Epilepsy in children Flashcards

1
Q

What is Epilepsy?

A

Epilepsy is an umbrella term for a condition where there is a tendency to have seizures.

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2
Q

What are seizures?

A

Seizures are transient episodes of abnormal electrical activity in the brain.

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3
Q

Generalized Tonic-Clonic Seizures

A

There is loss of consciousness and tonic (muscle tensing) and clonic (muscle jerking) movements. Typically the tonic phase comes before the clonic phase.

There may be associated *tongue biting, incontinence, groaning, and irregular breathing.

Post-ictal phase: After the seizure, there is a prolonged post-ictal period where the person is confused, drowsy, and feels irritable or low.

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4
Q

Maintance management of tonic-clonic seizures is with:

A
  1. First line: Sodium Valproate

OR

Phenobarbitone (< 6 months old)

  1. Second line: Lamotrigine
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5
Q

Focal Seizures

A

Focal seizures start in the temporal lobes. They affect hearing, speech, memory, and emotions. There are various ways that focal seizures can present:

  1. Hallucinations
  2. Memory flashbacks
  3. Déjà vu
  4. Doing strange things on autopilot
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6
Q

Focal seizures management maintenance:

A

One way to remember the treatment is that the choice of medication is the reverse of tonic-clonic seizures:

  1. First line: Carbamazepine
  2. Second line: Lamotrigine and Topiramate
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7
Q

Absence seizures/ Petitmal

A
Absence seizures typically happen in children and are sometimes mistaken for daydreaming and inattentiveness.  
1. Starring 
2. Loss of expression
3. Upward eye movements
4. Unresponsiveness
5. Eye blinking 
     lasts for 5-10 seconds

Post-ictal period: Person recovers immediately + resumes their previous activity with no memory of seizure.

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8
Q

Absence seizures maintenance management:

A
  1. First line: Sodium valproate

2. Second line: Lamotrigine

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9
Q

Atonic seizures?

A

Atonic seizures are also known as drop attacks. They are characterized by brief lapses in muscle tone. These don’t usually last more than 3 minutes. They typically begin in childhood.

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10
Q

Atonic seizures management:

A

They may be indicative of Lennox-Gastaut syndrome. Management is:

  1. First line: sodium valproate
  2. Second line: lamotrigine
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11
Q

Myoclonic seizures?

A

Myoclonic seizures present as sudden brief muscle contractions, like a sudden “jump”. The patient usually remains awake during the episode. They occur in various forms of epilepsy but typically happen in children as part of juvenile myoclonic epilepsy.

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12
Q

Myoclonic seizures Maintenance Management is:

A
  1. First line: Refer all for specialist investigation and initiation of therapy with Sodium valproate.
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13
Q

DIAGNOSTIC CRITERIA

A

A child may be diagnosed:

°With a specific anatomical or systemic cause for the seizure type (see table of possible causes);

°As having an epileptic syndrome, i.e. a specific seizure type associated with a characteristic EEG, natural history, response to anticonvulsant therapy and prognosis;

°With cryptogenic epilepsy.

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14
Q

Investigations

A

° MRI of the brain is the preferred investigation for recurrent seizures in children. If not available, a CT scan of the brain is indicated.

° EEG: is indicated for recurrent or syndromic seizures where a diagnosis cannot be made on clinical grounds alone. Delay an EEG for at least one week after the convulsive episode.

° If atypical, a 12 lead ECG should be considered in diagnostic uncertainty – it is important to consider prolonged QT interval syndromes.

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15
Q

GENERAL AND SUPPORTIVE MEASURES

A

° Minimise the impact of the epilepsy by obtaining complete seizure control to maximise the child’s full potential.

° Educate the patient and caregiver about epilepsy and associated complications and comorbidities, i.e. learning difficulties and ADHD.

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16
Q

Maintenance Therapy in detail

A

Monotherapy is preferred but combination therapy may be necessary.

Combination therapy should be specialist initiated.
Caution:potential drug-drug interactions.

As a general rule, start with small doses and titrate slowly upwards.

Aim for low to mid-therapeutic dose range and accept the lowest dose at which seizures are controlled.

If seizures continue, titrate to high therapeutic doses, if there are no unacceptable TB side-effects.

Measuring drug levels is rarely indicated unless there is concern about toxicity or adherence and in polytherapy.

17
Q

Maintenance Therapy for Sodium Valproate

A

Valproate, oral, 5 mg/kg/dose (starting dose), 8–12 hourly.

Increase by 5 mg/kg weekly to 15–20 mg/kg/day given 8–12 hourly over 4 weeks.

Maximum total daily dose: 40 mg/kg/day.

Exclude liver dysfunction prior to initiating therapy (at least ALT), in children under 2 years or if clinical suspicion of liver dysfunction or metabolic disease

Monitor at least clinically for hepatotoxicity.

18
Q

Maintenance Therapy for Carbamazepine

A

Carbamazepine, oral, 5 mg/kg/day (starting dose), 8-12 hourly.

Increase slowly by 0.2 mg/kg at 2 weekly intervals to 5–10 mg/kg/dose 8–12 hourly.

Usual maintenance total daily dose: 10–20 mg/kg/day.

Maximum total daily dose: 20 mg/kg/day.

Dosage intervals: syrup 8 hourly, tablets 12 hourly.

Exacerbates myoclonic seizures and absence seizures.

19
Q

Maintenance Therapy for Lamotrigine

A

Lamotrigine, oral, 0.2 mg/kg/dose starting daily dose. (Specialist initiated.)

Increase slowly at 2 weekly intervals to 1–5 mg/kg/dose 12–24 hourly.

Rapid escalation associated with side adverse effect of skin rash.

Maximum total daily dose when given with valproate: 5 mg/kg/day.

Lamotrigine is given as add-on therapy for different seizure types and in drug-resistant paediatric epileptic syndromes, such as Lennox-Gastaut syndrome.

Double the maximum dose of lamotrigine when using carbamazepine or phenobarbitone and,

Lamotrigine must be given at a reduced dosage, of no more than half the above recommended dose in patients using valproate,

20
Q

Maintenance Therapy for Phenobarbitone

A

Phenobarbitone, oral, 3–5 mg/kg/dose as single dose at night.

May be used in children under six months of age.

Is not recommended as maintenance therapy for children older than 2 years due to undesirable side effects such as sedation, behaviour disturbances, hyperkinesia and dependence, except in situations where there is poor adherence to other drugs.

Exacerbates absence seizures.

21
Q

REFERRAL

A

REFERRAL

Suspected but undiagnosed secondary cause for seizures.

Focal seizures for neuro-imaging (MRI preferred), if facilities or expertise not available.

All seizures other than typical febrile convulsions in children < 2 years.

Seizures that are not controlled within 2 months on one agent with minimal side effects.

Neuroregression.

Mixed seizure types in one patient.

All myoclonic seizures and epileptic spasms at presentation.

If need to add a second medicine.