Seizures and Epilepsy Flashcards

1
Q

Classification of epileptic seizures?

A
  1. partial
  2. generalised
  3. unclassified
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2
Q

Partial seizures?

A

involve part of one cerebral hemisphere
1. ‘simple’, - consciousness not impaired
2. ‘complex’ - consciousness is impaired

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3
Q

Generalized seizures?

A

involve both cerebral hemispheres
- may or may not be convulsive

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4
Q

Unclassified seizure?

A

which do not fit in the other groups

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5
Q

General history questions to ask in epilepsy?
(Describe seizure episode?)

A

The classification of the seizure (e.g generalized tonic-clonic, absence).
Any prodromal symptoms (e.g irritability, pallor).
Any aura (e.g a specific sensory symptom, rare in children)
Initial cry or scream
Initial localising sign (e.g. twitching of one hand)
Description of all the manifestations (motor and autonomic) of the seizure (e.g. eyes ‘rolling back’, cyanosis, jerking movements of limbs, urinary and/faecal incontinence).

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6
Q

History questions to ask about the seizure in epilepsy?
(What happens during the seizure?)

A

The duration of the seizures – the range and the usual time
The frequency of the seizures – range and the ‘usual’
Time of occurrence of the seizures (e.g. on waking, or on going to sleep)
The date and time of the last seizure
Any precipitating factors, e.g. tiredness, lack of sleep, fever, infectious illness, change of dosage or type of anticonvulsant, intake of other substances (in adolescents), falls or blows to the head, sensory stimuli such as flashing lights, television, computer games, sounds, startling by sudden noises or touch.
Postictal events (e.g. sleeping, confusion, headache, vomiting, Todd’s paralysis).

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7
Q

Past history of seizures?

A

Number of hospitalizations
Previous anticonvulsants used and why they were changed
Previous complications of seizures or their treatment
Whether febrile convulsions occurred at a younger age
Family history of seizure disorder or other neurological problems
Current anticonvulsants therapy: dose, recent dosage changes, and any current side effects

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8
Q

History questions specifically for the parents?

A

How the parents manage when the child is having a seizure
What contingency plan exists for a prolonged seizure
Criteria for seeking hospital treatment
How long it takes to get to hospital in an emergency
What restrictions are placed on the child because of the seizures (e.g climbing trees)
Evaluate parent’s understanding of seizures, e.g. in terms of prognosis, chances of remission, complications
Take a full social history: impact of the disease on the child, schooling, parents and siblings

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9
Q

Inspection in PE in epilepsy?

A

dysmorphic features
diagnostic rashes (e,g neurocutaneous syndromes)
Asymmetry (long-standing hemiplegia)

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10
Q

Blood pressure in epilepsy?

A

hypertension may be the cause

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11
Q

Head and neck physical exam in epilepsy?

A

Microcephaly: CP syndrome
Macrocephaly: hydrocephalus, intracranial tumors
Eyes: raised intracranial pressure (ICP)
Hearing: impairment with CP, congenital rubella
Cranial nerves

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12
Q

How to look for long tract signs in epilepsy?

A

gait exam

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13
Q

Investigations in epilepsy?

A

Electroencephalogram (EEG)
may help to confirm the diagnosis
normal EEG does not exclude the diagnosis
Biochemical evaluation (sodium, calcium, magnesium)
blood glucose level
Brain imaging (CT scan) indications:
Abnormal neurological findings (particularly focal signs)
Developmental delay/regression
Seizures that are difficult to control

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14
Q

Common Management Issues in Epilepsy

A

Increasing frequency of seizures and intractable epilepsy
Seizure worsening in duration or frequency
Seizures changing in nature (appearance different type of seizure)
Note: reconsider overall management

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15
Q

Name conditions that can mimic epilepsy?

A

Syncope
Breath-holding attacks
Undiagnosed structural causes (e.g brain tumor)

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16
Q

Medication management issues in epilepsy?

A

Wrong dose (non-compliance, ‘outgrowing’
Wrong drug (e.g carbamazepine can ‘unmask’ absence seizure)
Adverse drug interactions

17
Q

What are intercurrent problems in epilepsy?

A

Electrolyte imbalances consequent on drug side effects (e.g. hyponatremia with carbamazepine, via SIADH)
Intercurrent infections (e.g UTI)

18
Q

What are potential unrecognised precipitating factors in epilepsy?

A

Television, video games, open fires

19
Q

Is there a form of epilepsy which is commonly a treatment problem?

A

Lennox-Gastaut and infantile spasms

20
Q

What is Lennox-Gastaut?

A

Lennox-Gastautsyndrome is a severe form of epilepsy. Seizures begin in early childhood, usually before the age of 4 years. Children, adolescents, and adults withLennox-Gastautsyndrome have multiple types of seizures that vary among individuals.

21
Q

What are infantile spasms?

A

Infantile spasms (IS) is a seizure disorder in babies. Theseizures(or spasms) make muscles in the arms and legs stiff and bend the baby’s head forward. They look very much like a startle.
Babies also might have slowed development or loss of skills (like babbling, sitting, or crawling). Although the spasms usually go away by the time a child is 4 years old, many babies with IS will have other kinds ofepilepsylater in life.

22
Q

Advice to give parents and teachers on taking care of a child with epilepsy?

A
  1. management during a seizure
  2. safety considerations
  3. avoid known precipitants
    - Photosensitive epilepsy, avoid sitting close to open fires, television and changing TV channels
23
Q

Management during a seizure?

A

Lie the child on the side
Do not put things in the mouth
Move away nearby objects to avoid child hurting himself or herself
Have a time plan (For example, if a seizure lasts more than 15 minutes, seek medical attention)

24
Q

Safety considerations for a child with epilepsy?

A

No climbing on a height e.g. trees, ladders
No swimming
No bathing alone in younger children
No riding bicycles in busy roads
Use helmets when riding on less busy roads

25
Q

What to communicate with parents on treatment for epilepsy?

A

Rationale for treatment
Explain to parents
reasons for recommending treatment
benefits and possible side effects of chosen drug
Probable duration of treatment
All parents will wish to know about this
Stop if seizures free for between 2 and 4 years

26
Q

How to administer anticonvulsant medications?

A

Start at a low dosage, and gradually increased until the appropriate dosage is reached
If one drug given at the correct dosage, is unsuccessful in controlling the seizure, then commence the next most appropriate agent
Only once the second drug’s dosage has been optimized should the first drug be withdrawn

27
Q

Generalised tonic clonic seizure anticonvulsants?

A
28
Q

Abscence seizure anticonvulsant medication?

A
29
Q

Simple partial seizure anticonvulsants?

A
30
Q

Complex partial seizures anticonvulsants?

A
31
Q

Infantile spasms anticonvulsant?

A

prednisolone

32
Q

What are the Likely Side Effects of Anticonvulsants?

A

Acute toxicities (e.g. nystagmus and ataxia with carbamazepine and phenytoin)
Acute idiosyncratic reactions (e.g. skin manifestations such as Stevens-Johnson syndrome)
Chronic toxicities (e.g various effects on haematological system, bones, connective tissue, cosmetic effects and teratogenicity effects)
Drug interactions between anticonvulsants (e.g carbamazepine lowering phenytoin levels, valproate increasing phenobarbitone levels)
Drug interactions with other drugs (e.g erythromycin increasing carbamazepine levels)

33
Q

What are idiosyncratic drug reactions?

A

adverse effects that cannot be explained by the known mechanisms of action of the offending agent, do not occur at any dose in most patients, and develop mostly unpredictably in susceptible individuals only

34
Q

The chance of further seizure recurring after a single seizure, at 5 years of age is?

A

normal neurodevelopmental status, EEG, and MRI: 20%
- treatment is usually not started
neurodevelopmentally normal: 40%
mild neurological problems: 70%
severe neurological problems (e.g. CP): 90%
Note: If the patient has abnormal EEG, MRI, development, and/or neurologic exam, and/or a positive family history of epilepsy, then the risk is higher and often treatment is started.

35
Q

What are febrile sezures?

A

Febrile seizures occur between the ages of 6 and 60 mo (peak 12-18 mo)
There is usually a temperature of 38°C (100.4°F) or higher
Not a result of CNS infection or any metabolic imbalance
No prior history of afebrile seizures

36
Q

What are simple febrile seizures?

A

A primary generalized
Usually tonic-clonic
Associated with fever
Lasting for a maximum of 15 min
Not recurrent within a 24-hr period

37
Q

What is a complex febrile seizure?

A

Acomplex febrile seizureis more prolonged (>15 min) and/or
Focal and/or
Recurs within 24 hr

38
Q

What is febrile status epilepticus?

A

Febrile status epilepticusis a febrile seizure lasting longer than 30 min

39
Q
A