Epilepsy in children Flashcards

1
Q

What are infantile spasms also known as

A

west syndrome

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2
Q

define infantile spasms and when they occur

A

breif spasms beginning in the first few months of life

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3
Q

key features of infantile spasms

A

flexion of head trunk and limbs-> extension of arms (Salaam attack)
-lasts 1-2 secs
-repeat up to 50 times

-progressive mental handicap
-EEG: hypsarrhythmia

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4
Q

what are infantile spasms usally secondary to

A

serious neurological abnormality
-eg tuberous sclerosis
-encephalitis
-birth asphyxia

CAN BE IDIOPATHIC

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5
Q

possible treatment / prognois for infnantile spams

A

vigabatrin and sterorids

poor prognosis

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6
Q

onset of typical (petit mal) absence seizures

A

4-8yrs

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7
Q

duration of typical (petit mal) absence seizures

A

duration 3-30 seconds

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8
Q

presentation of typical (petit mal) absence seizures 3

A

no warning -blank out or stare into space for a few seconds/ lip smacking/ fluttering eyelids

symettircal
quick recovery

pften multiople per day

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9
Q

EEG in typical (petit mal) absence seizures

A

3Hz generalized

symmetrical

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10
Q

treatment for typical (petit mal) absence seizures 2

A

sodium valoprate

ethosuximide

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11
Q

prognosis for typical (petit mal) absence seizures

A

good prognosi - 90-95% seizure free in adolescence

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12
Q

what type of seziures can be an extension of infantile spasms

A

lennox-gastaut syndrome

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13
Q

onset of lennox-gastaut syndrome

A

1-5 yrs

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14
Q

features of lennox-gastaut syndrome 3

A

atypical absences , falls,jerks

90% moderate-sever mental handicap

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15
Q

EEG on lennox-gastaut syndrome

A

slow spike

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16
Q

treatment for lennox-gastaut syndrome 1

A

ketogenic diet may help

17
Q

who gets benign rolandic epilepsy (age, gender)

A

most common inchildhood and amongst males

18
Q

features of benign rolandic epilepsy 1

-treatment

A

paraestheia (unilateral face)
-usually on waking up]

-levetriceratam

19
Q

who gets juvenile myoclonic epilepsy (Janz syndrome)

A

teenage years , more common in girls

20
Q

features of juvenile myoclonic epilepsy (Janz syndrome) 4

A

infrequent generalised seizures
- often in morning/ following sleep deprivation
-daytime absences
-sudden, shock like myoclonic seziures (these may develop before seizures)

21
Q

treatment for juvenile myoclonic epilepsy (Janz syndrome) 1

A

good response to sodium valporate

22
Q

features of an epilepsy history 8

A

WITNESS CRUCIAL

where
when
what was person doing before
first signs
detailed descriptiong of event
aftermath
timing
video/ mimicry

23
Q

define febrile convulsions

A

seizures provoked by fever in otherwise normal children

24
Q

who gets febrile convulsions

A

-typically occur between ages of 6 months and 5 years
-seen in 3% of children

25
Q

clinical features of febrile convulsions 3

A

early viral infection as temperature rises rapidly

usually brief last less than 5 mins

most commonly tonic-clonic

26
Q

types of febrile convulsions 3

A

simple

complex

status epilepticus

27
Q

length of time in simple febrile convulsions

A

<15 mins

28
Q

length of time in complex febrile convulsions

A

15-30mins

29
Q

length of time in febrile status epilepticus

A

> 30mins

30
Q

type of seizure in simple febrile sezirues

would it recur within 24 hours

A

generalised seziures

typically would not recur within 24hrs

*-should have complete recovery within an hour

31
Q

type of seziure in complex febrile seizures

would it recur within 24 hours

A

focal seizure

may repated within 24 hours

32
Q

when should children with febrile seizures be admitted to paediatrics 2

A

first seizure

or

complex

33
Q

managemtn of febrile seizures

A

advise paretns to call abulance if >5 minutes seizure

antipyretics do not reduced chance pf febrile zeizure occuring

if recurrnet febrile convulsions occur -> benzo as resuce mdication may be considered
-only started on adivce of specialist
-rectal diazepam or buccal midazolma

34
Q

recurrence rate of febirle convulsison

A

1 in 3