Epilepsy Flashcards

1
Q

What qualifies epilepsy

A
  • At least 2 unprovoked seizures
  • 1 unprovoked + high probability of recurrence (over 10yrs)
  • Epilepsy syndrome
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2
Q

How common is it

A

1% prevalence

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3
Q

Who gets it

A

Starts in children or +60yrs

+++ likely if disabled

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4
Q

What are the causes/risk factors

A
  • 2/3rds idiopathic - familial
  • CV disease - cerebral infarct/haem, venous thrombosis
  • Head injury - cortical scarring
  • Cranial surgery
  • CNS infection - meningitis, encephalitis
  • Alzheimers
  • AI/ brain neoplasm / space occupying lesion / structural development (e.g. neuro-epithelial tumour)
  • DRUGS - phenothiazines, isoniazid, tricyclic antidepressants, binge drinking, recreational drugs (e.g. BZs), alcohol withdrawal
  • Metabolic disorder - Uraemia, hypoglycaemia, +Na, -Na, +Ca or -Ca
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5
Q

How do you classify seizures

A
  • Partial - focal onset w/ features referable to 1 hemisphere (usually underlying structural disease)
  • Primary generalised - simultaneous onset electrical discharge throughout cortex –> no localising feat
  • Focal seizure - originate w/in network limited to 1 hemisphere (mixed whether awareness retained)
  • Aura
  • Post-ictally - drowsiness, headache, confusion, myalgia, sore tongue, temporal weakness (Todd’s palsy)
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6
Q

Describe a simple partial seizure

A
  • Awareness unimpaired
  • focal motor/sensory (olfactory, visual) / autonomic pr psychic symptoms
  • No post-ictal symptoms
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7
Q

Describe a complex partial seizure + where does it happen most commonly

A
  • Awareness impaired
  • Either simple partial onset (aura) or impaired awareness at onset
  • Most common = temporal lobe
  • Post-ictal confusion common
    (if in frontal lobe recovery = rapid)
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8
Q

Describe a partial seizure w/ 2o generalisation

A
  • 2/3rd pt w. partial seizures –> electrical disturbances spreads causing 2o generalised seizure (generally convulsive)
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9
Q

What types of generalised seizures are there

A
  • Absent
  • Tonic clonic
  • Myoclonic
  • Atonic
  • Infantile
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10
Q

Describe an absent seizure

A
  • Brief (<10sec) pauses e.g. stop talking mid sentence
  • continue where left off
  • presents in childhood
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11
Q

Describe a tonic-clonic seizure

A
  • Loss of consciousness
  • Limbs stiffen (tonic) + then jerk (clonic)
  • May have 1 w/out other
  • Post-ictal drowsiness/confusion
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12
Q

Describe a myoclonic seizure

A
  • Sudden jerk limb, face or trunk

- May be thrown to ground or have violently disobedient lung

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13
Q

Describe an atonic (akinetic) seizure

A
  • Sudden loss of muscle tone
  • fall (rag-doll)
  • No LOC
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14
Q

What is an infantile seizure associated with

A

tubular sclerosis

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15
Q

How does genetic generalised epilepsy present

A
  • Childhood/teen onset
  • Triggered by sleep deprivation + alcohol
  • Early morning (tonic-clonic or myoclonic jerks)
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16
Q

How does focal epilepsy present

A
  • Hx potential cause
  • Aura
  • Focal motor activities during
  • Automatisms
17
Q

How do complex focal seizures present

A
  • Motor = automatisms, lip-smacking, plucking at hair/clothes
  • Sensory = transient paraesthesiae
  • Autonomic = odd epigastric sensation, nausea, abnormal taste/smell
  • Psychiatric = deja vu, fear, unreality
18
Q

What are the signs of epilepsy

A
  • Examination usually unremarkable

- Skin –> cafe-au-lait spots (neurofibromatosis) + adenoma sebaceum (tuberous sclerosis)

19
Q

What investigations do you perform

A
  • Full physical exam
  • FBC, U+E, LFTs, glucose, Ca
  • ECG, EEG
20
Q

How do you treat it

A
  • AVOID DANGEROUS ACTIVITIES - SWIM/DRIVE

DRUGS

  • Generalised tonic-clonic = SODIUM VALPORATE or LAMOTRIGINE 1st line –> carbamazepine 2nd line
  • Absence = sodium valporate, lamotrigine, ethosuximide
  • Myoclonic = same tonic-clonic but AVOID carbamazepine (may worsen)
  • Partial +/- 2o generalisation - carbamazepine

SURGERY
- If single epileptogenic focus found - neurological resection (70% freedom symptoms)

21
Q

What are the side effects of epilepsy medication

A
  • Carbamazepine – GI upset (N+V), dizziness, ataxia, hypersensitivity (mild maculopapular rash)
  • Lamotrigine – SJS or TENs –> maculopapular rash (occurs in 10%) typically in 1st 8wks. Diplopia, blurred vision, photosensitivity, tremor, agitation, vomiting, aplastic anaemia
  • Phenytoin – coarse facial features, acne, hirsutism, cerebellar toxicity (nystagmus, ataxia, discoordination), osteomalacia, hypersensitivity rash, cardiac collapse + resp distress
  • Sodium valproate - ^ appetite + weight gain, liver failure, pancreatitis, reversible hair loss (grows back curly), oedema, ataxia, teratogenicity, tremor, thrombocytopenia, encephalopathy
22
Q

What must you tell women who have epilepsy about medication

A
  • give advice before becoming sexually active – 5% fetal abnormality
  • Enzyme-inducing antiepileptic drugs may reduce effectiveness of hormonal contraceptives
  • Teratogenicity of AEDs – women should take folic acid (valproate should be avoided use Lamotrigine)