Paeds: Epilepsy georgie Flashcards

1
Q

AED for partial seizures

A
•	Carbamezapine (first libe treatment)
•	Sodium valporate
•	Lamotrigine 
•	Topiramate 
Levetiracetam
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2
Q

AEDs for Generalized

A

• Sodium valporate (first line teatment)
• Lamotrigine
• Topiramate
Levetiracetam

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3
Q

Complex partial

Prevalence

A

60%

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4
Q

Prevalence Secondary generalized tonic-clonic

A

60%

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5
Q

Prevalence Primary generalized tonic-clonic

A

30%

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6
Q

Prevalence Generalized absence

A

5%

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7
Q

Prevalence Generalized myoclonus

A

5%

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8
Q

Simple partial Prevalence

A

rare

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9
Q

West syndrome

age and comments

A

4-6 months
• Violent flexor spasms of the head, trunk and limbs followed by extension of the arms (so-called ‘salaam spasms’). Flexor spasms last 1–2 s, often multiple bursts of 20–30 spasms, often on waking, but may occur many times a day.
• Many causes; two-thirds have underlying neurological cause.
Most will subsequently lose skills and develop learning disability or epilepsy

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10
Q

Management of west syndorme

A

• Treatment is with vigabatrin or corticosteroids good response in 30-40%

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11
Q

Childhood absence syndrome

A

4-12 Years

• It is associated with brief interruptions of 3-5s in awareness, with minimal or no motor manifestation
• Accounts for 2% of epilepsy
• Prognosis is good, with 95% remission in adolescence; 5–10% may develop tonic-clonic seizures in adult life

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12
Q

childhood absence syndrome management

A

It responds to sodium valporate or ethosuximide

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13
Q

Juvenile myoclonic epilepsy age and presentation

A
  • Associated with early morning myoclonic jerks
  • Generalized tonic-clonic seizures occur in most
  • Childhood absence seizures in 30%
  • Precipitants: sleep deprivation, alcohol
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14
Q

Juvenile myoclonic epilepsy management

A

Best response to sodium valproate

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15
Q

Tonic-clonic generalised seizures first-line Rx

A

Valproate, carbamazepine

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16
Q

Tonic-clonic generalised second line

A

Lamotrigine

Topiramate

17
Q

Absence generalised seizures first-line

A

Valproate, ethosuximide

18
Q

Absence generalized seizures second line

A

Lamotrigine

19
Q

Myoclonic generalised seizures first line

A

Valproate

20
Q

Focal seizures first line

A

Carbamazepine or valproate

Lamotrigine shown since to be most effective - but slow titration

21
Q

Focal seizures second line

A

Topiramate, levetricatam, oxcarbazepine, gabapentin, tiagabine, vigabatrin

22
Q

Treatment info for parents

A

-70% of epilepsy controlled on AED therapy
- of these 80% on monotherapy, 10-15% on two drugs
30% not controlled

23
Q

If the response is poor to AED

A
  1. Switch to another 1st line AED as monotherapy
  2. Add 2nd AED
  3. Explore full range of doses
  4. Avoid polytherapy
  5. Surgery
24
Q

Valproate SE

A

weight gain
Hair loss
Rare idiosyncratic liver failure

25
Q

Carbamazepine/oxcarbazepine SE

A
Rash
Neutropenia
Hyponatraemia
Liver enzyma induction
Can interfere with other medication
26
Q

Vigabatrin SE

A

Restriction of visual fields, which has limited its use

Sedation

27
Q

Lamotrigine SE

A

Rash

28
Q

Ethosuximide SE

A

N and V

29
Q

Topiramate SE

A

Drowsiness, withdrawal and weight loss

30
Q

Gabapentin SE

A

Insomnia

31
Q

Levetiracetam SE

A

Sedation - rare

32
Q

Benzos SE

A

Sedation
tolerance to effect
Increased secretion

33
Q

Sudden death in epilepsy (SUDEP)

A
  • Risk of SUDEP should be discussed with all patients (NICE)
  • Not only patients with poorly controlled seizures are at risk.
  • Mainly respiratory arrest (central hypoventilation)
  • Risk highest in Generalized tonic-clonic seizures, also complex partial seizures of temporal origin (bradyarrythmia/ asystole)