• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/36

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

36 Cards in this Set

  • Front
  • Back

PRODROMAL PHASE:

subjective feeling or sensation that may serve as a warning sign of seizure onset for those who experience it

AURAL PHASE

considered an early part of the seizure

ICTAL PHASE

most people are familiar with and would identify as a seizure which manifests in different ways for each person with epilepsy

POST ICTAL PHASE

recovery period following a seizure where some people recover immediately, while others may require minutes, hours or days to feel like they’re back at their baseline.

Simple Partial Seizure

No impairment of consciousness. Usually last for 20-60 sec

Complex Partial Seizure

Most common and consciousness may be impaired. Usually last for 30 sec–2 min

Partial w/ Secondarily Generalized Seizure

Simple or complex that may evolve in generalize seizures

TONIC

Sudden stiffness or tension in the muscles of the arms, legs or trunk that lasts about 20 second

CLONIC

Repeated jerking movements of the arms and legs on one or both sides of the body, sometimes with numbness or tingling

Tonic-Clonic (Grand Mal)

Characterized by sudden loss of consciousness followed by sustained contraction of muscles (tonic – 1 min) then series of jerks (clonic-2-4min)

ATONIC DROP ATTACKS

Characterized by sudden loss of postural tone and head drops for few seconds or drop to ground.

EPILEPTIC SPASMS

sudden flexion, extension or mixed flexion-extension of proximal and truncal muscles, lasting 1-2 seconds

ABSENCE SEIZURES

Brief episodes of unconsciousness (4–20 seconds, usually <10 seconds) with no warning and immediate resumption of consciousness (no postictal abnormality).

GENERALIZED SEIURES (general onset)

Affects the whole brain.

Partial seizures ( focal brain region)

Begin foscally in the cortex

Epilepsy

common neurologic disorder affecting -0.5-1% of the population worldwide. • Characterized by recurrent seizures often accompanied by episodes of unconsciousness and / or amnesia.

Seizure

transcient alteration in behaviour because of disordered firing of groups od brain neurons.

Convulsion

involuntary, violent and spasmodic / prolonged contraction of the skeletetal muscle

Behavior arrest

characterized by a decrease in amplitude and/or rate or arrest of ongoing motor activity during the seizure. Because brief _________ is common and difficult to identify at the start of many seizures, the arrest must be persistent and dominant through the entire seizure.

Status epilepticus

Abnormal electrical activity in the brain that lasts longer than 5 minutes, or having more than 1 seizure within a 5 minutes period, without returning to a normal level of consciousness between episodes is called

Convulsive status epilictus

Status epilepticus with convulsions may be more likely to lead to long-term injury. Convulsions may involve jerking motions, grunting sounds, drooling, and rapid eye movements.

Nonconvulsive status epilictus

People with this type may appear confused or look like they're daydreaming. They may be unable to speak and may be behaving in an irrational way.

LENNOX-GASTAUT SYNDROME

A type of epilepsy with multiple different types of seizures, particularly tonic (stiffening) and atonic (drop) seizures.

LENNOX-GASTAUT SYNDROME

Intellectual development is usually delayed and often worsens over time. Behavioral problems, including hyperactivity, agitation, aggression and autism, are common.

Lennox-gastaut syndrome

is a type of “epileptic encephalopathy.”

Lennox-gastaut syndrome

Accounts for only 2 to 5% of childhood epilepsies.

Dravet syndrome

(Severe myoclonic epilepsy of infancy) is a rare genetic epileptic encephalopathy characterized by diverse generalized and focal seizure types, including myoclonic seizures, tonic-clonic seizures, absence seizures, atonic seizures, and one-sided hemi-convulsive and focal seizures.

Dravet's syndrome

are caused by mutation in the SCN1A gene, which is required for the proper function of brain cells.

Mild seizures

use of a single drug is preferred ( Monotherapy)

Hard-To-Control Seizures

multiple drugs are usually used simultaneously (Multidrug therapy) • Treatment is Palliative

temporal lobe resection

The most commonly performed epilepsy surgery is ___________ for mesial temporal lobe epilepsy; extratemporal cortical resection, when indicated, is less successful.

Convulsive status epilepticus

consisting of repeated generalized tonic-clonic seizures with persistent postictal depression of neurologic function between seizures

Nonconvulsive status epilepticus

persistent change in behavior or mental processes with continuous epileptiform EEG but without major motor signs

Focal status epilepticus

with or without altered awareness

IV Diazepam/Lorazepam is the DOC

For Absence Seizures going into status epilepticus:

Teratogenicity

Most women with epilepsy who become pregnant require continued antiseizure drug therapy for seizure control.