Seizure Disorders Flashcards

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1
Q

What is a seizure and what is epilepsy

A

Seizures are a sudden uncontrolled electrical discharge of neurons in the brain that interrupts normal function.
•May be symptom of an underlying illness
•Any seizure resulting from a systemic or metabolic disturbance that is resolved when the underlying problem is corrected is not epilepsy.
• Epilepsy is a condition in which a person has spontaneously recurring seizures (even if a long interval separates each attack).

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2
Q

State ten causes of seizures
State three specifically in these age groups 2-20,20-30,after 50

A

V: vascular-Vascular, eg. cerebral infarction,AVM, Subarachnoid hemorrhage
Stroke
Hypertensive crisis
Increased ICP secondary to clogged shunt
I: infection-Encephalitis,sepsis,meningitis and inflammatory conditions, eg. herpes simplex, MS
T: trauma,temperature,toxins-Pyrexia ,Alcohol withdrawal, Drugs.eg. ciclosporin, lidocaine, quinolones, SSRIs, interferons, cocaine lithium withdrawal of amphetamines, anti seizure drugs ingestion,barbiturates, Brain trauma and surgery, Epidural hematoma
Subdural hematoma
Intracranial hematoma
Cerebral contusion
Traumatic birth injury
A: AV malformation.
D(diseases;Neural degenerative disorders. eg. Alzheimer’s, Developmental eg.neuronal migration abnormalities,harmatomas
•Hippocampal sclerosis, Heart, liver, lung, or kidney disease
Systemic lupus erythematosus
M: metabolic-Metabolic abnormalities, eg. porphyria, hypocalcaemia,hypoglycemia, Seizures can be induced by electrolyte disturbances such as hyponatremia, hypernatremia, hypocalcemia, and hypomagnesemia.(hyponatremia causes seizures by-too much water that dilutes the Na+ value. As a result, water moves into body cells, causing them to swell. This swelling causes a major problem in brain cells, which is a change in mental status that can progress to seizures or coma)

I: idiopathic-Genetic predisposition, Provoked seizures, eg.photosensitivity, sleep deprivation
N: neoplasm-Intracranial mass lesions, eg. tumour, neurocysticercosis

OTIS CAMPBELL(for drugs that cause seizures)
Organophosphates
Tricyclic antidepressants
Isoniazid, Insulin
Sympathomimetics Cocaine, Clozapine Amphetamines, Antiepileptics
Methylxanthines (theophylline, caffeine)
Phencyclidine (PCP)
Benzodiazepine/Barbiturate withdrawal
Ethanol withdrawal
Lidocaine
Lithium

First 6 months of life – severe birth injury, congenital defects involving the central nervous system, infections, and inborn errors of metabolism.

2 – 20 years of age – birth injury, infection, trauma, and genetic factors.

20 – 30 years of age – structural lesions, such as trauma, brain tumors, or vascular disease.

After 50 years of age – cerebrovascular lesions and metastatic brain tumors.

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3
Q

Seizures occur due to problems in a part of the brain. State the two main types of seizures and define them(part of brain affected and presence of aura or not)
What is Todd’s paralysis
Which type of airway adjunct is best in seizures?

A

Generalized
Partial

GENERALIZED SEIZURES: Involves both sides of the brain.
Bilateral synchronous discharges in the brain from the onset of a seizure.
Entire brain is affected.
Usually no warning or “aura”.

PARTIAL SEIZURES: Begins in a specific region of the cortex.
Caused by focal irritations.
Unilateral manifestation arising from a localized area of the brain.
Exception:
Partial seizures may spread to involve the whole brain leading to a generalized tonic-clonic seizure.
A tonic-clonic seizure that is preceded by an aura or warning is a partial seizure that generalizes secondarily.
Many tonic-clonic seizures sometimes appear to be primarily generalized, but the partial component can be missed.
Postictally, secondary generalized seizures can result in a temporary neurological deficit called Todd”s paralysis.

Nasopharyngeal airway adjunct

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4
Q

State the subtypes of generalized seizures

A

Subtypes
-Tonic-Clonic ( Grand Mal)
-Typical Absence(Petit Mal)
- Atypical absence
-Myoclonic
-Tonic
-Akinetic

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5
Q

What are the clinical manifestations of tonic clonic seizures

A

Clinical Manifestations:
Loss of consciousness.
Stiffening of the body for 10-20 sec. (Tonic. Tonic Latin means tone, tension. If muscles are tensed, they become stiff. So tonic seizures, stiffening of body)
Jerking movements of the extremities. (Clonic,clonic means muscle spasms or rapid relaxation and contraction of muscles. Spasms lead to jerking movements or shaking. So Clonic seizures cause shaking or jerking)
May appear cyanotic, have excess salivation, bite their tongue or cheek, and may experience incontinence.
During postictal phase(phase after the seizure. Ictal phase is during the seizure phase) , usually sore, tired, and confused; may sleep for several hours.

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6
Q

What are the clinical manifestations of absence seizures (typical and atypical)

A

-Abscence
Typical Absence (Petit Mal)
Usually occurs in children; rarely goes beyond adolescence.
May develop into another type of seizure.
3 Hz spike-and-wave discharge
Clinical Manifestations:
Brief staring spell lasting a few seconds.
Brief loss of consciousness.
May occur up to 100 times a day if untreated. (these children usually don’t do well in school)

Atypical Absence
Clinical Manifestations: Staring spells. Brief warnings.  Peculiar behavior during the seizure. Confusion after the seizure. Has other EEG changes
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7
Q

What are myoclonic seizures
What are tonic seizures?
What are akinetic seizures?

A

-Myoclonic seizures
Isolated muscle jerking

-Tonic Seizures
Intense stiffening of the body, not followed by jerking

-Akinetic or atonic Seizures
Cessation of movement,
falling
loss of consciousness

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8
Q

What are the subtypes of partial seizures
State their clinical features
(So in generalized seizures they lose consciousness but in partial seizures they don’t lose consciousness. Generalized seizure there’s no aura but in partial seizures they have an aura. Remember this by specialized aura. It’s not general. It’s specialized so partial)

A

-Simple or focal Partial seizures
Clinical Manifestations:
No loss of consciousness. Patient is Alert
Usually last < 1 minute.
May involve an alteration in motor, sensory, or autonomic system(Sensory nerve damage often results in tingling, numbness, pain, and extreme sensitivity to touch. Autonomic nerves control involuntary or semi-voluntary functions, such as heart rate, blood pressure, digestion, and sweating. Motor involves movement)
Eg. of focal motor seizure- Jacksonian.(Jacksonian seizure is a type of simple partial seizure characterized by abnormal movements that begin in one group of muscles and progress to adjacent groups of muscles.)

-Complex Partial Clinical Manifestations: Usually in the temporal lobe. Lasts > 1 minute. Assoc. with loss of awareness or altered consciousness  Psychomotor sx: Lip-smacking, continuing an activity before seizure began, or fumbling with objects. Psychosensory sx: vertigo, déjà vu, visual or auditory sensations, altered thought processes (Visual and auditory disturbances cause the temporal lobe is affected)
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9
Q

What are the phases of seizures and define each.

A

Prodromal Phase:
Sign or activity which precedes a seizure.

Aural Phase:
Sensory warning.

Ictal Phase:
Full seizure.

Postictal Phase:
Period of recovery after the seizure.

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10
Q

How do you diagnose seizures?
When should EEG be done when there’s a suspected seizure
How do you describe a seizure?(pofd)
State five diagnostic tests for seizures

A

Accurate and comprehensive description of the seizures
Patient’s health history.
Recent illness, trauma,
Medication (new and old and whether patient is compliant. If defaulted, ask how long patient has defaulted), and
Recent social activity such and change in consumption of drugs or alcohol.

EEG is a useful adjuvant to the history if it shows abnormalities.
EEG should be done within 24 hours of a suspected seizure

Correct classification of the seizure type - The choice of treatment depends on the classification of the type of seizure.

Physical Examination
Birth and developmental history, Significant illness and injuries, Family history, Febrile seizures, Comprehensive neurologic assessment.
Seizure History
Precipitating factors, Antecedent events, Seizure description (including onset, duration, frequency, postictal state. (POFD) )

Diagnostic Studies
CBC, electrolytes, LFP’s(local field potentials), fasting glucose, BUN, creatinine
Lumbar puncture for CSF analysis(do CT scan before LP in a seizure, meningitis,encephalitis)
Electroencephalography (EEG)
CT, MRI, MRA, MRS, PET (positron emission tomography) scan
We don’t do contrast CT in seizures. We only do contrast CT if we suspect there’s a tumor causing it.
You ought to do a BUEandCr before giving contrast dye cuz it can cause renal impairment

Do a Ct to rule out a tumor before doing Lumbar puncture cuz LP can cause Herniation of brain stem if there’s a tumor.
You can also do LP for a subarachnoid haemorrhage.

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11
Q

How do you asses seizures in the emergency (signs of seizures)
What health information is important to obtain during assessment ?

A

Tonic- Clonic seizures

In an emergent situation it is critical for the nurse to assess for the signs of an oncoming seizure, or symptoms that the patient is in the midst of a seizure episode in order to apply appropriate life saving interventions. Some of these symptoms include:
Presence of an aura
Loss of consciousness
Signs of bowel/bladder incontinence
Tachycardia, diaphoresis
Pallor, flushing or cyanosis
Confusion and headache
Signs associated with tonic, hypertonic, clonic and postictal phases of a seizure
Presence of repeated clonic tonic seizures for several minutes in a row

Health information that is important to obtain during an assessment would include:
the last episode of a seizure and any co morbidities related to it.
compliance with their drug regimen

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12
Q

How do you intervene in emergency for a seizure patient and after the seizure

A

Emergent interventions for our patient center around the ABC’s and prevention of injury which include:

Maintaining the patients airway - Position the patients head and body to one side to lessen the risk of aspiration. Assist with suctioning, oxygen therapy, and assisted ventilation as needed after the seizure episode ends.

Maintaining patient safety - If sitting or standing, clear the area around the patient and ease them down to the floor supporting their neck and head in your lap, and loosen any constrictive clothing.

Never restrain or force objects into the mouth of a person during a seizure. This can lead to further injury of the patient and possibly to the care giver.

Stay with the patient through the entire seizure episode and carefully observe the exact onset, and events that preceded it. Assessment of the course and nature of the seizure is critical in order to help diagnose the type of seizure, and identify subsequent treatment to follow.

Continued assessment of vitals and LOC after the episode has completed is important as well as providing explanation of events, reassurance, and a period of rest for the patient.

post seizure:
Regular meals and snacks in between if feeling shaky, faint, or hungry

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13
Q

When giving drugs for seizures what is the goal?

A

Therapy is aimed toward preventing seizure occurrence.
Anti-seizure drugs act by stabilizing nerve cell membranes and preventing spread of the epileptic discharge.
The principle for drug therapy is to begin with a single drug based on patient age, weight, type, frequency, and cause of the seizures and to increase the dosage until the seizures are controlled or until toxic side effects occur.

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14
Q

Name four drugs for tonic clonic and partial seizures and three for absence, myoclonic and akinetic seizures
What are the side effects of Valproic acid and carbamazepine

A

Carbamazepine
Phenobarbital
Phenytoin
Levetiracetam (keppra)
Valproic acid

The other types of seizures:
Valproic acid
Phenobarbital

Carbamazepine:
Ataxia, aplastic anemia, thrombocytopenia,

Valproic:
Hepatotoxicity, pancreatitis, hyperammonemia

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15
Q

A significant number of patients whose epilepsy cannot be controlled with drug therapy are candidates for surgical intervention
Some examples of surgeries are: limbic resection, multilobar resections, anterior temporal lobe resections, and amygdalohippocampectomy
True or false

OTHER THERAPIES:
Vagal nerve stimulation
Biofeedback

A

True

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16
Q

What is status epilepticus
What is refractory status epilepticus

A

ILAE Task force), 2015 new definition for SE
Seizure that is prolonged after initiation of mechanisms to terminate the seizure within 5 minutes

Refractory status epilepticus (RSE) that persists despite adequate administration of benzo. and at least one antiepileptic drug

17
Q

Why is SE life threatening
Which type of seizure is the most dangerous and why

A

Life Threatening Emergency
Brain uses enormous amount of energy.

Neurons may cease to function-brain damage.

Tonic-clonic is the most dangerous - hypoxia, cardiac dysrhythmias, hyperthermia, systemic acidosis, and death.

High morbidity and mortality

It is a manifestation of a disease so its mandatory to look for an underlying cause

18
Q

Which forms do SE present in?

A
  1. Convulsive SE-repeated generalized tonicclonic seizures with persistent postictal depression of neurologic function between seizures

2.Non convulsive SE-seizures produce a continuous or fluctuating “epileptic twilight” state

  1. Repeated partial seizures-focal motor signs, focal sensory symptoms, or focal impairment of function (e.g aphasia) not associated with altered awareness (epilepsia partialis continua).
19
Q

State two CNS consequences of SE

A

Prolonged status:
Damage to cerebral cortex, cerebellum, thalamus, amygdaloid body, hippocampus

Childhood status: May lead to hippocampal sclerosis
and complex partial seizures later in life

Mechanisms:
Reduced GABA Inhibition
Enhanced glutaminergic excitation
Calcium mediated cell damage

20
Q

State ten causes of SE

A

VASCULAR Causes:
STROKE
SAH(sub arachnoid haemorrhage)
SUB OR
EPIDURAL
VASCULITIS

Toxic causes:
Cocaine
Tricyclics
Anticholinerg.
Isoniazid
Withdrawal

TUMORS and ECLAMPSIA

INFECTIOUS causes:
MENINGITIS
ENCEPHALITIS
BRAIN
ABSCESS

METABOLIC causes:
HYPONATREMIA
HYPOGLYCEMIA
HYPOCALCEMIA
HYPO MG

21
Q

State six diagnostic tests for SE

A

Serum electrolytes
Ca, Mg
Glucose
Renal and Liver function testing
Antiepileptic drug levels
Toxicology screen

Neuroimaging: A noncontrast Brain CT should be considered for all SE patients once they have been stabilized

Lumbar puncture:
If you suspect CNS infection
Empiric antibiotic or antiviral therapy
Obtain CT

EEG monitoring:

Nonconvulsive SE.
Comatose after generalized seizure
Paralytics where neuro examination is impossible

22
Q

What are the first drugs of choice for SE
What other popular drug can be used?
What is it’s dosage? Stat and maintenance
What are the limitations of this drug

A

Benzodiazepines such as diazepam and lorazepam

Phenytoin-20mls/kg/min stat in a non glucose solution(it crystallizes in a glucose solution)

5ml/kg/min is the maintenance dose for phenytoin
Target level or max dose is 15-20mg/L

Limitations-
Rate limited to 50 mg/min (25 mg/min in the elderly and patients with cardiovascular disease)

Hypotension, due to the propylene glycol diluent.

QT prolongation, (causes arrhythmias)cardiac monitoring is recommended

Extravasation can be disastrous extensive necrosis, namely the “purple glove syndrome.” need large IV

23
Q

How does phenobarbital work?
What are the limitations of using phenobarbital

A

It works on (GABAA) receptor, similar to benzodiazepines.

Problems
Profound respiratory depression and hypotension from its vasodilatory and cardiodepressant effects.

long half-life, which can make complications difficult to manage.

24
Q

In refractory SE(remember that refractory sounds like an an aesthetic something so an aesthetic agents) what drugs are suggested to be used

A

midazolam-Midazolam preferred for continuous infusion in because of its short duration. Given to people you plan to intubate cuz the seizures aren’t stopping. Midazolam will make them sleep
barbiturate
propofol-GABA antagonist

25
Q

When do you avoid phenobarbital and valproate acid

A

avoid phenobarbital where the risk of hypotension or respiratory depression are significant
avoid valproate where there is a particular susceptibility to hyperammonaemia or hepatic failure (possibly in children with mental handicap)

26
Q

In trauma, what is the anticonvulsant of choice
Which drug is used as third line for alcohol withdrawal syndrome

Scenario: patient comes seizing. a.What drug will you give immediately?
b. It didn’t work. What do you give Again?
C. It didn’t work. What do you give again
D. It didn’t work. What do you give again

A

Phenytoin is the anticonvulsant of choice

Phenobarbital is used

A. Diazepam
B. Diazepam
C. Phenytoin
D. Give midazolam to knock patient out to intubate patient and stop seizures

27
Q

Respiratory and cardiac symptoms are the most common encountered adverse events with IV anticonvulsant
True or false

What are the complications of SE

A

Cerebral hypoxia
Direct neuronal death
Systemic effects such as:
Hypoxia
• Hypoperfusion
* Metabolic acidosis
* Hyperthermia
* Rhabdomyolysis
* Hypoglycemia

28
Q

What are the Interventions for emergency department, in-patient setting, or prehospital setting with trained paramedics for seizures within 0-5 minutes?

A

Time Line
0-5 Minutes
Stabilization
Phase
1. Stabilize patient (airway, breathing, circulation, disability - neurologic exam)
2. Time seizure from its onset, monitor vital signs
3. Assess oxygenation, give oxygen via nasal cannula/mask, consider intubation if respiratory assistance needed
4. Initiate ECG monitoring
5. finger stick blood glucose. If glucose < 60 mg/d then
Adults: 100 mg thiamine IV then 50 ml D50W IV
Children ≥ 2 years: 2 ml/kg D25W IV Children < 2 years: 4 ml/kg
D12.5W IV
6. Attempt IV access and collect electrolytes, hematology, toxicology screen, (if appropriate) anticonvulsant drug levels

Within 0-5 minutes
Obtain vital signs, establish airway, administer oxygen if needed.
Observe seizures briefly to ascertain that patient is really in status.
Draw baseline blood work (CBC, chemistry panel, antiepileptic drug levels), draw ABGs (for pO2 and pH), draw toxicology screen.
Quickly assess patient for signs of cardio-respiratory compromise, hyperpyrexia, focal neurologic signs, head trauma, CNS infection.

29
Q

What is the intervention from 6-9 minuted

A

Start IV infusion with saline solution.
Administer 100 mg thiamine, IV(for alcohol abusers)
Administer 50 ml of 50% glucose solution, IV, if blood sugar is low or unobtainable. Do not give glucose if blood sugar is normal or high.
Always have CPR equipment at bedside of a patient in status.

30
Q

What is the intervention from 10-45 minutes

A

Infuse lorazepam (Ativan), 0.1 mg/kg, at 2 mg/min.
Begin IV loading dose of fosphenytoin (Cerebyx), 20 mg PE/kg, at 150 mg/min.
Monitor patient’s B/P, pulse, EKG, and respirations while giving IV fosphenytoin and lorazepam.
Side effects: hypotension, arrhythmia, paresthesias, and respiratory depression.

31
Q

What is the intervention from 46-60 minutes

A

If seizures persist, intubate and give phenobarbital, 20 mg/kg, at 100 mg/min.
Never use Valium and phenobarbital sequentially in the treatment of status, unless the patient is intubated and in an ICU. Their hypotensive and respiratory depressant actions synergize. Serious and abrupt side effects can occur with these two drugs when given together.

32
Q

What is the intervention from 1 hour

Summary:
Benzo followed by a phenytoin is the way to go
IV phenoba. or valproate in special cases.
EEG

True or false

A

Frame Procedure
1 hour If seizures persist, the patient should be placed in a drug induced coma with pentobarbital, a benzodiazepine, or other anesthetic agent to prevent life threatening lactic acidosis, hypoxia, hyperthermia, and permanent seizure-induced neuronal damage.
The patient must be in an ICU, and outcome should be monitored and treatment guided by EEG with the goal being suppression of seizure activity on EEG.

True