Anti Epileptic Flashcards

(37 cards)

1
Q

What is a seizure

A

sudden irregular discharge of electrical activity in the brain causing a physical manifestation such as sensory disturbance, unconsciousness or convulsions

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2
Q

What is a convulsion

A

uncontrolled shaking movements of the body due to rapid and repeated contraction and relaxation of muscles

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3
Q

What is an aura

A

a perceptual disturbance experienced by some prior to a seizure, e.g. strange light, unpleasant smell, confusing thoughts

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4
Q

What is epilepsy

A

neurological disorder marked by sudden recurrent episodes of sensory disturbance, LOC or convulsions, associated with abnormal electrical activity in the brain

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5
Q

What is status epilepticus

A

epileptic seizures occurring continuously without recovery of consciousness in between

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6
Q

How can seizures be classified

A

-

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7
Q

Compare partial vs generalised seizures

A

Partial happens in a single focus - one part of the brain. Generalised - seizure all over the brain - might start as a focus nd the spread uncontrolled throughout the brain

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8
Q

What are partia lseizures

A

PARTIAL SEIZURES • Part of the brain
• Simple or complex – Simple = Same consciousness - no loc
– Complex —> COnsciousness is iMPaired - loc

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9
Q

What are common types of partial seizures

A

• Temporal lobe epilepsy
– 1st/2nd decade in most people, following seizure with fever or an early injury to the brain
– auras –e.g. auditory hallucination, rush of memories
• Frontal lobe epilepsy – next most common
- Abnormal movements when motor areas affected (contralateral side)

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10
Q

What are types of generalised seizures

A
  • Tonic-clonic: 2 parts - 1st tonic (muscles Tense), 2nd clonic (Convulsions)
  • Absence:‘daydreaming’
  • Statusepilepticus:medicalemergency
  • Myoclonic:briefshock-likemusclejerks
  • Atonic:‘without tone’ – drop attack
  • Tonic:increasedtone
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11
Q

What are the vestigatins to confirm/exclude diagnosis

A

INVESTIGATIONS
• Clinical history • EEG
• MRI
• (ECG,bloods)

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12
Q

What should be asked about when asking a history abt seizure

A

Before

  • pmh, fh
  • triggers
  • auras
  • first sign/symptoms

During

  • description of seizure
  • duration
  • abrupt or gradual Ed

After

  • post-coal state
  • tongue biting
  • incontnence
  • neurological defecit

Vial to take collateral history where possible

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13
Q

What are causes of epilepsy

A
• Can be primary or secondary
• Primary (idiopathic) 
– No apparent cause 
– May be inherited
• Secondary (symptomatic)
– Known cause for epilepsy
  • Vascular:Stroke,TIA
  • Infection: Abscess, Meningitis
  • Trauma:Intracerebralhaemorrhage
  • Autoimmune:SLE
  • Metabolic:Hypoxia,Electrolyteimbalance, Hypoglycaemia,Thyroid dysfunction
  • Iatrogenic: Drugs, Alcohol Withdrawal
  • Neoplastic:Intracerebralmass
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14
Q

What is an eeg

A

EEG
• EEG not diagnostic - supports diagnosis
• In first unprovoked seizure – assess risk of seizure recurrence (unequivocal epileptiform
activity on EEG)
• Standard EEG assessment involves photic stimulation and hyperventilation - patient warned that it may induce a seizure
• Do NOT use if:
– Probable syncope (risk of false positive result)
– Clinical presentation supports diagnosis of non-epileptic event – In isolation to make a diagnosis of epilepsy
• Ifunclear,consider:
– Repeated standard EEGs
– Sleep EEGs (sleep deprivation or melatonin in children/young people) – Long-term video or ambulatory EEG

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15
Q

What are other investigations

A

OTHER INVESTIGATIONS
• To exclude other suspected causes of seizure • ECG as standard in adults
• MRI – in all patients with new-onset seizures

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16
Q

What are some classes of anti epileptic drugs

A
  • Na channel blockers • GABA potentiators • Ca channel blockers
  • Other drugs affecting GABA • Levetiracetam
17
Q

How to Na+ channels work and what are some examples

A
• Cause Na channels to remain in an inactive state
• Prevent axons from firing repetitively
• Examples
– Carbamazepine
– Phenytoin
– Lamotrigine
– Sodium valproate – Topiramate
18
Q

What are ccbs and how do they work

A
CALCIUM CHANNEL BLOCKERS
• Prevent activity of Ca channels
• Prevent depolarisation causing “spike and wave” discharge 
• Used in absence seizures
• Examples
– Ethosuximide
– Sodium valproate
19
Q

What are gaba potentiators and gaba

A
• GABA = inhibitory neurotransmitter, so rapidly alters excitability
• Involved with neurotransmitter modulation in a third of brain impulses
• GABA potentiators enhance the effect of GABA at the synaptic junction
– Examples
• Barbiturates (Phenobarbital)
• Benzodiazepines (Midazolam)
• GABA-transaminase inhibitors 
– Prevent breakdown of GABA 
– Vigabatrin
• Increased GABA production
– Improve utilisation of glutamate 
– Gabapentin
20
Q

What is levetiracetam

A

• Trade name Keppra
• Binds to synaptic vesicles (SV2A glycoprotein)
to inhibit pre-synaptic calcium channel activity
• Therefore, inhibiting neurotransmitterrelease from the pre-synaptic neuron

21
Q

When would antiepileptic be considered for use

A

• Epilepsy specialist/neurologist once diagnosis confirmed
• Considered if first unprovoked seizure and…
– Neurological deficit
– EEG shows unequivocal epileptic activity
– Risk of a further seizure is unacceptable
– Imaging reveals a structural abnormality
• Take into account the seizure type, patient’s age, lifestyle and preferences

22
Q

How are antiepileptics initiated

A

• Start with monotherapy and if ineffective change to monotherapy with different AED
• First-line for generalised or tonic-clonic seizures – sodium valproate (or lamotrigine)
– If ineffective, other adjuncts considered (e.g. Levetiracetam, topiramate or sodium valproate AND lamotrigine)
• Titrate up to achieve a balance of therapeutic effect vs adverse side effects

23
Q

What are ways anti epileptics can interact with other drugs

A
• Beware of interactions
– Liver enzyme inducers 
• Carbamazepine
• Phenyotin
– Liver enzyme inhibitors
• Sodium valproate
24
Q

What are some side effects of aeds

25
Why may aeds be changed
• Change if unacceptable side effects, failure of treatment or on inappropriate drug • Start at initial dose and slowly increase to middle of recommended therapeutic range • Then slowly withdraw old drug over about 6 weeks Keep patient on the drug, start a new one, slowly titrations up until middle of therapeutic range, then take the old one away. Want them to overlap - initial one may have had some kind of effect
26
When might aeds be stopped
• Consider if patient seizure free for at least 2 years – 60% will have no further seizure when medication withdrawn • However, bear in mind the increased risk of seizure compared to those who continue on treatment – Epilepsy since childhood – Patients on more than one drug – Myoclonic or tonic-clonic seizures – Abnormal EEG in last year – Known underlying brain damage • Need to think about patient’s livelihood • DVLA recommends no driving for 6 months after stopping medication
27
How are aeds stopped
CESSATION OF ANTIEPILEPTICS • Gradually taper off • Aim is to avoid withdrawal features – Recurrent seizures – Anxiety and restlessness • Lamotrigine, carbamazepine, phenytoin, sodiumvalproate, vigabatrin – Reduce dose by 10% every 2-4 weeks • Ethosuximide, barbiturates, benzodiazepines – Reduce dose by 10% every 4-8 weeks • If on more than one drug, withdraw from one drug at a time – 1 month between complete withdrawal from one drug and starting withdrawal from another
28
What are the effects of some aeds in pregancy
• Risk of congenital malformations – E.g.neuraltubedefects, hypospadias, cardiacdefects • Carbamazepine – Generally perceived as safe in pregnancy, although still carries risks • Sodium Valproate – Thought to cause decreased serum folate -> neural tube defects – Craniofacial and skeletal abnormalities – Developmental disorders after birth (mental and physical) • Try not to prescribe sodium valproate to females of childbearing age • Prescribe lowest effective dose – Divided over the day – Controlled-release tablets • Start folate supplementation before pregnancy • If no suitable alternative, counsel on risks and appropriate contraception • Specialist prenatal monitoring
29
What are the effects of phenytoin
``` PHENYTOIN • Common congenital malformations – Cleft lip and palate – Congenital heart defects (septal defects) • Anticonvulsant (epilepsy) • Cardiac depressant (arrhythmias) • Levels peak at 3 – 9 hours post dose • Therapeuticlevels:10mg/l–20mg/l • Toxicity  nausea, CNS dysfunction (confusion, nystagmus, ataxia), decreased consciousness, coma! ```
30
Describe teh pk of phenytoin
• Narrow therapeutic window • Non-linear pharmacokinetics • Therapeutic drug monitoring to: – Establish individual therapeutic concentration – Aid diagnosis of clinical toxicity – Assess compliance – Guide dose adjustments in patients with greater pharmacokinetic variability • Following loading dose, checked at 3-4 days, then 3-12 monthly if stable
31
What are treatments for partial seizures
Treatment of partial seizures (simple & complex) • Lamb – Lamotrigine • Top – Topiramate: can’t be explained off the Top a Ma Head – Also used in migraines • Gave – Gabapentin: wishes it worked like GABA but has pent up frustration • Funny – Phenytoin: can’t be funny for too long, so use in Status Epilepticus • Carbs – Carbamazepine: keeps Na channels inactive like phenytoin
32
What are the treatment of general seizures
eneral seizures: • Barbara – PheNObarbitol: NO barb means don’t use unless desperate • Valiantly – Sodium valproate: valiantly tries to do many things (including “attacking the liver enzymes”) • Sux – Ethosuximide: Sucks to learn it, but make sure it doesn’t go absent from revision • Good-Pam – Ends in Pam, so it’s a benzo – Acts quickly, so it’s good 1st line for status epilepticus
33
Describe the initial management of seizures
ABCDE -> lorazepam or midazolam benzodiazepines) | Pre-hospital: PR or buccal Hospital: IV
34
What is status epilepticus
= epileptic seizures occurring continuously without recovery of consciousness in between Neither Funny nor Good So use Phenytoin or Benzodiazepines
35
What is first fit c.liic
• Following first seizure, patient deemed safe for discharge • Referral to First Fit Clinic follows • Advise patient of lifestyle changes in the meantime • If treatment initiated: AIM = CONTROL of seizures on FEWEST drugs with LOWEST dose and LEAST side effects
36
What are daily living considerations
• Driving: – Epilepsy when awake, licence is taken away until 1 year seizure-free – If due to medication change: 6 months seizure-free – Seizures whilst asleep or don’t affect driving or consciousness – assessment of case by DVLA – If one-off seizure then can apply when 6 months seizure-free and assessment by DVLA • Do not operate dangerous machinery • Avoid potentially dangerous work or activities, e.g. swimming, climbing ladders • Bathe with supervision or leave bathroom door unlocked • Do not bathe babies alone • Do not cycle on busy roads • Avoid consuming alcohol
37
What are the long term considerations
• Annual review – Check seizure control and if any precipitants – Compliance – Consider advice on contraception, pregnancy, employment issues and benefits • SUDEP (sudden unexpected death in epilepsy) – Increased risk in patient with uncontrolled seizures – Risk increases to 1 in 150 with poorly controlled seizures • Increased risk of mental health illness – Abnormal activity of neurotransmitters – Structural abnormalities – Functional abnormalities