Epilepsy in children Flashcards

(34 cards)

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
clinical features of febrile convulsions 3
early viral infection as temperature rises rapidly usually brief last less than 5 mins most commonly tonic-clonic
26
types of febrile convulsions 3
simple complex status epilepticus
27
length of time in simple febrile convulsions
<15 mins
28
length of time in complex febrile convulsions
15-30mins
29
length of time in febrile status epilepticus
>30mins
30
type of seizure in simple febrile sezirues would it recur within 24 hours
generalised seziures typically would not recur within 24hrs *-should have complete recovery within an hour
31
type of seziure in complex febrile seizures would it recur within 24 hours
focal seizure may repated within 24 hours
32
when should children with febrile seizures be admitted to paediatrics 2
first seizure or complex
33
managemtn of febrile seizures
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
recurrence rate of febirle convulsison
1 in 3