Epilepsy Flashcards

1
Q

Suggest 4 fts in a history that point towards a diagnosis of a seizure as opposed to syncope/dissociative attack?

A
  • LOC/amnesia > 5 mins
  • aura: prodromal focal features or none
  • motor fts e.g. head turning unusual posturing, prolonged, prominent, rigid, rhythmic
  • lateral tongue biting, incontinence, injury
  • confused behaviour, post event headache/myalgia
  • unprovoked
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2
Q

Sheldon’s Questionnaire, scores for liklihood of seizure > syncope, give 3 of the features on this questionnaire

A
  • lateral tongue biting
  • deja or jamais vu before LOC
  • emotional stress associated with LoC
  • confusion following LoC
  • head turning during attack
  • unresponsive/unusual posturing/amnesia
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3
Q

How to initially manage syncope? Initial after transient loss of consciousness, what is the 1st ix to do?
-then for simple faint
-for pathological syncope (what are 4 red flags?)
Next step if present, is refer to___ ?

A
  • ECG!! (and document findings)
  • dx: uncomplicated vasovagal syncope, no red flags then can just explain and reassure, appropriate safety advice and discharge
  • dx: path. syncope - refer to CARDIO WITHIN 24hrs
  • red flags: any ECG abnormality, HF, murmur, new unexplained SOB, transient LOC on exertion, or unprovoked/at rest or Fam Hx of sudden cardiac death <40yrs, >65yrs t LOC with no prodrome
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4
Q

Dissociative vs Epileptic Seizure differentiation

-what fts favour dissociative seizures (aka non-epileptic functional seizures)

A
  • > 5mins duration of individual events
  • fluctuating course (wax and wanes)
  • asynchronous rhythmic movements
  • pelvic thrusting
  • side to side head/body movements
  • closed eyes
  • ictal crying
  • recall of items during event
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5
Q

If new onset suspected seizure/epilepsy what ix and management will be needed?

  • tests? imaging?
  • advice on what?
  • referral to who?
A
  • ECG and exclude acute metabolic cause
  • CT if focal fts, prolonged or recurrent
  • Provide suspected seizure info (DVLA, safety, lifestyle) - bathing/heights/machinery/occupational/parenting/swimming
  • consider home video if recurrent episodes
  • say “by law no driving until you’ve seen the specialist”
  • first fit neurology referral (will organise MRI/EEG if needed
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6
Q

If known epileptic presents to you with change in attacks or more frequent attacks, what should you do in terms of history ?

A
  • ensure dx is right (go through same process as initial seizure presentation, document hx that supports type of seizure/epilpsy)
  • worst and best seizure frequency to gage seriousness
  • document co-morbidities
  • current medication and what’s been tried before/recent changes to medication
  • ask re: compliance
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7
Q

If known epileptic presents to you with change in attacks or more frequent attacks, what should you do in terms of assessment/management?

A
  • consider triggers e.g. stress, infection, ETOH
  • FBC, biochem (rule out metabolic causes)
  • AED LEVELS (anti-epileptic drug levels)
  • seek advice from neurologist/epilepsy clinic that manages that pt
  • advise home video if diagnostic doubt of epilepsy
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8
Q
Basic First Aid Advice for a tonic clonic seizure:
A
C
T
I
O
N

+(call for help and consider rescue meds)

A

Assess - ensure safe, minimise injury risk
Cushion
Time
Identity (bracelet/ID card)
Over (recovery position, consider O2, gueddel airway..)
Never: restrain, put anything in mouth

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9
Q

What is status epilepticus?
NB: there are multiple types of SE for all seizures, but one is an emergency, which is?
-what are the T1 T2 time points

A

Prolonged seizure
Unlikely to self-terminate (T1) = 5mins
Risk of damage due to seizure itself and metabolic consequences (T2) = 30mins
-convulsive (tonic-clonic) SE is a MEDICAL EMERGENCY

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10
Q

What do these refer to in SE?
(T1) = 5mins
(T2) = 30mins

A
  • > 5mins is defined as SE as is v unlikely to self-terminate
  • > 30mins is timepoint of risk of damage due to seizure itself and metabolic consequences

NB: sooner rx is started, the more likely it will work so don’t delay!

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11
Q

Why does T2 ->30mins is timepoint of risk of damage due to seizure itself and metabolic consequences happen?

  • phase 1 of seizures what happens?
  • phase 2?
A
  • Phase 1: BP, O2, glucose utilisation and blood flow to brain increases. More lactate generated from muscles activity
  • Phase 2: ~30mins, due to the electrical storm, the brain and muscles cannot keep up with the demands so –> BP normal/low, glucose falls, lactate rises more and pH drops
  • can lead to respiratory compromise and hypothermia
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12
Q

What is the convulsive SE overview for management?

A
  • resuscitation and general medical support (ABCDE)
  • give 250mg thiamine and 30% glucose (as alcohol withdrawal is a common cause, and if not doesn’t do much harm)
  • confirm the dx (video if doubt, is it dissociative?)
  • stop the seizures
  • identify/treat the cause
  • establish maintenance anti-epileptic drugs.
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13
Q

How to stop the seizures of SE?
-Premonitory/Initial SE
NB: sooner given the better

A

Initial

  • benzodiazepines e.g. 10mg buccal midazolam/rectal diazepam or if have IV access give 4mg IV lorazepam
  • maximum x2 doses
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14
Q
  • How to stop the seizures of SE?
  • Established SE (SE that hasn’t responded to benzos therefore aka benzo refractory SE)
  • who should be notified at this stage?
A
Established:
-Valproate 40mg/KG or 
-Levetiracetam 60mg/KG
(phenytoin 20gm/kg no longer 1st line)
(call anaesthetist to notify pt - relates to next step if rx unsuccessful)
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15
Q

-How to stop the seizures of SE?

if refractory to benzos and valproate/levetiracetam?

A

-anaesthesia/ITU management

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16
Q

General principle of which drugs are best for following:

  • new onset focal epilepsies:
  • most effective for generalised seizures:
  • broad spectrum for either above:
A
  • new onset focal epilepsies: lamotrigine
  • most effective for generalised seizures: valproate
  • broad spectrum for either above: levetiracetam
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17
Q

Drug resistant epilepsy (can’t achieve complete seizure control) meds still help so should be continued, but what else may be poss to help?

A
  • surgery for localisation related with identifiable lesion e.g. hippocampal sclerosis, cavernoma, tumour.. can be curative but rare
  • electrical stimulation therapies (VNS-vagal nerve stimulation, DBS)
  • newer agents in clinical trials
18
Q

Long-term management of epilepsy: (holistic ideas, suggest 3 aspects)

A
  • shared care (primary, 2nry and 3ry care) that is flexible and responsive to pt needs
  • decisions about initiation/change and discontinuation of AEDs made by specialist
  • pt education, encourage autonomy
  • access to info (lifestyle, occupation, meds, preg, contraception)
  • access to specialist advice
19
Q

Drug resistant epilepsy (can’t achieve complete seizure control) meds still help so should be continued, but what else may be poss to help?

A
  • surgery for localisation related with identifiable lesion e.g. hippocampal sclerosis, cavernoma, tumour.. can be curative but rare
  • electrical stimulation therapies (VNS-vagal nerve stimulation, DBS)
  • newer agents in clinical trials
20
Q

As antiepileptic drugs (AEDs) as a group dampen down excessive neuronal activity, suggest 3 common SEs?
-what v dangerous allergic reaction can occur with a few AEDs in a small%?

A
  • CNS: sedation, unsteadiness, diplopia
  • Weight (gain or loss due to appetite sensors/gut)
  • behavioural/psychiatric SEs
  • GIT nausea/vomiting

-rare: allergic rash can –> steven johnson’s syndrome (!)

21
Q

As antiepileptic drugs (AEDs) as a group dampen down excessive neuronal activity, suggest 3 common SEs?
-what v dangerous allergic reaction can occur with a few AEDs in a small%?

A
  • CNS: sedation, unsteadiness, diplopia
  • Weight (gain or loss due to appetite sensors/gut)
  • behavioural/psychiatric SEs
  • GIT nausea/vomiting

-rare: allergic rash upon initiation can –> steven johnson’s syndrome (!)

22
Q

Which AED is commonly associated with agranularcytosis so warn pts about a severe sore throat?

A

Carbamazepine

23
Q

What guides choice of AED for treatment?

-pt factors

A
  • seizure type, frequency, severity
  • syndromic classification (focal, generalised, other)
  • women of child bearing age
  • co-morbidities e.g. overweight, anxiety disorder
24
Q

What guides choice of AED for treatment?

-drug factors

A
  • ease of use (interactions, formulation, speed) e.g. can they swallow tablets, can they take BD pill burden
  • effectiveness, tolerability and safety (trial and error)
  • cost effectiveness / availability
25
Roughly what % of pts diagnoses with epilepsy will achieve good control? What about remainder?
~70% (may need years of rx to remain in remission) ~5% progressive, relentless seizures ~25% rx-refractory, ongoing seizures
26
What often matters most to pts with drug-refractory epilepsy more than being seizure free? Suggest 3
- drug SEs e.g. dose related, long-term effects, pregnancy issues - mood complaints - memory complaints
27
Contraception and Epilepsy | -name 2 which are enzymes inducers, what effect does this have?
- Phenytoin, Carbamazepine, Topiramate, Oxcarbazepine, Phenobarbitone, primidone - these are CYP enzyme inducers so decrease effectiveness of COCP, POP, morning after pills and progestogen implants
28
-Phenytoin, Carbamazepine, Topiramate are CYP enzyme inducers so decrease effectiveness of COCP, POP, what 2 contraceptives are the exception?
- IM depo provera (but increases osteoporosis risk) | - progesterone containing IUDs and -mechanical IUDS
29
Teratogenicity and Fertility, name 5 confouding factors in epilepsy:
- AEDs - concurrent meds - concurrent disease - Epilepsy type - seizure frequency - genetics - maternal IQ, paternal IQ - folic acid - socio-economic class - education
30
AEDs and teratogenicity: -name a drug related with - heart abnormalities - mouth abnormalities - and spine abnormalities
- holes in heart, cardiac malformations esp. w carbamazepine - cleft palate w. phenytoin and phenobarbitone - spina bifida w. valproate and carbamazepine
31
What are the 2 highest risk of congenital malformation AEDs
-HIGH risk (!): valproate, phenytoin, topiramate, polytherapy
32
What are 3 bad effects of Valproate on foetal/child development? What is the issue with this for generalised epilepsy?
- greatest risk of teratogenicity >10% risk - IQ of child -7-10pts on average - x3 higher risk of autistic spectrum disorder - x5 higher risk of autism - maybe increased ADHD risk - it should be avoided where poss, but is best seizure control w/o SE medication for certain seizure types
33
Due to serious bad effects of valproate on women of childbearing age in terms of foetal and child development (teratogenic, lower IQ, more autism..) what is guidance in advice giving?
-discuss repeatedly prior to conception and written up to date information given before starting AEDs -requirement now for contraception and pregnancy testing -weigh up risk/benefit on individualised basis, start w lowest dose, monotherapy where poss -5mg folic acid prophylaxis (rarely but sometimes esp. in generalised sz, despite CI, continuing valproate through preg. may be the appropriate informed decision)
34
What is the most common co-morbidity with epilepsy? - important as big predictor of what? - what vicious cycle can occur?
- Up to 40% have at least 1 mood disorder, - anxiety and depression commonest - predictor of quality of life - more depressed correlates with seizure control
35
Suggest 3 multifactorial reasons, 40%+ epileptics have a mood disorder?
- biological factors e.g. temporal/frontal lobe disease - psychological and personality factors - sociological factors e.g. driving, work, family links to occupation and financial implications - perceived stigma and prejudice
36
Are anti-depressants CI in epileptic pts?
-no (!) treat as usual, with support, CBT and medical management (if anything, lower threshold for rx) -treating depression can improve QoL and seizure control (it is often underdiagnosed and undertreated)
37
What is a common complaint of pts with epilepsy relating to cognition? What impacts can this have?
- memory and cognitive complaints very common - highly variable - impacts: education, employment, QoL
38
How can we help epileptic pts with complaints of memory issues?
- some problems are unfixable - we can optimise seizure control and drug treatment - understand the specific problems, carry out a neuropsychological assessment
39
Bone health in epilepsy, what do we know?
- people with epilepsy have an increased risk of fractures (similar to osteoporosis) - fall over in seizures can contribute to this - pts often have more non-seizure related falls (e.g. neurodisability/subtle balance difficulties/2dnry to medication) - most of bone health is genetic related but AEDs play a small part to
40
As people with epilepsy have an increased risk of fractures on AEDs, what should we do?
- give dietary and lifestyle advice to minimise risk of osteoporosis - routine bloods (vit D, bone profile) 2-5yrly - consider vit D supplementation for all pts on AEDs - use QFracture and DEXA fragility scores to screen for issues