Seizures and Infantile spasms Flashcards

1
Q

What is West syndrome

A

Rare disorder starting at age 6 months where there are clusters of full body spasms. Poor prognosis

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2
Q

What are benign rolandic seizures

A

Characteristly have tonic seizures overnight

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3
Q

What are seizures

A

Transient episodes of abnormal electrical activity in the brain. Many different types

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4
Q

Generalised tonic clonic seizures

A

Loss of consciousness.
Tonic and clonic movements (tensing and jerking).
Associated tongue biting, incontinence, groaning and irregular breathing.

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5
Q

Phase after tonic clonic seizures

A

Post-ictal period - confused, drowsy, feels irritable or low

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6
Q

First line management of tonic clonic seizures

A

Sodium valproate

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7
Q

Second line management of tonic clonic seizures

A

Lamotrigine or carbamazepine

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8
Q

Focal seizures

A

Start in temporal lobes.
Affect hearing, speech, memory and emotions.

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9
Q

Presentation of focal seizures

A

Hallucinations.
Memory flashbacks
Deja vu
Dong strange things on autopilot

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10
Q

First line treatment of focal seizures

A

Carbamazepine or lamotrigine

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11
Q

Second line treatment of focal seizures

A

Sodium valproate or levetiracetam

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12
Q

Absent seizures

A

Patient becomes blank, stares into space, abruptly returns to normal. During episodes are unaware of surroudings and won’t respond. 10 - 20 seconds

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13
Q

Management of absent seizures

A

Sodium valproate or ethosuximide

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14
Q

Prognosis of absent seizures

A

Most grow out of them as they get older

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15
Q

Atonic seizures

A

Characterised by brief lapses in muscle tone. They don’t usually lastmore then 3 minutes. They typically begin in childhood.

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16
Q

What can atonic seizures be indicative of

A

Lennox-Gastaut syndrome

17
Q

First line treatment for atonic seizures

A

Sodium valproate

18
Q

Second line treatment for atonic seizures

A

Lamotrigine

19
Q

Myoclonic seizures

A

Present as sudden brief muscle contractions. Usually remains awake, like a sudden jump

20
Q

When do children experience myoclonic seizures

A

Typically happen as part of juvenile myoclonic epilepsy

21
Q

First line treatment of myoclonic seizures

A

Sodium valproate

22
Q

Other treatment options for myoclonic seizures

A

Lamotrigine, levetiracetam or topiramate

23
Q

Treatments for West syndrome

A

Prednisolone and Vigabatrin

24
Q

Prognosis of West syndrome

A

1/3 die by age 25, 1/3 seizure free

25
Q

When is an EEG performed

A

After second simple tonic-clonic seizure, used to support diagnosis

26
Q

When is an MRI brain performed

A

First seizure is in child under 2 years.
Focal seizure.
No response to anti-epileptic medications.

27
Q

Investigations to exclude differentials

A

ECG - heart
Blood electrolytes
Blood glucose - hypos
Blood, urine cultues, LP - sepsis, enceph or meningitis

28
Q

Side effects of sodium valproate

A

Teratogenic, liver damage and hepatitis, hair loss, tremor

29
Q

Side effects of carbamazepine

A

Agranulocytosis, aplastic anaemia, induces P450 enzyme so drug interactions

30
Q

Side effects of phenytoin

A

Folate and vitamin D deficiency, megaloblastic anaemia (folate deficiency) and osteomalacia (vit D def)

31
Q

Side effects of ethosuximide

A

Night terrors and rashes