resistance to passive eye opening.

Continence Incontinence often occurs with generalized seizure Incontinence often reported but uncommon on examination after an event. This is not a helpful differentiating historical feature.
EEG Electrographic seizure activity but may be at least partly obscured by movement artifact. Normal or muscle/movement artifact. May be difficult to rule-out electrical seizure if muscle artifact dominates the EEG or if there is prominent rhythmic artifact.
Prolactin level Often elevated briefly after generalized tonic-clonic seizures. Normal.
Provocation Usually unprovoked, but can be provoked by injury, stroke, brain infection, and, in patients with epilepsy, can be triggered by stress, illness, sleep deprivation, and certain medications. Often precipitated by stressful situation.

Hospital neurologists are often asked to differentiate seizure from syncope (see Table 19.2).




Table 19.2 Differentiation of seizure from syncope































Feature Seizure Syncope
Motor activity Longer duration, more that 15 seconds. Brief multifocal myoclonus, lasting less than 15 seconds.
Position No positional provocation. Upright posture or sitting, if there is an orthostatic component.
Appearance Normal color, flushed, or cyanotic with long-duration. Pale at onset.
Post-episode appearance Often lethargic and confused for minutes Post-episode disorientation is brief, if present at all.
Vital signs Often tachycardic and hypertensive during and shortly after the episode. Hypotensive during the episode but normotensive or even hypertensive after.
Prolactin level Often briefly elevated after a generalized tonic-clonic seizure and to a lesser extent after a focal seizure involving the temporal lobe. Often elevated after syncope; this is not a differentiating feature.

Vital signs are particularly problematic, since the report is frequently given that BP was normal or elevated after syncope is over. Determining timing and patient status at the time of the vital signs is key.


Prolactin levels are not as helpful as we would like, partly because of the brief time of elevation and the multitude of other reasons for prolactin elevation. Prolactin does not help in the distinction of seizure and syncope because it can be increased after both. Prolactin is usually not increased with psychogenic nonepileptic seizures unless elevated for another reason. Meds that can give elevated prolactin levels include select antipsychotics, antidepressants, antihypertensive meds (e.g., verapamil), opiates, and H2 antagonists.1


The summary statement of the Therapeutics and Technology Assessment Subcommittee reports that elevated prolactin measured 10–20 minutes after a seizure can be an adjunct in differentiating generalized tonic-clonic and complex partial seizure from psychogenic nonepileptic seizure.2


Symptomatic Seizure


The epilepsies will be discussed in detail in the section entitled “Epilepsy.” Here, we are considering seizures, which are symptomatic of another medical condition in hospitalized patients. Features of some important symptomatic seizures are shown in Table 19.3.




Table 19.3 Symptomatic seizures
































































Disorder Type Elements
Trauma Closed head injury Seizures occur acutely and/or remotely from the injury. Acute seizures are less likely to result in long-term seizure disorder. Late seizures predict development of epilepsy.
Penetrating injury Acute seizures are common in this setting, and recurrence is very frequent; the risk of epilepsy is increased 580 times
Infection Encephalitis HSV: Seizures and encephalopathy with febrile presentation.
Meningitis Seizures can occur with meningitis but less so than with encephalitis.
Sepsis Seizures with sepsis must have CNS infection ruled-out, but the seizures are usually secondary—medications, vascular.
Prion disease Seizures may occur with myoclonus and dementia
Autoimmune encephalitis Limbic encephalitis

Anti-NMDA receptor encephalitis: seizures with psychiatric symptoms, often with ovarian teratoma


Anti-voltage-gated potassium channel-complex antibody encephalitis: may start with very brief facio-brachial dystonic seizures. May be associated with hyponatremia, episodic bradycardia, neuromyotonia, increased sweating


Other limbic encephalitides (anti-GABAB receptor, anti-AMPA receptor, anti-GAD, onconeural antibody encephalitis)


Limbic encephalitis can be a paraneoplastic condition, most commonly with small cell lung cancer

Metabolic Electrolyte

Hypernatremia: Weakness, lethargy, seizures, coma.


Hyponatremia: Nausea, vomiting, encephalopathy, seizures, respiratory failure.

Glucose

Hyperglycemia: focal seizures are common


Hypoglycemia: autonomic symptoms with confusion, agitation, tremor, generalized convulsive seizure.

Hepatic Acute failure: Confusion, inattention, delirium, tremor, asterixis, lethargy, coma. Seizures may occur but are not the most prominent finding.
Renal Confusion, encephalopathy, tremor, myoclonus, asterixis, seizures, which may be generalized or focal.
Medications and toxins Antibiotics Multiple antibiotics can trigger seizures in individuals with low seizure threshold (e.g., cefepime, meropenem).
Chemotherapeutics PRES can develop from some chemotherapies producing seizures and encephalopathy.
Antiepileptics Seizures can be a manifestation of toxicity with several seizure medications in patients with epilepsy, particularly phenytoin. Tiagabine may trigger nonconvulsive status epilepticus in individuals who do not have epilepsy.
Neoplastic disease Brain tumors

Low-grade brain tumors can present with seizures. The risk of recurrence is very high, and these patients can be considered to have epilepsy.


High-grade tumors are less likely to present with seizures; focal symptoms are more common.

Metastases Seizures with known cancer can be from metastases, but also consider medications and metabolic causes.
Non-neurologic tumors Limbic encephalitis: These may present with seizures, most commonly focal from the temporal lobe, but there is often associated memory deficit or psychotic features.

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May 14, 2017 | Posted by in NEUROLOGY | Comments Off on Seizures and Epilepsy

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