epilepsy Flashcards

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1
Q

What are common triggers/precipitants for seizures?

What are the common facilitators of seizures in susceptable individuals?

A

Obligatory triggers: flashing lights, hyperventilation

Facilitators: stress, alcohol, febrile illness, sleep deprivation

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2
Q

What is the difference between epilepsy and seizures?

A

Epilepsy is a condition where brain disorders predispose to seizures.

seizures are the clinical manifestation of abnormal, excessive excitation of cortical neurons. Excessive excitation can be brought on by many things including epilepsy, drug intoxication or metabolic problems

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3
Q

If you suspect a patient has epilepsy, what disorders must you keep on the differential?

A

syncope attacks from orthostatic hypertention (but jerks can make it look like seizures)

cardiac arrhythmias - can lead to syncope

migraine - basilar migrane can make someone lose consciousness

hypoglycemia

narcolepsy

pain attacks

pseudoseizures

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4
Q

What patient populations have high incidences of epilepsy? What is the most common etiologies in each population?

A

children - developmental abnormality

elderly - strokes and scars from strokes

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5
Q

What is the concept of kindling in regards to epilepsy?

A

Seizures may be progressive and the number of foci might grow over time if not treated

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6
Q

What are the two main categories of epilepsy? How is the onset of the seizures different? How is the etiology different?

A

1) generalized epilepsy: seizure starts diffusely all over the brain at once. Usually due to genetic defect.
2) focal epilepsy: seizure starts at a particular focus in the brain. Can be due to trauma, infection, tumors, stroke or unknown

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7
Q

What are the types of seizures seen in generalized epilepsy? What are the types of seziures seen in focal epilepsy?

A

Generalized: absence seizures (“petit mal”), myoclonic jerks, primary generalized tonic-clonic seizures (“grand mal”)

focal: temporal, occipital, frontal lobe seizures, secondary generalized tonic-clonic seizures. Focal seizures can be simple (no loss of awareness) or complex (loss of awareness).

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8
Q

What are some of the common auras at the beginning of epileptic seizures?

A

sudden intense fear

deja vu

olfactory or gustatory hallucinations

rising abdominal sensation

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9
Q

What are the clinical findings in a generalized tonic-clonic seizure (grand mal seizure)?

A

generalized spikes on EEG

no auras (because no focus)

last for 2-3 minutes

post-ictal (post-epileptic episode) period of confusion

don’t remember the event

Tonic phase - The patient will quickly lose consciousness, and the skeletal muscles will suddenly tense, often causing the extremities to be pulled towards the body or rigidly pushed away from it

Clonic phase - The patient’s muscles will start to contract and relax rapidly, causing convulsions

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10
Q

What are the clincial findings in an absence seizure?

A

sudden behavioral arrest

staring, unresponsive

abrupt onset and abrupt return to normal

don’t remember the event/pick up conversation right where they left off/don’t know they had an episode

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11
Q

What are the clinical features of juvenile myoclonic seizures?

A

affect adolescents

myoclonus in the morning (makes them drop things)

usually a family history/genetic

initially exhibit myoclonic seizures, then absence seizures and generalized tonic-clonic seizures

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12
Q

What are the areas of the brain that are most prone to epilepsy?

A

amygdala, hippocampus, enterorhinal complex (all three are in the medial temporal lobe)

Temporal lobe seizures are most common

frontal lobe seizures are 2nd most common

occipital lobe seizures are rare

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13
Q

What is Todd’s postictal paralysis/Todd’s paresis?

A

The parts of the brain that have a seizure can be paralyzed for hours to days after the seizure. This leads to a transient weakness of a hand, arm, or leg after partial seizure activity within the motor cortex. The weakness may range in severity from mild to complete paralysis.

Must be distinguished from a stroke!

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14
Q

How does mesial temporal sclerosis present? What is the pathogenesis of MTS? What is the treatment?

A

MTS presents as temporal lobe epilepsy with an aura of rising stomach sensation, lip smacking and impaired consciousness.

Pathogenesis is neuronal loss in the hippocampus that forms a glial scar. The scar is the focus of the seizures. These seizures are commonly intractable so the treatment is to excise the glial scar.

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15
Q

Patients are usually not aware when then get bilateral seizures. What is the exception to this?

A

Frontal seizures can be bilateral but the patient is aware.

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16
Q

What are the characteristics of benign Rolandic seizures?

A

Usually affect children but resolve by adolescence

unilateral paresthesias involving the lip, cheek and tongue

unilateral clonic activity involving the face, lip and larynx causes speech arrest

Drooling

intact consciousness before secondary generalization

Onset is usually shortly after falling asleep

17
Q

What are the characteristics of West Syndrome? What is the treatment?

A

Infantile seizures that cause

18
Q

What is the difference between a simple partial seizure and a complex partial seizure?

A

patients do not have impaired consciousness during a simple partial seizure but will have impaired consciousness during a complex partial seizure

19
Q

What are the types of generalized seizures?

A

atonic

tonic-clonic

clonic

tonic

myoclonic

absence

20
Q
A