seizures / epilepsy / convulsions Flashcards

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1
Q

WHAT IS STATUS epilepticus ?

A

seizures lasting for >30min, or repeated seizures without intervening
consciousness. Mortality and the risk of permanent brain damage increase with the
length of attack

time threshold after which a seizure is considered SE differs according to the type of a seizure:
≥ 5 minutes for tonic-clonic seizures
≥ 10 minutes for focal seizures with impaired consciousness
10–15 minutes for absence seizures

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2
Q

what is the difference between seizure , epilepsy and convulsion?

A

seizure - abnormal electrical discharge in your brain
single seizure doesn’t mean you have epilepsy

Epilepsy is defined as having chronic seizures
characterized by a predisposition to seizures

convulsion - general term that people use to describe uncontrollable muscle contractions

Not all seizures are characterized by convulsions. if you have a seizure you can simply feel confused without a physical reaction

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3
Q

for epilepsy to be diagnosed what needs to be demonstrated ?

A

Two or more unprovoked or reflex seizures separated by more than 24 hours

or

unprovoked or reflex seizure in an individual with a high risk of subsequent seizures (e.g., after traumatic brain injury, stroke, CNS infections)

==========

A single seizure or multiple provoked or triggered seizures (e.g., febrile seizures) without an underlying predisposition to seizures do not suffice for the diagnosis of epilepsy.

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4
Q

what is the aetiology of seizures ?

A

Seizure triggers are stimuli that can precipitate seizures both in people with and without epilepsy.

Excessive physical exertion
Alcohol consumption
Fever (febrile seizures) 
Sleep deprivation
Flashing lights (e.g., strobe lights, video games)
Music 
Hormonal changes - after menopause
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5
Q

etiology of epilepsy ?

A

genetic

Genetic mutations affecting ion channels or transmitter receptors

Chromosomal abnormalities (e.g., Angelman syndrome, Prader-Willi syndrome, Rett syndrome)

Genetic metabolic disorders (e.g., PKU !!!!, congenital disorders of glycosylation, lysosomal storage diseases,

Mitochondrial diseases (e.g., MELAS)

============

structural - cerebral lesion or abnormality

Perinatal injury, e.g., hypoxic-ischemic injury 
Brain tumors and metastases 
Traumatic brain injury (TBI) 
Hippocampal sclerosis
Tuberous sclerosis

===========

Metabolic
Inborn errors of metabolism - PKU

============

Immune: autoimmune encephalitides

============

Infectious: chronic CNS infection (e.g., toxoplasmosis, malaria, neurocysticercosis) or complication of acute CNS infection

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6
Q

what is the classification of seizure according to location

A

1) location of abnormal activity

focal - Originates within the networks of a single hemisphere

Generalized - Originates from both hemispheres

Unknown

Focal to bilateral tonic-clonic: focal progresses to a tonic-clonic pattern (characteristic of bilateral brain involvement)

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7
Q

what are the different types of seizures according to clinical manfestation ?

A

Simple partial (focal)

no loss of consciousness

seizures or ‘auras’
“rising” feeling in your tummy – like the sensation in your stomach when on a fairground ride

can be motor - jerking movements of a foot, the face, an arm or another part of the body
sensory - hearing problems, hallucinations
unusual smells or tastes

Autonomic : may cause changes in blood pressure, heart rhythm, or bowel or bladder function
psychic

a feeling that events have happened before (déjà vu)

tingling in your arms and legs

=============

Complex partial (focal) seizures
 lose your sense of awareness and make random body movements, automatisms  such as:
smacking your lips
rubbing your hands
making random noises (grunting shouting)
moving your arms around
unresponive and have no memory of it 

==============

Tonic-clonic seizures
happen in 2 stages

============

Absence

================
Myoclonic seizures

================

Clonic seizures

===================

Tonic seizures

====================

Atonic seizures

======

febrile seizures

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8
Q

what are the different types of epilepsy ?

A

Reflex epilepsy

Epilepsy in which seizures are consistently provoked by a certain trigger (e.g., lights, music, hormonal changes during menstrual cycle). Subtypes can be determined based on the trigger and include:
Photosensitive epilepsy
Musicogenic epilepsy
Catamenial epilepsy

=========

Drug-resistant epilepsy: epilepsy in which at least two antiepileptic drugs have failed to prevent seizures

=========

Resolved epilepsy

age‐dependent epilepsy syndrome that has not recurred in individuals who are now past the applicable age.

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9
Q

Under generalised onset seizures what are the common symptoms of all the types of seizures

A

Symptoms are produced by bilateral cerebral cortex disturbances.
Start with loss of consciousness.
Patients do not recall the seizure.

Aura is uncommon

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10
Q

clinical manifestation of Tonic-clonic seizure (grand mal) ?

A

ICTAL

Prodromal symptoms
sleep disturbances, lightheadedness, mood changes, anxiety/irritability, impaired concentration

Loss of consciousness (sudden and without warning)

Motor symptoms

1) Tonic phase
Generalized muscle contraction: muscles go stiff
!! ROTATED EYES, APNEA, LATERAL TONGUE BITING !!
pooled oral secretions, cyanosis,
Increased sympathetic tone: dilated, unresponsive pupils,
↑ heart rate,
↑ blood pressure

=====

Clonic phase: rhythmic muscle twitching

=========

Bladder or bowel incontinence

Usually lasts 1–3 minutes

============

POST - ICTAL

Unresponsiveness - last a few seconds or up to an hour

Confusion
Amnesia of the event
Aphasia
Fatigue
Muscular flaccidity and muscle pain
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11
Q

clinical manifestation of clonic seizure ?

A

ICTAL

Loss of consciousness - if general

Bilateral rhythmic jerking (of the entire body or only a part)

typically lasts a few minutes

=======

post - ictal

Amnesia of the event

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12
Q

Under generalised motor seizures, what are the clinical manifestation of tonic seizure ?

A

ICTAL

Often occurs when the patient is drowsy, asleep, or after waking

Loss of consciousness

Muscle stiffening (extension or flexion of the head, trunk, and/or extremities)

can be bilateral or unilateral
Can be accompanied by

autonomic symptoms (e.g., tachycardia, flushing)

This might mean you lose balance and fall over

Can be followed by atypical absence seizure

===========

POST ICTAL

Amnesia of the event
Drowsiness or confusion may occur

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13
Q

Under generalised motor seizures, what are the clinical manifestation of myoclonic seizure ?

A

Positive myoclonus: sudden jerk-like muscle twitching

Negative myoclonus: a brief loss of muscle activity during tonic contraction of a muscle

can affect the entire body or only a part.

Myoclonic seizures
often happen soon after waking up.
normally remain awake during them

only last a fraction of a second, but several can sometimes occur in a short space of time.

are nonrhythmic (i.e., jerks occur at different intervals) and irregular (i.e., jerks are asymmetric and may change laterality)

==========

post ictal

amnesia

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14
Q

Under generalised motor seizures, what are the clinical manifestation of

1) myoclonic - atonic seizure ?
2) Myoclonic-tonic seizure?
3) Atonic seizure (also known as “drop seizure” or “drop attack”?

A

ICTAL

1) Myoclonus followed by a brief loss of tone
2) Myoclonus followed by a brief increase in tone
3) Sudden loss of muscle tone: sudden head drop or collapse (lasts < 15 seconds)

===========

post ictal

amnesia

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15
Q

clinical manifestation of Typical Generalized nonmotor seizure (absence seizure)

A

Sudden onset and stop

They mainly affect children

you lose awareness of your surroundings for a short time.

stare blankly into space
look like they’re “daydreaming”
blank stare, unresponsiveness
with sudden stop in motion

Subtle automatisms (often go unnoticed): lip-smacking, eye fluttering, or head nodding are common.

may fall to the ground.

======
Can occur several hundred times a day and usually lasts < 10 seconds
tend to be very brief and They can happen several times a day.

=========

post ictal

awareness returns rapidly, without any impairment
Amnesia is common

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16
Q

clinical manifestation of ATypical Generalized nonmotor seizure (absence seizure)

A

Gradual onset and stop

Interrupted motion or activity, blank stare

Patients may be responsive

Automatisms: lip-smacking, eye fluttering, chewing

Small hand movements (e.g., rubbing of the fingers)

Longer than typical form (10–30 seconds)

==========

post ictal

awareness returns rapidly, without any impairment
Amnesia is common

17
Q

what is the diagnosis of seizures ?

A

important to distinguish between focal/bilateral tonic-clonic seizures and generalized tonic-clonic seizures, as they manifest similarly but are managed differently.

==========
CONFIRMATION OF SEIZURE

History
description of the event by the patient (aware seizure) and/or witnesses (seizure with impaired awareness)
Potential triggers (e.g., sleep deprivation, excessive alcohol intake)
Prodromal symptoms (e.g., aura)
Ictal symptoms
Postictal symptoms

Past medical history
History of epilepsy
History of other potential underlying conditions (e.g., head trauma, stroke, tumor, CNS infection)

Physical examination: attention should be paid to visual inspection e.g., for bruises from falls, tongue bites, phakomatosis-specific skin manifestations and evaluation for cardiovascular disorders

==========
EEG

Performed in individuals who present with first seizure, with insufficient information for seizure classification

During the seizure (ictal)
Epileptiform discharges (e.g., spikes, sharp waves, spike waves) are usually detected.

3 Hz spike-and-wave in typical absence seizures

  • After a seizure or between seizures (postictal or interictal)

=======

Video-EEG telemetry in hospitalized patients

Continuous EEG in ambulatory patients

===============

Evaluation for underlying conditions

ECG: Rule out cardiogenic causes (e.g., cardiac arrhythmias resulting in cerebral hypoxia)

MRI: Modality of choice for investigating potential underlying structural abnormalities.
All patients with first-time focal seizures

Angiography: if vascular cause (e.g., cerebral arteriovenous malformation) is suspected

laboratory screening: to identify metabolic disorders and infectious diseases, if suspected
Blood
CBC
Glucose!
Electrolytes!
Prolactin 
Toxicology screening!

In adults, an isolated unprovoked focal or focal to bilateral tonic-clonic seizure typically indicates a structural or metabolic origin and should receive further evaluation

18
Q

dd

A

patient be pregnant - If so, eclampsia check the urine and BP: call a senior obstetrician—immediate delivery
may be needed

=========

Psychogenic nonepileptic seizures

Female sex
Psychiatric disorders (e.g., obsessive-compulsive disorder, posttraumatic stress disorder)
History of physical or sexual maltreatment
Substance use

Usually occur in presence of eyewitnesses
Generalized asynchronous motor activity
Forced eye closure

Tongue-biting and other types of self-injury are rare.
Awareness is usually unimpaired
Individuals with PNES can recall the event

Typically > 5 minutes

diagnostics - Video-EEG monitoring

=============

Panic attack

due to Genetic predisposition
Anxiety disorders
Stress

Palpitations
Chest pain
Sweating
Dyspnea

Seconds to hours

===========

Syncope

trigger - Emotional stress
Pain
Sudden changes in body position
Dehydration

Transient loss of consciousness and muscle tone
Prodromal symptoms
Dizziness
Palpitations
Pallor
Sweating

1–2 minutes

19
Q

what is the management of seizures?

A

to terminate seizures lasting more than a few minutes as soon as possible (<20min) because brain damage increases

Seizures are usually self-limiting and may not require administration of antiseizure drugs.
Long-term therapy with antiepileptic drugs is required for individuals who meet the criteria for epilepsy

===========

Acute management

A-E

chin lift head thrust - look for airway obstruction - suction or finger sweep

adjuncts as necessary
Oropharyngeal airway
Nasopharyngeal airway

Place the patient in the recovery position to prevent injury.

call for help early using an appropriate SBARR handover structure.

====

B - give 100 percent oxygen and suction as required

=====
C - IV access
take blood: U&E, LFT, FBC, glucose, Ca2+ Toxicology screen if indicated

check glucose levels !!!

=======

Remove cause or provoking factors (e.g., cessation of recreational drug use, treatment of underlying disorders)

========
Acute seizures are usually self-limiting and do not require pharmacological treatment.

If a seizure has not ceased after 5 minutes (indicating status epilepticus), the patient should receive antiseizure medications, starting with benzodiazepines
(lorazepam 4mg) as a slow bolus into a large vein, midazolam, or clonazepam)
IV route is preferred.
if not rectal route
if not Buccal midazolam

Give 2nd dose of lorazepam if no response after 10–20min

========

Stage 2
40 minutes after the onset of a seizure or after stage 1 treatment failed: a single dose of IV phenytoin or valproic acid

WITH MONITORING OF BP and ECG

=======

Stage 3
60-90 minutes after the onset of seizures or after stage 1 and 2 treatment failed): induction of coma with IV propofol, midazolam, thiopental,
BUT WITH EXPERT HELP

and ventilation with continuous EEG monitoring in ICU. NB: never spend longer than 20min on someone with status epilepticus without having help at the bedside from an anaesthetist

20
Q

what are the first line and second line treatment for Focal seizures ?

A

LAMOTRIGINE

LEVETIRACETAM

PHENYTOIN

====

second line

gabapentin
valproate

21
Q

what are the first line treatment for generalised seizures ?

A

TONIC-CLONIC

Lamotrigine
Valproate

=============

MYOCLONIC
ATONIC
ATYPICAL ABSENCE

Valproate
Lamotrigine
Topiramate

==========

TYPICAL ABSENCE

Ethosuximide
Valproate

22
Q

how is drug resistant epilepsy managed ?

A

nonpharmacological methods (e.g., with surgery, neurostimulation, ketogenic diet).

23
Q

how is termination of a seizure concluded ?

A

evaluated on a case‑by‑case basis

considered if the patient has < 2 seizures/year, an inconspicuous provocation

EEG, normal psychological findings, and no hereditary predisposition

Generally possible after 2–5 seizure‑free years with normal EEG results

24
Q

complication of epilepsy?

A

acute
Hyperthermia,
cardiorespiratory deficits, and excitatory toxicity potentially causing irreversible tissue damage (especially to the CNS; e.g., cortical laminar necrosis) and, in turn, increase the risk of further seizures.

Tongue biting
Posterior dislocation of the glenohumeral joint from falling

Long‑term
Psychiatric
Anxiety
Depression and risk of suicide

Sleep disturbances and insomnia

Sudden unexpected death in epilepsy

25
Q

difference between myoclonic and clonic seizure

A

clonic seizures are rapid rhythmically recurrent events, whereas myoclonic seizures are single or irregularly recurrent events

26
Q

if alcohol or malnourishment suspected cause for seizure ?

A

thiamine 250mg IV over 30min